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    <description>The Blood Podcast summarizes content recently published in Blood, the most cited peer-reviewed publication in the field of hematology.</description>
    <copyright>© 2026 American Society of Hematology</copyright>
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    <pubDate>Thu, 16 Apr 2026 12:33:22 -0400</pubDate>
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      <title>Blood Podcast</title>
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    <itunes:summary>The Blood Podcast summarizes content recently published in Blood, the most cited peer-reviewed publication in the field of hematology.</itunes:summary>
    <itunes:subtitle>The Blood Podcast summarizes content recently published in Blood, the most cited peer-reviewed publication in the field of hematology..</itunes:subtitle>
    <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
    <itunes:owner>
      <itunes:name>American Society of Hematology</itunes:name>
      <itunes:email>sjohnson@hematology.org</itunes:email>
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    <itunes:complete>No</itunes:complete>
    <itunes:explicit>No</itunes:explicit>
    <item>
      <title>Real-world availability of CAR T-cell therapies </title>
      <itunes:season>11</itunes:season>
      <podcast:season>11</podcast:season>
      <itunes:title>Real-world availability of CAR T-cell therapies </itunes:title>
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      <description>
        <![CDATA[<p>In this week's episode, <em>Blood </em>podcast editor Laurie Sehn interviews Drs. Edward Cliff on his latest research published in volume 147 issue 14 of <em>Blood</em>. Dr. Cliff discusses "<a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025030872">Global access to commercial CAR T-cell therapies: a cross-sectional study of health technology assessment across the G20 countries</a>" which maps the mismatch between innovation and implementation across high-income and selected-upper-middle-income countries for US Food and Drug Administration–approved products and indications. </p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, <em>Blood </em>podcast editor Laurie Sehn interviews Drs. Edward Cliff on his latest research published in volume 147 issue 14 of <em>Blood</em>. Dr. Cliff discusses "<a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025030872">Global access to commercial CAR T-cell therapies: a cross-sectional study of health technology assessment across the G20 countries</a>" which maps the mismatch between innovation and implementation across high-income and selected-upper-middle-income countries for US Food and Drug Administration–approved products and indications. </p>]]>
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      <pubDate>Thu, 16 Apr 2026 12:33:22 -0400</pubDate>
      <author>American Society of Hematology</author>
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      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>598</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, <em>Blood </em>podcast editor Laurie Sehn interviews Drs. Edward Cliff on his latest research published in volume 147 issue 14 of <em>Blood</em>. Dr. Cliff discusses "<a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025030872">Global access to commercial CAR T-cell therapies: a cross-sectional study of health technology assessment across the G20 countries</a>" which maps the mismatch between innovation and implementation across high-income and selected-upper-middle-income countries for US Food and Drug Administration–approved products and indications. </p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3mjmtfmrpcq2c"/>
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    <item>
      <title>Consequences of p53 loss and Gastrin for aGVHD of the Stomach</title>
      <itunes:season>11</itunes:season>
      <podcast:season>11</podcast:season>
      <itunes:title>Consequences of p53 loss and Gastrin for aGVHD of the Stomach</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
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      <description>
        <![CDATA[<p>In this week's episode, <em>Blood</em> podcast editor Dr. James Griffin interviews authors Drs. Steffen Boettcher and Robert Zeiser on their recent publications in <em>Blood</em>. Dr. Boettcher discusses "<a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025030230">Bone marrow failure, somatic rescue by p53 inactivation, and enhanced leukemogenesis in germ line ERCC6L2 disease</a>", which provides insights to disease evolution by demonstrating that p53 loss can rescue BMF phenotypes caused by biallelic mutations in <em>ERCC6L2</em>, but at the cost of profound genome instability, increasing DNA damage and leading to the onset of aggressive erythroid leukemia. Dr. Zeiser discusses "<a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025031080">Gastrin for the treatment of acute graft-versus-host-disease of the stomach</a>", which delineates the protective role of gastrin in aGVHD of the stomach in mice and patients and provides a rationale for therapeutic use of pentagastrin in a clinical trial for patients with aGVHD.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, <em>Blood</em> podcast editor Dr. James Griffin interviews authors Drs. Steffen Boettcher and Robert Zeiser on their recent publications in <em>Blood</em>. Dr. Boettcher discusses "<a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025030230">Bone marrow failure, somatic rescue by p53 inactivation, and enhanced leukemogenesis in germ line ERCC6L2 disease</a>", which provides insights to disease evolution by demonstrating that p53 loss can rescue BMF phenotypes caused by biallelic mutations in <em>ERCC6L2</em>, but at the cost of profound genome instability, increasing DNA damage and leading to the onset of aggressive erythroid leukemia. Dr. Zeiser discusses "<a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025031080">Gastrin for the treatment of acute graft-versus-host-disease of the stomach</a>", which delineates the protective role of gastrin in aGVHD of the stomach in mice and patients and provides a rationale for therapeutic use of pentagastrin in a clinical trial for patients with aGVHD.</p>]]>
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      <pubDate>Thu, 09 Apr 2026 12:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
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      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1212</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, <em>Blood</em> podcast editor Dr. James Griffin interviews authors Drs. Steffen Boettcher and Robert Zeiser on their recent publications in <em>Blood</em>. Dr. Boettcher discusses "<a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025030230">Bone marrow failure, somatic rescue by p53 inactivation, and enhanced leukemogenesis in germ line ERCC6L2 disease</a>", which provides insights to disease evolution by demonstrating that p53 loss can rescue BMF phenotypes caused by biallelic mutations in <em>ERCC6L2</em>, but at the cost of profound genome instability, increasing DNA damage and leading to the onset of aggressive erythroid leukemia. Dr. Zeiser discusses "<a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025031080">Gastrin for the treatment of acute graft-versus-host-disease of the stomach</a>", which delineates the protective role of gastrin in aGVHD of the stomach in mice and patients and provides a rationale for therapeutic use of pentagastrin in a clinical trial for patients with aGVHD.</p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3mj36ibplkp2g"/>
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    <item>
      <title>Review Series on Myeloproliferative Neoplasms</title>
      <itunes:season>11</itunes:season>
      <podcast:season>11</podcast:season>
      <itunes:title>Review Series on Myeloproliferative Neoplasms</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
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      <link>https://share.transistor.fm/s/5cf8c948</link>
      <description>
        <![CDATA[<p>In this episode, <em>Blood </em>Associate Editor Dr. Jason Gotlib discusses the Review Series "<a href="https://ashpublications.org/blood/article/147/12/1239/567079/Introduction-to-a-review-series-on-the-new-wave-of?searchresult=1">The New Wave of Targeted Therapeutics for MPN’s</a>", with authors Drs. Stefan Constantinescu, Ann Mullally, and Marina Kremyanskaya. This Review Series covers 3 areas where exciting advances are occurring. Dr. Constantinescu discusses “<a href="https://ashpublications.org/blood/article/147/12/1255/565933/Next-generation-JAK-inhibitors-in-the-treatment-of">Next-generation JAK inhibitors in the treatment of myeloproliferative neoplasms</a>” which describes how new ways to switch off JAK signaling are delivering a suite of new small-molecule drugs with potential. Dr. Mullally discusses “<a href="https://ashpublications.org/blood/article/147/12/1267/546893/Novel-strategies-targeting-mutant-calreticulin-in">Novel strategies targeting mutant calreticulin in essential thrombocythemia and myelofibrosis</a>” which reviews the biology of calreticulin mutations in myelofibrosis and ET and how multiple different modalities can be brought to bear against this mutant surface protein, including monoclonal antibodies, bispecific T-cell engagers, and cellular and vaccine therapies. Dr. Kremyanskaya discusses “<a href="https://ashpublications.org/blood/article/147/12/1278/547823/Modulators-of-the-hepcidin-pathway-in-polycythemia">Modulators of the hepcidin pathway in polycythemia vera and myelofibrosis</a>” which outlines the major recent progress being made in controlling excessive erythropoiesis through pharmacological modulation of iron metabolism.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this episode, <em>Blood </em>Associate Editor Dr. Jason Gotlib discusses the Review Series "<a href="https://ashpublications.org/blood/article/147/12/1239/567079/Introduction-to-a-review-series-on-the-new-wave-of?searchresult=1">The New Wave of Targeted Therapeutics for MPN’s</a>", with authors Drs. Stefan Constantinescu, Ann Mullally, and Marina Kremyanskaya. This Review Series covers 3 areas where exciting advances are occurring. Dr. Constantinescu discusses “<a href="https://ashpublications.org/blood/article/147/12/1255/565933/Next-generation-JAK-inhibitors-in-the-treatment-of">Next-generation JAK inhibitors in the treatment of myeloproliferative neoplasms</a>” which describes how new ways to switch off JAK signaling are delivering a suite of new small-molecule drugs with potential. Dr. Mullally discusses “<a href="https://ashpublications.org/blood/article/147/12/1267/546893/Novel-strategies-targeting-mutant-calreticulin-in">Novel strategies targeting mutant calreticulin in essential thrombocythemia and myelofibrosis</a>” which reviews the biology of calreticulin mutations in myelofibrosis and ET and how multiple different modalities can be brought to bear against this mutant surface protein, including monoclonal antibodies, bispecific T-cell engagers, and cellular and vaccine therapies. Dr. Kremyanskaya discusses “<a href="https://ashpublications.org/blood/article/147/12/1278/547823/Modulators-of-the-hepcidin-pathway-in-polycythemia">Modulators of the hepcidin pathway in polycythemia vera and myelofibrosis</a>” which outlines the major recent progress being made in controlling excessive erythropoiesis through pharmacological modulation of iron metabolism.</p>]]>
      </content:encoded>
      <pubDate>Thu, 02 Apr 2026 12:06:14 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/5cf8c948/d2a34c21.mp3" length="31424017" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/-sYhQfD_NgZTiYu9Vn7ObBE9jJCB5oZ8hCHUvI0VPn0/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS9hMGE4/NjcwOTZjNTBjMGZi/NGY4OWZhMTQxYTlk/NDkzMS5qcGc.jpg"/>
      <itunes:duration>1569</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this episode, <em>Blood </em>Associate Editor Dr. Jason Gotlib discusses the Review Series "<a href="https://ashpublications.org/blood/article/147/12/1239/567079/Introduction-to-a-review-series-on-the-new-wave-of?searchresult=1">The New Wave of Targeted Therapeutics for MPN’s</a>", with authors Drs. Stefan Constantinescu, Ann Mullally, and Marina Kremyanskaya. This Review Series covers 3 areas where exciting advances are occurring. Dr. Constantinescu discusses “<a href="https://ashpublications.org/blood/article/147/12/1255/565933/Next-generation-JAK-inhibitors-in-the-treatment-of">Next-generation JAK inhibitors in the treatment of myeloproliferative neoplasms</a>” which describes how new ways to switch off JAK signaling are delivering a suite of new small-molecule drugs with potential. Dr. Mullally discusses “<a href="https://ashpublications.org/blood/article/147/12/1267/546893/Novel-strategies-targeting-mutant-calreticulin-in">Novel strategies targeting mutant calreticulin in essential thrombocythemia and myelofibrosis</a>” which reviews the biology of calreticulin mutations in myelofibrosis and ET and how multiple different modalities can be brought to bear against this mutant surface protein, including monoclonal antibodies, bispecific T-cell engagers, and cellular and vaccine therapies. Dr. Kremyanskaya discusses “<a href="https://ashpublications.org/blood/article/147/12/1278/547823/Modulators-of-the-hepcidin-pathway-in-polycythemia">Modulators of the hepcidin pathway in polycythemia vera and myelofibrosis</a>” which outlines the major recent progress being made in controlling excessive erythropoiesis through pharmacological modulation of iron metabolism.</p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3mijlkw3h3k2f"/>
    </item>
    <item>
      <title>CH in children with SCD and Asciminib for CML in the ASC4FIRST trial</title>
      <itunes:season>11</itunes:season>
      <podcast:season>11</podcast:season>
      <itunes:title>CH in children with SCD and Asciminib for CML in the ASC4FIRST trial</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
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      <description>
        <![CDATA[<p>In this week's episode, <em>Blood </em>editor Dr. Laura Michaelis interviews Drs. Alexander Bick and Jorge Cortes on their latest papers published in <em>Blood</em>. Dr. Cortes, the current EIC of<em> Blood Global Hematology </em>discusses "<a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025029210">Asciminib Demonstrates Superior Efficacy and Safety in Newly Diagnosed Chronic Myeloid Leukemia in the ASC4FIRST Trial</a>" wherein the planned secondary analysis showed a further efficacy advantage and a consistently favorable safety profile for asciminib relative to investigator-selected TKIs, especially second-generation TKIs. Dr. Bick discusses "<a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025030898">Increased prevalence of clonal hematopoiesis in children with sickle cell disease</a>" where targeted sequencing for CH mutations in 2318 children with SCD and 2957 controls and found that children with SCD have a higher prevalence of CH, and majority of CH cases identified were very small “micro-CH” clones, more work is needed to define the clinical significance of these clones.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, <em>Blood </em>editor Dr. Laura Michaelis interviews Drs. Alexander Bick and Jorge Cortes on their latest papers published in <em>Blood</em>. Dr. Cortes, the current EIC of<em> Blood Global Hematology </em>discusses "<a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025029210">Asciminib Demonstrates Superior Efficacy and Safety in Newly Diagnosed Chronic Myeloid Leukemia in the ASC4FIRST Trial</a>" wherein the planned secondary analysis showed a further efficacy advantage and a consistently favorable safety profile for asciminib relative to investigator-selected TKIs, especially second-generation TKIs. Dr. Bick discusses "<a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025030898">Increased prevalence of clonal hematopoiesis in children with sickle cell disease</a>" where targeted sequencing for CH mutations in 2318 children with SCD and 2957 controls and found that children with SCD have a higher prevalence of CH, and majority of CH cases identified were very small “micro-CH” clones, more work is needed to define the clinical significance of these clones.</p>]]>
      </content:encoded>
      <pubDate>Thu, 26 Mar 2026 12:43:47 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/f8bc777b/476751ab.mp3" length="16325125" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>815</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, <em>Blood </em>editor Dr. Laura Michaelis interviews Drs. Alexander Bick and Jorge Cortes on their latest papers published in <em>Blood</em>. Dr. Cortes, the current EIC of<em> Blood Global Hematology </em>discusses "<a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025029210">Asciminib Demonstrates Superior Efficacy and Safety in Newly Diagnosed Chronic Myeloid Leukemia in the ASC4FIRST Trial</a>" wherein the planned secondary analysis showed a further efficacy advantage and a consistently favorable safety profile for asciminib relative to investigator-selected TKIs, especially second-generation TKIs. Dr. Bick discusses "<a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025030898">Increased prevalence of clonal hematopoiesis in children with sickle cell disease</a>" where targeted sequencing for CH mutations in 2318 children with SCD and 2957 controls and found that children with SCD have a higher prevalence of CH, and majority of CH cases identified were very small “micro-CH” clones, more work is needed to define the clinical significance of these clones.</p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3mhy2g4tvzc25"/>
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    <item>
      <title>Emerging Mechanisms: Neutrophils and Immune thrombocytopenia from ICI</title>
      <itunes:season>11</itunes:season>
      <podcast:season>11</podcast:season>
      <itunes:title>Emerging Mechanisms: Neutrophils and Immune thrombocytopenia from ICI</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
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      <link>https://share.transistor.fm/s/1995031d</link>
      <description>
        <![CDATA[<p>In this week's episode of the <em>Blood </em>podcast, editor Dr. James Griffin interviews Drs. Christian Gorzelanny and Rebecca Leaf on their latest articles published in this week's issue of <em>Blood</em>. Dr. Gorzelanny discusses compelling evidence for a new mechanism that amplifies their proinflammatory actions in "<a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025029974">Lipid nanotubes unmask neutrophils for complement attack</a>", demonstrating the pathological role of this process in a range of inflammatory disorders in order to stimulate intense study of how to regulate nanotube formation for therapeutic benefit. In "<a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025031449">Immune thrombocytopenia in patients treated with immune checkpoint inhibitors</a>" Dr. Leaf and colleagues define the incidence, clinical features, and outcomes of ICI-induced immune thrombocytopenia. Showing that ICI-induced immune thrombocytopenia is associated with excess mortality, these data should provide an impetus to greater recognition and to protocolization of effective interventions.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode of the <em>Blood </em>podcast, editor Dr. James Griffin interviews Drs. Christian Gorzelanny and Rebecca Leaf on their latest articles published in this week's issue of <em>Blood</em>. Dr. Gorzelanny discusses compelling evidence for a new mechanism that amplifies their proinflammatory actions in "<a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025029974">Lipid nanotubes unmask neutrophils for complement attack</a>", demonstrating the pathological role of this process in a range of inflammatory disorders in order to stimulate intense study of how to regulate nanotube formation for therapeutic benefit. In "<a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025031449">Immune thrombocytopenia in patients treated with immune checkpoint inhibitors</a>" Dr. Leaf and colleagues define the incidence, clinical features, and outcomes of ICI-induced immune thrombocytopenia. Showing that ICI-induced immune thrombocytopenia is associated with excess mortality, these data should provide an impetus to greater recognition and to protocolization of effective interventions.</p>]]>
      </content:encoded>
      <pubDate>Thu, 19 Mar 2026 12:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
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      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1172</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode of the <em>Blood </em>podcast, editor Dr. James Griffin interviews Drs. Christian Gorzelanny and Rebecca Leaf on their latest articles published in this week's issue of <em>Blood</em>. Dr. Gorzelanny discusses compelling evidence for a new mechanism that amplifies their proinflammatory actions in "<a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025029974">Lipid nanotubes unmask neutrophils for complement attack</a>", demonstrating the pathological role of this process in a range of inflammatory disorders in order to stimulate intense study of how to regulate nanotube formation for therapeutic benefit. In "<a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025031449">Immune thrombocytopenia in patients treated with immune checkpoint inhibitors</a>" Dr. Leaf and colleagues define the incidence, clinical features, and outcomes of ICI-induced immune thrombocytopenia. Showing that ICI-induced immune thrombocytopenia is associated with excess mortality, these data should provide an impetus to greater recognition and to protocolization of effective interventions.</p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3mhgepm2cqe23"/>
    </item>
    <item>
      <title>Hepcidin-DMT1 interaction and GPRC5D-targeting bispecific antibody for MM</title>
      <itunes:season>11</itunes:season>
      <podcast:season>11</podcast:season>
      <itunes:title>Hepcidin-DMT1 interaction and GPRC5D-targeting bispecific antibody for MM</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">f6a053d4-f732-427d-b46a-736a0b44969d</guid>
      <link>https://share.transistor.fm/s/f752e487</link>
      <description>
        <![CDATA[<p>In this week's episode, <em>Blood </em>editor Dr. Laura Michaelis interviews authors Drs. Marion Falabrègue and Ajai Chari on their papers published in volume 146 issue 24 of <em>Blood</em>. The work of Dr. Falabrègue and colleagues in "<a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025028370">Intestinal hepcidin overexpression promotes iron deficiency anemia and counteracts iron overload via DMT1 downregulation</a>" indicates that iron absorption from the apical surface of enterocytes can be modulated through manipulation of the hepcidin-DMT1 interaction, opening new avenues for research and therapeutic manipulation. "<a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025029360">Talquetamab plus daratumumab in multiple myeloma</a>" features a phase 1b/2 trial of 65 heavily pretreated patients with MM, where Chari et al combined daratumumab and talquetamab, a GPRC5D-targeting bispecific antibody, reporting depletion of CD38-expressing regulatory T cells following daratumumab and impressive efficacy, with an 80% overall (57% complete) response rate and median progression-free survival of 23.3 months. This regimen is now being evaluated in a phase 3 trial. </p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, <em>Blood </em>editor Dr. Laura Michaelis interviews authors Drs. Marion Falabrègue and Ajai Chari on their papers published in volume 146 issue 24 of <em>Blood</em>. The work of Dr. Falabrègue and colleagues in "<a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025028370">Intestinal hepcidin overexpression promotes iron deficiency anemia and counteracts iron overload via DMT1 downregulation</a>" indicates that iron absorption from the apical surface of enterocytes can be modulated through manipulation of the hepcidin-DMT1 interaction, opening new avenues for research and therapeutic manipulation. "<a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025029360">Talquetamab plus daratumumab in multiple myeloma</a>" features a phase 1b/2 trial of 65 heavily pretreated patients with MM, where Chari et al combined daratumumab and talquetamab, a GPRC5D-targeting bispecific antibody, reporting depletion of CD38-expressing regulatory T cells following daratumumab and impressive efficacy, with an 80% overall (57% complete) response rate and median progression-free survival of 23.3 months. This regimen is now being evaluated in a phase 3 trial. </p>]]>
      </content:encoded>
      <pubDate>Thu, 12 Mar 2026 12:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/f752e487/c3b26e69.mp3" length="18666568" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>932</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, <em>Blood </em>editor Dr. Laura Michaelis interviews authors Drs. Marion Falabrègue and Ajai Chari on their papers published in volume 146 issue 24 of <em>Blood</em>. The work of Dr. Falabrègue and colleagues in "<a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025028370">Intestinal hepcidin overexpression promotes iron deficiency anemia and counteracts iron overload via DMT1 downregulation</a>" indicates that iron absorption from the apical surface of enterocytes can be modulated through manipulation of the hepcidin-DMT1 interaction, opening new avenues for research and therapeutic manipulation. "<a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025029360">Talquetamab plus daratumumab in multiple myeloma</a>" features a phase 1b/2 trial of 65 heavily pretreated patients with MM, where Chari et al combined daratumumab and talquetamab, a GPRC5D-targeting bispecific antibody, reporting depletion of CD38-expressing regulatory T cells following daratumumab and impressive efficacy, with an 80% overall (57% complete) response rate and median progression-free survival of 23.3 months. This regimen is now being evaluated in a phase 3 trial. </p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3mgurh6nzke2n"/>
    </item>
    <item>
      <title>PETAL Consortium Survival Prognosticators and How Inflammation Impacts Hematopoiesis</title>
      <itunes:season>11</itunes:season>
      <podcast:season>11</podcast:season>
      <itunes:title>PETAL Consortium Survival Prognosticators and How Inflammation Impacts Hematopoiesis</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">44467d22-d715-4fa9-b7fd-83ab6f5d88fa</guid>
      <link>https://share.transistor.fm/s/65259fd5</link>
      <description>
        <![CDATA[<p>In this week's episode, <em>Blood </em>associate editor Dr. Laura Michaelis interviews Drs. Mark Sorial and Emmanuelle Passegue on their articles published in volume 147 issue 7 of <em>Blood</em>. Dr. Sorial discusses "<a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025030149">Early time to relapse as a survival prognosticator in nodal mature T-cell lymphomas: results from the PETAL consortium</a>" where he and his team evaluated the prognostic significance of early relapse in a large retrospective cohort. They report a time to relapse of &lt;12 months as a strong predictive factor independent of the prognostic index for T-cell lymphoma and histology, with results validated in 2 independent cohorts. Dr. Emmanuelle Passegue discusses "<a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025029513">Inflammation perturbs hematopoiesis by remodeling specific compartments of the bone marrow niche</a>". Using a combination of single-cell RNA sequencing profiling and flow cytometry, the team characterized the bone marrow niche compartments in mice subjected to inflammation. They show that inter-feron-mediated inflammation preferentially targets central marrow leptin receptor–expressing mesenchymal cells, triggering cytokine release that affects monocyte dynamics in the bone marrow microenvironment.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, <em>Blood </em>associate editor Dr. Laura Michaelis interviews Drs. Mark Sorial and Emmanuelle Passegue on their articles published in volume 147 issue 7 of <em>Blood</em>. Dr. Sorial discusses "<a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025030149">Early time to relapse as a survival prognosticator in nodal mature T-cell lymphomas: results from the PETAL consortium</a>" where he and his team evaluated the prognostic significance of early relapse in a large retrospective cohort. They report a time to relapse of &lt;12 months as a strong predictive factor independent of the prognostic index for T-cell lymphoma and histology, with results validated in 2 independent cohorts. Dr. Emmanuelle Passegue discusses "<a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025029513">Inflammation perturbs hematopoiesis by remodeling specific compartments of the bone marrow niche</a>". Using a combination of single-cell RNA sequencing profiling and flow cytometry, the team characterized the bone marrow niche compartments in mice subjected to inflammation. They show that inter-feron-mediated inflammation preferentially targets central marrow leptin receptor–expressing mesenchymal cells, triggering cytokine release that affects monocyte dynamics in the bone marrow microenvironment.</p>]]>
      </content:encoded>
      <pubDate>Thu, 05 Mar 2026 12:00:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/65259fd5/7a73e32c.mp3" length="15632500" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>780</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, <em>Blood </em>associate editor Dr. Laura Michaelis interviews Drs. Mark Sorial and Emmanuelle Passegue on their articles published in volume 147 issue 7 of <em>Blood</em>. Dr. Sorial discusses "<a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025030149">Early time to relapse as a survival prognosticator in nodal mature T-cell lymphomas: results from the PETAL consortium</a>" where he and his team evaluated the prognostic significance of early relapse in a large retrospective cohort. They report a time to relapse of &lt;12 months as a strong predictive factor independent of the prognostic index for T-cell lymphoma and histology, with results validated in 2 independent cohorts. Dr. Emmanuelle Passegue discusses "<a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025029513">Inflammation perturbs hematopoiesis by remodeling specific compartments of the bone marrow niche</a>". Using a combination of single-cell RNA sequencing profiling and flow cytometry, the team characterized the bone marrow niche compartments in mice subjected to inflammation. They show that inter-feron-mediated inflammation preferentially targets central marrow leptin receptor–expressing mesenchymal cells, triggering cytokine release that affects monocyte dynamics in the bone marrow microenvironment.</p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3mgdbjyyupy2y"/>
    </item>
    <item>
      <title>Review Series on the Structural Underpinnings of Hemostatic Plugs and Thrombotic Occulsions</title>
      <itunes:season>11</itunes:season>
      <podcast:season>11</podcast:season>
      <itunes:title>Review Series on the Structural Underpinnings of Hemostatic Plugs and Thrombotic Occulsions</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">d3d5ac6f-8544-48e7-a279-495989fcb9c7</guid>
      <link>https://share.transistor.fm/s/d7be0206</link>
      <description>
        <![CDATA[<p>This review series focuses on recent advances in resolving macro and molecular structures that have driven the field of occlusive thrombus structure and function forward. Covering multiple contributions to thrombosis, eg, platelets, factor XIII, and the contact system, the series also looks to put this new knowledge into the context of future advances in diagnostic and therapeutic tools to enhance normal hemostasis while preventing and treating unwanted thrombosis. <em>Blood </em>Associate Editor, Dr. Thomas Ortel discusses this series with Drs. Alisa Wolberg, Jonas Emsley, and John Weisel, who all contributed to articles in the <a href="https://ashpublications.org/blood/article/146/12/1377/547225/Introduction-to-a-review-series-on-the-structural">Review Series on the Structural Underpinnings of Hemostatic Plugs and Thrombotic Occulsions</a> which can be found in volume 146, issue 12 of <em>Blood</em>. </p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>This review series focuses on recent advances in resolving macro and molecular structures that have driven the field of occlusive thrombus structure and function forward. Covering multiple contributions to thrombosis, eg, platelets, factor XIII, and the contact system, the series also looks to put this new knowledge into the context of future advances in diagnostic and therapeutic tools to enhance normal hemostasis while preventing and treating unwanted thrombosis. <em>Blood </em>Associate Editor, Dr. Thomas Ortel discusses this series with Drs. Alisa Wolberg, Jonas Emsley, and John Weisel, who all contributed to articles in the <a href="https://ashpublications.org/blood/article/146/12/1377/547225/Introduction-to-a-review-series-on-the-structural">Review Series on the Structural Underpinnings of Hemostatic Plugs and Thrombotic Occulsions</a> which can be found in volume 146, issue 12 of <em>Blood</em>. </p>]]>
      </content:encoded>
      <pubDate>Thu, 26 Feb 2026 12:00:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/d7be0206/84a707ff.mp3" length="34230588" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/wV4uJdNvwoiW9A5HZZk_Y4WylPjzEt-OpdYFZ-uyAbk/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS81ZGVi/YTczMjIwOGEwMzBj/ZjljYTI2ODU0NmI5/MzU1NC5qcGc.jpg"/>
      <itunes:duration>1710</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>This review series focuses on recent advances in resolving macro and molecular structures that have driven the field of occlusive thrombus structure and function forward. Covering multiple contributions to thrombosis, eg, platelets, factor XIII, and the contact system, the series also looks to put this new knowledge into the context of future advances in diagnostic and therapeutic tools to enhance normal hemostasis while preventing and treating unwanted thrombosis. <em>Blood </em>Associate Editor, Dr. Thomas Ortel discusses this series with Drs. Alisa Wolberg, Jonas Emsley, and John Weisel, who all contributed to articles in the <a href="https://ashpublications.org/blood/article/146/12/1377/547225/Introduction-to-a-review-series-on-the-structural">Review Series on the Structural Underpinnings of Hemostatic Plugs and Thrombotic Occulsions</a> which can be found in volume 146, issue 12 of <em>Blood</em>. </p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3mfrobxfqcx2l"/>
    </item>
    <item>
      <title>VTE Risk Model in Children and a Novel Tri-specific T-cell-engager for MM</title>
      <itunes:season>11</itunes:season>
      <podcast:season>11</podcast:season>
      <itunes:title>VTE Risk Model in Children and a Novel Tri-specific T-cell-engager for MM</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">ccd7d018-e915-43c9-a893-e033c28d138d</guid>
      <link>https://share.transistor.fm/s/97e8c581</link>
      <description>
        <![CDATA[<p>In this week's episode, <em>Blood </em>editor Dr. Laurie Sehn interviews authors Drs. Julie Jaffray and Ulrike Philippar on their latest articles published in <em>Blood</em>. Dr. Jaffray discusses her CME article, "<a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025029841">Multisite validation of a venous thrombosis risk model in critically ill children through the CHAT Consortium</a>", identifying patients with risks as high as 17% and taking research one step closer to the goal of personalized thromboprophylaxis for safe and effective care of high-risk children. Dr. Philippar discusses her article "<a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025030027">Ramantamig (JNJ-79635322), a novel T-cell-engaging trispecific antibody targeting BCMA, GPRC5D, and CD3, in multiple myeloma models</a>", where the extensive in vitro and in vivo preclinical studies with cell lines and patient samples indicate strong potential for this agent to have efficacy against MM expressing either or both of these antigens.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, <em>Blood </em>editor Dr. Laurie Sehn interviews authors Drs. Julie Jaffray and Ulrike Philippar on their latest articles published in <em>Blood</em>. Dr. Jaffray discusses her CME article, "<a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025029841">Multisite validation of a venous thrombosis risk model in critically ill children through the CHAT Consortium</a>", identifying patients with risks as high as 17% and taking research one step closer to the goal of personalized thromboprophylaxis for safe and effective care of high-risk children. Dr. Philippar discusses her article "<a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025030027">Ramantamig (JNJ-79635322), a novel T-cell-engaging trispecific antibody targeting BCMA, GPRC5D, and CD3, in multiple myeloma models</a>", where the extensive in vitro and in vivo preclinical studies with cell lines and patient samples indicate strong potential for this agent to have efficacy against MM expressing either or both of these antigens.</p>]]>
      </content:encoded>
      <pubDate>Thu, 19 Feb 2026 12:00:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/97e8c581/58f569a8.mp3" length="20451207" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1021</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, <em>Blood </em>editor Dr. Laurie Sehn interviews authors Drs. Julie Jaffray and Ulrike Philippar on their latest articles published in <em>Blood</em>. Dr. Jaffray discusses her CME article, "<a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025029841">Multisite validation of a venous thrombosis risk model in critically ill children through the CHAT Consortium</a>", identifying patients with risks as high as 17% and taking research one step closer to the goal of personalized thromboprophylaxis for safe and effective care of high-risk children. Dr. Philippar discusses her article "<a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025030027">Ramantamig (JNJ-79635322), a novel T-cell-engaging trispecific antibody targeting BCMA, GPRC5D, and CD3, in multiple myeloma models</a>", where the extensive in vitro and in vivo preclinical studies with cell lines and patient samples indicate strong potential for this agent to have efficacy against MM expressing either or both of these antigens.</p>]]>
      </itunes:summary>
      <itunes:keywords>pediatric hematology, pediatric thrombosis, CME, CHAT consortium, multiple myeloma, VTE</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3mfa2z5smhu2s"/>
    </item>
    <item>
      <title>CAR-iNKT cell immunotherapy and Jagged2/Notch regulation of HSC</title>
      <itunes:season>11</itunes:season>
      <podcast:season>11</podcast:season>
      <itunes:title>CAR-iNKT cell immunotherapy and Jagged2/Notch regulation of HSC</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">21993ccb-6962-4d02-9294-1783018bfd6d</guid>
      <link>https://share.transistor.fm/s/a342d949</link>
      <description>
        <![CDATA[<p>In this week's episode, <em>Blood </em>editor Dr. Laurie Sehn interviews authors Drs. Anastasios Karadimitris and Maria Carolina Florian on their papers published in Volume 147 Issue 2 of <em>Blood</em>. Dr. Karadimitris' paper "<a href="https://ashpublications.org/blood/article/147/2/180/547084/Off-the-shelf-dual-CAR-iNKT-cell-immunotherapy">Off-the-shelf dual CAR-iNKT cell immunotherapy eradicates medullary and leptomeningeal high-risk <em>KMT2A</em>-rearranged leukemia</a>", discusses the success of bispecific CAR-iNKT cells targeting CD19 and CD133 in pre-clinical models, prompting the clinical development of this class of product. Dr. Florian's paper, "<a href="https://ashpublications.org/blood/article/147/2/164/547604/A-Notch-trans-activation-to-cis-inhibition-switch">A Notch <em>trans</em>-activation to <em>cis</em>-inhibition switch underlies hematopoietic stem cell aging</a>" proposes that the Jagged2/Notch interaction is a key regulator of hematopoietic stem cell divisional symmetry during aging and offers insights that may inform strategies to restore regenerative function in aged hematopoiesis. </p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, <em>Blood </em>editor Dr. Laurie Sehn interviews authors Drs. Anastasios Karadimitris and Maria Carolina Florian on their papers published in Volume 147 Issue 2 of <em>Blood</em>. Dr. Karadimitris' paper "<a href="https://ashpublications.org/blood/article/147/2/180/547084/Off-the-shelf-dual-CAR-iNKT-cell-immunotherapy">Off-the-shelf dual CAR-iNKT cell immunotherapy eradicates medullary and leptomeningeal high-risk <em>KMT2A</em>-rearranged leukemia</a>", discusses the success of bispecific CAR-iNKT cells targeting CD19 and CD133 in pre-clinical models, prompting the clinical development of this class of product. Dr. Florian's paper, "<a href="https://ashpublications.org/blood/article/147/2/164/547604/A-Notch-trans-activation-to-cis-inhibition-switch">A Notch <em>trans</em>-activation to <em>cis</em>-inhibition switch underlies hematopoietic stem cell aging</a>" proposes that the Jagged2/Notch interaction is a key regulator of hematopoietic stem cell divisional symmetry during aging and offers insights that may inform strategies to restore regenerative function in aged hematopoiesis. </p>]]>
      </content:encoded>
      <pubDate>Thu, 12 Feb 2026 13:43:14 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/a342d949/01365364.mp3" length="24225870" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1210</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, <em>Blood </em>editor Dr. Laurie Sehn interviews authors Drs. Anastasios Karadimitris and Maria Carolina Florian on their papers published in Volume 147 Issue 2 of <em>Blood</em>. Dr. Karadimitris' paper "<a href="https://ashpublications.org/blood/article/147/2/180/547084/Off-the-shelf-dual-CAR-iNKT-cell-immunotherapy">Off-the-shelf dual CAR-iNKT cell immunotherapy eradicates medullary and leptomeningeal high-risk <em>KMT2A</em>-rearranged leukemia</a>", discusses the success of bispecific CAR-iNKT cells targeting CD19 and CD133 in pre-clinical models, prompting the clinical development of this class of product. Dr. Florian's paper, "<a href="https://ashpublications.org/blood/article/147/2/164/547604/A-Notch-trans-activation-to-cis-inhibition-switch">A Notch <em>trans</em>-activation to <em>cis</em>-inhibition switch underlies hematopoietic stem cell aging</a>" proposes that the Jagged2/Notch interaction is a key regulator of hematopoietic stem cell divisional symmetry during aging and offers insights that may inform strategies to restore regenerative function in aged hematopoiesis. </p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3meoninau2y2d"/>
    </item>
    <item>
      <title>Biologic Insights and Clinical Trial Design for AML</title>
      <itunes:season>11</itunes:season>
      <podcast:season>11</podcast:season>
      <itunes:title>Biologic Insights and Clinical Trial Design for AML</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">5cbe4609-3885-4852-8a89-45d374ee4cb2</guid>
      <link>https://share.transistor.fm/s/1ae254c6</link>
      <description>
        <![CDATA[<p>In this week's episode, <em>Blood </em>editor Dr. James Griffin interviews Drs. Paresh Vyas and Andrew Hantel on their research published in this week's issue of <em>Blood</em>. Dr. Vyas discusses his paper, "<a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027948">Rapid clonal selection within early hematopoietic cell compartments presages outcome to ivosidenib combination therapy</a>", which provided new insights as to when and how to intervene to circumvent resistance to AML remission. Dr. Hantel will speak about his paper, "<a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025030741">Impact of Modernizing Eligibility Criteria on Enrollment and Representation in AML Clinical Trials</a>". For a real-world cohort of more than 2200 patients with AML, they reported that modernized, safety-based criteria could nearly double trial eligibility, with especially pronounced gains among historically underserved groups.  Both studies highlight how biologic insight and thoughtful trial design can drive more effective, inclusive advances in AML treatment and research.  <br> <em> </em></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, <em>Blood </em>editor Dr. James Griffin interviews Drs. Paresh Vyas and Andrew Hantel on their research published in this week's issue of <em>Blood</em>. Dr. Vyas discusses his paper, "<a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027948">Rapid clonal selection within early hematopoietic cell compartments presages outcome to ivosidenib combination therapy</a>", which provided new insights as to when and how to intervene to circumvent resistance to AML remission. Dr. Hantel will speak about his paper, "<a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025030741">Impact of Modernizing Eligibility Criteria on Enrollment and Representation in AML Clinical Trials</a>". For a real-world cohort of more than 2200 patients with AML, they reported that modernized, safety-based criteria could nearly double trial eligibility, with especially pronounced gains among historically underserved groups.  Both studies highlight how biologic insight and thoughtful trial design can drive more effective, inclusive advances in AML treatment and research.  <br> <em> </em></p>]]>
      </content:encoded>
      <pubDate>Thu, 05 Feb 2026 13:59:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/1ae254c6/2d122dd6.mp3" length="27538385" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1376</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, <em>Blood </em>editor Dr. James Griffin interviews Drs. Paresh Vyas and Andrew Hantel on their research published in this week's issue of <em>Blood</em>. Dr. Vyas discusses his paper, "<a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027948">Rapid clonal selection within early hematopoietic cell compartments presages outcome to ivosidenib combination therapy</a>", which provided new insights as to when and how to intervene to circumvent resistance to AML remission. Dr. Hantel will speak about his paper, "<a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025030741">Impact of Modernizing Eligibility Criteria on Enrollment and Representation in AML Clinical Trials</a>". For a real-world cohort of more than 2200 patients with AML, they reported that modernized, safety-based criteria could nearly double trial eligibility, with especially pronounced gains among historically underserved groups.  Both studies highlight how biologic insight and thoughtful trial design can drive more effective, inclusive advances in AML treatment and research.  <br> <em> </em></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3me534hljkd2j"/>
    </item>
    <item>
      <title>How I Treat Series on Acute Lymphoblastic Leukemia</title>
      <itunes:season>11</itunes:season>
      <podcast:season>11</podcast:season>
      <itunes:title>How I Treat Series on Acute Lymphoblastic Leukemia</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">ee2e6c65-89a6-4b9f-b6c6-9159f09cff8b</guid>
      <link>https://share.transistor.fm/s/411e1898</link>
      <description>
        <![CDATA[<p>In this week's episode, <em>Blood </em>Associate editor Dr. Hervé Dombret interviews authors Drs. Sarah K. Tasian and David T. Teachey on their contributions to the How I Treat Series on acute lymphoblastic leukemia. Dr. Tasian's paper, “<a href="https://ashpublications.org/blood/article/145/1/20/515891/How-I-treat-Philadelphia-chromosome-like-acute">How I treat Philadelphia chromosome-like acute lymphoblastic leukemia in children, adolescents, and young adults</a>” discusses the different classes of Ph-like ALL and reviews the recent trials investigating TKIs and immunotherapy specifically for this high-risk patient population. Dr. Teachey's paper, “<a href="https://ashpublications.org/blood/article/145/1/43/514992/How-I-treat-ETP-ALL-in-children">How I treat ETP-ALL in children</a>”, discusses the best current and emerging therapies that may be used in patients with ETP ALL, including nelarabine and other new agents, immunotherapy, and allogeneic HSCT.</p><p><br></p><p><a href="https://ashpublications.org/blood/article/145/1/1/534797/Introduction-to-a-How-I-Treat-series-on-acute">See the full How I Treat series in volume 145 issue 1 of <em>Blood</em>.</a></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, <em>Blood </em>Associate editor Dr. Hervé Dombret interviews authors Drs. Sarah K. Tasian and David T. Teachey on their contributions to the How I Treat Series on acute lymphoblastic leukemia. Dr. Tasian's paper, “<a href="https://ashpublications.org/blood/article/145/1/20/515891/How-I-treat-Philadelphia-chromosome-like-acute">How I treat Philadelphia chromosome-like acute lymphoblastic leukemia in children, adolescents, and young adults</a>” discusses the different classes of Ph-like ALL and reviews the recent trials investigating TKIs and immunotherapy specifically for this high-risk patient population. Dr. Teachey's paper, “<a href="https://ashpublications.org/blood/article/145/1/43/514992/How-I-treat-ETP-ALL-in-children">How I treat ETP-ALL in children</a>”, discusses the best current and emerging therapies that may be used in patients with ETP ALL, including nelarabine and other new agents, immunotherapy, and allogeneic HSCT.</p><p><br></p><p><a href="https://ashpublications.org/blood/article/145/1/1/534797/Introduction-to-a-How-I-Treat-series-on-acute">See the full How I Treat series in volume 145 issue 1 of <em>Blood</em>.</a></p>]]>
      </content:encoded>
      <pubDate>Thu, 29 Jan 2026 13:23:18 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/411e1898/107d09d3.mp3" length="31768607" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/l47EeJ3ne8aAI9Hf98b3PZp8U5a8rfIRepsqxE3gue8/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS84N2Jk/NTM5ZDMxNzIwMDFh/YTUyNWNhNDg4ZWNm/MzY0Yi5qcGc.jpg"/>
      <itunes:duration>1587</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, <em>Blood </em>Associate editor Dr. Hervé Dombret interviews authors Drs. Sarah K. Tasian and David T. Teachey on their contributions to the How I Treat Series on acute lymphoblastic leukemia. Dr. Tasian's paper, “<a href="https://ashpublications.org/blood/article/145/1/20/515891/How-I-treat-Philadelphia-chromosome-like-acute">How I treat Philadelphia chromosome-like acute lymphoblastic leukemia in children, adolescents, and young adults</a>” discusses the different classes of Ph-like ALL and reviews the recent trials investigating TKIs and immunotherapy specifically for this high-risk patient population. Dr. Teachey's paper, “<a href="https://ashpublications.org/blood/article/145/1/43/514992/How-I-treat-ETP-ALL-in-children">How I treat ETP-ALL in children</a>”, discusses the best current and emerging therapies that may be used in patients with ETP ALL, including nelarabine and other new agents, immunotherapy, and allogeneic HSCT.</p><p><br></p><p><a href="https://ashpublications.org/blood/article/145/1/1/534797/Introduction-to-a-How-I-Treat-series-on-acute">See the full How I Treat series in volume 145 issue 1 of <em>Blood</em>.</a></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3mdlfu5vzry2w"/>
    </item>
    <item>
      <title>How I Treat Series on the 25th anniversary of Tyrosine Kinase Inhibitors in Chronic Myeloid Leukemia</title>
      <itunes:season>11</itunes:season>
      <podcast:season>11</podcast:season>
      <itunes:title>How I Treat Series on the 25th anniversary of Tyrosine Kinase Inhibitors in Chronic Myeloid Leukemia</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">0dc33165-c86f-4b26-aed8-f35eb4bde4aa</guid>
      <link>https://share.transistor.fm/s/11b920ba</link>
      <description>
        <![CDATA[<p>In this week's episode, <em>Blood </em>Associate Editor, Dr. Jason Gotlib leads a discussion about the How I Treat Series commemorating the 25th anniversary of the introduction of tyrosine kinase inhibitors in CML, featuring Drs. Neil Shah, Simona Soverini, Elisabetta Abruzzese, and Yves Chalandon. The introduction of TKIs revolutionized patient outcomes in CML, turning a poor prognosis—3 to 5 years life expectancy—to a manageable chronic condition. In this conversation, we'll cover management techniques for CML during relapse, pregnancy, and explore indications for hematopoietic stem cell transplantation. </p><p><a href="https://ashpublications.org/blood/article/147/4/319/565948/Introduction-to-a-How-I-Treat-series-on-chronic">See the full How I Treat series in Volume 147 issue 4 of <em>Blood</em>.</a></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, <em>Blood </em>Associate Editor, Dr. Jason Gotlib leads a discussion about the How I Treat Series commemorating the 25th anniversary of the introduction of tyrosine kinase inhibitors in CML, featuring Drs. Neil Shah, Simona Soverini, Elisabetta Abruzzese, and Yves Chalandon. The introduction of TKIs revolutionized patient outcomes in CML, turning a poor prognosis—3 to 5 years life expectancy—to a manageable chronic condition. In this conversation, we'll cover management techniques for CML during relapse, pregnancy, and explore indications for hematopoietic stem cell transplantation. </p><p><a href="https://ashpublications.org/blood/article/147/4/319/565948/Introduction-to-a-How-I-Treat-series-on-chronic">See the full How I Treat series in Volume 147 issue 4 of <em>Blood</em>.</a></p>]]>
      </content:encoded>
      <pubDate>Thu, 22 Jan 2026 12:02:07 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/11b920ba/aa30b175.mp3" length="41910596" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/0uyhud6WD0hw7yDWVsI9vIgwi1axciMuwznVs21Lvqk/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS9hY2Yw/ODY4ZDk3MDM2MzRh/MjIxOTU0MTU2OGQ2/ODFhZi5qcGc.jpg"/>
      <itunes:duration>2094</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, <em>Blood </em>Associate Editor, Dr. Jason Gotlib leads a discussion about the How I Treat Series commemorating the 25th anniversary of the introduction of tyrosine kinase inhibitors in CML, featuring Drs. Neil Shah, Simona Soverini, Elisabetta Abruzzese, and Yves Chalandon. The introduction of TKIs revolutionized patient outcomes in CML, turning a poor prognosis—3 to 5 years life expectancy—to a manageable chronic condition. In this conversation, we'll cover management techniques for CML during relapse, pregnancy, and explore indications for hematopoietic stem cell transplantation. </p><p><a href="https://ashpublications.org/blood/article/147/4/319/565948/Introduction-to-a-How-I-Treat-series-on-chronic">See the full How I Treat series in Volume 147 issue 4 of <em>Blood</em>.</a></p>]]>
      </itunes:summary>
      <itunes:keywords>TKIs, CML, hematology, oncology, leukemia, drug therapy</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3mczo2wo3no2d"/>
    </item>
    <item>
      <title>How I Treat Series on Hematologic Complications in Pregnancy</title>
      <itunes:season>11</itunes:season>
      <podcast:season>11</podcast:season>
      <itunes:title>How I Treat Series on Hematologic Complications in Pregnancy</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">627c87a5-5227-4523-b070-78e45d2571ed</guid>
      <link>https://share.transistor.fm/s/db0f6b74</link>
      <description>
        <![CDATA[<p>In this week's episode, <em>Blood </em>Associate editor Dr. Thomas Ortel interviews authors Drs. Ware Branch and J.J. Strouse on their contributions to How I Treat hematologic complications in pregnancy. Dr. Branch's paper, “<a href="https://ashpublications.org/blood/article/143/9/757/506724/How-I-diagnose-and-treat-antiphospholipid-syndrome">How I diagnose and treat antiphospholipid syndrome in pregnancy</a>” discusses the evolving clinical and laboratory features of APS, and the treatment of cases meeting ACR/EULAR classification criteria. Dr. Strouse stresses the unique problems posed to both the mother and fetus during pregnancy in his paper "<a href="https://ashpublications.org/blood/article/143/9/769/498771/How-I-treat-sickle-cell-disease-in-pregnancy">How I treat sickle cell disease in pregnancy</a>”.</p><p><a href="https://ashpublications.org/blood/article/143/9/739/515060/Introduction-to-a-How-I-Treat-series-on">See the full How I Treat series in volume 143 issue 9 of <em>Blood </em>journal. </a></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, <em>Blood </em>Associate editor Dr. Thomas Ortel interviews authors Drs. Ware Branch and J.J. Strouse on their contributions to How I Treat hematologic complications in pregnancy. Dr. Branch's paper, “<a href="https://ashpublications.org/blood/article/143/9/757/506724/How-I-diagnose-and-treat-antiphospholipid-syndrome">How I diagnose and treat antiphospholipid syndrome in pregnancy</a>” discusses the evolving clinical and laboratory features of APS, and the treatment of cases meeting ACR/EULAR classification criteria. Dr. Strouse stresses the unique problems posed to both the mother and fetus during pregnancy in his paper "<a href="https://ashpublications.org/blood/article/143/9/769/498771/How-I-treat-sickle-cell-disease-in-pregnancy">How I treat sickle cell disease in pregnancy</a>”.</p><p><a href="https://ashpublications.org/blood/article/143/9/739/515060/Introduction-to-a-How-I-Treat-series-on">See the full How I Treat series in volume 143 issue 9 of <em>Blood </em>journal. </a></p>]]>
      </content:encoded>
      <pubDate>Thu, 15 Jan 2026 12:00:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/db0f6b74/45c899f4.mp3" length="21800476" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/Y105-vqeCDRznN9cjsAeonJ_RcpqngMZX18QpmqInOs/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS80ZjRh/YjNmMWUyNGU5YmQ5/YmFkYjE5YTA3YjEy/YWQ2Yi5qcGc.jpg"/>
      <itunes:duration>1089</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, <em>Blood </em>Associate editor Dr. Thomas Ortel interviews authors Drs. Ware Branch and J.J. Strouse on their contributions to How I Treat hematologic complications in pregnancy. Dr. Branch's paper, “<a href="https://ashpublications.org/blood/article/143/9/757/506724/How-I-diagnose-and-treat-antiphospholipid-syndrome">How I diagnose and treat antiphospholipid syndrome in pregnancy</a>” discusses the evolving clinical and laboratory features of APS, and the treatment of cases meeting ACR/EULAR classification criteria. Dr. Strouse stresses the unique problems posed to both the mother and fetus during pregnancy in his paper "<a href="https://ashpublications.org/blood/article/143/9/769/498771/How-I-treat-sickle-cell-disease-in-pregnancy">How I treat sickle cell disease in pregnancy</a>”.</p><p><a href="https://ashpublications.org/blood/article/143/9/739/515060/Introduction-to-a-How-I-Treat-series-on">See the full How I Treat series in volume 143 issue 9 of <em>Blood </em>journal. </a></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3mci2pflw3d2i"/>
    </item>
    <item>
      <title>Review Series on Marginal Zone Lymphoma </title>
      <itunes:season>11</itunes:season>
      <podcast:season>11</podcast:season>
      <itunes:title>Review Series on Marginal Zone Lymphoma </itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">2fbd31ed-aa15-4b80-a00b-162d708b1c62</guid>
      <link>https://share.transistor.fm/s/bf2851cf</link>
      <description>
        <![CDATA[<p>This week's episode accompanies the Review Series on Marginal Zone Lymphoma published in this week's issue of <em>Blood</em>. Associate editor, Dr. Philippe Armand interviews authors Dr. Juan Pablo Alderuccio and Dr. Ariela Noy on their contribution to this review series titled "<a href="https://ashpublications.org/blood/article/doi/10.1182/blood.2024028269/546195/The-Treatment-of-Marginal-Zone-Lymphoma">The treatment of marginal zone lymphoma</a>". The article is crucial in highlighting the clinically and biologically heterogenous nature of MZL diseases, and how current treatment options and available research do not allow for comprehensive MZL specific therapies. Drs. Alderuccio and Noy share their insights on specific avenues for the expansion of the MZL care landscape. </p><p><a href="https://ashpublications.org/blood/article/147/2/95/557532/Introduction-to-a-review-series-on-marginal-zone">Find the full review series in volume 147 issue 2 of <em>Blood </em>journal.<br></a><br></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>This week's episode accompanies the Review Series on Marginal Zone Lymphoma published in this week's issue of <em>Blood</em>. Associate editor, Dr. Philippe Armand interviews authors Dr. Juan Pablo Alderuccio and Dr. Ariela Noy on their contribution to this review series titled "<a href="https://ashpublications.org/blood/article/doi/10.1182/blood.2024028269/546195/The-Treatment-of-Marginal-Zone-Lymphoma">The treatment of marginal zone lymphoma</a>". The article is crucial in highlighting the clinically and biologically heterogenous nature of MZL diseases, and how current treatment options and available research do not allow for comprehensive MZL specific therapies. Drs. Alderuccio and Noy share their insights on specific avenues for the expansion of the MZL care landscape. </p><p><a href="https://ashpublications.org/blood/article/147/2/95/557532/Introduction-to-a-review-series-on-marginal-zone">Find the full review series in volume 147 issue 2 of <em>Blood </em>journal.<br></a><br></p>]]>
      </content:encoded>
      <pubDate>Thu, 08 Jan 2026 12:28:27 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/bf2851cf/30471b1f.mp3" length="32261611" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/xLJZs3PaXdh6A5Fak_auEyvfiD60HfjAzlQ9OIjKJv0/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS83OGYy/ZThjM2Y2ZGQyODE2/NTc1OGZlZDYzMWI1/MzVhMi5qcGc.jpg"/>
      <itunes:duration>1611</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>This week's episode accompanies the Review Series on Marginal Zone Lymphoma published in this week's issue of <em>Blood</em>. Associate editor, Dr. Philippe Armand interviews authors Dr. Juan Pablo Alderuccio and Dr. Ariela Noy on their contribution to this review series titled "<a href="https://ashpublications.org/blood/article/doi/10.1182/blood.2024028269/546195/The-Treatment-of-Marginal-Zone-Lymphoma">The treatment of marginal zone lymphoma</a>". The article is crucial in highlighting the clinically and biologically heterogenous nature of MZL diseases, and how current treatment options and available research do not allow for comprehensive MZL specific therapies. Drs. Alderuccio and Noy share their insights on specific avenues for the expansion of the MZL care landscape. </p><p><a href="https://ashpublications.org/blood/article/147/2/95/557532/Introduction-to-a-review-series-on-marginal-zone">Find the full review series in volume 147 issue 2 of <em>Blood </em>journal.<br></a><br></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3mbwizmgqid2l"/>
    </item>
    <item>
      <title>VTE Recurrence Risk Factors and poor-response AML Transplant Outcome Indicators</title>
      <itunes:season>11</itunes:season>
      <podcast:season>11</podcast:season>
      <itunes:title>VTE Recurrence Risk Factors and poor-response AML Transplant Outcome Indicators</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">6613cc41-e09e-473c-85ab-dcb5f2f0e71c</guid>
      <link>https://share.transistor.fm/s/9988c2c1</link>
      <description>
        <![CDATA[<p>In this week's episode we've pulled a vault recording from 2025! <em>Blood </em>editor Dr. Laurie Sehn interviews authors Drs. David-Alexandre Trégouët and Johannes Schetelig on their research published in volume 146 issue 19 of <em>Blood </em>journal. Dr. Trégouët's study conducted a genome-wide association study supplemented by transcriptome and Mendelian randomization analyses to identify 28 loci and proteins associated with VTE recurrence risk. This work provides genomic evidence that inherited variants contribute to the risk of VTE recurrence, raising the possibility of a more personalized approach to the prevention of recurrent VTE. The study conducted by Dr. Schetelig and colleagues report the results of a long term trial on patients with poor-response AML, comparing outcomes between patients who received salvage chemotherapy versus immediate transplantation. With no difference in survival rates at 5 years, outcomes seem to be determined mainly by genetic risk factors, age, and comorbidities, therefore challenging the routine use of intensive remission induction before allogeneic transplant in patients with an available donor and underscore the need for novel therapeutic strategies for poor-risk AML.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027879">Molecular Determinants of Thrombosis Recurrence Risk Across Venous Thromboembolism Subtypes </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025028730">Disease risk but not remission status determines transplant outcomes in AML: long-term outcomes of the ASAP trial <br></a><br></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we've pulled a vault recording from 2025! <em>Blood </em>editor Dr. Laurie Sehn interviews authors Drs. David-Alexandre Trégouët and Johannes Schetelig on their research published in volume 146 issue 19 of <em>Blood </em>journal. Dr. Trégouët's study conducted a genome-wide association study supplemented by transcriptome and Mendelian randomization analyses to identify 28 loci and proteins associated with VTE recurrence risk. This work provides genomic evidence that inherited variants contribute to the risk of VTE recurrence, raising the possibility of a more personalized approach to the prevention of recurrent VTE. The study conducted by Dr. Schetelig and colleagues report the results of a long term trial on patients with poor-response AML, comparing outcomes between patients who received salvage chemotherapy versus immediate transplantation. With no difference in survival rates at 5 years, outcomes seem to be determined mainly by genetic risk factors, age, and comorbidities, therefore challenging the routine use of intensive remission induction before allogeneic transplant in patients with an available donor and underscore the need for novel therapeutic strategies for poor-risk AML.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027879">Molecular Determinants of Thrombosis Recurrence Risk Across Venous Thromboembolism Subtypes </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025028730">Disease risk but not remission status determines transplant outcomes in AML: long-term outcomes of the ASAP trial <br></a><br></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 01 Jan 2026 12:00:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/9988c2c1/89596193.mp3" length="17897125" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>893</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we've pulled a vault recording from 2025! <em>Blood </em>editor Dr. Laurie Sehn interviews authors Drs. David-Alexandre Trégouët and Johannes Schetelig on their research published in volume 146 issue 19 of <em>Blood </em>journal. Dr. Trégouët's study conducted a genome-wide association study supplemented by transcriptome and Mendelian randomization analyses to identify 28 loci and proteins associated with VTE recurrence risk. This work provides genomic evidence that inherited variants contribute to the risk of VTE recurrence, raising the possibility of a more personalized approach to the prevention of recurrent VTE. The study conducted by Dr. Schetelig and colleagues report the results of a long term trial on patients with poor-response AML, comparing outcomes between patients who received salvage chemotherapy versus immediate transplantation. With no difference in survival rates at 5 years, outcomes seem to be determined mainly by genetic risk factors, age, and comorbidities, therefore challenging the routine use of intensive remission induction before allogeneic transplant in patients with an available donor and underscore the need for novel therapeutic strategies for poor-risk AML.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027879">Molecular Determinants of Thrombosis Recurrence Risk Across Venous Thromboembolism Subtypes </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025028730">Disease risk but not remission status determines transplant outcomes in AML: long-term outcomes of the ASAP trial <br></a><br></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3mbeu5ptgy42t"/>
    </item>
    <item>
      <title>Novel Treatment Targets for Hemophilia A and AML</title>
      <itunes:season>10</itunes:season>
      <podcast:season>10</podcast:season>
      <itunes:title>Novel Treatment Targets for Hemophilia A and AML</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">296e0a55-bb65-448d-b93f-84eab10cdec8</guid>
      <link>https://share.transistor.fm/s/25be2371</link>
      <description>
        <![CDATA[<p>In this week's episode, <em>Blood </em>editor Dr. James Griffin interviews authors Drs. Vincent Muczynski and Mark Geyer on their latest research published in <em>Blood</em>. Dr. Muczynski's research asks if there could there be a better gene than the factor VIII (FVIII) gene to transfer for curative treatment of hemophilia A? Dr. Geyer then explores CAR T cells armed with interleukin-18 (IL-18) secretion that target CD371, a transmembrane glycoprotein with high expression on AML and leukemia-initiating cells. Both studies explore finding novel targets for these powerful treatment modalities. </p><p><br>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027709">Alternative AAV gene therapy for hemophilia A using expression of Bi8, a novel single-chain FVIII-mimetic antibody</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025029532">CD371-targeted CAR T cells secreting interleukin-18 exhibit robust expansion and clear refractory acute myeloid leukemia</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, <em>Blood </em>editor Dr. James Griffin interviews authors Drs. Vincent Muczynski and Mark Geyer on their latest research published in <em>Blood</em>. Dr. Muczynski's research asks if there could there be a better gene than the factor VIII (FVIII) gene to transfer for curative treatment of hemophilia A? Dr. Geyer then explores CAR T cells armed with interleukin-18 (IL-18) secretion that target CD371, a transmembrane glycoprotein with high expression on AML and leukemia-initiating cells. Both studies explore finding novel targets for these powerful treatment modalities. </p><p><br>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027709">Alternative AAV gene therapy for hemophilia A using expression of Bi8, a novel single-chain FVIII-mimetic antibody</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025029532">CD371-targeted CAR T cells secreting interleukin-18 exhibit robust expansion and clear refractory acute myeloid leukemia</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 25 Dec 2025 12:00:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/25be2371/4fbb3e03.mp3" length="28467665" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1422</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, <em>Blood </em>editor Dr. James Griffin interviews authors Drs. Vincent Muczynski and Mark Geyer on their latest research published in <em>Blood</em>. Dr. Muczynski's research asks if there could there be a better gene than the factor VIII (FVIII) gene to transfer for curative treatment of hemophilia A? Dr. Geyer then explores CAR T cells armed with interleukin-18 (IL-18) secretion that target CD371, a transmembrane glycoprotein with high expression on AML and leukemia-initiating cells. Both studies explore finding novel targets for these powerful treatment modalities. </p><p><br>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027709">Alternative AAV gene therapy for hemophilia A using expression of Bi8, a novel single-chain FVIII-mimetic antibody</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025029532">CD371-targeted CAR T cells secreting interleukin-18 exhibit robust expansion and clear refractory acute myeloid leukemia</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3matavytags2w"/>
    </item>
    <item>
      <title>Novel Differentiation Therapies for AML and Prognostic Value of PET in MM</title>
      <itunes:season>10</itunes:season>
      <podcast:season>10</podcast:season>
      <itunes:title>Novel Differentiation Therapies for AML and Prognostic Value of PET in MM</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
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      <link>https://share.transistor.fm/s/749211ae</link>
      <description>
        <![CDATA[<p>In this week's episode, <em>Blood </em>editor Dr. Laurie Sehn interviews three of the latest <em>Blood </em>authors: Drs. Vijay Sankaran, Ruud Delwel, Françoise Kraeber-Bodere. Two studies on the MECOM gene have been paired in this episode, analyzing new groundwork for potential novel myeloid differentiation therapies via repression of MECOM restoring enhancer mediated <em>CEBPA </em>expression. We'll also hear about the results of CASSIOPET, imaging companion study of the CASSIOPEIA trial, and how achieving negativity in PET before starting maintenance therapy is significant even in patients who still show residual disease in the bone marrow.</p><p>Featured Articles</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025028954">CEBPA repression by MECOM blocks differentiation to drive aggressive leukemias</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025028914">MECOM is a master repressor of myeloid differentiation through dose control of CEBPA in acute myeloid leukemia </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025030084">Prognostic value of premaintenance FDG PET/CT response in patients with newly diagnosed from the CASSIOPEIA trial</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, <em>Blood </em>editor Dr. Laurie Sehn interviews three of the latest <em>Blood </em>authors: Drs. Vijay Sankaran, Ruud Delwel, Françoise Kraeber-Bodere. Two studies on the MECOM gene have been paired in this episode, analyzing new groundwork for potential novel myeloid differentiation therapies via repression of MECOM restoring enhancer mediated <em>CEBPA </em>expression. We'll also hear about the results of CASSIOPET, imaging companion study of the CASSIOPEIA trial, and how achieving negativity in PET before starting maintenance therapy is significant even in patients who still show residual disease in the bone marrow.</p><p>Featured Articles</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025028954">CEBPA repression by MECOM blocks differentiation to drive aggressive leukemias</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025028914">MECOM is a master repressor of myeloid differentiation through dose control of CEBPA in acute myeloid leukemia </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025030084">Prognostic value of premaintenance FDG PET/CT response in patients with newly diagnosed from the CASSIOPEIA trial</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 18 Dec 2025 12:00:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/749211ae/8a1e1e16.mp3" length="23871690" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1192</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, <em>Blood </em>editor Dr. Laurie Sehn interviews three of the latest <em>Blood </em>authors: Drs. Vijay Sankaran, Ruud Delwel, Françoise Kraeber-Bodere. Two studies on the MECOM gene have been paired in this episode, analyzing new groundwork for potential novel myeloid differentiation therapies via repression of MECOM restoring enhancer mediated <em>CEBPA </em>expression. We'll also hear about the results of CASSIOPET, imaging companion study of the CASSIOPEIA trial, and how achieving negativity in PET before starting maintenance therapy is significant even in patients who still show residual disease in the bone marrow.</p><p>Featured Articles</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025028954">CEBPA repression by MECOM blocks differentiation to drive aggressive leukemias</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025028914">MECOM is a master repressor of myeloid differentiation through dose control of CEBPA in acute myeloid leukemia </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025030084">Prognostic value of premaintenance FDG PET/CT response in patients with newly diagnosed from the CASSIOPEIA trial</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3mabnndkdo22l"/>
    </item>
    <item>
      <title>Review Series on Platelet Heterogeneity</title>
      <itunes:season>10</itunes:season>
      <podcast:season>10</podcast:season>
      <itunes:title>Review Series on Platelet Heterogeneity</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
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      <link>https://share.transistor.fm/s/225eb97f</link>
      <description>
        <![CDATA[<p>In this Review Series episode, <em>Blood </em>Associate Editor, Dr. Elisabeth Battinelli discusses the Platelet Heterogeneity with authors Drs. Craig Morrell, Larry Frelinger, and Leo Nicolai.  </p><p><a href="https://ashpublications.org/blood/article/146/24/2847/556815/Introduction-to-a-review-series-on-platelet">Find the full review series in volume 146 issue 24 of <em>Blood</em>. </a></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this Review Series episode, <em>Blood </em>Associate Editor, Dr. Elisabeth Battinelli discusses the Platelet Heterogeneity with authors Drs. Craig Morrell, Larry Frelinger, and Leo Nicolai.  </p><p><a href="https://ashpublications.org/blood/article/146/24/2847/556815/Introduction-to-a-review-series-on-platelet">Find the full review series in volume 146 issue 24 of <em>Blood</em>. </a></p>]]>
      </content:encoded>
      <pubDate>Thu, 11 Dec 2025 12:00:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/225eb97f/09c66231.mp3" length="22821476" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/i3ZE9Fm8WHQTdjXXlCkQV8JDvgcchKDsV7-AHAk1VnE/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS83ODk4/YzQyM2QyMzFjMmM0/M2RlMzY0MzM2NDM1/YzU3MC5qcGc.jpg"/>
      <itunes:duration>1140</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this Review Series episode, <em>Blood </em>Associate Editor, Dr. Elisabeth Battinelli discusses the Platelet Heterogeneity with authors Drs. Craig Morrell, Larry Frelinger, and Leo Nicolai.  </p><p><a href="https://ashpublications.org/blood/article/146/24/2847/556815/Introduction-to-a-review-series-on-platelet">Find the full review series in volume 146 issue 24 of <em>Blood</em>. </a></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3m7q2ekbcul26"/>
    </item>
    <item>
      <title>Special Episode: Maternal Health in Hematology</title>
      <itunes:season>10</itunes:season>
      <podcast:season>10</podcast:season>
      <itunes:title>Special Episode: Maternal Health in Hematology</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">363f7038-dc4e-496f-b7d3-52de84284b9a</guid>
      <link>https://share.transistor.fm/s/0b114bcf</link>
      <description>
        <![CDATA[<p>In this special episode, <em>Blood </em>editor Dr. Laura Michaelis interviews Dr. Arielle Langer and Blood Associate editor Dr. Marc Blondon for this special Maternal Health episode. In honor of the second Maternal Health compendium, both discuss their papers featured in this special collection. </p><p>Featured Articles: </p><ul><li><a href="https://doi.org/10.1182/blood.2024026736">β-Thalassemia minor is associated with high rates of worsening anemia in pregnancy</a></li><li><a href="https://doi.org/10.1182/blood.2023021717">Longitudinal profile of estrogen-related thrombotic biomarkers after cessation of combined hormonal contraceptives</a></li></ul><p><a href="https://ashpublications.org/collection/42819/Maternal-Health-Compendium-2025">See the entire Maternal Health Compendium Second Edition</a></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this special episode, <em>Blood </em>editor Dr. Laura Michaelis interviews Dr. Arielle Langer and Blood Associate editor Dr. Marc Blondon for this special Maternal Health episode. In honor of the second Maternal Health compendium, both discuss their papers featured in this special collection. </p><p>Featured Articles: </p><ul><li><a href="https://doi.org/10.1182/blood.2024026736">β-Thalassemia minor is associated with high rates of worsening anemia in pregnancy</a></li><li><a href="https://doi.org/10.1182/blood.2023021717">Longitudinal profile of estrogen-related thrombotic biomarkers after cessation of combined hormonal contraceptives</a></li></ul><p><a href="https://ashpublications.org/collection/42819/Maternal-Health-Compendium-2025">See the entire Maternal Health Compendium Second Edition</a></p>]]>
      </content:encoded>
      <pubDate>Fri, 05 Dec 2025 18:08:38 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/0b114bcf/dcdb02ed.mp3" length="24968463" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1247</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this special episode, <em>Blood </em>editor Dr. Laura Michaelis interviews Dr. Arielle Langer and Blood Associate editor Dr. Marc Blondon for this special Maternal Health episode. In honor of the second Maternal Health compendium, both discuss their papers featured in this special collection. </p><p>Featured Articles: </p><ul><li><a href="https://doi.org/10.1182/blood.2024026736">β-Thalassemia minor is associated with high rates of worsening anemia in pregnancy</a></li><li><a href="https://doi.org/10.1182/blood.2023021717">Longitudinal profile of estrogen-related thrombotic biomarkers after cessation of combined hormonal contraceptives</a></li></ul><p><a href="https://ashpublications.org/collection/42819/Maternal-Health-Compendium-2025">See the entire Maternal Health Compendium Second Edition</a></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3m7bm5qvwws2l"/>
    </item>
    <item>
      <title>Analysis of IELSG37 Trial Results and PF4 in Stem Cell Aging</title>
      <itunes:season>10</itunes:season>
      <podcast:season>10</podcast:season>
      <itunes:title>Analysis of IELSG37 Trial Results and PF4 in Stem Cell Aging</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">39e77f7f-ad6c-410d-ba7b-253aaf2bb0d3</guid>
      <link>https://share.transistor.fm/s/52e2e68a</link>
      <description>
        <![CDATA[<p> In this week's episode, <em>Blood </em>editor Dr. James Griffin speaks with Drs. Emanuele Zucca and Sandra Pinho about their latest articles published in <em>Blood</em>. Dr. Zucca discusses his second analysis of the IELSG37 trial, where findings suggested that R-CHOP21 rituximab, cyclophosphamide,<br>doxorubicin, vincristine, and prednisone, administered every 21 days) may be a suboptimal frontline regimen for PMBCL. Dr. Pinho discusses the aging megakaryocytic niche and its influence on the age-associated decline in HSC and progenitor cell function. The authors demonstrate that remodeling of the megakaryocytic niche and associated platelet factor 4 (PF4) downregulation are central mechanisms driving HSC aging.</p><p>Featured Articles: </p><ul><li><a href="https://ashpublications.org/blood/article/146/23/2758/548472/Impact-of-immunochemotherapy-regimens-on-outcomes">Impact of immunochemotherapy regimens on outcomes of patients with primary mediastinal B-cell lymphoma in the IELSG37 trial </a></li><li><a href="https://ashpublications.org/blood/article/146/23/2765/548479/Platelet-factor-4-regulates-hematopoietic-stem">Platelet Factor 4 (PF4) Regulates Hematopoietic Stem Cell Aging</a> </li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p> In this week's episode, <em>Blood </em>editor Dr. James Griffin speaks with Drs. Emanuele Zucca and Sandra Pinho about their latest articles published in <em>Blood</em>. Dr. Zucca discusses his second analysis of the IELSG37 trial, where findings suggested that R-CHOP21 rituximab, cyclophosphamide,<br>doxorubicin, vincristine, and prednisone, administered every 21 days) may be a suboptimal frontline regimen for PMBCL. Dr. Pinho discusses the aging megakaryocytic niche and its influence on the age-associated decline in HSC and progenitor cell function. The authors demonstrate that remodeling of the megakaryocytic niche and associated platelet factor 4 (PF4) downregulation are central mechanisms driving HSC aging.</p><p>Featured Articles: </p><ul><li><a href="https://ashpublications.org/blood/article/146/23/2758/548472/Impact-of-immunochemotherapy-regimens-on-outcomes">Impact of immunochemotherapy regimens on outcomes of patients with primary mediastinal B-cell lymphoma in the IELSG37 trial </a></li><li><a href="https://ashpublications.org/blood/article/146/23/2765/548479/Platelet-factor-4-regulates-hematopoietic-stem">Platelet Factor 4 (PF4) Regulates Hematopoietic Stem Cell Aging</a> </li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 04 Dec 2025 12:00:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/52e2e68a/fc20cbe0.mp3" length="19513766" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>974</itunes:duration>
      <itunes:summary>
        <![CDATA[<p> In this week's episode, <em>Blood </em>editor Dr. James Griffin speaks with Drs. Emanuele Zucca and Sandra Pinho about their latest articles published in <em>Blood</em>. Dr. Zucca discusses his second analysis of the IELSG37 trial, where findings suggested that R-CHOP21 rituximab, cyclophosphamide,<br>doxorubicin, vincristine, and prednisone, administered every 21 days) may be a suboptimal frontline regimen for PMBCL. Dr. Pinho discusses the aging megakaryocytic niche and its influence on the age-associated decline in HSC and progenitor cell function. The authors demonstrate that remodeling of the megakaryocytic niche and associated platelet factor 4 (PF4) downregulation are central mechanisms driving HSC aging.</p><p>Featured Articles: </p><ul><li><a href="https://ashpublications.org/blood/article/146/23/2758/548472/Impact-of-immunochemotherapy-regimens-on-outcomes">Impact of immunochemotherapy regimens on outcomes of patients with primary mediastinal B-cell lymphoma in the IELSG37 trial </a></li><li><a href="https://ashpublications.org/blood/article/146/23/2765/548479/Platelet-factor-4-regulates-hematopoietic-stem">Platelet Factor 4 (PF4) Regulates Hematopoietic Stem Cell Aging</a> </li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3m76h4qycpx25"/>
    </item>
    <item>
      <title>Fixed-Duration Epcoritamab Combination Therapy for Relapsed or Refractory Follicular Lymphoma and Pre-Transplant Strategies for GVHD post-HSCT</title>
      <itunes:season>10</itunes:season>
      <podcast:season>10</podcast:season>
      <itunes:title>Fixed-Duration Epcoritamab Combination Therapy for Relapsed or Refractory Follicular Lymphoma and Pre-Transplant Strategies for GVHD post-HSCT</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">d0239572-ea14-4daa-ba82-b9ad68b13f72</guid>
      <link>https://share.transistor.fm/s/f44e8a53</link>
      <description>
        <![CDATA[<p>In this week's episode, <em>Blood </em>editor Dr. Laurie Sehn interviews authors Drs. Lorenzo Falchi and Robert Levy on their latest papers published in <em>Blood </em>Journal. Dr. Falchi discusses his work on an open-label, multicenter phase 1b/2 study evaluating fixed-duration epcoritamab with rituximab and lenalidomide in 108 patients with relapsed or refractory follicular lymphoma. Dr. Levy shares his work on demonstrating that in vivo expansion of Tregs in recipients prior to transplant is possible by activating TNFRSF25 (also known as death receptor 3) in combination with low-dose interleukin-2 in preclinical models. Both papers showed impressive and promising results for the treatment of lymphoma and GVHD.</p><p>Featured Articles</p><ul><li><a href="https://doi.org/10.1182/blood.2025029909">Fixed-Duration Epcoritamab Plus R2 Drives Favorable Outcomes in Relapsed or Refractory Follicular Lymphoma</a></li><li><a href="https://doi.org/10.1182/blood.2025028418">Pre-transplant targeting of TNFRSF25 and CD25 stimulates recipient Tregs in target tissues ameliorating GVHD post-HSCT</a></li></ul><p><br></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, <em>Blood </em>editor Dr. Laurie Sehn interviews authors Drs. Lorenzo Falchi and Robert Levy on their latest papers published in <em>Blood </em>Journal. Dr. Falchi discusses his work on an open-label, multicenter phase 1b/2 study evaluating fixed-duration epcoritamab with rituximab and lenalidomide in 108 patients with relapsed or refractory follicular lymphoma. Dr. Levy shares his work on demonstrating that in vivo expansion of Tregs in recipients prior to transplant is possible by activating TNFRSF25 (also known as death receptor 3) in combination with low-dose interleukin-2 in preclinical models. Both papers showed impressive and promising results for the treatment of lymphoma and GVHD.</p><p>Featured Articles</p><ul><li><a href="https://doi.org/10.1182/blood.2025029909">Fixed-Duration Epcoritamab Plus R2 Drives Favorable Outcomes in Relapsed or Refractory Follicular Lymphoma</a></li><li><a href="https://doi.org/10.1182/blood.2025028418">Pre-transplant targeting of TNFRSF25 and CD25 stimulates recipient Tregs in target tissues ameliorating GVHD post-HSCT</a></li></ul><p><br></p>]]>
      </content:encoded>
      <pubDate>Thu, 27 Nov 2025 12:00:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/f44e8a53/ef5e72cb.mp3" length="26438379" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1321</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, <em>Blood </em>editor Dr. Laurie Sehn interviews authors Drs. Lorenzo Falchi and Robert Levy on their latest papers published in <em>Blood </em>Journal. Dr. Falchi discusses his work on an open-label, multicenter phase 1b/2 study evaluating fixed-duration epcoritamab with rituximab and lenalidomide in 108 patients with relapsed or refractory follicular lymphoma. Dr. Levy shares his work on demonstrating that in vivo expansion of Tregs in recipients prior to transplant is possible by activating TNFRSF25 (also known as death receptor 3) in combination with low-dose interleukin-2 in preclinical models. Both papers showed impressive and promising results for the treatment of lymphoma and GVHD.</p><p>Featured Articles</p><ul><li><a href="https://doi.org/10.1182/blood.2025029909">Fixed-Duration Epcoritamab Plus R2 Drives Favorable Outcomes in Relapsed or Refractory Follicular Lymphoma</a></li><li><a href="https://doi.org/10.1182/blood.2025028418">Pre-transplant targeting of TNFRSF25 and CD25 stimulates recipient Tregs in target tissues ameliorating GVHD post-HSCT</a></li></ul><p><br></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3m6mtu3nthw2j"/>
    </item>
    <item>
      <title>Advancing Blood Disorder Treatments Through Precision Therapeutics</title>
      <itunes:season>10</itunes:season>
      <podcast:season>10</podcast:season>
      <itunes:title>Advancing Blood Disorder Treatments Through Precision Therapeutics</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
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      <link>https://share.transistor.fm/s/878dade1</link>
      <description>
        <![CDATA[<p>In this week's episode, <em>Blood </em>editor Dr. Laura Michaelis interviews authors Drs. Terri Parker and Peter Lenting on their latest papers published in <em>Blood </em>Journal. Dr. Lenting discusses his work on introducing a new therapeutic approach to von Willebrand disease with the development of a novel bispecific antibody (KB-V13A12) that links endogenous mouse VWF to albumin, extending VWF half-life twofold with cessation of provoked bleeding. Dr Parker shares the results of a 43-patient phase 2 study that evaluates the single agent isatuximab, a CD38 monoclonal antibody, in patients with relapsed/refractory AL amyloidosis. With a hematological response rate of 77%, organ response rates between 50 and 57%, and an excellent safety profile, the current study lays the foundation for future use of isatuximab across treatment settings and combination strategies.</p><p>Featured Articles</p><ul><li><a href="https://ashpublications.org/blood/article/146/21/2507/547199/Isatuximab-for-relapsed-and-or-refractory-AL">Isatuximab for Relapsed and/or Refractory AL Amyloidosis: Results of a Prospective Phase 2 Trial (SWOG S1702)</a></li><li><a href="https://ashpublications.org/blood/article/146/21/2597/547103/A-bispecific-nanobody-for-the-treatment-of-von">A bispecific nanobody for the treatment of von Willebrand disease type 1</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, <em>Blood </em>editor Dr. Laura Michaelis interviews authors Drs. Terri Parker and Peter Lenting on their latest papers published in <em>Blood </em>Journal. Dr. Lenting discusses his work on introducing a new therapeutic approach to von Willebrand disease with the development of a novel bispecific antibody (KB-V13A12) that links endogenous mouse VWF to albumin, extending VWF half-life twofold with cessation of provoked bleeding. Dr Parker shares the results of a 43-patient phase 2 study that evaluates the single agent isatuximab, a CD38 monoclonal antibody, in patients with relapsed/refractory AL amyloidosis. With a hematological response rate of 77%, organ response rates between 50 and 57%, and an excellent safety profile, the current study lays the foundation for future use of isatuximab across treatment settings and combination strategies.</p><p>Featured Articles</p><ul><li><a href="https://ashpublications.org/blood/article/146/21/2507/547199/Isatuximab-for-relapsed-and-or-refractory-AL">Isatuximab for Relapsed and/or Refractory AL Amyloidosis: Results of a Prospective Phase 2 Trial (SWOG S1702)</a></li><li><a href="https://ashpublications.org/blood/article/146/21/2597/547103/A-bispecific-nanobody-for-the-treatment-of-von">A bispecific nanobody for the treatment of von Willebrand disease type 1</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 20 Nov 2025 12:40:15 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/878dade1/aed5e9d6.mp3" length="18189983" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>908</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, <em>Blood </em>editor Dr. Laura Michaelis interviews authors Drs. Terri Parker and Peter Lenting on their latest papers published in <em>Blood </em>Journal. Dr. Lenting discusses his work on introducing a new therapeutic approach to von Willebrand disease with the development of a novel bispecific antibody (KB-V13A12) that links endogenous mouse VWF to albumin, extending VWF half-life twofold with cessation of provoked bleeding. Dr Parker shares the results of a 43-patient phase 2 study that evaluates the single agent isatuximab, a CD38 monoclonal antibody, in patients with relapsed/refractory AL amyloidosis. With a hematological response rate of 77%, organ response rates between 50 and 57%, and an excellent safety profile, the current study lays the foundation for future use of isatuximab across treatment settings and combination strategies.</p><p>Featured Articles</p><ul><li><a href="https://ashpublications.org/blood/article/146/21/2507/547199/Isatuximab-for-relapsed-and-or-refractory-AL">Isatuximab for Relapsed and/or Refractory AL Amyloidosis: Results of a Prospective Phase 2 Trial (SWOG S1702)</a></li><li><a href="https://ashpublications.org/blood/article/146/21/2597/547103/A-bispecific-nanobody-for-the-treatment-of-von">A bispecific nanobody for the treatment of von Willebrand disease type 1</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3m63ctm4zz525"/>
    </item>
    <item>
      <title>New Research: Mitochondrial DNA in TRALI and Venetoclax-Obinituzumab in CLL Trials</title>
      <itunes:season>10</itunes:season>
      <podcast:season>10</podcast:season>
      <itunes:title>New Research: Mitochondrial DNA in TRALI and Venetoclax-Obinituzumab in CLL Trials</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
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      <link>https://share.transistor.fm/s/00c6f013</link>
      <description>
        <![CDATA[<p>In this week's episode, associate editor Dr. James Griffin interviews researchers Dr. John Semple and Dr. Othman Al-Sawaf on their groundbreaking studies on transfusion-related acute lung injury and chronic lymphocytic leukemia treatment. Dr. Semple explored how mitochondrial DNA could act as a first hit in lung injury, while Dr. Al-Sawaf revealed that patient fitness may not significantly impact the efficacy of targeted CLL treatments. Both studies challenge existing medical assumptions and suggest new approaches to understanding disease mechanisms and treatment responses.</p><p>Featured Articles</p><ul><li><a href="https://ashpublications.org/blood/article/146/20/2406/548058/The-impact-of-fitness-and-dose-intensity-on">The impact of fitness and dose intensity on clinical outcomes with venetoclax-obinutuzumab in CLL</a></li><li><a href="https://ashpublications.org/blood/article/146/20/2479/548060/Mitochondrial-DNA-via-recipient-TLR9-acts-as-a">Mitochondrial DNA via recipient TLR9 acts as a potent first-hit in murine transfusion-related acute lung injury (TRALI)</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, associate editor Dr. James Griffin interviews researchers Dr. John Semple and Dr. Othman Al-Sawaf on their groundbreaking studies on transfusion-related acute lung injury and chronic lymphocytic leukemia treatment. Dr. Semple explored how mitochondrial DNA could act as a first hit in lung injury, while Dr. Al-Sawaf revealed that patient fitness may not significantly impact the efficacy of targeted CLL treatments. Both studies challenge existing medical assumptions and suggest new approaches to understanding disease mechanisms and treatment responses.</p><p>Featured Articles</p><ul><li><a href="https://ashpublications.org/blood/article/146/20/2406/548058/The-impact-of-fitness-and-dose-intensity-on">The impact of fitness and dose intensity on clinical outcomes with venetoclax-obinutuzumab in CLL</a></li><li><a href="https://ashpublications.org/blood/article/146/20/2479/548060/Mitochondrial-DNA-via-recipient-TLR9-acts-as-a">Mitochondrial DNA via recipient TLR9 acts as a potent first-hit in murine transfusion-related acute lung injury (TRALI)</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 13 Nov 2025 12:00:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/00c6f013/209bac38.mp3" length="22338639" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1116</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, associate editor Dr. James Griffin interviews researchers Dr. John Semple and Dr. Othman Al-Sawaf on their groundbreaking studies on transfusion-related acute lung injury and chronic lymphocytic leukemia treatment. Dr. Semple explored how mitochondrial DNA could act as a first hit in lung injury, while Dr. Al-Sawaf revealed that patient fitness may not significantly impact the efficacy of targeted CLL treatments. Both studies challenge existing medical assumptions and suggest new approaches to understanding disease mechanisms and treatment responses.</p><p>Featured Articles</p><ul><li><a href="https://ashpublications.org/blood/article/146/20/2406/548058/The-impact-of-fitness-and-dose-intensity-on">The impact of fitness and dose intensity on clinical outcomes with venetoclax-obinutuzumab in CLL</a></li><li><a href="https://ashpublications.org/blood/article/146/20/2479/548060/Mitochondrial-DNA-via-recipient-TLR9-acts-as-a">Mitochondrial DNA via recipient TLR9 acts as a potent first-hit in murine transfusion-related acute lung injury (TRALI)</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3m5jnde6beo2y"/>
    </item>
    <item>
      <title>Bispecific Antibodies in Aggressive B-Cell Lymphoma: Real-World Insights and Future Directions</title>
      <itunes:season>10</itunes:season>
      <podcast:season>10</podcast:season>
      <itunes:title>Bispecific Antibodies in Aggressive B-Cell Lymphoma: Real-World Insights and Future Directions</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
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      <link>https://share.transistor.fm/s/2a7d2c4a</link>
      <description>
        <![CDATA[<p>In this week's episode, <em>Blood </em>editor Dr. Laura Michaelis interviews author Dr. Taylor Brooks on his latest paper published in volume 146 issue 18 of <em>Blood</em> Journal. The conversation discusses outcomes of bispecific antibodies (epcoritamab or glofitamab) in treating aggressive B-cell lymphoma in a study with 245 patients. Findings show a tentative way forward in treatment for patients with relapsed or refractory (R/R) diffuse large B-cell lymphoma (DLBCL).</p><p>Featured Article:</p><ul><li><a href="https://ashpublications.org/blood/article/146/18/2177/546196/Real-world-outcomes-of-patients-with-aggressive-B?searchresult=1">Real-world outcomes of patients with aggressive B-cell lymphoma treated with epcoritamab or glofitamab</a></li></ul><p><br></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, <em>Blood </em>editor Dr. Laura Michaelis interviews author Dr. Taylor Brooks on his latest paper published in volume 146 issue 18 of <em>Blood</em> Journal. The conversation discusses outcomes of bispecific antibodies (epcoritamab or glofitamab) in treating aggressive B-cell lymphoma in a study with 245 patients. Findings show a tentative way forward in treatment for patients with relapsed or refractory (R/R) diffuse large B-cell lymphoma (DLBCL).</p><p>Featured Article:</p><ul><li><a href="https://ashpublications.org/blood/article/146/18/2177/546196/Real-world-outcomes-of-patients-with-aggressive-B?searchresult=1">Real-world outcomes of patients with aggressive B-cell lymphoma treated with epcoritamab or glofitamab</a></li></ul><p><br></p>]]>
      </content:encoded>
      <pubDate>Thu, 06 Nov 2025 14:29:21 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/2a7d2c4a/1f2b61fa.mp3" length="11546331" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>576</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, <em>Blood </em>editor Dr. Laura Michaelis interviews author Dr. Taylor Brooks on his latest paper published in volume 146 issue 18 of <em>Blood</em> Journal. The conversation discusses outcomes of bispecific antibodies (epcoritamab or glofitamab) in treating aggressive B-cell lymphoma in a study with 245 patients. Findings show a tentative way forward in treatment for patients with relapsed or refractory (R/R) diffuse large B-cell lymphoma (DLBCL).</p><p>Featured Article:</p><ul><li><a href="https://ashpublications.org/blood/article/146/18/2177/546196/Real-world-outcomes-of-patients-with-aggressive-B?searchresult=1">Real-world outcomes of patients with aggressive B-cell lymphoma treated with epcoritamab or glofitamab</a></li></ul><p><br></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3m4ycfjyfd42k"/>
    </item>
    <item>
      <title>Review Series on Follicular Lymphoma</title>
      <itunes:season>10</itunes:season>
      <podcast:season>10</podcast:season>
      <itunes:title>Review Series on Follicular Lymphoma</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
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      <link>https://share.transistor.fm/s/0d71c6ee</link>
      <description>
        <![CDATA[<p>In this Review Series episode, Associate Editor Dr. Philippe Armand speaks with multiple authors about what it might look like to improve treatments follicular lymphoma, a disease that has been put on the backburner of innovation due to its generally treatable nature. Dr. Armand discusses "<a href="https://ashpublications.org/blood/article/146/15/1782/546730/Treatment-of-relapsed-and-refractory-follicular">Treatment of relapsed and refractory follicular lymphoma: which treatment for which patient for which line of therapy?</a>" with author Dr. Carla Casulo,  "<a href="https://ashpublications.org/blood/article/146/15/1792/535794/The-future-of-follicular-lymphoma-management">The future of follicular lymphoma management: strategies on the horizon</a>” with author Dr. Sarah C. Rutherford, and "<a href="https://ashpublications.org/blood/article/146/15/1812/537307/An-updated-understanding-of-follicular-lymphoma">An updated understanding of follicular lymphoma transformation</a>” with Dr. Erin M. Parry.</p><p><a href="https://ashpublications.org/blood/article/146/15/1739/547574/Introduction-to-a-review-series-on-follicular?searchresult=1">Find the whole review series on follicular lymphoma in volume 146 issue 15 of <em>Blood </em>Journal.  </a></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this Review Series episode, Associate Editor Dr. Philippe Armand speaks with multiple authors about what it might look like to improve treatments follicular lymphoma, a disease that has been put on the backburner of innovation due to its generally treatable nature. Dr. Armand discusses "<a href="https://ashpublications.org/blood/article/146/15/1782/546730/Treatment-of-relapsed-and-refractory-follicular">Treatment of relapsed and refractory follicular lymphoma: which treatment for which patient for which line of therapy?</a>" with author Dr. Carla Casulo,  "<a href="https://ashpublications.org/blood/article/146/15/1792/535794/The-future-of-follicular-lymphoma-management">The future of follicular lymphoma management: strategies on the horizon</a>” with author Dr. Sarah C. Rutherford, and "<a href="https://ashpublications.org/blood/article/146/15/1812/537307/An-updated-understanding-of-follicular-lymphoma">An updated understanding of follicular lymphoma transformation</a>” with Dr. Erin M. Parry.</p><p><a href="https://ashpublications.org/blood/article/146/15/1739/547574/Introduction-to-a-review-series-on-follicular?searchresult=1">Find the whole review series on follicular lymphoma in volume 146 issue 15 of <em>Blood </em>Journal.  </a></p>]]>
      </content:encoded>
      <pubDate>Thu, 30 Oct 2025 12:11:45 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/0d71c6ee/81d5b27d.mp3" length="21186628" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/5EG85o31pqM3FDNxMeY1teL3_gixCwuQlR7ZcqXWbII/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS9hNDhj/MGNjYjhiN2ZlZWE5/ZmZmZjM2NmNiOTI0/NzI0Ny5qcGc.jpg"/>
      <itunes:duration>1058</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this Review Series episode, Associate Editor Dr. Philippe Armand speaks with multiple authors about what it might look like to improve treatments follicular lymphoma, a disease that has been put on the backburner of innovation due to its generally treatable nature. Dr. Armand discusses "<a href="https://ashpublications.org/blood/article/146/15/1782/546730/Treatment-of-relapsed-and-refractory-follicular">Treatment of relapsed and refractory follicular lymphoma: which treatment for which patient for which line of therapy?</a>" with author Dr. Carla Casulo,  "<a href="https://ashpublications.org/blood/article/146/15/1792/535794/The-future-of-follicular-lymphoma-management">The future of follicular lymphoma management: strategies on the horizon</a>” with author Dr. Sarah C. Rutherford, and "<a href="https://ashpublications.org/blood/article/146/15/1812/537307/An-updated-understanding-of-follicular-lymphoma">An updated understanding of follicular lymphoma transformation</a>” with Dr. Erin M. Parry.</p><p><a href="https://ashpublications.org/blood/article/146/15/1739/547574/Introduction-to-a-review-series-on-follicular?searchresult=1">Find the whole review series on follicular lymphoma in volume 146 issue 15 of <em>Blood </em>Journal.  </a></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3m4ge35plum2l"/>
    </item>
    <item>
      <title>Breakthroughs in Multiple Myeloma Treatment and Von Willebrand Disease Mechanisms</title>
      <itunes:season>10</itunes:season>
      <podcast:season>10</podcast:season>
      <itunes:title>Breakthroughs in Multiple Myeloma Treatment and Von Willebrand Disease Mechanisms</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
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      <link>https://share.transistor.fm/s/ba4aedec</link>
      <description>
        <![CDATA[<p>In this week's episode of the <em>Blood</em> Podcast, Associate Editor Dr. James Griffin interviews Drs. Binod Dhakal and Ruben Bierings about their respective papers published in this week's issue of <em>Blood</em>. Dr. Dhakal presents his study on using talquetamab, a bispecific antibody, as a bridging therapy before BCMA-targeted CAR T-cell therapy in multiple myeloma patients, showing promising results with high response rates and manageable toxicities. Next, Dr. Bierings identified patients with genetic variants in the guanine exchange factor MAP kinase–activating death domain (<em>MADD</em>) that impair VWF secretion from endothelial cells and possibly cause VWD type 1. </p><p>Featured Articles</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027935">A novel cause of type 1 von Willebrand disease: impaired exocytosis of Weibel-Palade bodies due to biallelic MADD variants</a><br>Sophie Hordijk, Stijn A. Groten, Petra E. Bürgisser, Sebastiaan N. J. Laan, Georg Christoph Korenke, Tomáš Honzík, Diane Beysen, Frank W. G. Leebeek, Paul A. Skehel, Maartje van den Biggelaar, Tom Carter, Ruben Bierings</li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025029773">Sequential targeting in multiple myeloma: talquetamab, a GPRC5D bispecific antibody, as a bridge to BCMA CAR-T therapy</a><br>Binod Dhakal, Othman S. Akhtar, David Fandrei, Alexandria Jensen, Rahul Banerjee, Darren Pan, Shambavi Richard, Reed Friend, Matthew Rees, Patrick Costello, Mariola Vazquez Martinez, Oren Pasvolsky, Charlotte Wagner, James A. Davis, Omar Castaneda Puglianini, Ran Reshef, Aimaz Afrough, Danai Dima, Manisha Bhutani, Omar Nadeem, Ricardo Parrondo, Ciara Freeman, Lekha Mikkilineni, Shahzad Raza, Larry D. Anderson Jr, Prashant Kapoor, Hitomi Hosoya, Saurabh Chhabra, Ariel Grajales-Cruz, Mahmoud Gaballa, Shonali Midha, Melissa Alsina, Douglas Sborov, Krina Patel, Yi Lin, Christopher Ferreri, Nico Gagelmann, Anupama Kumar, Doris Hansen, Andrew Cowan, Luciano J. Costa, Maximilian Merz, Surbhi Sidana</li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode of the <em>Blood</em> Podcast, Associate Editor Dr. James Griffin interviews Drs. Binod Dhakal and Ruben Bierings about their respective papers published in this week's issue of <em>Blood</em>. Dr. Dhakal presents his study on using talquetamab, a bispecific antibody, as a bridging therapy before BCMA-targeted CAR T-cell therapy in multiple myeloma patients, showing promising results with high response rates and manageable toxicities. Next, Dr. Bierings identified patients with genetic variants in the guanine exchange factor MAP kinase–activating death domain (<em>MADD</em>) that impair VWF secretion from endothelial cells and possibly cause VWD type 1. </p><p>Featured Articles</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027935">A novel cause of type 1 von Willebrand disease: impaired exocytosis of Weibel-Palade bodies due to biallelic MADD variants</a><br>Sophie Hordijk, Stijn A. Groten, Petra E. Bürgisser, Sebastiaan N. J. Laan, Georg Christoph Korenke, Tomáš Honzík, Diane Beysen, Frank W. G. Leebeek, Paul A. Skehel, Maartje van den Biggelaar, Tom Carter, Ruben Bierings</li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025029773">Sequential targeting in multiple myeloma: talquetamab, a GPRC5D bispecific antibody, as a bridge to BCMA CAR-T therapy</a><br>Binod Dhakal, Othman S. Akhtar, David Fandrei, Alexandria Jensen, Rahul Banerjee, Darren Pan, Shambavi Richard, Reed Friend, Matthew Rees, Patrick Costello, Mariola Vazquez Martinez, Oren Pasvolsky, Charlotte Wagner, James A. Davis, Omar Castaneda Puglianini, Ran Reshef, Aimaz Afrough, Danai Dima, Manisha Bhutani, Omar Nadeem, Ricardo Parrondo, Ciara Freeman, Lekha Mikkilineni, Shahzad Raza, Larry D. Anderson Jr, Prashant Kapoor, Hitomi Hosoya, Saurabh Chhabra, Ariel Grajales-Cruz, Mahmoud Gaballa, Shonali Midha, Melissa Alsina, Douglas Sborov, Krina Patel, Yi Lin, Christopher Ferreri, Nico Gagelmann, Anupama Kumar, Doris Hansen, Andrew Cowan, Luciano J. Costa, Maximilian Merz, Surbhi Sidana</li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 23 Oct 2025 12:43:16 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/ba4aedec/e2f1fa95.mp3" length="29042798" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1451</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode of the <em>Blood</em> Podcast, Associate Editor Dr. James Griffin interviews Drs. Binod Dhakal and Ruben Bierings about their respective papers published in this week's issue of <em>Blood</em>. Dr. Dhakal presents his study on using talquetamab, a bispecific antibody, as a bridging therapy before BCMA-targeted CAR T-cell therapy in multiple myeloma patients, showing promising results with high response rates and manageable toxicities. Next, Dr. Bierings identified patients with genetic variants in the guanine exchange factor MAP kinase–activating death domain (<em>MADD</em>) that impair VWF secretion from endothelial cells and possibly cause VWD type 1. </p><p>Featured Articles</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027935">A novel cause of type 1 von Willebrand disease: impaired exocytosis of Weibel-Palade bodies due to biallelic MADD variants</a><br>Sophie Hordijk, Stijn A. Groten, Petra E. Bürgisser, Sebastiaan N. J. Laan, Georg Christoph Korenke, Tomáš Honzík, Diane Beysen, Frank W. G. Leebeek, Paul A. Skehel, Maartje van den Biggelaar, Tom Carter, Ruben Bierings</li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025029773">Sequential targeting in multiple myeloma: talquetamab, a GPRC5D bispecific antibody, as a bridge to BCMA CAR-T therapy</a><br>Binod Dhakal, Othman S. Akhtar, David Fandrei, Alexandria Jensen, Rahul Banerjee, Darren Pan, Shambavi Richard, Reed Friend, Matthew Rees, Patrick Costello, Mariola Vazquez Martinez, Oren Pasvolsky, Charlotte Wagner, James A. Davis, Omar Castaneda Puglianini, Ran Reshef, Aimaz Afrough, Danai Dima, Manisha Bhutani, Omar Nadeem, Ricardo Parrondo, Ciara Freeman, Lekha Mikkilineni, Shahzad Raza, Larry D. Anderson Jr, Prashant Kapoor, Hitomi Hosoya, Saurabh Chhabra, Ariel Grajales-Cruz, Mahmoud Gaballa, Shonali Midha, Melissa Alsina, Douglas Sborov, Krina Patel, Yi Lin, Christopher Ferreri, Nico Gagelmann, Anupama Kumar, Doris Hansen, Andrew Cowan, Luciano J. Costa, Maximilian Merz, Surbhi Sidana</li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3m3uslblovh2l"/>
    </item>
    <item>
      <title>Spotlight on Acute Myeloid Leukemia</title>
      <itunes:season>10</itunes:season>
      <podcast:season>10</podcast:season>
      <itunes:title>Spotlight on Acute Myeloid Leukemia</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">73487d85-ad61-4b6e-9a62-e6eece21692e</guid>
      <link>https://share.transistor.fm/s/3db1ad88</link>
      <description>
        <![CDATA[<p>In this Spotlight series episode on Acute Myeloid Leukemia, <em>Blood </em>Editor, Dr. Selina Luger interviews Drs. Laura Michaelis and Alexander Perl on their paper in the series titled “<a href="https://ashpublications.org/blood/article/145/24/2840/535274/The-fit-older-adult-with-acute-myeloid-leukemia">The fit older adult with acute myeloid leukemia: clinical challenges to providing evidence-based frontline treatment</a>”. The conversation explores challenges in treating AML across different patient populations. They also focus on treatment approaches for fit older adults with AML, highlighting the need for less toxic therapies and ongoing randomized trials to better understand treatment efficacy. </p><p><a href="https://ashpublications.org/blood/article/145/24/2801/537608/Introduction-to-a-Blood-Spotlight-series-on-acute?searchresult=1">See the full spotlight series on Acute Myeloid Leukemia in Volume 145 Issue 24 of <em>Blood </em>journal. </a></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this Spotlight series episode on Acute Myeloid Leukemia, <em>Blood </em>Editor, Dr. Selina Luger interviews Drs. Laura Michaelis and Alexander Perl on their paper in the series titled “<a href="https://ashpublications.org/blood/article/145/24/2840/535274/The-fit-older-adult-with-acute-myeloid-leukemia">The fit older adult with acute myeloid leukemia: clinical challenges to providing evidence-based frontline treatment</a>”. The conversation explores challenges in treating AML across different patient populations. They also focus on treatment approaches for fit older adults with AML, highlighting the need for less toxic therapies and ongoing randomized trials to better understand treatment efficacy. </p><p><a href="https://ashpublications.org/blood/article/145/24/2801/537608/Introduction-to-a-Blood-Spotlight-series-on-acute?searchresult=1">See the full spotlight series on Acute Myeloid Leukemia in Volume 145 Issue 24 of <em>Blood </em>journal. </a></p>]]>
      </content:encoded>
      <pubDate>Thu, 16 Oct 2025 12:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/3db1ad88/fb78d7e3.mp3" length="26015390" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/x2wehtfRwlYAfqetq0Jc_pOWKVZBj3SLrn2CgbZjTNc/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS85MTA1/YzI1M2Y1ODNjMGZk/NjdjMjlmM2IyNDNl/YmQ3Zi5wbmc.jpg"/>
      <itunes:duration>1299</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this Spotlight series episode on Acute Myeloid Leukemia, <em>Blood </em>Editor, Dr. Selina Luger interviews Drs. Laura Michaelis and Alexander Perl on their paper in the series titled “<a href="https://ashpublications.org/blood/article/145/24/2840/535274/The-fit-older-adult-with-acute-myeloid-leukemia">The fit older adult with acute myeloid leukemia: clinical challenges to providing evidence-based frontline treatment</a>”. The conversation explores challenges in treating AML across different patient populations. They also focus on treatment approaches for fit older adults with AML, highlighting the need for less toxic therapies and ongoing randomized trials to better understand treatment efficacy. </p><p><a href="https://ashpublications.org/blood/article/145/24/2801/537608/Introduction-to-a-Blood-Spotlight-series-on-acute?searchresult=1">See the full spotlight series on Acute Myeloid Leukemia in Volume 145 Issue 24 of <em>Blood </em>journal. </a></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3m3d4wsquex22"/>
    </item>
    <item>
      <title>Busulfan-melphalan conditioning in newly diagnosed, transplant-eligible multiple myeloma; and use of spatial transcriptomics to probe the three-dimensional properties of multiple myeloma bone marrow microenvironments</title>
      <itunes:season>10</itunes:season>
      <podcast:season>10</podcast:season>
      <itunes:title>Busulfan-melphalan conditioning in newly diagnosed, transplant-eligible multiple myeloma; and use of spatial transcriptomics to probe the three-dimensional properties of multiple myeloma bone marrow microenvironments</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">07b1df34-6ab8-4021-bead-dd10e50048be</guid>
      <link>https://share.transistor.fm/s/b25f032b</link>
      <description>
        <![CDATA[<p>In this week's episode we’ll learn more about a study comparing busulfan-melphalan with melphalan alone as the conditioning protocol for newly diagnosed, transplant-eligible multiple myeloma; then we will discuss data on how three-dimensional transcriptomics can reveal complex interactions between plasma cells and bone marrow microenvironments.</p><p>Featured Articles</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025028313">High-dose busulfan-melphalan vs melphalan and reinforced VRD for newly diagnosed multiple myeloma: a phase 3 GEM trial</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025028896">Profiling the spatial architecture of multiple myeloma in human bone marrow trephine biopsy specimens with spatial transcriptomics</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025028863">Preclinical advances in glofitamab combinations: a new frontier for non-Hodgkin lymphoma</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we’ll learn more about a study comparing busulfan-melphalan with melphalan alone as the conditioning protocol for newly diagnosed, transplant-eligible multiple myeloma; then we will discuss data on how three-dimensional transcriptomics can reveal complex interactions between plasma cells and bone marrow microenvironments.</p><p>Featured Articles</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025028313">High-dose busulfan-melphalan vs melphalan and reinforced VRD for newly diagnosed multiple myeloma: a phase 3 GEM trial</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025028896">Profiling the spatial architecture of multiple myeloma in human bone marrow trephine biopsy specimens with spatial transcriptomics</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025028863">Preclinical advances in glofitamab combinations: a new frontier for non-Hodgkin lymphoma</a></li></ul>]]>
      </content:encoded>
      <pubDate>Tue, 14 Oct 2025 17:55:33 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/b25f032b/ef025b7e.mp3" length="15880716" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>793</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we’ll learn more about a study comparing busulfan-melphalan with melphalan alone as the conditioning protocol for newly diagnosed, transplant-eligible multiple myeloma; then we will discuss data on how three-dimensional transcriptomics can reveal complex interactions between plasma cells and bone marrow microenvironments.</p><p>Featured Articles</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025028313">High-dose busulfan-melphalan vs melphalan and reinforced VRD for newly diagnosed multiple myeloma: a phase 3 GEM trial</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025028896">Profiling the spatial architecture of multiple myeloma in human bone marrow trephine biopsy specimens with spatial transcriptomics</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025028863">Preclinical advances in glofitamab combinations: a new frontier for non-Hodgkin lymphoma</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3m36ptbp3wj2s"/>
    </item>
    <item>
      <title>How I Treat Wiskott-Alrich syndrome</title>
      <itunes:season>10</itunes:season>
      <podcast:season>10</podcast:season>
      <itunes:title>How I Treat Wiskott-Alrich syndrome</itunes:title>
      <itunes:episodeType>bonus</itunes:episodeType>
      <guid isPermaLink="false">a766a521-6b28-4c97-980a-f955308915bd</guid>
      <link>https://share.transistor.fm/s/172b64c6</link>
      <description>
        <![CDATA[<p>In this How I Treat podcast episode, Laura Michaelis, MD interviews Sung-Yun Pai, MD about their recently published article in <em>Blood</em> journal "<a href="https://ashpublications.org/blood/article/146/1/41/536678/How-I-treat-Wiskott-Aldrich-syndrome">How I treat Wiskott-Alrich syndrome</a>". They highlight recent updates in treatment, including new risk-benefit calculations due to safer treatments and longer follow-ups. Challenges include late diagnosis, lack of well-matched donors, and limited gene therapy availability. They emphasize the importance of early referral to specialized centers and the need for discussions about curative intent therapies, including transplant and gene therapy. The conversation also covers the complexities of gene therapy, such as the need for better conditioning agents and the challenges of achieving full correction in all cell types.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this How I Treat podcast episode, Laura Michaelis, MD interviews Sung-Yun Pai, MD about their recently published article in <em>Blood</em> journal "<a href="https://ashpublications.org/blood/article/146/1/41/536678/How-I-treat-Wiskott-Aldrich-syndrome">How I treat Wiskott-Alrich syndrome</a>". They highlight recent updates in treatment, including new risk-benefit calculations due to safer treatments and longer follow-ups. Challenges include late diagnosis, lack of well-matched donors, and limited gene therapy availability. They emphasize the importance of early referral to specialized centers and the need for discussions about curative intent therapies, including transplant and gene therapy. The conversation also covers the complexities of gene therapy, such as the need for better conditioning agents and the challenges of achieving full correction in all cell types.</p>]]>
      </content:encoded>
      <pubDate>Thu, 02 Oct 2025 12:15:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/172b64c6/40a47b6c.mp3" length="15955524" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/J6qL_nDN2G1U_Tj3m6spKsIEyEc4EsaYaK3tRtwp3Vs/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS8wOGY2/MjFiZTc3ZTdkYzVm/M2FjMDg0MzlhOGVk/M2U3ZC5qcGc.jpg"/>
      <itunes:duration>796</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this How I Treat podcast episode, Laura Michaelis, MD interviews Sung-Yun Pai, MD about their recently published article in <em>Blood</em> journal "<a href="https://ashpublications.org/blood/article/146/1/41/536678/How-I-treat-Wiskott-Aldrich-syndrome">How I treat Wiskott-Alrich syndrome</a>". They highlight recent updates in treatment, including new risk-benefit calculations due to safer treatments and longer follow-ups. Challenges include late diagnosis, lack of well-matched donors, and limited gene therapy availability. They emphasize the importance of early referral to specialized centers and the need for discussions about curative intent therapies, including transplant and gene therapy. The conversation also covers the complexities of gene therapy, such as the need for better conditioning agents and the challenges of achieving full correction in all cell types.</p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3m27x7lle2j2y"/>
    </item>
    <item>
      <title>Use of Marstacimab for Prophylaxis in hemophilia A and B; matched-donor allogeneic CD19 CAR-T in adult B-ALL; a new prognostic index for T-cell cutaneous lymphomas</title>
      <itunes:season>10</itunes:season>
      <podcast:season>10</podcast:season>
      <itunes:title>Use of Marstacimab for Prophylaxis in hemophilia A and B; matched-donor allogeneic CD19 CAR-T in adult B-ALL; a new prognostic index for T-cell cutaneous lymphomas</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">b4f4ed7a-2461-413f-80c0-cc5fdedea644</guid>
      <link>https://share.transistor.fm/s/b899e46c</link>
      <description>
        <![CDATA[<p>In this week's episode we'll learn about targeting the tissue factor pathway inhibitor with a monoclonal antibody to rebalance HEMOSTASIS in hemophilia A and B. In the phase 3 BASIS trial, the monoclonal antibody marstacimab reduced bleeding events, and was generally well tolerated, with no unanticipated side effects. After that: matched-donor allogeneic CD19 CAR-T for adult B-ALL. Given after allogeneic transplantation, CAR-donor lymphocyte infusion after lymphodepleting chemotherapy was associated with favorable efficacy and a tolerable safety profile. Finally: a new prognostic index for mycosis fungoides and Sézary syndrome. Comprised of four prognostic factors, the “CLIPI” could enable more personalized treatment of cutaneous lymphomas, identifying patients who may benefit from intensified treatment.</p><p>Featured Articles</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027468">Marstacimab prophylaxis in hemophilia A/B without inhibitors: results from the phase 3 BASIS trial</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025028790">Matched donor allogeneic CAR-T for adult B-ALL: toxicity, efficacy, repeat dosing, and the importance of lymphodepletion</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025029628">A new prognostic index (CLIPI) for advanced cutaneous lymphoma enables precise patient risk stratification</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we'll learn about targeting the tissue factor pathway inhibitor with a monoclonal antibody to rebalance HEMOSTASIS in hemophilia A and B. In the phase 3 BASIS trial, the monoclonal antibody marstacimab reduced bleeding events, and was generally well tolerated, with no unanticipated side effects. After that: matched-donor allogeneic CD19 CAR-T for adult B-ALL. Given after allogeneic transplantation, CAR-donor lymphocyte infusion after lymphodepleting chemotherapy was associated with favorable efficacy and a tolerable safety profile. Finally: a new prognostic index for mycosis fungoides and Sézary syndrome. Comprised of four prognostic factors, the “CLIPI” could enable more personalized treatment of cutaneous lymphomas, identifying patients who may benefit from intensified treatment.</p><p>Featured Articles</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027468">Marstacimab prophylaxis in hemophilia A/B without inhibitors: results from the phase 3 BASIS trial</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025028790">Matched donor allogeneic CAR-T for adult B-ALL: toxicity, efficacy, repeat dosing, and the importance of lymphodepletion</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025029628">A new prognostic index (CLIPI) for advanced cutaneous lymphoma enables precise patient risk stratification</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 02 Oct 2025 12:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/b899e46c/0e37a04f.mp3" length="23684483" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1183</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we'll learn about targeting the tissue factor pathway inhibitor with a monoclonal antibody to rebalance HEMOSTASIS in hemophilia A and B. In the phase 3 BASIS trial, the monoclonal antibody marstacimab reduced bleeding events, and was generally well tolerated, with no unanticipated side effects. After that: matched-donor allogeneic CD19 CAR-T for adult B-ALL. Given after allogeneic transplantation, CAR-donor lymphocyte infusion after lymphodepleting chemotherapy was associated with favorable efficacy and a tolerable safety profile. Finally: a new prognostic index for mycosis fungoides and Sézary syndrome. Comprised of four prognostic factors, the “CLIPI” could enable more personalized treatment of cutaneous lymphomas, identifying patients who may benefit from intensified treatment.</p><p>Featured Articles</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027468">Marstacimab prophylaxis in hemophilia A/B without inhibitors: results from the phase 3 BASIS trial</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025028790">Matched donor allogeneic CAR-T for adult B-ALL: toxicity, efficacy, repeat dosing, and the importance of lymphodepletion</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025029628">A new prognostic index (CLIPI) for advanced cutaneous lymphoma enables precise patient risk stratification</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3m27wewoujx27"/>
    </item>
    <item>
      <title>Epstein-Barr virus genomic variants in human disease states, somatic GATA1 mutations and leukemia in Down syndrome, and new definitions for high-risk multiple myeloma</title>
      <itunes:season>10</itunes:season>
      <podcast:season>10</podcast:season>
      <itunes:title>Epstein-Barr virus genomic variants in human disease states, somatic GATA1 mutations and leukemia in Down syndrome, and new definitions for high-risk multiple myeloma</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">71f43fda-4b8d-4124-9753-31859999b19c</guid>
      <link>https://share.transistor.fm/s/95325add</link>
      <description>
        <![CDATA[<p>In this week's episode, we’ll learn more about relationships between Epstein-Barr virus genomic variants and human diseases, including hematological malignancies; the presence and timing of somatic GATA1 mutations and their relationship to a Down syndrome-specific form of leukemia; and new definitions for high-risk multiple myeloma that emphasize the presence of two or more high-risk cytogenetic abnormalities.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024028055">Association of Epstein-Barr virus genomic alterations with human pathologies</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025029250">Clinical significance of preleukemic somatic GATA1 mutations in children with Down syndrome</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024028107">Biallelic antigen escape is a mechanism of resistance to anti-CD38 antibodies in multiple myeloma</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, we’ll learn more about relationships between Epstein-Barr virus genomic variants and human diseases, including hematological malignancies; the presence and timing of somatic GATA1 mutations and their relationship to a Down syndrome-specific form of leukemia; and new definitions for high-risk multiple myeloma that emphasize the presence of two or more high-risk cytogenetic abnormalities.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024028055">Association of Epstein-Barr virus genomic alterations with human pathologies</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025029250">Clinical significance of preleukemic somatic GATA1 mutations in children with Down syndrome</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024028107">Biallelic antigen escape is a mechanism of resistance to anti-CD38 antibodies in multiple myeloma</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 25 Sep 2025 12:06:34 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/95325add/cfd648e5.mp3" length="21639098" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1081</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, we’ll learn more about relationships between Epstein-Barr virus genomic variants and human diseases, including hematological malignancies; the presence and timing of somatic GATA1 mutations and their relationship to a Down syndrome-specific form of leukemia; and new definitions for high-risk multiple myeloma that emphasize the presence of two or more high-risk cytogenetic abnormalities.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024028055">Association of Epstein-Barr virus genomic alterations with human pathologies</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025029250">Clinical significance of preleukemic somatic GATA1 mutations in children with Down syndrome</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024028107">Biallelic antigen escape is a mechanism of resistance to anti-CD38 antibodies in multiple myeloma</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3lzodik6xn42q"/>
    </item>
    <item>
      <title>Review Series on Acute Lymphoblastic Leukemia (ALL)</title>
      <itunes:season>10</itunes:season>
      <podcast:season>10</podcast:season>
      <itunes:title>Review Series on Acute Lymphoblastic Leukemia (ALL)</itunes:title>
      <itunes:episodeType>bonus</itunes:episodeType>
      <guid isPermaLink="false">e8920ea6-fd50-4a45-a0bd-23c26f513938</guid>
      <link>https://share.transistor.fm/s/196648ea</link>
      <description>
        <![CDATA[<p>In this Review Series episode, Associate Editor Dr. Hervé Dombret speaks with Dr. Mark Litzow about the latest immunotherapy advances for Acute Lymphoblastic Leukemia (ALL). The discussion highlights innovative treatments like blinatumomab and inotuzumab, which are showing remarkable success in clinical trials, including an 85% three-year survival rate and over 90% complete remission in elderly patients. Researchers are focusing on reducing chemotherapy intensity, developing personalized treatment approaches, and identifying optimal immunotherapy strategies for different ALL subtypes. The conversation underscores a promising shift towards more targeted, less toxic treatments that could significantly improve patient outcomes across various age groups and disease characteristics. These emerging therapies represent a potential paradigm shift in ALL treatment, offering hope for more effective and less aggressive therapeutic interventions.</p><p><a href="https://ashpublications.org/blood/article/145/14/1475/517665/Incorporation-of-immunotherapy-into-frontline">Read Dr. Litzow's paper “Incorporation of immunotherapy into frontline treatment for adults with B-cell precursor acute lymphoblastic leukemia”</a> <strong>or</strong> <a href="https://ashpublications.org/blood/article/145/14/1439/536403/Introduction-to-a-review-series-on-acute?searchresult=1">find the whole review series on acute lymphoblastic leukemia in volume 145 issue 14 of <em>Blood Journal</em>. </a></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this Review Series episode, Associate Editor Dr. Hervé Dombret speaks with Dr. Mark Litzow about the latest immunotherapy advances for Acute Lymphoblastic Leukemia (ALL). The discussion highlights innovative treatments like blinatumomab and inotuzumab, which are showing remarkable success in clinical trials, including an 85% three-year survival rate and over 90% complete remission in elderly patients. Researchers are focusing on reducing chemotherapy intensity, developing personalized treatment approaches, and identifying optimal immunotherapy strategies for different ALL subtypes. The conversation underscores a promising shift towards more targeted, less toxic treatments that could significantly improve patient outcomes across various age groups and disease characteristics. These emerging therapies represent a potential paradigm shift in ALL treatment, offering hope for more effective and less aggressive therapeutic interventions.</p><p><a href="https://ashpublications.org/blood/article/145/14/1475/517665/Incorporation-of-immunotherapy-into-frontline">Read Dr. Litzow's paper “Incorporation of immunotherapy into frontline treatment for adults with B-cell precursor acute lymphoblastic leukemia”</a> <strong>or</strong> <a href="https://ashpublications.org/blood/article/145/14/1439/536403/Introduction-to-a-review-series-on-acute?searchresult=1">find the whole review series on acute lymphoblastic leukemia in volume 145 issue 14 of <em>Blood Journal</em>. </a></p>]]>
      </content:encoded>
      <pubDate>Thu, 18 Sep 2025 12:15:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/196648ea/1a121aeb.mp3" length="15178928" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/owrkFvlg03toGvuSFKnmSnwFdN-aOciqjtVGiNIwUko/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS9hOGE2/NTI1M2ZiOTFjODlk/YzQ2MGZjNzk0MmU1/YTVhNS5qcGc.jpg"/>
      <itunes:duration>758</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this Review Series episode, Associate Editor Dr. Hervé Dombret speaks with Dr. Mark Litzow about the latest immunotherapy advances for Acute Lymphoblastic Leukemia (ALL). The discussion highlights innovative treatments like blinatumomab and inotuzumab, which are showing remarkable success in clinical trials, including an 85% three-year survival rate and over 90% complete remission in elderly patients. Researchers are focusing on reducing chemotherapy intensity, developing personalized treatment approaches, and identifying optimal immunotherapy strategies for different ALL subtypes. The conversation underscores a promising shift towards more targeted, less toxic treatments that could significantly improve patient outcomes across various age groups and disease characteristics. These emerging therapies represent a potential paradigm shift in ALL treatment, offering hope for more effective and less aggressive therapeutic interventions.</p><p><a href="https://ashpublications.org/blood/article/145/14/1475/517665/Incorporation-of-immunotherapy-into-frontline">Read Dr. Litzow's paper “Incorporation of immunotherapy into frontline treatment for adults with B-cell precursor acute lymphoblastic leukemia”</a> <strong>or</strong> <a href="https://ashpublications.org/blood/article/145/14/1439/536403/Introduction-to-a-review-series-on-acute?searchresult=1">find the whole review series on acute lymphoblastic leukemia in volume 145 issue 14 of <em>Blood Journal</em>. </a></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3lz4qovb6ig24"/>
    </item>
    <item>
      <title>Azacitidine holds promise in VEXAS syndrome; a step forward in precision blood matching; identifying a new vulnerability in TP53-mutated AML</title>
      <itunes:season>10</itunes:season>
      <podcast:season>10</podcast:season>
      <itunes:title>Azacitidine holds promise in VEXAS syndrome; a step forward in precision blood matching; identifying a new vulnerability in TP53-mutated AML</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">d2e02661-a058-4bce-acd2-45e47ea3de26</guid>
      <link>https://share.transistor.fm/s/4fe28b82</link>
      <description>
        <![CDATA[<p>In this week's episode we'll learn about Azacitidine in VEXAS syndrome. Treatment can provide responses in patients with this complex autoinflammatory disorder. But relapse rates were high, so long-term therapy may be required to maintain disease control. After that: A step forward in precision blood matching. High-throughput array genotyping enables extended matching to reduce antibody formation. The results show the potential for reducing harm in regularly transfused patients. Finally, identifying a new vulnerability in TP53-mutated AML. Loss of the tumor suppressor BAP1 defines a unique subtype of TP53-mutated de novo AML. BAP1 loss also confers sensitivity to BCL-xL inhibitors in vivo, opening a new therapeutic avenue.</p><p>Featured Articles</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024028133">Efficacy and safety of azacitidine for VEXAS syndrome: a large-scale retrospective study from FRENVEX</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025028902">Array genotyping of transfusion-relevant blood cell antigens in 6946 ancestrally diverse study participants</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026417">Loss of <em>BAP1 </em>defines a unique subtype of <em>TP53</em>-mutated de novo AML and confers sensitivity to BCL-xL inhibitors</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we'll learn about Azacitidine in VEXAS syndrome. Treatment can provide responses in patients with this complex autoinflammatory disorder. But relapse rates were high, so long-term therapy may be required to maintain disease control. After that: A step forward in precision blood matching. High-throughput array genotyping enables extended matching to reduce antibody formation. The results show the potential for reducing harm in regularly transfused patients. Finally, identifying a new vulnerability in TP53-mutated AML. Loss of the tumor suppressor BAP1 defines a unique subtype of TP53-mutated de novo AML. BAP1 loss also confers sensitivity to BCL-xL inhibitors in vivo, opening a new therapeutic avenue.</p><p>Featured Articles</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024028133">Efficacy and safety of azacitidine for VEXAS syndrome: a large-scale retrospective study from FRENVEX</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025028902">Array genotyping of transfusion-relevant blood cell antigens in 6946 ancestrally diverse study participants</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026417">Loss of <em>BAP1 </em>defines a unique subtype of <em>TP53</em>-mutated de novo AML and confers sensitivity to BCL-xL inhibitors</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 18 Sep 2025 12:01:51 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/4fe28b82/a606f83a.mp3" length="22780623" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1138</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we'll learn about Azacitidine in VEXAS syndrome. Treatment can provide responses in patients with this complex autoinflammatory disorder. But relapse rates were high, so long-term therapy may be required to maintain disease control. After that: A step forward in precision blood matching. High-throughput array genotyping enables extended matching to reduce antibody formation. The results show the potential for reducing harm in regularly transfused patients. Finally, identifying a new vulnerability in TP53-mutated AML. Loss of the tumor suppressor BAP1 defines a unique subtype of TP53-mutated de novo AML. BAP1 loss also confers sensitivity to BCL-xL inhibitors in vivo, opening a new therapeutic avenue.</p><p>Featured Articles</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024028133">Efficacy and safety of azacitidine for VEXAS syndrome: a large-scale retrospective study from FRENVEX</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025028902">Array genotyping of transfusion-relevant blood cell antigens in 6946 ancestrally diverse study participants</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026417">Loss of <em>BAP1 </em>defines a unique subtype of <em>TP53</em>-mutated de novo AML and confers sensitivity to BCL-xL inhibitors</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3lz4px5wzhw24"/>
    </item>
    <item>
      <title>Diffuse large B-cell lymphoma’s long-term effects on immune profiles, plasminogen activation and prevention of venous thromboembolism, and PARP inhibitors in hematological malignancies carrying epigenetic mutations</title>
      <itunes:season>10</itunes:season>
      <podcast:season>10</podcast:season>
      <itunes:title>Diffuse large B-cell lymphoma’s long-term effects on immune profiles, plasminogen activation and prevention of venous thromboembolism, and PARP inhibitors in hematological malignancies carrying epigenetic mutations</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">d9abe608-79ef-4190-981c-f7f5055b2a7e</guid>
      <link>https://share.transistor.fm/s/c6c45a9a</link>
      <description>
        <![CDATA[<p>In this week's episode we'll learn about persistent changes in immune profiles in patients who have had diffuse large B-cell lymphoma, or DLBCL, and other cancers; that plasminogen activation and plasmin activity do not appear to play a role in routine physiological prevention of venous thromboembolism, or VTE; and about a novel mechanism that makes hematological malignancies carrying epigenetic mutations susceptible to PARP inhibitors.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027877">Large B-cell lymphoma imprints a dysfunctional immune phenotype that persists years after treatment</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025028680">Plasminogen activation and plasmin activity are not required to prevent venous thrombosis/thromboembolism</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025028560">Transposable elements as novel therapeutic targets for PARPi-induced synthetic lethality in PcG-mutated blood cancer</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we'll learn about persistent changes in immune profiles in patients who have had diffuse large B-cell lymphoma, or DLBCL, and other cancers; that plasminogen activation and plasmin activity do not appear to play a role in routine physiological prevention of venous thromboembolism, or VTE; and about a novel mechanism that makes hematological malignancies carrying epigenetic mutations susceptible to PARP inhibitors.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027877">Large B-cell lymphoma imprints a dysfunctional immune phenotype that persists years after treatment</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025028680">Plasminogen activation and plasmin activity are not required to prevent venous thrombosis/thromboembolism</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025028560">Transposable elements as novel therapeutic targets for PARPi-induced synthetic lethality in PcG-mutated blood cancer</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 11 Sep 2025 15:04:51 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/c6c45a9a/17076574.mp3" length="22244358" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1111</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we'll learn about persistent changes in immune profiles in patients who have had diffuse large B-cell lymphoma, or DLBCL, and other cancers; that plasminogen activation and plasmin activity do not appear to play a role in routine physiological prevention of venous thromboembolism, or VTE; and about a novel mechanism that makes hematological malignancies carrying epigenetic mutations susceptible to PARP inhibitors.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027877">Large B-cell lymphoma imprints a dysfunctional immune phenotype that persists years after treatment</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025028680">Plasminogen activation and plasmin activity are not required to prevent venous thrombosis/thromboembolism</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025028560">Transposable elements as novel therapeutic targets for PARPi-induced synthetic lethality in PcG-mutated blood cancer</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3lylgvrbrfq2o"/>
    </item>
    <item>
      <title>“Ironing out” Tet2-mutant HSPCs; A CAR-T “license to kill” in T cell leukemia/lymphoma; insights on cHL genetics, through the lens of ctDNA</title>
      <itunes:season>10</itunes:season>
      <podcast:season>10</podcast:season>
      <itunes:title>“Ironing out” Tet2-mutant HSPCs; A CAR-T “license to kill” in T cell leukemia/lymphoma; insights on cHL genetics, through the lens of ctDNA</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">9d285def-e324-479d-8bf6-9d52b13d79b7</guid>
      <link>https://share.transistor.fm/s/93fa5eac</link>
      <description>
        <![CDATA[<p>In this week's episode, we'll learn about how TET2 is often mutated in myeloid malignancies and clonal hematopoiesis. In new work, expansion of Tet2-mutant HSPCs was dependent on Ncoa4, the cargo receptor mediating ferritinophagy. We’ll iron out the implications. After that: a double-oh-seven license to kill in T-cell leukemia/lymphoma. WU-CART-007 is an off-the-shelf CAR T product with manageable safety and encouraging efficacy. With further work, it could become a new option for patients in urgent need of therapy. Finally: a comprehensive genetic study of classical Hodgkin lymphoma using circulating tumor DNA. This new research provides novel and complex insights on genetic subtypes, prognostic biomarkers, neoantigens in the disease environment, and more.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024028033">An in vivo barcoded CRISPR-Cas9 screen identifies <em>Ncoa4</em>-mediated ferritinophagy as a dependence in <em>Tet2</em>-deficient hematopoiesis</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025028387">Phase 1/2 trial of anti-CD7 allogeneic WU-CART-007 for patients with relapsed/refractory T-cell malignancies</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027355">A comprehensive genetic study of classic Hodgkin lymphoma using circulating tumor DNA</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, we'll learn about how TET2 is often mutated in myeloid malignancies and clonal hematopoiesis. In new work, expansion of Tet2-mutant HSPCs was dependent on Ncoa4, the cargo receptor mediating ferritinophagy. We’ll iron out the implications. After that: a double-oh-seven license to kill in T-cell leukemia/lymphoma. WU-CART-007 is an off-the-shelf CAR T product with manageable safety and encouraging efficacy. With further work, it could become a new option for patients in urgent need of therapy. Finally: a comprehensive genetic study of classical Hodgkin lymphoma using circulating tumor DNA. This new research provides novel and complex insights on genetic subtypes, prognostic biomarkers, neoantigens in the disease environment, and more.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024028033">An in vivo barcoded CRISPR-Cas9 screen identifies <em>Ncoa4</em>-mediated ferritinophagy as a dependence in <em>Tet2</em>-deficient hematopoiesis</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025028387">Phase 1/2 trial of anti-CD7 allogeneic WU-CART-007 for patients with relapsed/refractory T-cell malignancies</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027355">A comprehensive genetic study of classic Hodgkin lymphoma using circulating tumor DNA</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 04 Sep 2025 12:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/93fa5eac/fd878909.mp3" length="24881008" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1243</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, we'll learn about how TET2 is often mutated in myeloid malignancies and clonal hematopoiesis. In new work, expansion of Tet2-mutant HSPCs was dependent on Ncoa4, the cargo receptor mediating ferritinophagy. We’ll iron out the implications. After that: a double-oh-seven license to kill in T-cell leukemia/lymphoma. WU-CART-007 is an off-the-shelf CAR T product with manageable safety and encouraging efficacy. With further work, it could become a new option for patients in urgent need of therapy. Finally: a comprehensive genetic study of classical Hodgkin lymphoma using circulating tumor DNA. This new research provides novel and complex insights on genetic subtypes, prognostic biomarkers, neoantigens in the disease environment, and more.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024028033">An in vivo barcoded CRISPR-Cas9 screen identifies <em>Ncoa4</em>-mediated ferritinophagy as a dependence in <em>Tet2</em>-deficient hematopoiesis</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025028387">Phase 1/2 trial of anti-CD7 allogeneic WU-CART-007 for patients with relapsed/refractory T-cell malignancies</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027355">A comprehensive genetic study of classic Hodgkin lymphoma using circulating tumor DNA</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3lxzjcxtjhy23"/>
    </item>
    <item>
      <title>Targeting NPM1 in AML with a menin inhibitor; in primates, a CD137 ADC eliminates acute GVHD</title>
      <itunes:season>10</itunes:season>
      <podcast:season>10</podcast:season>
      <itunes:title>Targeting NPM1 in AML with a menin inhibitor; in primates, a CD137 ADC eliminates acute GVHD</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">2135908f-651a-4f99-81b8-a46278566bab</guid>
      <link>https://share.transistor.fm/s/4ab1ccb3</link>
      <description>
        <![CDATA[<p>In this week's episode we'll learn about targeting NPM1 in acute myeloid leukemia. Researchers report the first clinical evidence of a menin inhibitor inducing complete remissions in AML with a NPM1 mutation. This validates NPM1 as a new therapeutic target in AML, alongside FLT3, IDH1/2, and KMT2A. Also on the podcast: targeting CD137 to prevent graft-versus-host disease. In nonhuman primates, a single dose of a CD137 antibody-drug conjugate provided long-term protection, with one important caveat: the potential for viral reactivation.</p><p>Featured Articles: </p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025028357">Menin inhibition with revumenib for NPM1-mutated relapsed or refractory acute myeloid leukemia: the AUGMENT-101 study</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027239">A single dose of a CD137 antibody–drug conjugate protects rhesus macaque allogeneic HCT recipients against acute GVHD</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we'll learn about targeting NPM1 in acute myeloid leukemia. Researchers report the first clinical evidence of a menin inhibitor inducing complete remissions in AML with a NPM1 mutation. This validates NPM1 as a new therapeutic target in AML, alongside FLT3, IDH1/2, and KMT2A. Also on the podcast: targeting CD137 to prevent graft-versus-host disease. In nonhuman primates, a single dose of a CD137 antibody-drug conjugate provided long-term protection, with one important caveat: the potential for viral reactivation.</p><p>Featured Articles: </p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025028357">Menin inhibition with revumenib for NPM1-mutated relapsed or refractory acute myeloid leukemia: the AUGMENT-101 study</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027239">A single dose of a CD137 antibody–drug conjugate protects rhesus macaque allogeneic HCT recipients against acute GVHD</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 28 Aug 2025 16:44:38 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/4ab1ccb3/46db59e4.mp3" length="18228999" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>910</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we'll learn about targeting NPM1 in acute myeloid leukemia. Researchers report the first clinical evidence of a menin inhibitor inducing complete remissions in AML with a NPM1 mutation. This validates NPM1 as a new therapeutic target in AML, alongside FLT3, IDH1/2, and KMT2A. Also on the podcast: targeting CD137 to prevent graft-versus-host disease. In nonhuman primates, a single dose of a CD137 antibody-drug conjugate provided long-term protection, with one important caveat: the potential for viral reactivation.</p><p>Featured Articles: </p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025028357">Menin inhibition with revumenib for NPM1-mutated relapsed or refractory acute myeloid leukemia: the AUGMENT-101 study</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027239">A single dose of a CD137 antibody–drug conjugate protects rhesus macaque allogeneic HCT recipients against acute GVHD</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3lxifxepnzm25"/>
    </item>
    <item>
      <title>How I Treat Series on Iron Overload in Hematologic Disorders</title>
      <itunes:season>10</itunes:season>
      <podcast:season>10</podcast:season>
      <itunes:title>How I Treat Series on Iron Overload in Hematologic Disorders</itunes:title>
      <itunes:episodeType>bonus</itunes:episodeType>
      <guid isPermaLink="false">f15d52ac-ec90-4138-b1b5-33ecf867162a</guid>
      <link>https://share.transistor.fm/s/f5772b4c</link>
      <description>
        <![CDATA[<p><em>Blood </em>Editor, Dr. Thomas Coates interviews Dr. Emanuele Angelucci on his paper, "<a href="https://ashpublications.org/blood/article/145/4/372/516079/How-I-manage-iron-overload-in-the-hematopoietic">How I manage iron overload in the hematopoietic cell transplantation setting</a>" which is featured in <em>Blood's </em>"How I Treat Series on Iron Overload in Hematologic Disorders". </p><p><a href="https://ashpublications.org/blood/article/145/4/349/535088/Introduction-to-a-How-I-Treat-series-on-iron?searchresult=1">See the full How I Treat series in volume 145 issue 4 of <em>Blood</em>. </a></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p><em>Blood </em>Editor, Dr. Thomas Coates interviews Dr. Emanuele Angelucci on his paper, "<a href="https://ashpublications.org/blood/article/145/4/372/516079/How-I-manage-iron-overload-in-the-hematopoietic">How I manage iron overload in the hematopoietic cell transplantation setting</a>" which is featured in <em>Blood's </em>"How I Treat Series on Iron Overload in Hematologic Disorders". </p><p><a href="https://ashpublications.org/blood/article/145/4/349/535088/Introduction-to-a-How-I-Treat-series-on-iron?searchresult=1">See the full How I Treat series in volume 145 issue 4 of <em>Blood</em>. </a></p>]]>
      </content:encoded>
      <pubDate>Thu, 28 Aug 2025 13:39:05 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/f5772b4c/3632afaf.mp3" length="41183401" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/i4pnfP3FOkswXUcNnYtW1IhYGI9XUzV848s3-o6pfGw/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS8wMDgw/YTQxZDcyMTlmMmEx/ODQ0NmFjOTA2YzM5/YWFhYS5qcGc.jpg"/>
      <itunes:duration>2057</itunes:duration>
      <itunes:summary>
        <![CDATA[<p><em>Blood </em>Editor, Dr. Thomas Coates interviews Dr. Emanuele Angelucci on his paper, "<a href="https://ashpublications.org/blood/article/145/4/372/516079/How-I-manage-iron-overload-in-the-hematopoietic">How I manage iron overload in the hematopoietic cell transplantation setting</a>" which is featured in <em>Blood's </em>"How I Treat Series on Iron Overload in Hematologic Disorders". </p><p><a href="https://ashpublications.org/blood/article/145/4/349/535088/Introduction-to-a-How-I-Treat-series-on-iron?searchresult=1">See the full How I Treat series in volume 145 issue 4 of <em>Blood</em>. </a></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Early prediction of follicular lymphoma patients with poor survival; immune hotspots in aplastic anemia; role of allo-transplant for Hodgkin lymphoma in the checkpoint inhibitor era</title>
      <itunes:season>10</itunes:season>
      <podcast:season>10</podcast:season>
      <itunes:title>Early prediction of follicular lymphoma patients with poor survival; immune hotspots in aplastic anemia; role of allo-transplant for Hodgkin lymphoma in the checkpoint inhibitor era</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">b35a9207-8027-45ce-8963-170793033b83</guid>
      <link>https://share.transistor.fm/s/8356005b</link>
      <description>
        <![CDATA[<p>In this week's episode we'll learn about how by combining PET response with circulating tumor DNA, or  ctDNA, in newly treated patients with follicular lymphoma, investigators identify those patients likely to progress within 24 months of initial treatment, also known as POD24. After that: Immune hotspots in aplastic anemia. These newly identified hotspots potentially represent sites in the bone marrow where the active immune response takes place, driving the destruction of hematopoietic stem and progenitor cells. Finally, allogeneic transplantation for Hodgkin lymphoma in the checkpoint inhibitor era. In a large, retrospective study, patients with prior checkpoint inhibitor exposure had remarkable outcomes, particularly when post-transplant cyclophosphamide was used.</p><p>Featured Articles: </p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027727">Combined PET and ctDNA response as predictors of POD24 for follicular lymphoma after first-line induction treatment</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025028723">Imaging Mass Cytometry Reveals the Order of Events in the Pathogenesis of Immune-Mediated Aplastic Anemia</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027197">Outcomes of Allogeneic HCT in Hodgkin Lymphoma in the Era of Checkpoint Inhibitors: A Joint CIBMTR and EBMT Analysis</a></li></ul><p><br></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we'll learn about how by combining PET response with circulating tumor DNA, or  ctDNA, in newly treated patients with follicular lymphoma, investigators identify those patients likely to progress within 24 months of initial treatment, also known as POD24. After that: Immune hotspots in aplastic anemia. These newly identified hotspots potentially represent sites in the bone marrow where the active immune response takes place, driving the destruction of hematopoietic stem and progenitor cells. Finally, allogeneic transplantation for Hodgkin lymphoma in the checkpoint inhibitor era. In a large, retrospective study, patients with prior checkpoint inhibitor exposure had remarkable outcomes, particularly when post-transplant cyclophosphamide was used.</p><p>Featured Articles: </p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027727">Combined PET and ctDNA response as predictors of POD24 for follicular lymphoma after first-line induction treatment</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025028723">Imaging Mass Cytometry Reveals the Order of Events in the Pathogenesis of Immune-Mediated Aplastic Anemia</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027197">Outcomes of Allogeneic HCT in Hodgkin Lymphoma in the Era of Checkpoint Inhibitors: A Joint CIBMTR and EBMT Analysis</a></li></ul><p><br></p>]]>
      </content:encoded>
      <pubDate>Thu, 21 Aug 2025 12:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/8356005b/b4a9a1f7.mp3" length="23810933" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1189</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we'll learn about how by combining PET response with circulating tumor DNA, or  ctDNA, in newly treated patients with follicular lymphoma, investigators identify those patients likely to progress within 24 months of initial treatment, also known as POD24. After that: Immune hotspots in aplastic anemia. These newly identified hotspots potentially represent sites in the bone marrow where the active immune response takes place, driving the destruction of hematopoietic stem and progenitor cells. Finally, allogeneic transplantation for Hodgkin lymphoma in the checkpoint inhibitor era. In a large, retrospective study, patients with prior checkpoint inhibitor exposure had remarkable outcomes, particularly when post-transplant cyclophosphamide was used.</p><p>Featured Articles: </p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027727">Combined PET and ctDNA response as predictors of POD24 for follicular lymphoma after first-line induction treatment</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025028723">Imaging Mass Cytometry Reveals the Order of Events in the Pathogenesis of Immune-Mediated Aplastic Anemia</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027197">Outcomes of Allogeneic HCT in Hodgkin Lymphoma in the Era of Checkpoint Inhibitors: A Joint CIBMTR and EBMT Analysis</a></li></ul><p><br></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3lwwcs6gus62b"/>
    </item>
    <item>
      <title>Exogenous CD19 stimulation in B-cell acute lymphoblastic leukemia treated with CD19 CAR T-cell therapy, sequential rapid immune-assay in heparin-induced thrombocytopenia diagnosis, and new survival prediction models for chronic myelomonocytic leukemia</title>
      <itunes:season>10</itunes:season>
      <podcast:season>10</podcast:season>
      <itunes:title>Exogenous CD19 stimulation in B-cell acute lymphoblastic leukemia treated with CD19 CAR T-cell therapy, sequential rapid immune-assay in heparin-induced thrombocytopenia diagnosis, and new survival prediction models for chronic myelomonocytic leukemia</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">acc1d96e-319c-45d9-8d07-439f44781b5f</guid>
      <link>https://share.transistor.fm/s/345952ca</link>
      <description>
        <![CDATA[<p>In this week's episode, we’ll learn more about how exogenous CD19 stimulation affects CAR T-cell persistence in B-cell acute lymphoblastic leukemia treated with CD19 CAR T-cell therapy; new algorithms that incorporate sequential rapid immune-assays, intended to improve diagnosis of heparin-induced thrombocytopenia, and resource-adaptive survival prediction models to help guide management of patients with chronic myelomonocytic leukemia.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025028359">Outcomes of PLAT-02 and PLAT-03: evaluating CD19 CAR T-cell therapy and CD19-expressing T-APC support in pediatric B-ALL</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027517">Sequential combinations of rapid immunoassays for prompt recognition of heparin-induced thrombocytopenia</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027170">BLAST: a globally applicable and molecularly versatile survival model for chronic myelomonocytic leukemia</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, we’ll learn more about how exogenous CD19 stimulation affects CAR T-cell persistence in B-cell acute lymphoblastic leukemia treated with CD19 CAR T-cell therapy; new algorithms that incorporate sequential rapid immune-assays, intended to improve diagnosis of heparin-induced thrombocytopenia, and resource-adaptive survival prediction models to help guide management of patients with chronic myelomonocytic leukemia.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025028359">Outcomes of PLAT-02 and PLAT-03: evaluating CD19 CAR T-cell therapy and CD19-expressing T-APC support in pediatric B-ALL</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027517">Sequential combinations of rapid immunoassays for prompt recognition of heparin-induced thrombocytopenia</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027170">BLAST: a globally applicable and molecularly versatile survival model for chronic myelomonocytic leukemia</a></li></ul>]]>
      </content:encoded>
      <pubDate>Tue, 19 Aug 2025 16:22:05 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/345952ca/7011ac63.mp3" length="22474056" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1122</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, we’ll learn more about how exogenous CD19 stimulation affects CAR T-cell persistence in B-cell acute lymphoblastic leukemia treated with CD19 CAR T-cell therapy; new algorithms that incorporate sequential rapid immune-assays, intended to improve diagnosis of heparin-induced thrombocytopenia, and resource-adaptive survival prediction models to help guide management of patients with chronic myelomonocytic leukemia.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025028359">Outcomes of PLAT-02 and PLAT-03: evaluating CD19 CAR T-cell therapy and CD19-expressing T-APC support in pediatric B-ALL</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027517">Sequential combinations of rapid immunoassays for prompt recognition of heparin-induced thrombocytopenia</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027170">BLAST: a globally applicable and molecularly versatile survival model for chronic myelomonocytic leukemia</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3lwrqivioi42w"/>
    </item>
    <item>
      <title>How I Treat series on Acute Myeloid Leukemia</title>
      <itunes:season>10</itunes:season>
      <podcast:season>10</podcast:season>
      <itunes:title>How I Treat series on Acute Myeloid Leukemia</itunes:title>
      <itunes:episodeType>bonus</itunes:episodeType>
      <guid isPermaLink="false">e3d20353-c76a-4f09-9b68-bc9528a78d94</guid>
      <link>https://share.transistor.fm/s/0640afb6</link>
      <description>
        <![CDATA[<p>In this episode, Associate <em>Blood </em>editor Dr. Selina Luger leads a discussion with Drs. Courtney DiNardo, Eunice Wang, Andrew Wei and Gail Roboz about the advances in treatment options for Acute Myeloid Leukemia (AML). The conversation highlights new combinations like Venetoclax-azacitidine, challenges with differentiation syndrome, and emerging strategies for secondary AML patients. The authors emphasize moving beyond traditional one-size-fits-all treatments to more nuanced, patient-specific care that considers individual genetic profiles and potential complications. These insights provide a comprehensive overview of the latest innovations in AML treatment, offering healthcare professionals critical updates on managing this complex disease. </p><p><a href="https://ashpublications.org/blood/article/145/12/1227/535988/Introduction-to-a-How-I-Treat-series-on-acute">See the full How I Treat series on Acute Myeloid Leukemia in volume 145 issue 12 of <em>Blood </em>journal.</a></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this episode, Associate <em>Blood </em>editor Dr. Selina Luger leads a discussion with Drs. Courtney DiNardo, Eunice Wang, Andrew Wei and Gail Roboz about the advances in treatment options for Acute Myeloid Leukemia (AML). The conversation highlights new combinations like Venetoclax-azacitidine, challenges with differentiation syndrome, and emerging strategies for secondary AML patients. The authors emphasize moving beyond traditional one-size-fits-all treatments to more nuanced, patient-specific care that considers individual genetic profiles and potential complications. These insights provide a comprehensive overview of the latest innovations in AML treatment, offering healthcare professionals critical updates on managing this complex disease. </p><p><a href="https://ashpublications.org/blood/article/145/12/1227/535988/Introduction-to-a-How-I-Treat-series-on-acute">See the full How I Treat series on Acute Myeloid Leukemia in volume 145 issue 12 of <em>Blood </em>journal.</a></p>]]>
      </content:encoded>
      <pubDate>Thu, 14 Aug 2025 12:10:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/0640afb6/629cbca6.mp3" length="51532652" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/7B_aQuoIzCNhYgh-GVTP3xz7qXin-qyHOLfZKk1jEOs/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS80ZGJh/YmM1Mjk5ZDcyZDE4/MzdlYTlmOWJlNDJl/YWYzMS5qcGc.jpg"/>
      <itunes:duration>2575</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this episode, Associate <em>Blood </em>editor Dr. Selina Luger leads a discussion with Drs. Courtney DiNardo, Eunice Wang, Andrew Wei and Gail Roboz about the advances in treatment options for Acute Myeloid Leukemia (AML). The conversation highlights new combinations like Venetoclax-azacitidine, challenges with differentiation syndrome, and emerging strategies for secondary AML patients. The authors emphasize moving beyond traditional one-size-fits-all treatments to more nuanced, patient-specific care that considers individual genetic profiles and potential complications. These insights provide a comprehensive overview of the latest innovations in AML treatment, offering healthcare professionals critical updates on managing this complex disease. </p><p><a href="https://ashpublications.org/blood/article/145/12/1227/535988/Introduction-to-a-How-I-Treat-series-on-acute">See the full How I Treat series on Acute Myeloid Leukemia in volume 145 issue 12 of <em>Blood </em>journal.</a></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3lweq45ykxo2p"/>
    </item>
    <item>
      <title>Daratumumab maintenance in newly-diagnosed, transplant-eligible multiple myeloma; the role of neutrophils in myeloproliferative neoplasms; and novel genetic loci associated with the risk of heavy menstrual bleeding</title>
      <itunes:season>10</itunes:season>
      <podcast:season>10</podcast:season>
      <itunes:title>Daratumumab maintenance in newly-diagnosed, transplant-eligible multiple myeloma; the role of neutrophils in myeloproliferative neoplasms; and novel genetic loci associated with the risk of heavy menstrual bleeding</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">32ed553d-4238-4db4-8949-9a7a17699243</guid>
      <link>https://share.transistor.fm/s/66317918</link>
      <description>
        <![CDATA[<p>In this week's episode, we’ll learn more about the effects of daratumumab maintenance on minimal residual disease in patients with newly diagnosed, transplant-eligible multiple myeloma; the role of neutrophils in the pathophysiology of myeloproliferative neoplasms; and a genome-wide association study that identified novel genetic loci associated with the risk of heavy menstrual bleeding.</p><p>Featured Articles</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027620">Daratumumab-bortezomib-thalidomide-dexamethasone for newly diagnosed myeloma: CASSIOPEIA minimal residual disease results</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027455">Defective neutrophil clearance in <em>JAK2^V617F</em> myeloproliferative neoplasms drives myelofibrosis via immune checkpoint CD24</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027382">Genome-wide meta-analysis of heavy menstrual bleeding reveals 36 risk loci</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, we’ll learn more about the effects of daratumumab maintenance on minimal residual disease in patients with newly diagnosed, transplant-eligible multiple myeloma; the role of neutrophils in the pathophysiology of myeloproliferative neoplasms; and a genome-wide association study that identified novel genetic loci associated with the risk of heavy menstrual bleeding.</p><p>Featured Articles</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027620">Daratumumab-bortezomib-thalidomide-dexamethasone for newly diagnosed myeloma: CASSIOPEIA minimal residual disease results</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027455">Defective neutrophil clearance in <em>JAK2^V617F</em> myeloproliferative neoplasms drives myelofibrosis via immune checkpoint CD24</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027382">Genome-wide meta-analysis of heavy menstrual bleeding reveals 36 risk loci</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 07 Aug 2025 12:05:28 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/66317918/65fe497f.mp3" length="18241660" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>911</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, we’ll learn more about the effects of daratumumab maintenance on minimal residual disease in patients with newly diagnosed, transplant-eligible multiple myeloma; the role of neutrophils in the pathophysiology of myeloproliferative neoplasms; and a genome-wide association study that identified novel genetic loci associated with the risk of heavy menstrual bleeding.</p><p>Featured Articles</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027620">Daratumumab-bortezomib-thalidomide-dexamethasone for newly diagnosed myeloma: CASSIOPEIA minimal residual disease results</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027455">Defective neutrophil clearance in <em>JAK2^V617F</em> myeloproliferative neoplasms drives myelofibrosis via immune checkpoint CD24</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027382">Genome-wide meta-analysis of heavy menstrual bleeding reveals 36 risk loci</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3lvt4tkkp7v2m"/>
    </item>
    <item>
      <title>Hematopoietic stem cells with enhanced transplantability, ruxolitinib for refractory macrophage activation syndrome, and magrolimab in newly diagnosed acute myeloid leukemia</title>
      <itunes:season>10</itunes:season>
      <podcast:season>10</podcast:season>
      <itunes:title>Hematopoietic stem cells with enhanced transplantability, ruxolitinib for refractory macrophage activation syndrome, and magrolimab in newly diagnosed acute myeloid leukemia</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">312cb7c6-7af8-4ac2-ae8d-74c14bc9a5a9</guid>
      <link>https://share.transistor.fm/s/17ab2d31</link>
      <description>
        <![CDATA[<p>In this week's episode we'll learn more about enhanced transplant characteristics; targeting the JAK-STAT pathway with ruxolitinib in patients with adult-onset Still’s disease and macrophage activation syndrome; and a pair of trials demonstrating lack of benefit for the anti-CD47 monoclonal antibody magrolimab in newly diagnosed acute myeloid leukemia.</p><p>Featured Articles</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027872">Heterogeneity of high-potency multilineage hematopoietic stem cells and identification of “Super” transplantability</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024362">Ruxolitinib targets JAK-STAT signaling to modulate neutrophil activation in refractory macrophage activation syndrome</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027408">Magrolimab plus azacitidine vs physician’s choice for untreated TP53-mutated acute myeloid leukemia: the ENHANCE-2 study</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027506">The ENHANCE-3 study: venetoclax and azacitidine plus magrolimab or placebo for untreated AML unfit for intensive therapy</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we'll learn more about enhanced transplant characteristics; targeting the JAK-STAT pathway with ruxolitinib in patients with adult-onset Still’s disease and macrophage activation syndrome; and a pair of trials demonstrating lack of benefit for the anti-CD47 monoclonal antibody magrolimab in newly diagnosed acute myeloid leukemia.</p><p>Featured Articles</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027872">Heterogeneity of high-potency multilineage hematopoietic stem cells and identification of “Super” transplantability</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024362">Ruxolitinib targets JAK-STAT signaling to modulate neutrophil activation in refractory macrophage activation syndrome</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027408">Magrolimab plus azacitidine vs physician’s choice for untreated TP53-mutated acute myeloid leukemia: the ENHANCE-2 study</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027506">The ENHANCE-3 study: venetoclax and azacitidine plus magrolimab or placebo for untreated AML unfit for intensive therapy</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 31 Jul 2025 12:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/17ab2d31/f778c8cd.mp3" length="22746696" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1136</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we'll learn more about enhanced transplant characteristics; targeting the JAK-STAT pathway with ruxolitinib in patients with adult-onset Still’s disease and macrophage activation syndrome; and a pair of trials demonstrating lack of benefit for the anti-CD47 monoclonal antibody magrolimab in newly diagnosed acute myeloid leukemia.</p><p>Featured Articles</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027872">Heterogeneity of high-potency multilineage hematopoietic stem cells and identification of “Super” transplantability</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024362">Ruxolitinib targets JAK-STAT signaling to modulate neutrophil activation in refractory macrophage activation syndrome</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027408">Magrolimab plus azacitidine vs physician’s choice for untreated TP53-mutated acute myeloid leukemia: the ENHANCE-2 study</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027506">The ENHANCE-3 study: venetoclax and azacitidine plus magrolimab or placebo for untreated AML unfit for intensive therapy</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3lvbntijmdw2w"/>
    </item>
    <item>
      <title>A JAK inhibitor for CRS and ICANS prevention; ChAdOx1-platelet interactions and post-vaccination arterial thrombosis; lineage switch, an emerging mechanism of leukemia relapse </title>
      <itunes:season>10</itunes:season>
      <podcast:season>10</podcast:season>
      <itunes:title>A JAK inhibitor for CRS and ICANS prevention; ChAdOx1-platelet interactions and post-vaccination arterial thrombosis; lineage switch, an emerging mechanism of leukemia relapse </itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">5c6f9a8c-af57-4e4b-a251-ec718304f21f</guid>
      <link>https://share.transistor.fm/s/88449966</link>
      <description>
        <![CDATA[<p>In this week's episode, we'll learn about a JAK inhibitor to prevent complications of CD19-directed CAR T-cell therapy. In a phase 2 study, itacitinib was well tolerated and demonstrated promising reductions in the incidence of cytokine release syndrome and neurotoxicity. After that: investigators report direct interactions between ChAdOx1 and platelets under arterial shear conditions. Investigators say it’s a novel biophysical mechanism that potentially contributes to post-vaccination arterial thrombosis. Finally, we explore lineage switch, an emerging form of acute leukemia relapse with dismal outcomes. It arises rapidly following antigen-targeted immunotherapy, highlighting the importance of advanced methods for detection and treatment.</p><p>Featured Articles: </p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026586">Itacitinib for the prevention of IEC therapy–associated CRS: results from the 2-part phase 2 INCB 39110-211 study</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027675">Shear-dependent platelet aggregation by ChAdOx1 nCoV-19 vaccine: a novel biophysical mechanism for arterial thrombosis</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026655">Project EVOLVE: an international analysis of postimmunotherapy lineage switch, an emergent form of relapse in leukemia</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, we'll learn about a JAK inhibitor to prevent complications of CD19-directed CAR T-cell therapy. In a phase 2 study, itacitinib was well tolerated and demonstrated promising reductions in the incidence of cytokine release syndrome and neurotoxicity. After that: investigators report direct interactions between ChAdOx1 and platelets under arterial shear conditions. Investigators say it’s a novel biophysical mechanism that potentially contributes to post-vaccination arterial thrombosis. Finally, we explore lineage switch, an emerging form of acute leukemia relapse with dismal outcomes. It arises rapidly following antigen-targeted immunotherapy, highlighting the importance of advanced methods for detection and treatment.</p><p>Featured Articles: </p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026586">Itacitinib for the prevention of IEC therapy–associated CRS: results from the 2-part phase 2 INCB 39110-211 study</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027675">Shear-dependent platelet aggregation by ChAdOx1 nCoV-19 vaccine: a novel biophysical mechanism for arterial thrombosis</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026655">Project EVOLVE: an international analysis of postimmunotherapy lineage switch, an emergent form of relapse in leukemia</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 24 Jul 2025 12:14:59 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/88449966/177f9840.mp3" length="22649001" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1131</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, we'll learn about a JAK inhibitor to prevent complications of CD19-directed CAR T-cell therapy. In a phase 2 study, itacitinib was well tolerated and demonstrated promising reductions in the incidence of cytokine release syndrome and neurotoxicity. After that: investigators report direct interactions between ChAdOx1 and platelets under arterial shear conditions. Investigators say it’s a novel biophysical mechanism that potentially contributes to post-vaccination arterial thrombosis. Finally, we explore lineage switch, an emerging form of acute leukemia relapse with dismal outcomes. It arises rapidly following antigen-targeted immunotherapy, highlighting the importance of advanced methods for detection and treatment.</p><p>Featured Articles: </p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026586">Itacitinib for the prevention of IEC therapy–associated CRS: results from the 2-part phase 2 INCB 39110-211 study</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027675">Shear-dependent platelet aggregation by ChAdOx1 nCoV-19 vaccine: a novel biophysical mechanism for arterial thrombosis</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026655">Project EVOLVE: an international analysis of postimmunotherapy lineage switch, an emergent form of relapse in leukemia</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3lupwl5hbqb2j"/>
    </item>
    <item>
      <title>Ruxolitinib plus dexamethasone in newly diagnosed adult hemophagocytic lymphohistiocytosis; lysine-specific demethylase-1 inhibitors in sickle cell disease; and clinical characteristics of patients with low von Willebrand factor</title>
      <itunes:season>10</itunes:season>
      <podcast:season>10</podcast:season>
      <itunes:title>Ruxolitinib plus dexamethasone in newly diagnosed adult hemophagocytic lymphohistiocytosis; lysine-specific demethylase-1 inhibitors in sickle cell disease; and clinical characteristics of patients with low von Willebrand factor</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">b3f6d873-0815-4a4c-8157-bf4e4d9358e4</guid>
      <link>https://share.transistor.fm/s/df26fcb8</link>
      <description>
        <![CDATA[<p>In this week's episode we’ll learn more about the use of ruxolitinib plus dexamethasone to treat newly diagnosed patients with adult hemophagocytic lymphohistiocytosis; lysine-specific demethylase-1 inhibitors as a potential new class of therapies for sickle cell disease and other beta-globinopathies; and insights into clinical characteristics of patients with von Willebrand factor levels that are lower than normal but higher than those typically used to diagnose von Willebrand disease.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026139">Ruxolitinib combined with dexamethasone for adult patients with newly diagnosed hemophagocytic lymphohistiocytosis in China</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024028006">Novel, potent, and orally bioavailable LSD1 inhibitors induce fetal hemoglobin synthesis in a sickle cell disease mouse model</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024028035">Clinical phenotype and pathophysiological mechanisms underlying qualitative low VWF</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we’ll learn more about the use of ruxolitinib plus dexamethasone to treat newly diagnosed patients with adult hemophagocytic lymphohistiocytosis; lysine-specific demethylase-1 inhibitors as a potential new class of therapies for sickle cell disease and other beta-globinopathies; and insights into clinical characteristics of patients with von Willebrand factor levels that are lower than normal but higher than those typically used to diagnose von Willebrand disease.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026139">Ruxolitinib combined with dexamethasone for adult patients with newly diagnosed hemophagocytic lymphohistiocytosis in China</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024028006">Novel, potent, and orally bioavailable LSD1 inhibitors induce fetal hemoglobin synthesis in a sickle cell disease mouse model</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024028035">Clinical phenotype and pathophysiological mechanisms underlying qualitative low VWF</a></li></ul>]]>
      </content:encoded>
      <pubDate>Mon, 21 Jul 2025 14:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/df26fcb8/04626348.mp3" length="22686669" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1133</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we’ll learn more about the use of ruxolitinib plus dexamethasone to treat newly diagnosed patients with adult hemophagocytic lymphohistiocytosis; lysine-specific demethylase-1 inhibitors as a potential new class of therapies for sickle cell disease and other beta-globinopathies; and insights into clinical characteristics of patients with von Willebrand factor levels that are lower than normal but higher than those typically used to diagnose von Willebrand disease.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026139">Ruxolitinib combined with dexamethasone for adult patients with newly diagnosed hemophagocytic lymphohistiocytosis in China</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024028006">Novel, potent, and orally bioavailable LSD1 inhibitors induce fetal hemoglobin synthesis in a sickle cell disease mouse model</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024028035">Clinical phenotype and pathophysiological mechanisms underlying qualitative low VWF</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:transcript url="https://share.transistor.fm/s/df26fcb8/transcription.vtt" type="text/vtt" rel="captions"/>
      <podcast:transcript url="https://share.transistor.fm/s/df26fcb8/transcription.srt" type="application/x-subrip" rel="captions"/>
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      <podcast:transcript url="https://share.transistor.fm/s/df26fcb8/transcription" type="text/html"/>
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    </item>
    <item>
      <title>Review series on mantle cell lymphoma </title>
      <itunes:season>10</itunes:season>
      <podcast:season>10</podcast:season>
      <itunes:title>Review series on mantle cell lymphoma </itunes:title>
      <itunes:episodeType>bonus</itunes:episodeType>
      <guid isPermaLink="false">19bbe65d-01f9-44ae-815d-9bd012d22758</guid>
      <link>https://share.transistor.fm/s/ca4fb1a2</link>
      <description>
        <![CDATA[<p>In this episode, Associate Editor Dr. Philippe Armand discusses the Review Series on mantle cell lymphoma with author Dr. Christine Ryan. Both were authors of "<a href="https://ashpublications.org/blood/article/145/7/663/515338/Frontline-management-of-mantle-cell-lymphoma">Frontline management of mantle cell lymphoma</a>", and discuss shifts in treatments and new research.</p><p><br><a href="https://ashpublications.org/blood/article/145/7/653/535441/Introduction-to-a-review-series-on-mantle-cell">Find the full review series in Volume 145 Issue 7 of <em>Blood: "</em>Review series on mantle cell lymphoma: sands shifting in the darkness"</a></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this episode, Associate Editor Dr. Philippe Armand discusses the Review Series on mantle cell lymphoma with author Dr. Christine Ryan. Both were authors of "<a href="https://ashpublications.org/blood/article/145/7/663/515338/Frontline-management-of-mantle-cell-lymphoma">Frontline management of mantle cell lymphoma</a>", and discuss shifts in treatments and new research.</p><p><br><a href="https://ashpublications.org/blood/article/145/7/653/535441/Introduction-to-a-review-series-on-mantle-cell">Find the full review series in Volume 145 Issue 7 of <em>Blood: "</em>Review series on mantle cell lymphoma: sands shifting in the darkness"</a></p>]]>
      </content:encoded>
      <pubDate>Thu, 17 Jul 2025 12:06:51 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/ca4fb1a2/97e8f3cf.mp3" length="20713829" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/s5Uz-cHK9YQeLCXVnvyw3WWtu-TD2_yOtMEpqGaeDN0/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS9hOGNm/MGQyMmUzMGY1MGZj/NDEzMmNjNTc4YzI3/MDcxYy5qcGc.jpg"/>
      <itunes:duration>1034</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this episode, Associate Editor Dr. Philippe Armand discusses the Review Series on mantle cell lymphoma with author Dr. Christine Ryan. Both were authors of "<a href="https://ashpublications.org/blood/article/145/7/663/515338/Frontline-management-of-mantle-cell-lymphoma">Frontline management of mantle cell lymphoma</a>", and discuss shifts in treatments and new research.</p><p><br><a href="https://ashpublications.org/blood/article/145/7/653/535441/Introduction-to-a-review-series-on-mantle-cell">Find the full review series in Volume 145 Issue 7 of <em>Blood: "</em>Review series on mantle cell lymphoma: sands shifting in the darkness"</a></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3lu6cun5bxe2u"/>
    </item>
    <item>
      <title>Rapid, high-sensitivity ADAMTS13 assays for TTP; combination CD38/PD-1 blockade in extranodal NK/T-cell lymphoma; a “zombie enzyme” in CREBBP-mutant lymphomas</title>
      <itunes:season>10</itunes:season>
      <podcast:season>10</podcast:season>
      <itunes:title>Rapid, high-sensitivity ADAMTS13 assays for TTP; combination CD38/PD-1 blockade in extranodal NK/T-cell lymphoma; a “zombie enzyme” in CREBBP-mutant lymphomas</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">a5361667-6ae3-4220-8a76-bf492b5da9dc</guid>
      <link>https://share.transistor.fm/s/b06721f3</link>
      <description>
        <![CDATA[<p>In this week's episode, we'll learn about rapid, high-sensitivity diagnostic assays for TTP, or thrombotic thrombocytopenic purpura, that can reduce unnecessary treatments. After that: enhancing PD-1 blockade in relapsed/refractory extranodal NK/T-cell lymphoma. In a single-arm, phase 2 study, combined CD38 and PD-1 inhibition demonstrated durable responses and manageable safety. Finally, a lymphoma horror story with a happy ending. <em>CREBBP </em>mutations create a zombie enzyme that competes with its wild-type counterparts. By enforcing CD40 signaling, a bispecific antibody overcomes this effect and induces lymphoma cell death.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025028416">Rapid ADAMTS13 activity assays for thrombotic thrombocytopenic purpura: a systematic review and meta-analysis</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027109">Efficacy of combined CD38 and PD-1 inhibition with isatuximab and cemiplimab for relapsed/refractory NK/T-cell lymphoma</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026664">Blunted CD40-responsive enhancer activation in <em>CREBBP</em>-mutant lymphomas can be restored by enforced CD4 T-cell engagement</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, we'll learn about rapid, high-sensitivity diagnostic assays for TTP, or thrombotic thrombocytopenic purpura, that can reduce unnecessary treatments. After that: enhancing PD-1 blockade in relapsed/refractory extranodal NK/T-cell lymphoma. In a single-arm, phase 2 study, combined CD38 and PD-1 inhibition demonstrated durable responses and manageable safety. Finally, a lymphoma horror story with a happy ending. <em>CREBBP </em>mutations create a zombie enzyme that competes with its wild-type counterparts. By enforcing CD40 signaling, a bispecific antibody overcomes this effect and induces lymphoma cell death.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025028416">Rapid ADAMTS13 activity assays for thrombotic thrombocytopenic purpura: a systematic review and meta-analysis</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027109">Efficacy of combined CD38 and PD-1 inhibition with isatuximab and cemiplimab for relapsed/refractory NK/T-cell lymphoma</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026664">Blunted CD40-responsive enhancer activation in <em>CREBBP</em>-mutant lymphomas can be restored by enforced CD4 T-cell engagement</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 10 Jul 2025 12:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/b06721f3/53ff1238.mp3" length="24194546" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1208</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, we'll learn about rapid, high-sensitivity diagnostic assays for TTP, or thrombotic thrombocytopenic purpura, that can reduce unnecessary treatments. After that: enhancing PD-1 blockade in relapsed/refractory extranodal NK/T-cell lymphoma. In a single-arm, phase 2 study, combined CD38 and PD-1 inhibition demonstrated durable responses and manageable safety. Finally, a lymphoma horror story with a happy ending. <em>CREBBP </em>mutations create a zombie enzyme that competes with its wild-type counterparts. By enforcing CD40 signaling, a bispecific antibody overcomes this effect and induces lymphoma cell death.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2025028416">Rapid ADAMTS13 activity assays for thrombotic thrombocytopenic purpura: a systematic review and meta-analysis</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027109">Efficacy of combined CD38 and PD-1 inhibition with isatuximab and cemiplimab for relapsed/refractory NK/T-cell lymphoma</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026664">Blunted CD40-responsive enhancer activation in <em>CREBBP</em>-mutant lymphomas can be restored by enforced CD4 T-cell engagement</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3ltmp7gbohc2u"/>
    </item>
    <item>
      <title>A novel mouse model of sickle cell SC disease; multiple myeloma induction therapy with isatuximab, carfilzomib, lenalidomide, and dexamethasone; and splicing factor mutations in myelodysplastic syndromes</title>
      <itunes:season>10</itunes:season>
      <podcast:season>10</podcast:season>
      <itunes:title>A novel mouse model of sickle cell SC disease; multiple myeloma induction therapy with isatuximab, carfilzomib, lenalidomide, and dexamethasone; and splicing factor mutations in myelodysplastic syndromes</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">2df2bee9-4c07-4111-a113-6f959c8e4702</guid>
      <link>https://share.transistor.fm/s/5b8ce549</link>
      <description>
        <![CDATA[<p>In this week's episode we’ll learn more about a novel mouse model that recapitulates many of the properties of human sickle cell SC disease; results from the induction phase of the risk-adapted MIDAS trial of isatuximab, carfilzomib, lenalidomide, and dexamethasone in newly diagnosed, transplant-eligible multiple myeloma; and a link between splicing factor mutations and competitive fitness in myelodysplastic syndrome stem cells.</p><p>Featured articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024028136">A novel mouse model of hemoglobin SC disease reveals mechanisms underlying beneficial effects of hydroxyurea</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026230">Isatuximab, carfilzomib, lenalidomide, and dexamethasone induction in newly diagnosed myeloma: analysis of the MIDAS trial</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025670">Cell-autonomous dysregulation of interferon signaling drives clonal expansion of SRSF2-mutant MDS stem/progenitor cells</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we’ll learn more about a novel mouse model that recapitulates many of the properties of human sickle cell SC disease; results from the induction phase of the risk-adapted MIDAS trial of isatuximab, carfilzomib, lenalidomide, and dexamethasone in newly diagnosed, transplant-eligible multiple myeloma; and a link between splicing factor mutations and competitive fitness in myelodysplastic syndrome stem cells.</p><p>Featured articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024028136">A novel mouse model of hemoglobin SC disease reveals mechanisms underlying beneficial effects of hydroxyurea</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026230">Isatuximab, carfilzomib, lenalidomide, and dexamethasone induction in newly diagnosed myeloma: analysis of the MIDAS trial</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025670">Cell-autonomous dysregulation of interferon signaling drives clonal expansion of SRSF2-mutant MDS stem/progenitor cells</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 03 Jul 2025 12:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/5b8ce549/0272b053.mp3" length="22984439" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1148</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we’ll learn more about a novel mouse model that recapitulates many of the properties of human sickle cell SC disease; results from the induction phase of the risk-adapted MIDAS trial of isatuximab, carfilzomib, lenalidomide, and dexamethasone in newly diagnosed, transplant-eligible multiple myeloma; and a link between splicing factor mutations and competitive fitness in myelodysplastic syndrome stem cells.</p><p>Featured articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024028136">A novel mouse model of hemoglobin SC disease reveals mechanisms underlying beneficial effects of hydroxyurea</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026230">Isatuximab, carfilzomib, lenalidomide, and dexamethasone induction in newly diagnosed myeloma: analysis of the MIDAS trial</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025670">Cell-autonomous dysregulation of interferon signaling drives clonal expansion of SRSF2-mutant MDS stem/progenitor cells</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3lt33xj3pad2a"/>
    </item>
    <item>
      <title>An AI model for transplant risk in myelofibrosis; preventing priapism in men with sickle cell anemia; hallmarks of T cell exhaustion absent in newly diagnosed MM</title>
      <itunes:season>9</itunes:season>
      <podcast:season>9</podcast:season>
      <itunes:title>An AI model for transplant risk in myelofibrosis; preventing priapism in men with sickle cell anemia; hallmarks of T cell exhaustion absent in newly diagnosed MM</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">af62e9ea-34d2-40d8-b7ba-a2a65891f968</guid>
      <link>https://share.transistor.fm/s/ec3e4a1c</link>
      <description>
        <![CDATA[<p>In this week's episode, we'll learn about using AI to assess transplant risk in myelofibrosis. In a step toward personalized medicine, researchers report on a machine learning model that identifies 25% of patients with poor outcomes. After that: preventing priapism in men with sickle cell anemia. A recent phase 2 feasibility study shows high rates of recruitment, retention, and adherence to oral therapies, coupled with a significant reduction in the risk of this difficult complication. Finally, new research indicates that hallmarks of terminal T-cell exhaustion are absent in multiple myeloma, from diagnosis through maintenance therapy. We explore these provocative and counterintuitive findings arising from profiling of blood and marrow samples.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027287">Use of machine learning techniques to predict poor survival after hematopoietic cell transplantation for myelofibrosis</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027898">A controlled trial for preventing priapism in sickle cell anemia: hydroxyurea plus placebo vs hydroxyurea plus tadalafil</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025655">Hallmarks of T-cell exhaustion and antigen experience are absent in multiple myeloma from diagnosis to maintenance therapy</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, we'll learn about using AI to assess transplant risk in myelofibrosis. In a step toward personalized medicine, researchers report on a machine learning model that identifies 25% of patients with poor outcomes. After that: preventing priapism in men with sickle cell anemia. A recent phase 2 feasibility study shows high rates of recruitment, retention, and adherence to oral therapies, coupled with a significant reduction in the risk of this difficult complication. Finally, new research indicates that hallmarks of terminal T-cell exhaustion are absent in multiple myeloma, from diagnosis through maintenance therapy. We explore these provocative and counterintuitive findings arising from profiling of blood and marrow samples.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027287">Use of machine learning techniques to predict poor survival after hematopoietic cell transplantation for myelofibrosis</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027898">A controlled trial for preventing priapism in sickle cell anemia: hydroxyurea plus placebo vs hydroxyurea plus tadalafil</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025655">Hallmarks of T-cell exhaustion and antigen experience are absent in multiple myeloma from diagnosis to maintenance therapy</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 26 Jun 2025 12:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/ec3e4a1c/c7d89fd6.mp3" length="22113997" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1104</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, we'll learn about using AI to assess transplant risk in myelofibrosis. In a step toward personalized medicine, researchers report on a machine learning model that identifies 25% of patients with poor outcomes. After that: preventing priapism in men with sickle cell anemia. A recent phase 2 feasibility study shows high rates of recruitment, retention, and adherence to oral therapies, coupled with a significant reduction in the risk of this difficult complication. Finally, new research indicates that hallmarks of terminal T-cell exhaustion are absent in multiple myeloma, from diagnosis through maintenance therapy. We explore these provocative and counterintuitive findings arising from profiling of blood and marrow samples.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027287">Use of machine learning techniques to predict poor survival after hematopoietic cell transplantation for myelofibrosis</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027898">A controlled trial for preventing priapism in sickle cell anemia: hydroxyurea plus placebo vs hydroxyurea plus tadalafil</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025655">Hallmarks of T-cell exhaustion and antigen experience are absent in multiple myeloma from diagnosis to maintenance therapy</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3lsjiqjscj22t"/>
    </item>
    <item>
      <title>Social determinants of health and access to allogeneic hematopoietic cell transplantation, megakaryocyte growth factor receptor-based pretransplant conditioning for ex vivo autologous gene therapy, and novel protein biomarkers for risk stratification in a</title>
      <itunes:season>9</itunes:season>
      <podcast:season>9</podcast:season>
      <itunes:title>Social determinants of health and access to allogeneic hematopoietic cell transplantation, megakaryocyte growth factor receptor-based pretransplant conditioning for ex vivo autologous gene therapy, and novel protein biomarkers for risk stratification in a</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">8776b6f1-e81a-4b6e-bd2f-a53a51b7312b</guid>
      <link>https://share.transistor.fm/s/c423bfa3</link>
      <description>
        <![CDATA[<p>In this week's episode, we’ll learn more about social determinants of health that impact access to allogeneic hematopoietic cell transplantation in patients with acute myeloid leukemia, or AML; use of megakaryocyte growth factor receptor-based stem cell depletion as part of pretransplant conditioning in <em>ex vivo</em> autologous gene therapy; and identification of an eight-protein risk signature as well as a novel single protein biomarker, soluble oncostatin M receptor, for risk stratification in AML.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027543"><strong>Social Determinants of Health and Access to Allogeneic Hematopoietic Cell Transplantation for Acute Myeloid Leukemia</strong></a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024636"><strong>cMPL-Based Purification and Depletion of Human Hematopoietic Stem Cells: Implications for Pretransplant Conditioning</strong></a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027244"><strong>Blood-Based Proteomic Profiling Identifies OSMR as a Novel Biomarker of AML Outcomes</strong></a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, we’ll learn more about social determinants of health that impact access to allogeneic hematopoietic cell transplantation in patients with acute myeloid leukemia, or AML; use of megakaryocyte growth factor receptor-based stem cell depletion as part of pretransplant conditioning in <em>ex vivo</em> autologous gene therapy; and identification of an eight-protein risk signature as well as a novel single protein biomarker, soluble oncostatin M receptor, for risk stratification in AML.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027543"><strong>Social Determinants of Health and Access to Allogeneic Hematopoietic Cell Transplantation for Acute Myeloid Leukemia</strong></a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024636"><strong>cMPL-Based Purification and Depletion of Human Hematopoietic Stem Cells: Implications for Pretransplant Conditioning</strong></a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027244"><strong>Blood-Based Proteomic Profiling Identifies OSMR as a Novel Biomarker of AML Outcomes</strong></a></li></ul>]]>
      </content:encoded>
      <pubDate>Mon, 23 Jun 2025 09:23:02 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/c423bfa3/fe145edb.mp3" length="23581651" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1178</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, we’ll learn more about social determinants of health that impact access to allogeneic hematopoietic cell transplantation in patients with acute myeloid leukemia, or AML; use of megakaryocyte growth factor receptor-based stem cell depletion as part of pretransplant conditioning in <em>ex vivo</em> autologous gene therapy; and identification of an eight-protein risk signature as well as a novel single protein biomarker, soluble oncostatin M receptor, for risk stratification in AML.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027543"><strong>Social Determinants of Health and Access to Allogeneic Hematopoietic Cell Transplantation for Acute Myeloid Leukemia</strong></a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024636"><strong>cMPL-Based Purification and Depletion of Human Hematopoietic Stem Cells: Implications for Pretransplant Conditioning</strong></a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027244"><strong>Blood-Based Proteomic Profiling Identifies OSMR as a Novel Biomarker of AML Outcomes</strong></a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3lsbojipkkw2v"/>
    </item>
    <item>
      <title>Aggressive non-Hodgkin lymphoma: defining and managing high-risk subsets</title>
      <itunes:season>9</itunes:season>
      <podcast:season>9</podcast:season>
      <itunes:title>Aggressive non-Hodgkin lymphoma: defining and managing high-risk subsets</itunes:title>
      <itunes:episodeType>bonus</itunes:episodeType>
      <guid isPermaLink="false">9840159b-8a06-4e2f-b3e6-27b4ebe0f567</guid>
      <link>https://share.transistor.fm/s/e89ee027</link>
      <description>
        <![CDATA[<p><em>Blood </em>editor Dr. Laurie Sehn discusses the topic of "Aggressive non-Hodgkin lymphoma: defining and managing high-risk subsets" featuring Drs. Mark Roschewski, Grzegorz Nowakowski, and Neha Mehta-Shah, who each contributed to the articles featured in the review series on high-risk aggressive lymphoma.</p><p><br></p><p><a href="https://ashpublications.org/blood/article/144/25/2561/534557/Introduction-to-a-review-series-on-high-risk">See the full review series on high risk lymphoma in volume 144, issue 25 of <em>Blood</em>.</a></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p><em>Blood </em>editor Dr. Laurie Sehn discusses the topic of "Aggressive non-Hodgkin lymphoma: defining and managing high-risk subsets" featuring Drs. Mark Roschewski, Grzegorz Nowakowski, and Neha Mehta-Shah, who each contributed to the articles featured in the review series on high-risk aggressive lymphoma.</p><p><br></p><p><a href="https://ashpublications.org/blood/article/144/25/2561/534557/Introduction-to-a-review-series-on-high-risk">See the full review series on high risk lymphoma in volume 144, issue 25 of <em>Blood</em>.</a></p>]]>
      </content:encoded>
      <pubDate>Thu, 19 Jun 2025 12:05:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/e89ee027/d1f3cb93.mp3" length="49786504" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/jr7ubSC9oAVlB51YiPZYTnHsiyxo3pqb2Rar2MTJwHU/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS9jNjc1/MTIwOWQ4Yjg2NWM1/MzhhODY2NTVmZGI4/M2U4MC5qcGc.jpg"/>
      <itunes:duration>2488</itunes:duration>
      <itunes:summary>
        <![CDATA[<p><em>Blood </em>editor Dr. Laurie Sehn discusses the topic of "Aggressive non-Hodgkin lymphoma: defining and managing high-risk subsets" featuring Drs. Mark Roschewski, Grzegorz Nowakowski, and Neha Mehta-Shah, who each contributed to the articles featured in the review series on high-risk aggressive lymphoma.</p><p><br></p><p><a href="https://ashpublications.org/blood/article/144/25/2561/534557/Introduction-to-a-review-series-on-high-risk">See the full review series on high risk lymphoma in volume 144, issue 25 of <em>Blood</em>.</a></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3lrxvpdeibh25"/>
    </item>
    <item>
      <title>A key role for T-cell TET3 in chronic GVHD; a BTK inhibitor for ITP; co-inhibition of pre-TCR and IL-7R pathways in a T-ALL patient subset </title>
      <itunes:season>9</itunes:season>
      <podcast:season>9</podcast:season>
      <itunes:title>A key role for T-cell TET3 in chronic GVHD; a BTK inhibitor for ITP; co-inhibition of pre-TCR and IL-7R pathways in a T-ALL patient subset </itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">7208db7c-1fca-47f8-85a2-98f13fda5ceb</guid>
      <link>https://share.transistor.fm/s/ff138053</link>
      <description>
        <![CDATA[<p>In this week's episode, we' ll learn about how TET3 has a key role in GVHD. In mice, a deficiency of Tet3 in donor T cells inhibited pathogenic immunoglobulin class switching and suppressed lung fibrosis. Accordingly, TET3 may be a new therapeutic target in chronic GVHD. After that: rilzabrutinib, a BTK inhibitor for ITP. In a randomized, placebo-controlled trial, treatment produced rapid and durable platelet responses, with acceptable safety, in adults with immune thrombocytopenia who had failed multiple previous therapies. Finally: exploring pre-TCR surface expression patterns in T-cell ALL. Co-inhibition of the interleukin-7 receptor and pre-T cell receptor pathways may play a therapeutic role for a subset of T-lymphoblastic leukemias.</p><p>Featured Articles: </p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025036">Deficiency of T follicular helper cell Tet3 DNA demethylation inhibits pathogenic IgG2c class switching and chronic GVHD</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027336">Safety and efficacy of rilzabrutinib vs placebo in adults with immune thrombocytopenia: the phase 3 LUNA3 study</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027982">Surface pTα expression predicts LCK activation and preclinical synergy of LCK and JAK coinhibition in adult T-ALL</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, we' ll learn about how TET3 has a key role in GVHD. In mice, a deficiency of Tet3 in donor T cells inhibited pathogenic immunoglobulin class switching and suppressed lung fibrosis. Accordingly, TET3 may be a new therapeutic target in chronic GVHD. After that: rilzabrutinib, a BTK inhibitor for ITP. In a randomized, placebo-controlled trial, treatment produced rapid and durable platelet responses, with acceptable safety, in adults with immune thrombocytopenia who had failed multiple previous therapies. Finally: exploring pre-TCR surface expression patterns in T-cell ALL. Co-inhibition of the interleukin-7 receptor and pre-T cell receptor pathways may play a therapeutic role for a subset of T-lymphoblastic leukemias.</p><p>Featured Articles: </p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025036">Deficiency of T follicular helper cell Tet3 DNA demethylation inhibits pathogenic IgG2c class switching and chronic GVHD</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027336">Safety and efficacy of rilzabrutinib vs placebo in adults with immune thrombocytopenia: the phase 3 LUNA3 study</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027982">Surface pTα expression predicts LCK activation and preclinical synergy of LCK and JAK coinhibition in adult T-ALL</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 12 Jun 2025 00:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/ff138053/c457d6ca.mp3" length="24618596" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1230</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, we' ll learn about how TET3 has a key role in GVHD. In mice, a deficiency of Tet3 in donor T cells inhibited pathogenic immunoglobulin class switching and suppressed lung fibrosis. Accordingly, TET3 may be a new therapeutic target in chronic GVHD. After that: rilzabrutinib, a BTK inhibitor for ITP. In a randomized, placebo-controlled trial, treatment produced rapid and durable platelet responses, with acceptable safety, in adults with immune thrombocytopenia who had failed multiple previous therapies. Finally: exploring pre-TCR surface expression patterns in T-cell ALL. Co-inhibition of the interleukin-7 receptor and pre-T cell receptor pathways may play a therapeutic role for a subset of T-lymphoblastic leukemias.</p><p>Featured Articles: </p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025036">Deficiency of T follicular helper cell Tet3 DNA demethylation inhibits pathogenic IgG2c class switching and chronic GVHD</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027336">Safety and efficacy of rilzabrutinib vs placebo in adults with immune thrombocytopenia: the phase 3 LUNA3 study</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027982">Surface pTα expression predicts LCK activation and preclinical synergy of LCK and JAK coinhibition in adult T-ALL</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3lrezxcbz5x2t"/>
    </item>
    <item>
      <title>Special Episode: Eliminating the Need for Sequential Confirmation of Response in Multiple Myeloma</title>
      <itunes:season>9</itunes:season>
      <podcast:season>9</podcast:season>
      <itunes:title>Special Episode: Eliminating the Need for Sequential Confirmation of Response in Multiple Myeloma</itunes:title>
      <itunes:episodeType>bonus</itunes:episodeType>
      <guid isPermaLink="false">e20de466-c65d-4bd3-8df4-aac5a6ad49de</guid>
      <link>https://share.transistor.fm/s/38b2a401</link>
      <description>
        <![CDATA[<p>In this special episode, Dr. Shaji Kumar from the Mayo Clinic speaks with <em>Blood </em>editor Dr. Laurie Sehn on a paper recently published in <em>Blood</em>, "<a href="https://ashpublications.org/blood/article-abstract/doi/10.1182/blood.2024027949/537693/Eliminating-The-Need-for-Sequential-Confirmation?redirectedFrom=fulltext">Eliminating the Need for Sequential Confirmation of Response in Multiple Myeloma</a>". The findings demonstrate eliminating the need for sequential confirmation of response in multiple myeloma. The study, involving 583 episodes of progression, found that simultaneous confirmation of disease progression using two different markers (e.g., serum protein electrophoresis and serum free light chain assay) was 98% accurate, compared to 82% for sequential confirmation. This suggests that simultaneous confirmation could improve clinical trial accuracy and reduce false censoring. The International Myeloma Working Group is set to revise its response criteria to incorporate these findings, potentially simplifying disease assessment and reducing the need for multiple blood draws.</p><p><br></p><p><br></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this special episode, Dr. Shaji Kumar from the Mayo Clinic speaks with <em>Blood </em>editor Dr. Laurie Sehn on a paper recently published in <em>Blood</em>, "<a href="https://ashpublications.org/blood/article-abstract/doi/10.1182/blood.2024027949/537693/Eliminating-The-Need-for-Sequential-Confirmation?redirectedFrom=fulltext">Eliminating the Need for Sequential Confirmation of Response in Multiple Myeloma</a>". The findings demonstrate eliminating the need for sequential confirmation of response in multiple myeloma. The study, involving 583 episodes of progression, found that simultaneous confirmation of disease progression using two different markers (e.g., serum protein electrophoresis and serum free light chain assay) was 98% accurate, compared to 82% for sequential confirmation. This suggests that simultaneous confirmation could improve clinical trial accuracy and reduce false censoring. The International Myeloma Working Group is set to revise its response criteria to incorporate these findings, potentially simplifying disease assessment and reducing the need for multiple blood draws.</p><p><br></p><p><br></p>]]>
      </content:encoded>
      <pubDate>Tue, 10 Jun 2025 08:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/38b2a401/38059445.mp3" length="11761372" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>587</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this special episode, Dr. Shaji Kumar from the Mayo Clinic speaks with <em>Blood </em>editor Dr. Laurie Sehn on a paper recently published in <em>Blood</em>, "<a href="https://ashpublications.org/blood/article-abstract/doi/10.1182/blood.2024027949/537693/Eliminating-The-Need-for-Sequential-Confirmation?redirectedFrom=fulltext">Eliminating the Need for Sequential Confirmation of Response in Multiple Myeloma</a>". The findings demonstrate eliminating the need for sequential confirmation of response in multiple myeloma. The study, involving 583 episodes of progression, found that simultaneous confirmation of disease progression using two different markers (e.g., serum protein electrophoresis and serum free light chain assay) was 98% accurate, compared to 82% for sequential confirmation. This suggests that simultaneous confirmation could improve clinical trial accuracy and reduce false censoring. The International Myeloma Working Group is set to revise its response criteria to incorporate these findings, potentially simplifying disease assessment and reducing the need for multiple blood draws.</p><p><br></p><p><br></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3lrattgiiyw2r"/>
    </item>
    <item>
      <title>How I Treat Series on Geriatric Hematology</title>
      <itunes:season>9</itunes:season>
      <podcast:season>9</podcast:season>
      <itunes:title>How I Treat Series on Geriatric Hematology</itunes:title>
      <itunes:episodeType>bonus</itunes:episodeType>
      <guid isPermaLink="false">0353edd7-7cc1-4cec-925a-2d677350096b</guid>
      <link>https://share.transistor.fm/s/2fdd67a2</link>
      <description>
        <![CDATA[<p>In this How I Treat Series episode Dr. Thomas Ortel leads a discussion with author Dr. Patrick Foy on his paper “<a href="https://ashpublications.org/blood/article/143/3/214/498686/How-I-diagnose-and-treat-thrombocytopenia-in">How I diagnose and treat thrombocytopenia in geriatric patients</a>”.<br> <br><a href="https://ashpublications.org/blood/article/143/3/185/507077/Introduction-to-a-How-I-Treat-series-on-geriatric?searchresult=1">See the full How I Treat series on geriatric hematology in volume 143 issue 3 of <em>Blood</em> Journal.</a></p><p><br></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this How I Treat Series episode Dr. Thomas Ortel leads a discussion with author Dr. Patrick Foy on his paper “<a href="https://ashpublications.org/blood/article/143/3/214/498686/How-I-diagnose-and-treat-thrombocytopenia-in">How I diagnose and treat thrombocytopenia in geriatric patients</a>”.<br> <br><a href="https://ashpublications.org/blood/article/143/3/185/507077/Introduction-to-a-How-I-Treat-series-on-geriatric?searchresult=1">See the full How I Treat series on geriatric hematology in volume 143 issue 3 of <em>Blood</em> Journal.</a></p><p><br></p>]]>
      </content:encoded>
      <pubDate>Thu, 05 Jun 2025 12:15:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/2fdd67a2/3c8a9bac.mp3" length="20807371" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/mlV3_1E_wDwt9zLRMbtNWppqxldmc2MnK_S5hmQ6g8M/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS9kYmI0/MWM4ZDM0M2E0Zjk2/MzJlOTIwZGVmYTkz/ZDIxMC5qcGc.jpg"/>
      <itunes:duration>1039</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this How I Treat Series episode Dr. Thomas Ortel leads a discussion with author Dr. Patrick Foy on his paper “<a href="https://ashpublications.org/blood/article/143/3/214/498686/How-I-diagnose-and-treat-thrombocytopenia-in">How I diagnose and treat thrombocytopenia in geriatric patients</a>”.<br> <br><a href="https://ashpublications.org/blood/article/143/3/185/507077/Introduction-to-a-How-I-Treat-series-on-geriatric?searchresult=1">See the full How I Treat series on geriatric hematology in volume 143 issue 3 of <em>Blood</em> Journal.</a></p><p><br></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3lqupqhzjva2v"/>
    </item>
    <item>
      <title>Single cell multi-omic analysis of leukemia stem cells, cyclophosphamide for non-immune effector cell-associated neurotoxicity, and glycosylation as a mediator of von Willebrand factor clearance</title>
      <itunes:season>9</itunes:season>
      <podcast:season>9</podcast:season>
      <itunes:title>Single cell multi-omic analysis of leukemia stem cells, cyclophosphamide for non-immune effector cell-associated neurotoxicity, and glycosylation as a mediator of von Willebrand factor clearance</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">0d36182e-9b2d-476d-a302-3a6e4962dfd9</guid>
      <link>https://share.transistor.fm/s/7c7e0674</link>
      <description>
        <![CDATA[<p>In this week's episode, we’ll learn more about the identification and characterization of stem cell-like leukemia blasts using single cell multi-omics, cyclophosphamide as a treatment for non-immune effector cell-associated neurotoxicity in patients treated with B-cell maturation antigen, or BCMA, targeted CAR T-cell therapies, and how differences in glycosylation affect the clearance of human plasma-derived and recombinant von Willebrand factor concentrates.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027270">Single-cell panleukemia signatures of HSPC-like blasts predict drug response and clinical outcome</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024028172">Cyclophosphamide mitigates non-ICANS neurotoxicities following ciltacabtagene autoleucel treatment</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027038">Enhanced α2-3–linked sialylation determines the extended half-life of CHO-rVWF</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, we’ll learn more about the identification and characterization of stem cell-like leukemia blasts using single cell multi-omics, cyclophosphamide as a treatment for non-immune effector cell-associated neurotoxicity in patients treated with B-cell maturation antigen, or BCMA, targeted CAR T-cell therapies, and how differences in glycosylation affect the clearance of human plasma-derived and recombinant von Willebrand factor concentrates.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027270">Single-cell panleukemia signatures of HSPC-like blasts predict drug response and clinical outcome</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024028172">Cyclophosphamide mitigates non-ICANS neurotoxicities following ciltacabtagene autoleucel treatment</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027038">Enhanced α2-3–linked sialylation determines the extended half-life of CHO-rVWF</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 05 Jun 2025 12:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/7c7e0674/3ddf1062.mp3" length="19339304" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>966</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, we’ll learn more about the identification and characterization of stem cell-like leukemia blasts using single cell multi-omics, cyclophosphamide as a treatment for non-immune effector cell-associated neurotoxicity in patients treated with B-cell maturation antigen, or BCMA, targeted CAR T-cell therapies, and how differences in glycosylation affect the clearance of human plasma-derived and recombinant von Willebrand factor concentrates.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027270">Single-cell panleukemia signatures of HSPC-like blasts predict drug response and clinical outcome</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024028172">Cyclophosphamide mitigates non-ICANS neurotoxicities following ciltacabtagene autoleucel treatment</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027038">Enhanced α2-3–linked sialylation determines the extended half-life of CHO-rVWF</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3lquovc7oe72q"/>
    </item>
    <item>
      <title>New insights on PU.1-mutated agammaglobulinemia; venetoclax-based induction therapy in younger AML patients; the link between ABO Blood groups and risk of future VTE </title>
      <itunes:season>9</itunes:season>
      <podcast:season>9</podcast:season>
      <itunes:title>New insights on PU.1-mutated agammaglobulinemia; venetoclax-based induction therapy in younger AML patients; the link between ABO Blood groups and risk of future VTE </itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">d0325e64-5be7-4d64-83f6-dfc99085dfaa</guid>
      <link>https://share.transistor.fm/s/b1a89729</link>
      <description>
        <![CDATA[<p>In this week's episode, we'll hear about new insights into PU.1-mutated agammaglobulinemia. Researchers show that haploinsufficiency of the master transcriptional regulator PU.1 causes agammaglobulinemia and dendritic cell deficiencies. These patients experience an array of infectious and non-infectious complications, but not leukemia. After that: venetoclax-based induction therapy in younger patients with AML. Venetoclax plus decitabine was associated with superior safety and non-inferior response rates compared to intensive chemotherapy. Is it time to consider lower-intensity therapy beyond older and unfit patients? Finally, a focus on venous thromboembolism. Researchers link BGAT, an enzyme pivotal to determining blood type, to risk of future VTE. They say high plasma levels of BGAT contribute to risk above and beyond what can be explained by von Willebrand factor and Factor VIII.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026683">One hundred thirty-four germ line PU.1 variants and the agammaglobulinemic patients carrying them</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027217">Venetoclax and decitabine vs intensive chemotherapy as induction for young patients with newly diagnosed AML</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025923">Histo–blood group ABO system transferase plasma levels and risk of future venous thromboembolism: the HUNT study</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, we'll hear about new insights into PU.1-mutated agammaglobulinemia. Researchers show that haploinsufficiency of the master transcriptional regulator PU.1 causes agammaglobulinemia and dendritic cell deficiencies. These patients experience an array of infectious and non-infectious complications, but not leukemia. After that: venetoclax-based induction therapy in younger patients with AML. Venetoclax plus decitabine was associated with superior safety and non-inferior response rates compared to intensive chemotherapy. Is it time to consider lower-intensity therapy beyond older and unfit patients? Finally, a focus on venous thromboembolism. Researchers link BGAT, an enzyme pivotal to determining blood type, to risk of future VTE. They say high plasma levels of BGAT contribute to risk above and beyond what can be explained by von Willebrand factor and Factor VIII.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026683">One hundred thirty-four germ line PU.1 variants and the agammaglobulinemic patients carrying them</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027217">Venetoclax and decitabine vs intensive chemotherapy as induction for young patients with newly diagnosed AML</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025923">Histo–blood group ABO system transferase plasma levels and risk of future venous thromboembolism: the HUNT study</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 29 May 2025 12:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/b1a89729/7b8eba87.mp3" length="23755017" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1186</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, we'll hear about new insights into PU.1-mutated agammaglobulinemia. Researchers show that haploinsufficiency of the master transcriptional regulator PU.1 causes agammaglobulinemia and dendritic cell deficiencies. These patients experience an array of infectious and non-infectious complications, but not leukemia. After that: venetoclax-based induction therapy in younger patients with AML. Venetoclax plus decitabine was associated with superior safety and non-inferior response rates compared to intensive chemotherapy. Is it time to consider lower-intensity therapy beyond older and unfit patients? Finally, a focus on venous thromboembolism. Researchers link BGAT, an enzyme pivotal to determining blood type, to risk of future VTE. They say high plasma levels of BGAT contribute to risk above and beyond what can be explained by von Willebrand factor and Factor VIII.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026683">One hundred thirty-four germ line PU.1 variants and the agammaglobulinemic patients carrying them</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027217">Venetoclax and decitabine vs intensive chemotherapy as induction for young patients with newly diagnosed AML</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025923">Histo–blood group ABO system transferase plasma levels and risk of future venous thromboembolism: the HUNT study</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3lqd3orwqfs25"/>
    </item>
    <item>
      <title>How I Treat Transfusion Medicine (part 2)</title>
      <itunes:season>9</itunes:season>
      <podcast:season>9</podcast:season>
      <itunes:title>How I Treat Transfusion Medicine (part 2)</itunes:title>
      <itunes:episodeType>bonus</itunes:episodeType>
      <guid isPermaLink="false">49eb05d1-cadb-499d-bd09-4fd3fb1ce3a6</guid>
      <link>https://share.transistor.fm/s/70cfb32a</link>
      <description>
        <![CDATA[<p>In part two of the How I Treat Series on Transfusion Medicine Dr. Erica Wood interviews the<a href="https://ashpublications.org/blood/article/145/20/2245/537115/How-I-manage-major-hemorrhage"> "How I Manage Major Hemorrhage</a>" author group: Drs. Jeannie Callium, Keyvan Karkouti, and Ron George.</p><p><a href="https://ashpublications.org/blood/article/145/20/2233/537120/Introduction-to-a-How-I-Treat-series-on">Find the full published review series in Volume 145 Issue 20 of <em>Blood </em>Journal.</a></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In part two of the How I Treat Series on Transfusion Medicine Dr. Erica Wood interviews the<a href="https://ashpublications.org/blood/article/145/20/2245/537115/How-I-manage-major-hemorrhage"> "How I Manage Major Hemorrhage</a>" author group: Drs. Jeannie Callium, Keyvan Karkouti, and Ron George.</p><p><a href="https://ashpublications.org/blood/article/145/20/2233/537120/Introduction-to-a-How-I-Treat-series-on">Find the full published review series in Volume 145 Issue 20 of <em>Blood </em>Journal.</a></p>]]>
      </content:encoded>
      <pubDate>Thu, 22 May 2025 12:15:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/70cfb32a/ec63030a.mp3" length="40772970" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/Asd2yfb4rHMXOFvPtCkPOsPAvqLoQWIaGx5_Ktuudps/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS9lMTVk/ZDMzMjUwOTk0MTU3/Zjk0NjUzMjk4ZTdl/ODQ4NC5qcGc.jpg"/>
      <itunes:duration>2037</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In part two of the How I Treat Series on Transfusion Medicine Dr. Erica Wood interviews the<a href="https://ashpublications.org/blood/article/145/20/2245/537115/How-I-manage-major-hemorrhage"> "How I Manage Major Hemorrhage</a>" author group: Drs. Jeannie Callium, Keyvan Karkouti, and Ron George.</p><p><a href="https://ashpublications.org/blood/article/145/20/2233/537120/Introduction-to-a-How-I-Treat-series-on">Find the full published review series in Volume 145 Issue 20 of <em>Blood </em>Journal.</a></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3lprj7jatkv2l"/>
    </item>
    <item>
      <title>Clonal hematopoiesis in frequent blood donors, immune microenvironment and bispecific antibody response in diffuse large B-cell lymphoma, and blinatumomab as part of early consolidation therapy in CD19-positive Ph-negative B-cell acute lymphoblastic lymphoma</title>
      <itunes:season>9</itunes:season>
      <podcast:season>9</podcast:season>
      <itunes:title>Clonal hematopoiesis in frequent blood donors, immune microenvironment and bispecific antibody response in diffuse large B-cell lymphoma, and blinatumomab as part of early consolidation therapy in CD19-positive Ph-negative B-cell acute lymphoblastic lymphoma</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">de87b7a5-1590-47b0-bcdf-e9134f4f5fea</guid>
      <link>https://share.transistor.fm/s/f2c85b3b</link>
      <description>
        <![CDATA[<p>In this week's episode we’ll learn about how frequent blood donation affects clonal hematopoiesis in older, male blood donors; the effect of immune microenvironment on response to bispecific antibodies in diffuse large B-cell lymphoma; and the feasibility of adding blinatumomab to early consolidation therapy in CD19-positive Ph-negative B-cell acute lymphoblastic lymphoma.</p><p>Featured Articles</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027999">Clonal Hematopoiesis Landscape in Frequent Blood Donors</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025355">Integrative genomic analysis of DLBCL identifies immune environments associated with bispecific antibody response</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027500">Upfront Blinatumomab Improves MRD Clearance and Outcome in Adult Ph-negative B-lineage ALL: The GIMEMA LAL2317 Phase 2 Study</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we’ll learn about how frequent blood donation affects clonal hematopoiesis in older, male blood donors; the effect of immune microenvironment on response to bispecific antibodies in diffuse large B-cell lymphoma; and the feasibility of adding blinatumomab to early consolidation therapy in CD19-positive Ph-negative B-cell acute lymphoblastic lymphoma.</p><p>Featured Articles</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027999">Clonal Hematopoiesis Landscape in Frequent Blood Donors</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025355">Integrative genomic analysis of DLBCL identifies immune environments associated with bispecific antibody response</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027500">Upfront Blinatumomab Improves MRD Clearance and Outcome in Adult Ph-negative B-lineage ALL: The GIMEMA LAL2317 Phase 2 Study</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 22 May 2025 12:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/f2c85b3b/f5bd2462.mp3" length="25174080" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1257</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we’ll learn about how frequent blood donation affects clonal hematopoiesis in older, male blood donors; the effect of immune microenvironment on response to bispecific antibodies in diffuse large B-cell lymphoma; and the feasibility of adding blinatumomab to early consolidation therapy in CD19-positive Ph-negative B-cell acute lymphoblastic lymphoma.</p><p>Featured Articles</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027999">Clonal Hematopoiesis Landscape in Frequent Blood Donors</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025355">Integrative genomic analysis of DLBCL identifies immune environments associated with bispecific antibody response</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027500">Upfront Blinatumomab Improves MRD Clearance and Outcome in Adult Ph-negative B-lineage ALL: The GIMEMA LAL2317 Phase 2 Study</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>How I Treat Transfusion Medicine (part 1)</title>
      <itunes:season>9</itunes:season>
      <podcast:season>9</podcast:season>
      <itunes:title>How I Treat Transfusion Medicine (part 1)</itunes:title>
      <itunes:episodeType>bonus</itunes:episodeType>
      <guid isPermaLink="false">6c5ad190-fb4d-40d5-bdb6-f309e18f7be7</guid>
      <link>https://share.transistor.fm/s/ce857169</link>
      <description>
        <![CDATA[<p>In this two-part series, Dr. Erica Wood talks with Drs. Masja de Haas, Helen Savoia, and Stella Chou about their articles in the How I Treat Series on Transfusion Medicine. Topics include noninvasive prenatal testing for red blood cell and platelet antigens, transfusion cases in sickle cell disease, and pregnant patients who are alloimmunized to RBC antigens. </p><p><a href="https://ashpublications.org/blood/article/145/20/2233/537120/Introduction-to-a-How-I-Treat-series-on">Find the full published review series in Volume 145 Issue 20 of <em>Blood</em> Journal.</a></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this two-part series, Dr. Erica Wood talks with Drs. Masja de Haas, Helen Savoia, and Stella Chou about their articles in the How I Treat Series on Transfusion Medicine. Topics include noninvasive prenatal testing for red blood cell and platelet antigens, transfusion cases in sickle cell disease, and pregnant patients who are alloimmunized to RBC antigens. </p><p><a href="https://ashpublications.org/blood/article/145/20/2233/537120/Introduction-to-a-How-I-Treat-series-on">Find the full published review series in Volume 145 Issue 20 of <em>Blood</em> Journal.</a></p>]]>
      </content:encoded>
      <pubDate>Thu, 15 May 2025 12:30:20 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/ce857169/0abf303e.mp3" length="38667690" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/0Bm9m2ZZgegLkt5KavgaO3FFYqRyCLWZXHSFIibztsg/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS82Zjcy/M2YxNjE3NzdlMmI5/NTUzYTRlOWY0ZTA0/ZGJmNS5qcGc.jpg"/>
      <itunes:duration>1932</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this two-part series, Dr. Erica Wood talks with Drs. Masja de Haas, Helen Savoia, and Stella Chou about their articles in the How I Treat Series on Transfusion Medicine. Topics include noninvasive prenatal testing for red blood cell and platelet antigens, transfusion cases in sickle cell disease, and pregnant patients who are alloimmunized to RBC antigens. </p><p><a href="https://ashpublications.org/blood/article/145/20/2233/537120/Introduction-to-a-How-I-Treat-series-on">Find the full published review series in Volume 145 Issue 20 of <em>Blood</em> Journal.</a></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3lp7wrtjebp2k"/>
    </item>
    <item>
      <title>Discontinuing lenalidomide maintenance in MM; congenital neutropenia syndrome linked to COPZ1 mutations; low GVHD rates with ruxolitinib after allogeneic HCT</title>
      <itunes:season>9</itunes:season>
      <podcast:season>9</podcast:season>
      <itunes:title>Discontinuing lenalidomide maintenance in MM; congenital neutropenia syndrome linked to COPZ1 mutations; low GVHD rates with ruxolitinib after allogeneic HCT</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">e58c42a5-58f7-41ac-962e-a73a9bf7a0b8</guid>
      <link>https://share.transistor.fm/s/4845ee97</link>
      <description>
        <![CDATA[<p>In this week's episode, we'll learn about stopping myeloma maintenance therapy in the modern era. New research suggests that many patients in remission can discontinue lenalidomide, remaining treatment-free, without jeopardizing disease response. After that: a novel congenital neutropenia syndrome. Mutations in the <em>COPZ1</em> gene impact myeloid differentiation and development of neutropenia. Researchers describe the mechanisms and propose a treatment strategy for restoring granulopoiesis. Finally, ruxolitinib maintenance therapy after allogeneic transplant. In a phase 2 study, this treatment strategy was associated with low rates of chronic graft-versus-host disease. Investigators say the use of JAK inhibitors in this context warrants further study.</p><p>Featured Articles: </p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027686">Sustained bone marrow and imaging MRD negativity for 3 years drives discontinuation of maintenance post-ASCT in myeloma</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022576">A new severe congenital neutropenia syndrome associated with autosomal recessive COPZ1 mutations</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024028005">Low rates of chronic graft-versus-host disease with ruxolitinib maintenance following allogeneic HCT<br></a><br></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, we'll learn about stopping myeloma maintenance therapy in the modern era. New research suggests that many patients in remission can discontinue lenalidomide, remaining treatment-free, without jeopardizing disease response. After that: a novel congenital neutropenia syndrome. Mutations in the <em>COPZ1</em> gene impact myeloid differentiation and development of neutropenia. Researchers describe the mechanisms and propose a treatment strategy for restoring granulopoiesis. Finally, ruxolitinib maintenance therapy after allogeneic transplant. In a phase 2 study, this treatment strategy was associated with low rates of chronic graft-versus-host disease. Investigators say the use of JAK inhibitors in this context warrants further study.</p><p>Featured Articles: </p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027686">Sustained bone marrow and imaging MRD negativity for 3 years drives discontinuation of maintenance post-ASCT in myeloma</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022576">A new severe congenital neutropenia syndrome associated with autosomal recessive COPZ1 mutations</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024028005">Low rates of chronic graft-versus-host disease with ruxolitinib maintenance following allogeneic HCT<br></a><br></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 15 May 2025 12:17:31 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/4845ee97/bfb23bbb.mp3" length="21918599" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1095</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, we'll learn about stopping myeloma maintenance therapy in the modern era. New research suggests that many patients in remission can discontinue lenalidomide, remaining treatment-free, without jeopardizing disease response. After that: a novel congenital neutropenia syndrome. Mutations in the <em>COPZ1</em> gene impact myeloid differentiation and development of neutropenia. Researchers describe the mechanisms and propose a treatment strategy for restoring granulopoiesis. Finally, ruxolitinib maintenance therapy after allogeneic transplant. In a phase 2 study, this treatment strategy was associated with low rates of chronic graft-versus-host disease. Investigators say the use of JAK inhibitors in this context warrants further study.</p><p>Featured Articles: </p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027686">Sustained bone marrow and imaging MRD negativity for 3 years drives discontinuation of maintenance post-ASCT in myeloma</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022576">A new severe congenital neutropenia syndrome associated with autosomal recessive COPZ1 mutations</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024028005">Low rates of chronic graft-versus-host disease with ruxolitinib maintenance following allogeneic HCT<br></a><br></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3lp7wa6me5s2t"/>
    </item>
    <item>
      <title>Measurable residual disease and maintenance therapy in acute myeloid leukemia (AML), stemness and chemotherapy resistance in AML, and effects of babesiosis on red blood cells in sickle cell disease</title>
      <itunes:season>9</itunes:season>
      <podcast:season>9</podcast:season>
      <itunes:title>Measurable residual disease and maintenance therapy in acute myeloid leukemia (AML), stemness and chemotherapy resistance in AML, and effects of babesiosis on red blood cells in sickle cell disease</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">e9e5df84-26db-4446-8cbe-afcc2366810d</guid>
      <link>https://share.transistor.fm/s/ef63e85b</link>
      <description>
        <![CDATA[<p>In this week's episode, we’ll learn more about how measurable residual disease might help guide decisions about post-transplant gilteritinib maintenance in <em>FLT3-ITD</em> acute myeloid leukemia, or AML; how stemness contributes to chemotherapy resistance in AML; and effects of babesiosis on red blood cells from individuals with sickle cell disease, sickle cell trait, and wild-type hemoglobin. </p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025154">Measurable residual disease and post-transplantation gilteritinib maintenance for patients with <em>FLT3-ITD</em>-mutated AML</a> </li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025761">GATA2 links stemness to chemotherapy resistance in acute myeloid leukemia </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027602">Babesiosis and Sickle Red Blood Cells: Loss of Deformability, Heightened Osmotic fragility and Hyper-vesiculation </a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, we’ll learn more about how measurable residual disease might help guide decisions about post-transplant gilteritinib maintenance in <em>FLT3-ITD</em> acute myeloid leukemia, or AML; how stemness contributes to chemotherapy resistance in AML; and effects of babesiosis on red blood cells from individuals with sickle cell disease, sickle cell trait, and wild-type hemoglobin. </p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025154">Measurable residual disease and post-transplantation gilteritinib maintenance for patients with <em>FLT3-ITD</em>-mutated AML</a> </li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025761">GATA2 links stemness to chemotherapy resistance in acute myeloid leukemia </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027602">Babesiosis and Sickle Red Blood Cells: Loss of Deformability, Heightened Osmotic fragility and Hyper-vesiculation </a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 08 May 2025 12:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/ef63e85b/58576b3b.mp3" length="23983893" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1198</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, we’ll learn more about how measurable residual disease might help guide decisions about post-transplant gilteritinib maintenance in <em>FLT3-ITD</em> acute myeloid leukemia, or AML; how stemness contributes to chemotherapy resistance in AML; and effects of babesiosis on red blood cells from individuals with sickle cell disease, sickle cell trait, and wild-type hemoglobin. </p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025154">Measurable residual disease and post-transplantation gilteritinib maintenance for patients with <em>FLT3-ITD</em>-mutated AML</a> </li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025761">GATA2 links stemness to chemotherapy resistance in acute myeloid leukemia </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027602">Babesiosis and Sickle Red Blood Cells: Loss of Deformability, Heightened Osmotic fragility and Hyper-vesiculation </a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3loobu4ukmw2f"/>
    </item>
    <item>
      <title>Uniquely programmed blood stem cells in the human lung; inclusive molecular classifier for DLBCL; new insights on NETs in the liver vasculature</title>
      <itunes:season>9</itunes:season>
      <podcast:season>9</podcast:season>
      <itunes:title>Uniquely programmed blood stem cells in the human lung; inclusive molecular classifier for DLBCL; new insights on NETs in the liver vasculature</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">56c693b2-f3a1-418d-a944-8d1a20b72e6a</guid>
      <link>https://share.transistor.fm/s/515c756b</link>
      <description>
        <![CDATA[<p>In this week's episode, we'll hear about how researchers look toward the lung, and find uniquely programmed blood stem cells. This study is the first to fully characterize hematopoietic stem and progenitor cells in the adult human lung. After that: researchers develop a neural network-based probabilistic classifier, DLB<em>class</em>, that assigns all diffuse large B-cell lymphomas into one of five genetic subtypes. It’s an inclusive taxonomy that they say provides actionable genetic information in almost all patients with DLBCL. Finally, new insights on NETS, or neutrophil extracellular traps. In the liver vasculature, NET removal leads to secondary inflammation, resulting in new waves of NETS that may impact future infection. We’ll review these and other findings from this recent mouse model study.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027884">Decoding functional hematopoietic progenitor cells in the adult human lung</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025652">DLB<em>class</em>: a probabilistic molecular classifier to guide clinical investigation and practice in diffuse large B-cell lymphoma</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026446">Donor regulatory T-cell therapy to prevent graft-versus-host disease</a></li></ul><p><br></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, we'll hear about how researchers look toward the lung, and find uniquely programmed blood stem cells. This study is the first to fully characterize hematopoietic stem and progenitor cells in the adult human lung. After that: researchers develop a neural network-based probabilistic classifier, DLB<em>class</em>, that assigns all diffuse large B-cell lymphomas into one of five genetic subtypes. It’s an inclusive taxonomy that they say provides actionable genetic information in almost all patients with DLBCL. Finally, new insights on NETS, or neutrophil extracellular traps. In the liver vasculature, NET removal leads to secondary inflammation, resulting in new waves of NETS that may impact future infection. We’ll review these and other findings from this recent mouse model study.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027884">Decoding functional hematopoietic progenitor cells in the adult human lung</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025652">DLB<em>class</em>: a probabilistic molecular classifier to guide clinical investigation and practice in diffuse large B-cell lymphoma</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026446">Donor regulatory T-cell therapy to prevent graft-versus-host disease</a></li></ul><p><br></p>]]>
      </content:encoded>
      <pubDate>Thu, 01 May 2025 12:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/515c756b/1c81b917.mp3" length="21863206" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1092</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, we'll hear about how researchers look toward the lung, and find uniquely programmed blood stem cells. This study is the first to fully characterize hematopoietic stem and progenitor cells in the adult human lung. After that: researchers develop a neural network-based probabilistic classifier, DLB<em>class</em>, that assigns all diffuse large B-cell lymphomas into one of five genetic subtypes. It’s an inclusive taxonomy that they say provides actionable genetic information in almost all patients with DLBCL. Finally, new insights on NETS, or neutrophil extracellular traps. In the liver vasculature, NET removal leads to secondary inflammation, resulting in new waves of NETS that may impact future infection. We’ll review these and other findings from this recent mouse model study.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027884">Decoding functional hematopoietic progenitor cells in the adult human lung</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025652">DLB<em>class</em>: a probabilistic molecular classifier to guide clinical investigation and practice in diffuse large B-cell lymphoma</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026446">Donor regulatory T-cell therapy to prevent graft-versus-host disease</a></li></ul><p><br></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3lo4ol5pxd22e"/>
    </item>
    <item>
      <title>Phosphoseryl-tRNA kinase inhibition in acute myeloid leukemia (AML), APOE gene variants and post-hematopoietic stem cell transplant outcomes in AML, and the role of chronic inflammation in sickle cell cardiomyopathy</title>
      <itunes:season>9</itunes:season>
      <podcast:season>9</podcast:season>
      <itunes:title>Phosphoseryl-tRNA kinase inhibition in acute myeloid leukemia (AML), APOE gene variants and post-hematopoietic stem cell transplant outcomes in AML, and the role of chronic inflammation in sickle cell cardiomyopathy</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">9bcf49d0-289f-4c2a-b43d-253f84346211</guid>
      <link>https://share.transistor.fm/s/adb234c0</link>
      <description>
        <![CDATA[<p>In this week's episode we’ll learn more about how phosphoseryl-tRNA kinase inhibition promotes cell death in acute myeloid leukemia, or AML; <em>APOE</em> gene variants and their association with post-hematopoietic stem cell transplant outcomes in AML; and pathways by which chronic inflammation and oxidative stress may lead to cardiomyopathy in patients with sickle cell disease.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026040">PSTK inhibition activates cGAS-STING, precipitating ferroptotic cell death in leukemic stem cells </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026886">Common Hereditary Variants of the APOE Gene and Posttransplant Outcome in Acute Myeloid Leukemia </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024768">17R-Resolvin D1 Protects Against Sickle Cell Related Inflammatory Cardiomyopathy in Humanized Mice </a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we’ll learn more about how phosphoseryl-tRNA kinase inhibition promotes cell death in acute myeloid leukemia, or AML; <em>APOE</em> gene variants and their association with post-hematopoietic stem cell transplant outcomes in AML; and pathways by which chronic inflammation and oxidative stress may lead to cardiomyopathy in patients with sickle cell disease.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026040">PSTK inhibition activates cGAS-STING, precipitating ferroptotic cell death in leukemic stem cells </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026886">Common Hereditary Variants of the APOE Gene and Posttransplant Outcome in Acute Myeloid Leukemia </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024768">17R-Resolvin D1 Protects Against Sickle Cell Related Inflammatory Cardiomyopathy in Humanized Mice </a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 24 Apr 2025 12:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/adb234c0/7fe01436.mp3" length="22951017" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1146</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we’ll learn more about how phosphoseryl-tRNA kinase inhibition promotes cell death in acute myeloid leukemia, or AML; <em>APOE</em> gene variants and their association with post-hematopoietic stem cell transplant outcomes in AML; and pathways by which chronic inflammation and oxidative stress may lead to cardiomyopathy in patients with sickle cell disease.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026040">PSTK inhibition activates cGAS-STING, precipitating ferroptotic cell death in leukemic stem cells </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026886">Common Hereditary Variants of the APOE Gene and Posttransplant Outcome in Acute Myeloid Leukemia </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024768">17R-Resolvin D1 Protects Against Sickle Cell Related Inflammatory Cardiomyopathy in Humanized Mice </a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3lnl3bvvko42f"/>
    </item>
    <item>
      <title>How I Treat Myeloproliferative Neoplasms</title>
      <itunes:season>9</itunes:season>
      <podcast:season>9</podcast:season>
      <itunes:title>How I Treat Myeloproliferative Neoplasms</itunes:title>
      <itunes:episodeType>bonus</itunes:episodeType>
      <guid isPermaLink="false">429226c2-9d4c-412a-8630-1e2024dd6cd6</guid>
      <link>https://share.transistor.fm/s/7e60e62e</link>
      <description>
        <![CDATA[<p>In this How I Treat series episode <em>Blood</em> Associate Editor, Dr. Jason Gotlib speaks with Drs. Aaron Gerds, Andreas Reiter, and Claire Harrison. The conversation focuses on the work and contributions of these authors to How I Treat Myeloproliferative Neoplasms, and exciting advances in the treatment and management of MPNs. </p><p><a href="https://ashpublications.org/blood/article/145/16/1707/536654/Introduction-to-a-How-I-Treat-series-on">See the full How I Treat series in volume 145 issue 16 of <em>Blood</em></a><em>.</em></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this How I Treat series episode <em>Blood</em> Associate Editor, Dr. Jason Gotlib speaks with Drs. Aaron Gerds, Andreas Reiter, and Claire Harrison. The conversation focuses on the work and contributions of these authors to How I Treat Myeloproliferative Neoplasms, and exciting advances in the treatment and management of MPNs. </p><p><a href="https://ashpublications.org/blood/article/145/16/1707/536654/Introduction-to-a-How-I-Treat-series-on">See the full How I Treat series in volume 145 issue 16 of <em>Blood</em></a><em>.</em></p>]]>
      </content:encoded>
      <pubDate>Thu, 17 Apr 2025 12:01:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/7e60e62e/d267fdcf.mp3" length="46357769" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/FulBA2sGpwVV_RHBrZF1diDRUAOPCL0zasLAT0CewmM/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS83MTZk/NjU3ODY1MGM5OWU3/NWQ5NGEwMjFkOTY3/YWY5Yy5qcGc.jpg"/>
      <itunes:duration>2316</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this How I Treat series episode <em>Blood</em> Associate Editor, Dr. Jason Gotlib speaks with Drs. Aaron Gerds, Andreas Reiter, and Claire Harrison. The conversation focuses on the work and contributions of these authors to How I Treat Myeloproliferative Neoplasms, and exciting advances in the treatment and management of MPNs. </p><p><a href="https://ashpublications.org/blood/article/145/16/1707/536654/Introduction-to-a-How-I-Treat-series-on">See the full How I Treat series in volume 145 issue 16 of <em>Blood</em></a><em>.</em></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3lmzi3jjbjj2q"/>
    </item>
    <item>
      <title>The decline of transplant for relapsed myeloma; DDAVP response in bleeding disorders; dual DOT1L/EZH2 targeting in DLBCL</title>
      <itunes:season>9</itunes:season>
      <podcast:season>9</podcast:season>
      <itunes:title>The decline of transplant for relapsed myeloma; DDAVP response in bleeding disorders; dual DOT1L/EZH2 targeting in DLBCL</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">841b72c7-71db-4c4d-8237-60f415365fd3</guid>
      <link>https://share.transistor.fm/s/1bf04e68</link>
      <description>
        <![CDATA[<p>In this week's episode we'll learn about the role of autologous transplant for relapsed myeloma. In an updated analysis of the GMMG ReLApsE trial, salvage autologous transplant offered no survival benefit compared to control chemotherapy. These findings may have clinical implications in an era of alternative, and highly effective, treatment options. After that: Response to DDAVP, or desmopressin, in bleeding disorders. This study is the first large scale meta-analysis to assess the response rate to DDAVP in bleeding disorders. Authors provide new insights into determinants of response, which vary according to the disease type. Finally, turning to diffuse large B cell lymphoma. Germinal center B cells depend on the activity of DOT1 and EZH2 to maintain their pro-proliferative identity. New research shows that combined treatment with DOT1L and EZH2 inhibitors has synergistic activity in vitro.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027342">Salvage autologous transplant in relapsed multiple myeloma: long-term follow-up of the phase 3 GMMG ReLApsE trial</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026804">DDAVP response and its determinants in bleeding disorders: a systematic review and meta-analysis</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025500">Targeting DOT1L and EZH2 synergizes in breaking the germinal center identity of diffuse large B-cell lymphoma</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we'll learn about the role of autologous transplant for relapsed myeloma. In an updated analysis of the GMMG ReLApsE trial, salvage autologous transplant offered no survival benefit compared to control chemotherapy. These findings may have clinical implications in an era of alternative, and highly effective, treatment options. After that: Response to DDAVP, or desmopressin, in bleeding disorders. This study is the first large scale meta-analysis to assess the response rate to DDAVP in bleeding disorders. Authors provide new insights into determinants of response, which vary according to the disease type. Finally, turning to diffuse large B cell lymphoma. Germinal center B cells depend on the activity of DOT1 and EZH2 to maintain their pro-proliferative identity. New research shows that combined treatment with DOT1L and EZH2 inhibitors has synergistic activity in vitro.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027342">Salvage autologous transplant in relapsed multiple myeloma: long-term follow-up of the phase 3 GMMG ReLApsE trial</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026804">DDAVP response and its determinants in bleeding disorders: a systematic review and meta-analysis</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025500">Targeting DOT1L and EZH2 synergizes in breaking the germinal center identity of diffuse large B-cell lymphoma</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 17 Apr 2025 12:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/1bf04e68/46aee1b2.mp3" length="22611852" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1129</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we'll learn about the role of autologous transplant for relapsed myeloma. In an updated analysis of the GMMG ReLApsE trial, salvage autologous transplant offered no survival benefit compared to control chemotherapy. These findings may have clinical implications in an era of alternative, and highly effective, treatment options. After that: Response to DDAVP, or desmopressin, in bleeding disorders. This study is the first large scale meta-analysis to assess the response rate to DDAVP in bleeding disorders. Authors provide new insights into determinants of response, which vary according to the disease type. Finally, turning to diffuse large B cell lymphoma. Germinal center B cells depend on the activity of DOT1 and EZH2 to maintain their pro-proliferative identity. New research shows that combined treatment with DOT1L and EZH2 inhibitors has synergistic activity in vitro.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027342">Salvage autologous transplant in relapsed multiple myeloma: long-term follow-up of the phase 3 GMMG ReLApsE trial</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026804">DDAVP response and its determinants in bleeding disorders: a systematic review and meta-analysis</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025500">Targeting DOT1L and EZH2 synergizes in breaking the germinal center identity of diffuse large B-cell lymphoma</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3lmzhztvzph2g"/>
    </item>
    <item>
      <title>Interleukin-1 signaling pathways in myelodysplastic syndromes, the immune checkpoint regulator VISTA as a target in graft-vs-host disease, and epcoritamab plus chemotherapy in transplant-ineligible relapsed/refractory diffuse large B-cell lymphoma</title>
      <itunes:season>9</itunes:season>
      <podcast:season>9</podcast:season>
      <itunes:title>Interleukin-1 signaling pathways in myelodysplastic syndromes, the immune checkpoint regulator VISTA as a target in graft-vs-host disease, and epcoritamab plus chemotherapy in transplant-ineligible relapsed/refractory diffuse large B-cell lymphoma</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">58826505-951b-4e6e-a86a-17f508aa8b4b</guid>
      <link>https://share.transistor.fm/s/ebbbbdcc</link>
      <description>
        <![CDATA[<p>In this week's episode we’ll learn about the role of interleukin-1 signaling in the bone marrow microenvironment in the development of myelodysplastic syndromes, the immune checkpoint regulator VISTA as a potential target for preventing graft-vs-host disease, and epcoritamab plus gemcitabine and oxaliplatin in transplant-ineligible relapsed/refractory diffuse large B-cell lymphoma.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024818">IL-1R1 and IL-18 signals regulate mesenchymal stromal cells in an aged murine model of myelodysplastic syndromes</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025884">Targeting cell-surface VISTA expression on allospecific naïve T cells promotes tolerance</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026830">Epcoritamab plus GemOx in transplant-ineligible relapsed/refractory DLBCL: results from the EPCORE NHL-2 trial</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we’ll learn about the role of interleukin-1 signaling in the bone marrow microenvironment in the development of myelodysplastic syndromes, the immune checkpoint regulator VISTA as a potential target for preventing graft-vs-host disease, and epcoritamab plus gemcitabine and oxaliplatin in transplant-ineligible relapsed/refractory diffuse large B-cell lymphoma.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024818">IL-1R1 and IL-18 signals regulate mesenchymal stromal cells in an aged murine model of myelodysplastic syndromes</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025884">Targeting cell-surface VISTA expression on allospecific naïve T cells promotes tolerance</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026830">Epcoritamab plus GemOx in transplant-ineligible relapsed/refractory DLBCL: results from the EPCORE NHL-2 trial</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 10 Apr 2025 12:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/ebbbbdcc/fdb5e68c.mp3" length="25211685" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1259</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we’ll learn about the role of interleukin-1 signaling in the bone marrow microenvironment in the development of myelodysplastic syndromes, the immune checkpoint regulator VISTA as a potential target for preventing graft-vs-host disease, and epcoritamab plus gemcitabine and oxaliplatin in transplant-ineligible relapsed/refractory diffuse large B-cell lymphoma.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024818">IL-1R1 and IL-18 signals regulate mesenchymal stromal cells in an aged murine model of myelodysplastic syndromes</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025884">Targeting cell-surface VISTA expression on allospecific naïve T cells promotes tolerance</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026830">Epcoritamab plus GemOx in transplant-ineligible relapsed/refractory DLBCL: results from the EPCORE NHL-2 trial</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3lmhurubsc32g"/>
    </item>
    <item>
      <title>Aging platelets shift to proinflammatory function; Odronextamab bispecific antibody therapy after CAR T in DLBCL; prizlon-cel, a novel bispecific CAR T, in B-NHL</title>
      <itunes:season>9</itunes:season>
      <podcast:season>9</podcast:season>
      <itunes:title>Aging platelets shift to proinflammatory function; Odronextamab bispecific antibody therapy after CAR T in DLBCL; prizlon-cel, a novel bispecific CAR T, in B-NHL</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">e35f64cb-7711-4f7b-884b-4498241fabc5</guid>
      <link>https://share.transistor.fm/s/7c38a2f2</link>
      <description>
        <![CDATA[<p>In this week's episode we'll learn about tracking the functional profile of aging platelets. Researchers demonstrate that over time, platelet function shifts away from hemostasis and toward a more immunomodulatory role. These finding could have important implications for transfusion medicine and certain platelet-related disease states. After that, use of odronextamab, a CD20×CD3 bispecific antibody, in patients with diffuse large B-cell lymphoma, or DLBCL, progressing after CAR T cell therapy. The study is the first to evaluate the efficacy and safety of this therapy in the post-CAR T cell treatment setting. Finally, we will recap findings from a study of a novel CAR T-cell product that utilizes specificity to two antigens common in diffuse large B-cell lymphoma.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024901">Aging platelets shift their hemostatic properties to inflammatory functions</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027044">Odronextamab monotherapy in R/R DLBCL after progression with CAR T-cell therapy: primary analysis of the ELM-1 study</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022197">Dissection of single-cell landscapes for the development of chimeric antigen receptor T cells in Hodgkin lymphoma</a></li></ul><p><br></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we'll learn about tracking the functional profile of aging platelets. Researchers demonstrate that over time, platelet function shifts away from hemostasis and toward a more immunomodulatory role. These finding could have important implications for transfusion medicine and certain platelet-related disease states. After that, use of odronextamab, a CD20×CD3 bispecific antibody, in patients with diffuse large B-cell lymphoma, or DLBCL, progressing after CAR T cell therapy. The study is the first to evaluate the efficacy and safety of this therapy in the post-CAR T cell treatment setting. Finally, we will recap findings from a study of a novel CAR T-cell product that utilizes specificity to two antigens common in diffuse large B-cell lymphoma.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024901">Aging platelets shift their hemostatic properties to inflammatory functions</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027044">Odronextamab monotherapy in R/R DLBCL after progression with CAR T-cell therapy: primary analysis of the ELM-1 study</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022197">Dissection of single-cell landscapes for the development of chimeric antigen receptor T cells in Hodgkin lymphoma</a></li></ul><p><br></p>]]>
      </content:encoded>
      <pubDate>Thu, 03 Apr 2025 12:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/7c38a2f2/4cfb227b.mp3" length="18555599" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>926</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we'll learn about tracking the functional profile of aging platelets. Researchers demonstrate that over time, platelet function shifts away from hemostasis and toward a more immunomodulatory role. These finding could have important implications for transfusion medicine and certain platelet-related disease states. After that, use of odronextamab, a CD20×CD3 bispecific antibody, in patients with diffuse large B-cell lymphoma, or DLBCL, progressing after CAR T cell therapy. The study is the first to evaluate the efficacy and safety of this therapy in the post-CAR T cell treatment setting. Finally, we will recap findings from a study of a novel CAR T-cell product that utilizes specificity to two antigens common in diffuse large B-cell lymphoma.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024901">Aging platelets shift their hemostatic properties to inflammatory functions</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027044">Odronextamab monotherapy in R/R DLBCL after progression with CAR T-cell therapy: primary analysis of the ELM-1 study</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022197">Dissection of single-cell landscapes for the development of chimeric antigen receptor T cells in Hodgkin lymphoma</a></li></ul><p><br></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3llwb4chrdy2s"/>
    </item>
    <item>
      <title>Blood Bonus Episode: What is a Blood group? </title>
      <itunes:season>9</itunes:season>
      <podcast:season>9</podcast:season>
      <itunes:title>Blood Bonus Episode: What is a Blood group? </itunes:title>
      <itunes:episodeType>bonus</itunes:episodeType>
      <guid isPermaLink="false">d11b60c9-106d-4eb3-82aa-5c529f47ce10</guid>
      <link>https://share.transistor.fm/s/03660e6e</link>
      <description>
        <![CDATA[<p>In this bonus episode of the <em>Blood </em>podcast, we'll hear from Dr. Nicole Thornton, senior author of the article “<a href="https://ashpublications.org/blood/article/144/26/2735/517404/Deletions-in-the-MAL-gene-result-in-loss-of-Mal">Deletions in the MAL gene result in loss of Mal protein, defining the rare inherited AnWj-negative blood group phenotype</a>”, speaks with <em>Blood </em>Associate Editor Dr. Erica Wood about the discovery of the genetic basis for the inherited AnWj-negative blood group phenotype. The discovery that Mal protein is expressed on red blood cell membranes of AnWj-positive, but not AnWj-negative individuals, and that homozygous deletion in MAL causes the AnWj-negative blood group phenotype, helps answer a decades-old mystery related to the high prevalence red blood cell antigen AnWj and forms the basis of a new blood group system. </p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this bonus episode of the <em>Blood </em>podcast, we'll hear from Dr. Nicole Thornton, senior author of the article “<a href="https://ashpublications.org/blood/article/144/26/2735/517404/Deletions-in-the-MAL-gene-result-in-loss-of-Mal">Deletions in the MAL gene result in loss of Mal protein, defining the rare inherited AnWj-negative blood group phenotype</a>”, speaks with <em>Blood </em>Associate Editor Dr. Erica Wood about the discovery of the genetic basis for the inherited AnWj-negative blood group phenotype. The discovery that Mal protein is expressed on red blood cell membranes of AnWj-positive, but not AnWj-negative individuals, and that homozygous deletion in MAL causes the AnWj-negative blood group phenotype, helps answer a decades-old mystery related to the high prevalence red blood cell antigen AnWj and forms the basis of a new blood group system. </p>]]>
      </content:encoded>
      <pubDate>Mon, 31 Mar 2025 12:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/03660e6e/849593bd.mp3" length="18017177" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>899</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this bonus episode of the <em>Blood </em>podcast, we'll hear from Dr. Nicole Thornton, senior author of the article “<a href="https://ashpublications.org/blood/article/144/26/2735/517404/Deletions-in-the-MAL-gene-result-in-loss-of-Mal">Deletions in the MAL gene result in loss of Mal protein, defining the rare inherited AnWj-negative blood group phenotype</a>”, speaks with <em>Blood </em>Associate Editor Dr. Erica Wood about the discovery of the genetic basis for the inherited AnWj-negative blood group phenotype. The discovery that Mal protein is expressed on red blood cell membranes of AnWj-positive, but not AnWj-negative individuals, and that homozygous deletion in MAL causes the AnWj-negative blood group phenotype, helps answer a decades-old mystery related to the high prevalence red blood cell antigen AnWj and forms the basis of a new blood group system. </p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3lloq4h3szc2b"/>
    </item>
    <item>
      <title>Itacitinib in haploidentical hematopoietic cell transplantation, diagnosis and management of purpura fulminans, and lack of evidence for sickle cell crisis-associated mortality in individuals with sickle cell trait</title>
      <itunes:season>9</itunes:season>
      <podcast:season>9</podcast:season>
      <itunes:title>Itacitinib in haploidentical hematopoietic cell transplantation, diagnosis and management of purpura fulminans, and lack of evidence for sickle cell crisis-associated mortality in individuals with sickle cell trait</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">c9c711eb-f921-40be-b726-99086a4c8c2c</guid>
      <link>https://share.transistor.fm/s/3c55c845</link>
      <description>
        <![CDATA[<p>In this week's episode, we’ll learn more about using itacitinib for the prevention of graft vs host disease in haploidentical transplants, diagnosis and management of purpura fulminans, and results of a systematic review seeking evidence for sickle cell crisis-associated mortality in individuals with sickle cell trait.</p><p><strong> <br></strong>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026497">Itacitinib for prevention of graft-versus-host disease and cytokine release syndrome in haploidentical transplantation</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025078">How I diagnose and treat acute infection–associated purpura fulminans</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026899">Sickle cell trait does not cause “sickle cell crisis” leading to exertion-related death: a systematic review</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, we’ll learn more about using itacitinib for the prevention of graft vs host disease in haploidentical transplants, diagnosis and management of purpura fulminans, and results of a systematic review seeking evidence for sickle cell crisis-associated mortality in individuals with sickle cell trait.</p><p><strong> <br></strong>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026497">Itacitinib for prevention of graft-versus-host disease and cytokine release syndrome in haploidentical transplantation</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025078">How I diagnose and treat acute infection–associated purpura fulminans</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026899">Sickle cell trait does not cause “sickle cell crisis” leading to exertion-related death: a systematic review</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 27 Mar 2025 12:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/3c55c845/e9a15171.mp3" length="23144322" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1156</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, we’ll learn more about using itacitinib for the prevention of graft vs host disease in haploidentical transplants, diagnosis and management of purpura fulminans, and results of a systematic review seeking evidence for sickle cell crisis-associated mortality in individuals with sickle cell trait.</p><p><strong> <br></strong>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026497">Itacitinib for prevention of graft-versus-host disease and cytokine release syndrome in haploidentical transplantation</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025078">How I diagnose and treat acute infection–associated purpura fulminans</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026899">Sickle cell trait does not cause “sickle cell crisis” leading to exertion-related death: a systematic review</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3lleoannlme2z"/>
    </item>
    <item>
      <title>Time-limited triplet therapy in relapsed/refractory CLL; patient-reported outcomes in chronic GVHD-related sclerosis; myeloid bias mechanisms in hematopoiesis</title>
      <itunes:season>9</itunes:season>
      <podcast:season>9</podcast:season>
      <itunes:title>Time-limited triplet therapy in relapsed/refractory CLL; patient-reported outcomes in chronic GVHD-related sclerosis; myeloid bias mechanisms in hematopoiesis</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">2d4ff251-ff47-48e5-a82c-b038269a8be1</guid>
      <link>https://share.transistor.fm/s/1930495c</link>
      <description>
        <![CDATA[<p>In today's episode, we'll discuss time-limited triplet therapy in relapsed or refractory CLL. Zanubrutinib, venetoclax and obinutuzumab induced deep remissions, and was well tolerated, even in very high-risk patients, and those with prior exposure to targeted therapies. After that: researchers chronicle the development of a patient-reported outcome measure for sclerosis associated with chronic GVHD—graft-versus-host disease. The new symptom scale—currently undergoing validation studies—may provide valuable information regarding severity, functional impact, and response to therapy. Finally, a study of changes in population dynamic rates that underlie inflammation-associated myeloid bias. The work demonstrates the use of mathematical models to deliver critical biological insights and uncover underlying mechanisms.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026685">MRD-guided zanubrutinib, venetoclax, and obinutuzumab in relapsed CLL: primary end point analysis from the CLL2-BZAG trial</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027334">Development of the Lee Symptom Scale–Skin Sclerosis for chronic GVHD–associated sclerosis</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025598">Population dynamics modeling reveals that myeloid bias involves both HSC differentiation and progenitor proliferation biases</a></li></ul><p><br></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In today's episode, we'll discuss time-limited triplet therapy in relapsed or refractory CLL. Zanubrutinib, venetoclax and obinutuzumab induced deep remissions, and was well tolerated, even in very high-risk patients, and those with prior exposure to targeted therapies. After that: researchers chronicle the development of a patient-reported outcome measure for sclerosis associated with chronic GVHD—graft-versus-host disease. The new symptom scale—currently undergoing validation studies—may provide valuable information regarding severity, functional impact, and response to therapy. Finally, a study of changes in population dynamic rates that underlie inflammation-associated myeloid bias. The work demonstrates the use of mathematical models to deliver critical biological insights and uncover underlying mechanisms.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026685">MRD-guided zanubrutinib, venetoclax, and obinutuzumab in relapsed CLL: primary end point analysis from the CLL2-BZAG trial</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027334">Development of the Lee Symptom Scale–Skin Sclerosis for chronic GVHD–associated sclerosis</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025598">Population dynamics modeling reveals that myeloid bias involves both HSC differentiation and progenitor proliferation biases</a></li></ul><p><br></p>]]>
      </content:encoded>
      <pubDate>Thu, 20 Mar 2025 13:02:46 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/1930495c/e86eae61.mp3" length="22977605" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1147</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In today's episode, we'll discuss time-limited triplet therapy in relapsed or refractory CLL. Zanubrutinib, venetoclax and obinutuzumab induced deep remissions, and was well tolerated, even in very high-risk patients, and those with prior exposure to targeted therapies. After that: researchers chronicle the development of a patient-reported outcome measure for sclerosis associated with chronic GVHD—graft-versus-host disease. The new symptom scale—currently undergoing validation studies—may provide valuable information regarding severity, functional impact, and response to therapy. Finally, a study of changes in population dynamic rates that underlie inflammation-associated myeloid bias. The work demonstrates the use of mathematical models to deliver critical biological insights and uncover underlying mechanisms.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026685">MRD-guided zanubrutinib, venetoclax, and obinutuzumab in relapsed CLL: primary end point analysis from the CLL2-BZAG trial</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024027334">Development of the Lee Symptom Scale–Skin Sclerosis for chronic GVHD–associated sclerosis</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025598">Population dynamics modeling reveals that myeloid bias involves both HSC differentiation and progenitor proliferation biases</a></li></ul><p><br></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3lkt6hul67j22"/>
    </item>
    <item>
      <title>Azacitidine plus venetoclax in high-risk myelodysplastic syndromes, post-CAR T-cell hematotoxicity in B-cell acute lymphoblastic leukemia (B-ALL), and inotuzumab ozogamicin resistance in B-ALL</title>
      <itunes:season>9</itunes:season>
      <podcast:season>9</podcast:season>
      <itunes:title>Azacitidine plus venetoclax in high-risk myelodysplastic syndromes, post-CAR T-cell hematotoxicity in B-cell acute lymphoblastic leukemia (B-ALL), and inotuzumab ozogamicin resistance in B-ALL</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">09a1a90f-dd0e-41c9-83f2-4494d8452248</guid>
      <link>https://share.transistor.fm/s/71521b54</link>
      <description>
        <![CDATA[<p>In this week's episode we’ll learn more about azacitidine-venetoclax combination therapy for first-line treatment of high-risk myelodysplastic syndromes; a new risk-scoring system for post-CAR T-cell hematotoxicity in B-cell acute lymphoblastic leukemia, also known as B-ALL; and a novel mechanism for inotuzumab ozogamicin resistance in B-ALL.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025464">Efficacy and safety of venetoclax plus azacitidine for patients with treatment-naive high-risk myelodysplastic syndromes</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025910">Development of ALL-Hematotox: predicting post-CAR T-cell hematotoxicity in B-cell acute lymphoblastic leukemia</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026085">DNTT-mediated DNA damage response drives inotuzumab ozogamicin resistance in B-cell acute lymphoblastic leukemia</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we’ll learn more about azacitidine-venetoclax combination therapy for first-line treatment of high-risk myelodysplastic syndromes; a new risk-scoring system for post-CAR T-cell hematotoxicity in B-cell acute lymphoblastic leukemia, also known as B-ALL; and a novel mechanism for inotuzumab ozogamicin resistance in B-ALL.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025464">Efficacy and safety of venetoclax plus azacitidine for patients with treatment-naive high-risk myelodysplastic syndromes</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025910">Development of ALL-Hematotox: predicting post-CAR T-cell hematotoxicity in B-cell acute lymphoblastic leukemia</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026085">DNTT-mediated DNA damage response drives inotuzumab ozogamicin resistance in B-cell acute lymphoblastic leukemia</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 13 Mar 2025 12:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/71521b54/47d9a646.mp3" length="25789459" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1288</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we’ll learn more about azacitidine-venetoclax combination therapy for first-line treatment of high-risk myelodysplastic syndromes; a new risk-scoring system for post-CAR T-cell hematotoxicity in B-cell acute lymphoblastic leukemia, also known as B-ALL; and a novel mechanism for inotuzumab ozogamicin resistance in B-ALL.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025464">Efficacy and safety of venetoclax plus azacitidine for patients with treatment-naive high-risk myelodysplastic syndromes</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025910">Development of ALL-Hematotox: predicting post-CAR T-cell hematotoxicity in B-cell acute lymphoblastic leukemia</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026085">DNTT-mediated DNA damage response drives inotuzumab ozogamicin resistance in B-cell acute lymphoblastic leukemia</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3lkbhpdplvu2l"/>
    </item>
    <item>
      <title>Mutations in AMBRA1 aggravate β-thalassemia; targeting MYD88 mutations in lymphomas; air pollution and incident VTE risk</title>
      <itunes:season>9</itunes:season>
      <podcast:season>9</podcast:season>
      <itunes:title>Mutations in AMBRA1 aggravate β-thalassemia; targeting MYD88 mutations in lymphomas; air pollution and incident VTE risk</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">19f43fc7-4666-487e-b940-8130c3c32834</guid>
      <link>https://share.transistor.fm/s/e5ad1753</link>
      <description>
        <![CDATA[<p>In this week's podcast, a potential new therapeutic target in beta-thalassemia. The E3 ubiquitin ligase <em>AMBRA1 </em>promotes autophagic clearance of free alpha-globin. Researchers describe mutations in the AMBRA1 gene that impair this clearance, exacerbating ineffective erythropoiesis and disease severity. After that: targeting <em>MYD88</em> mutations. Lasalocid-A is a compound that selectively binds to the MYD88 L265P mutant protein, which is found in a range of B-cell lymphomas. New research shows its potential to inhibit tumor growth, overcome ibrutinib resistance, and synergize with venetoclax. Finally: air pollution is linked to an increased risk of venous thromboembolism in a prospective, community-based cohort study. The findings highlight the harms of pollution, and support the case for global efforts to improve public health.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022688">Mutations in <em>AMBRA1</em> aggravate β-thalassemia by impairing autophagy-mediated clearance of free α-globin</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026781">Lasalocid A selectively induces the degradation of MYD88 in lymphomas harboring the MYD88 L265P mutation</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026399">Air pollution is associated with increased risk of venous thromboembolism: the Multi-Ethnic Study of Atherosclerosis</a></li></ul><p><br></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's podcast, a potential new therapeutic target in beta-thalassemia. The E3 ubiquitin ligase <em>AMBRA1 </em>promotes autophagic clearance of free alpha-globin. Researchers describe mutations in the AMBRA1 gene that impair this clearance, exacerbating ineffective erythropoiesis and disease severity. After that: targeting <em>MYD88</em> mutations. Lasalocid-A is a compound that selectively binds to the MYD88 L265P mutant protein, which is found in a range of B-cell lymphomas. New research shows its potential to inhibit tumor growth, overcome ibrutinib resistance, and synergize with venetoclax. Finally: air pollution is linked to an increased risk of venous thromboembolism in a prospective, community-based cohort study. The findings highlight the harms of pollution, and support the case for global efforts to improve public health.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022688">Mutations in <em>AMBRA1</em> aggravate β-thalassemia by impairing autophagy-mediated clearance of free α-globin</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026781">Lasalocid A selectively induces the degradation of MYD88 in lymphomas harboring the MYD88 L265P mutation</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026399">Air pollution is associated with increased risk of venous thromboembolism: the Multi-Ethnic Study of Atherosclerosis</a></li></ul><p><br></p>]]>
      </content:encoded>
      <pubDate>Thu, 06 Mar 2025 12:00:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/e5ad1753/191c9a4e.mp3" length="21398119" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1068</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's podcast, a potential new therapeutic target in beta-thalassemia. The E3 ubiquitin ligase <em>AMBRA1 </em>promotes autophagic clearance of free alpha-globin. Researchers describe mutations in the AMBRA1 gene that impair this clearance, exacerbating ineffective erythropoiesis and disease severity. After that: targeting <em>MYD88</em> mutations. Lasalocid-A is a compound that selectively binds to the MYD88 L265P mutant protein, which is found in a range of B-cell lymphomas. New research shows its potential to inhibit tumor growth, overcome ibrutinib resistance, and synergize with venetoclax. Finally: air pollution is linked to an increased risk of venous thromboembolism in a prospective, community-based cohort study. The findings highlight the harms of pollution, and support the case for global efforts to improve public health.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022688">Mutations in <em>AMBRA1</em> aggravate β-thalassemia by impairing autophagy-mediated clearance of free α-globin</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026781">Lasalocid A selectively induces the degradation of MYD88 in lymphomas harboring the MYD88 L265P mutation</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026399">Air pollution is associated with increased risk of venous thromboembolism: the Multi-Ethnic Study of Atherosclerosis</a></li></ul><p><br></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3ljpxsgmcfy2t"/>
    </item>
    <item>
      <title>Hypercalcemia in monoclonal gammopathy of undetermined significance, neutrophil gelatinase-associated lipocalin in hemostasis, and CD19-targeted NK- or T-cell therapy combined with anti-CD19 monoclonal antibodies</title>
      <itunes:season>9</itunes:season>
      <podcast:season>9</podcast:season>
      <itunes:title>Hypercalcemia in monoclonal gammopathy of undetermined significance, neutrophil gelatinase-associated lipocalin in hemostasis, and CD19-targeted NK- or T-cell therapy combined with anti-CD19 monoclonal antibodies</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">f8a36211-df6a-4508-8d17-cdb45796c429</guid>
      <link>https://share.transistor.fm/s/b648bf5f</link>
      <description>
        <![CDATA[<p>In this week's episode we’ll learn more about the significance of hypercalcemia in monoclonal gammopathy of undetermined significance, the role of neutrophil gelatinase-associated lipocalin in hemostasis, and the feasibility of combining CD19-targeted NK- or T-cell therapy with anti-CD19 monoclonal antibodies.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025624">Approaching Hypercalcemia in Gammopathy of Undetermined Significance: Insights from the iStopMM study </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025624">Deficiency of neutrophil gelatinase-associated lipocalin elicits Hemophilia-like bleeding and clotting disorder </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025673">Anti-CD19 antibody cotreatment enhances serial killing activity of anti-CD19 CAR-T/-NK cells and reduces trogocytosis </a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we’ll learn more about the significance of hypercalcemia in monoclonal gammopathy of undetermined significance, the role of neutrophil gelatinase-associated lipocalin in hemostasis, and the feasibility of combining CD19-targeted NK- or T-cell therapy with anti-CD19 monoclonal antibodies.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025624">Approaching Hypercalcemia in Gammopathy of Undetermined Significance: Insights from the iStopMM study </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025624">Deficiency of neutrophil gelatinase-associated lipocalin elicits Hemophilia-like bleeding and clotting disorder </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025673">Anti-CD19 antibody cotreatment enhances serial killing activity of anti-CD19 CAR-T/-NK cells and reduces trogocytosis </a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 27 Feb 2025 12:00:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/b648bf5f/a61678c0.mp3" length="23380691" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1168</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we’ll learn more about the significance of hypercalcemia in monoclonal gammopathy of undetermined significance, the role of neutrophil gelatinase-associated lipocalin in hemostasis, and the feasibility of combining CD19-targeted NK- or T-cell therapy with anti-CD19 monoclonal antibodies.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025624">Approaching Hypercalcemia in Gammopathy of Undetermined Significance: Insights from the iStopMM study </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025624">Deficiency of neutrophil gelatinase-associated lipocalin elicits Hemophilia-like bleeding and clotting disorder </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025673">Anti-CD19 antibody cotreatment enhances serial killing activity of anti-CD19 CAR-T/-NK cells and reduces trogocytosis </a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3lj6ejmy3sl2d"/>
    </item>
    <item>
      <title>Review Series on a Quarter Century of TKIs in CML</title>
      <itunes:season>9</itunes:season>
      <podcast:season>9</podcast:season>
      <itunes:title>Review Series on a Quarter Century of TKIs in CML</itunes:title>
      <itunes:episodeType>bonus</itunes:episodeType>
      <guid isPermaLink="false">305753b0-b0ad-44f8-9a5b-865e0447bc3a</guid>
      <link>https://share.transistor.fm/s/eecdddc8</link>
      <description>
        <![CDATA[<p>In this Review Series episode Reflections on a Quarter Century of TKIs in CML introduced by Associate Editor Dr. Jason Gottlieb, we’ll hear from contributing authors Drs. Brian Drucker, Francois Guillot, Tim Hughes and Michael Deininger, as they discuss how CML treatment has been impacted since the introduction of tyrosine kinase inhibitors 25 years ago.</p><p><a href="https://ashpublications.org/blood/article/145/9/909/534974/Introduction-to-a-series-of-reflections-on-a%20target=%22_blank%22">Click here to view the complete Review Series featured in Volume 145 Issue 9 of <em>Blood</em>.</a></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this Review Series episode Reflections on a Quarter Century of TKIs in CML introduced by Associate Editor Dr. Jason Gottlieb, we’ll hear from contributing authors Drs. Brian Drucker, Francois Guillot, Tim Hughes and Michael Deininger, as they discuss how CML treatment has been impacted since the introduction of tyrosine kinase inhibitors 25 years ago.</p><p><a href="https://ashpublications.org/blood/article/145/9/909/534974/Introduction-to-a-series-of-reflections-on-a%20target=%22_blank%22">Click here to view the complete Review Series featured in Volume 145 Issue 9 of <em>Blood</em>.</a></p>]]>
      </content:encoded>
      <pubDate>Thu, 27 Feb 2025 11:49:22 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/eecdddc8/1dda084b.mp3" length="39732648" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/UOzWWqAX2T7gETIlWX3vaT7VJQ77KO7UXYNXtL29Szw/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS9jMTVl/ODhiODQxNTdjN2I2/NDA5MTViN2E0Mjg3/MzUxOS5qcGc.jpg"/>
      <itunes:duration>1985</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this Review Series episode Reflections on a Quarter Century of TKIs in CML introduced by Associate Editor Dr. Jason Gottlieb, we’ll hear from contributing authors Drs. Brian Drucker, Francois Guillot, Tim Hughes and Michael Deininger, as they discuss how CML treatment has been impacted since the introduction of tyrosine kinase inhibitors 25 years ago.</p><p><a href="https://ashpublications.org/blood/article/145/9/909/534974/Introduction-to-a-series-of-reflections-on-a%20target=%22_blank%22">Click here to view the complete Review Series featured in Volume 145 Issue 9 of <em>Blood</em>.</a></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3lj6dwqg6ka2g"/>
    </item>
    <item>
      <title>A “belt and suspenders” approach to PNH; oral pathogens exacerbate chronic GVHD; microbial metabolome changes may adversely impact CAR-T outcomes </title>
      <itunes:season>9</itunes:season>
      <podcast:season>9</podcast:season>
      <itunes:title>A “belt and suspenders” approach to PNH; oral pathogens exacerbate chronic GVHD; microbial metabolome changes may adversely impact CAR-T outcomes </itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">f8c5ebee-048c-4f63-82ef-b372f042bdd8</guid>
      <link>https://share.transistor.fm/s/2918794f</link>
      <description>
        <![CDATA[<p>In this week's episode, we'll hear about a “belt and suspenders” approach to paroxysmal nocturnal hemoglobinuria, or PNH. We’ll review long-term efficacy data for danicopan—an oral complement factor D inhibitor recently approved as an add-on to C5 inhibitor therapy.<br>After that: researchers show how oral pathogens may exacerbate chronic graft-versus-host disease. And they assess targeted interventions to mitigate these effects. Finally, we move from the oral to the gut microbiome. New findings suggest that intestinal dysbiosis, induced by antibiotics, may adversely affect outcomes among patients who are receiving CAR-T cell therapy.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026299">Long-term efficacy and safety of danicopan as add-on therapy to ravulizumab or eculizumab in PNH with significant EVH</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024540">Oral inflammation and microbiome dysbiosis exacerbate chronic graft-versus-host disease</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025366">Antibiotic-induced loss of gut microbiome metabolic output correlates with clinical responses to CAR T-cell therapy</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, we'll hear about a “belt and suspenders” approach to paroxysmal nocturnal hemoglobinuria, or PNH. We’ll review long-term efficacy data for danicopan—an oral complement factor D inhibitor recently approved as an add-on to C5 inhibitor therapy.<br>After that: researchers show how oral pathogens may exacerbate chronic graft-versus-host disease. And they assess targeted interventions to mitigate these effects. Finally, we move from the oral to the gut microbiome. New findings suggest that intestinal dysbiosis, induced by antibiotics, may adversely affect outcomes among patients who are receiving CAR-T cell therapy.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026299">Long-term efficacy and safety of danicopan as add-on therapy to ravulizumab or eculizumab in PNH with significant EVH</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024540">Oral inflammation and microbiome dysbiosis exacerbate chronic graft-versus-host disease</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025366">Antibiotic-induced loss of gut microbiome metabolic output correlates with clinical responses to CAR T-cell therapy</a></li></ul>]]>
      </content:encoded>
      <pubDate>Fri, 21 Feb 2025 12:00:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/2918794f/4e8edd6d.mp3" length="22992597" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1149</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, we'll hear about a “belt and suspenders” approach to paroxysmal nocturnal hemoglobinuria, or PNH. We’ll review long-term efficacy data for danicopan—an oral complement factor D inhibitor recently approved as an add-on to C5 inhibitor therapy.<br>After that: researchers show how oral pathogens may exacerbate chronic graft-versus-host disease. And they assess targeted interventions to mitigate these effects. Finally, we move from the oral to the gut microbiome. New findings suggest that intestinal dysbiosis, induced by antibiotics, may adversely affect outcomes among patients who are receiving CAR-T cell therapy.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026299">Long-term efficacy and safety of danicopan as add-on therapy to ravulizumab or eculizumab in PNH with significant EVH</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024540">Oral inflammation and microbiome dysbiosis exacerbate chronic graft-versus-host disease</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025366">Antibiotic-induced loss of gut microbiome metabolic output correlates with clinical responses to CAR T-cell therapy</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
      <podcast:socialInteract protocol="atproto" uri="at://did:plc:76mgbwf3yum2vv7y75n7phww/app.bsky.feed.post/3lipbq3tgc324"/>
    </item>
    <item>
      <title>Mosunetuzumab in relapsed/refractory follicular lymphoma, CD70 CAR T-cells and an anti-CD33/anti-CD3 bispecific antibody in acute myeloid leukemia, and ferroptosis in stored red blood cells</title>
      <itunes:season>9</itunes:season>
      <podcast:season>9</podcast:season>
      <itunes:title>Mosunetuzumab in relapsed/refractory follicular lymphoma, CD70 CAR T-cells and an anti-CD33/anti-CD3 bispecific antibody in acute myeloid leukemia, and ferroptosis in stored red blood cells</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">4e47a930-8dc8-453c-b6f1-ead511f574ac</guid>
      <link>https://share.transistor.fm/s/8c695e06</link>
      <description>
        <![CDATA[<p>In this week's episode we’ll find out about longer term results from a pivotal trial of mosunetuzumab in relapsed/refractory follicular lymphoma, potential use of CD70 CAR T-cells that secrete an anti-CD33/anti-CD3 bispecific antibody as a therapy for acute myeloid leukemia, and how ferroptosis regulates hemolysis in stored red blood cells.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025454">Long-term 3-year follow-up of mosunetuzumab in relapsed or refractory follicular lymphoma after ≥2 prior therapies</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023210">CD70 CAR T cells secreting an anti-CD33/anti-CD3 dual-targeting antibody overcome antigen heterogeneity in AML</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026109">Ferroptosis regulates hemolysis in stored murine and human red blood cells</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we’ll find out about longer term results from a pivotal trial of mosunetuzumab in relapsed/refractory follicular lymphoma, potential use of CD70 CAR T-cells that secrete an anti-CD33/anti-CD3 bispecific antibody as a therapy for acute myeloid leukemia, and how ferroptosis regulates hemolysis in stored red blood cells.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025454">Long-term 3-year follow-up of mosunetuzumab in relapsed or refractory follicular lymphoma after ≥2 prior therapies</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023210">CD70 CAR T cells secreting an anti-CD33/anti-CD3 dual-targeting antibody overcome antigen heterogeneity in AML</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026109">Ferroptosis regulates hemolysis in stored murine and human red blood cells</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 13 Feb 2025 12:00:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/8c695e06/609a0248.mp3" length="27902986" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1394</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we’ll find out about longer term results from a pivotal trial of mosunetuzumab in relapsed/refractory follicular lymphoma, potential use of CD70 CAR T-cells that secrete an anti-CD33/anti-CD3 bispecific antibody as a therapy for acute myeloid leukemia, and how ferroptosis regulates hemolysis in stored red blood cells.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025454">Long-term 3-year follow-up of mosunetuzumab in relapsed or refractory follicular lymphoma after ≥2 prior therapies</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023210">CD70 CAR T cells secreting an anti-CD33/anti-CD3 dual-targeting antibody overcome antigen heterogeneity in AML</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026109">Ferroptosis regulates hemolysis in stored murine and human red blood cells</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title> Review Series on Basic/Translational Science of Factor VIII, Factor IX, and von Willebrand Factor</title>
      <itunes:season>9</itunes:season>
      <podcast:season>9</podcast:season>
      <itunes:title> Review Series on Basic/Translational Science of Factor VIII, Factor IX, and von Willebrand Factor</itunes:title>
      <itunes:episodeType>bonus</itunes:episodeType>
      <guid isPermaLink="false">62d0e3d4-49a4-4e3e-ba62-0fae487a9dc5</guid>
      <link>https://share.transistor.fm/s/8f96dde1</link>
      <description>
        <![CDATA[<p>In this Review Series episode on Basic/Translational Science of Factor VIII, Factor IX, and von Willebrand Factor introduced by Dr. Thomas Ortel, we’ll hear from contributing authors Drs. Ben Samuelson Jones, Mac Monroe and Peter Lenting as they discuss how the functional roles of these 3 proteins are interconnected. </p><p><a href="https://ashpublications.org/blood/article/144/21/2157/525958/Introduction-to-a-review-series-on-von-Willebrand?searchresult=1">Click here to view the complete Review Series featured in Volume 144 Issue 21 of <em>Blood</em>.</a></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this Review Series episode on Basic/Translational Science of Factor VIII, Factor IX, and von Willebrand Factor introduced by Dr. Thomas Ortel, we’ll hear from contributing authors Drs. Ben Samuelson Jones, Mac Monroe and Peter Lenting as they discuss how the functional roles of these 3 proteins are interconnected. </p><p><a href="https://ashpublications.org/blood/article/144/21/2157/525958/Introduction-to-a-review-series-on-von-Willebrand?searchresult=1">Click here to view the complete Review Series featured in Volume 144 Issue 21 of <em>Blood</em>.</a></p>]]>
      </content:encoded>
      <pubDate>Thu, 13 Feb 2025 11:59:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/8f96dde1/ba356af3.mp3" length="37976288" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/zEjdqmciivJJYGI3Y-2ZyulI-L2g_moWc0eijqy94xU/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS80ZWVl/ZTQzNzdmYTU1NGM1/OTk4MzJhOGQzNjE3/ZDE0Mi5qcGc.jpg"/>
      <itunes:duration>1898</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this Review Series episode on Basic/Translational Science of Factor VIII, Factor IX, and von Willebrand Factor introduced by Dr. Thomas Ortel, we’ll hear from contributing authors Drs. Ben Samuelson Jones, Mac Monroe and Peter Lenting as they discuss how the functional roles of these 3 proteins are interconnected. </p><p><a href="https://ashpublications.org/blood/article/144/21/2157/525958/Introduction-to-a-review-series-on-von-Willebrand?searchresult=1">Click here to view the complete Review Series featured in Volume 144 Issue 21 of <em>Blood</em>.</a></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Dual TKI targeting in Ph+ ALL; role of liver endothelial ferroportin in iron sensing and homeostasis; severe anemia in pregnant patients with beta-thalassemia minor</title>
      <itunes:season>9</itunes:season>
      <podcast:season>9</podcast:season>
      <itunes:title>Dual TKI targeting in Ph+ ALL; role of liver endothelial ferroportin in iron sensing and homeostasis; severe anemia in pregnant patients with beta-thalassemia minor</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">2abc0933-1a38-40f8-9e08-eb57d619d8fa</guid>
      <link>https://share.transistor.fm/s/bf06e6fe</link>
      <description>
        <![CDATA[<p>In this week's episode we'll learn about asciminib plus dasatinib in Philadelphia chromosome-positive acute leukemia. In a phase 1 study, combining two tyrosine kinase inhibitors with distinct mechanisms of action had encouraging activity in patients with de novo disease. After that: new research demonstrates that the iron exporter ferroportin contributes to the iron-sensing properties of liver endothelial cells. But is it the primary mediator of systemic iron homeostasis? Finally: anemia in pregnant patients with beta-thalassemia minor. In the third trimester, about one-third of patients have hemoglobin levels of 9 grams per deciliter or lower. This report may help to guide the appropriate diagnosis of anemia while limiting unnecessary testing and interventions. </p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025800">Asciminib plus dasatinib and prednisone for Philadelphia chromosome–positive acute leukemia</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024795">The hepcidin-ferroportin axis modulates liver endothelial cell BMP expression to influence iron homeostasis in mice</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026736">β-Thalassemia minor is associated with high rates of worsening anemia in pregnancy</a></li></ul><p><br></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we'll learn about asciminib plus dasatinib in Philadelphia chromosome-positive acute leukemia. In a phase 1 study, combining two tyrosine kinase inhibitors with distinct mechanisms of action had encouraging activity in patients with de novo disease. After that: new research demonstrates that the iron exporter ferroportin contributes to the iron-sensing properties of liver endothelial cells. But is it the primary mediator of systemic iron homeostasis? Finally: anemia in pregnant patients with beta-thalassemia minor. In the third trimester, about one-third of patients have hemoglobin levels of 9 grams per deciliter or lower. This report may help to guide the appropriate diagnosis of anemia while limiting unnecessary testing and interventions. </p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025800">Asciminib plus dasatinib and prednisone for Philadelphia chromosome–positive acute leukemia</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024795">The hepcidin-ferroportin axis modulates liver endothelial cell BMP expression to influence iron homeostasis in mice</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026736">β-Thalassemia minor is associated with high rates of worsening anemia in pregnancy</a></li></ul><p><br></p>]]>
      </content:encoded>
      <pubDate>Thu, 06 Feb 2025 12:00:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/bf06e6fe/37f0631a.mp3" length="22446504" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1121</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we'll learn about asciminib plus dasatinib in Philadelphia chromosome-positive acute leukemia. In a phase 1 study, combining two tyrosine kinase inhibitors with distinct mechanisms of action had encouraging activity in patients with de novo disease. After that: new research demonstrates that the iron exporter ferroportin contributes to the iron-sensing properties of liver endothelial cells. But is it the primary mediator of systemic iron homeostasis? Finally: anemia in pregnant patients with beta-thalassemia minor. In the third trimester, about one-third of patients have hemoglobin levels of 9 grams per deciliter or lower. This report may help to guide the appropriate diagnosis of anemia while limiting unnecessary testing and interventions. </p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025800">Asciminib plus dasatinib and prednisone for Philadelphia chromosome–positive acute leukemia</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024795">The hepcidin-ferroportin axis modulates liver endothelial cell BMP expression to influence iron homeostasis in mice</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026736">β-Thalassemia minor is associated with high rates of worsening anemia in pregnancy</a></li></ul><p><br></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>First-line zanubrutinib, obinutuzumab, and venetoclax in mantle cell lymphoma; hyperdiploidy in multiple myeloma; and pegcrisantaspase plus venetoclax in relapsed/refractory acute myeloid leukemia</title>
      <itunes:season>9</itunes:season>
      <podcast:season>9</podcast:season>
      <itunes:title>First-line zanubrutinib, obinutuzumab, and venetoclax in mantle cell lymphoma; hyperdiploidy in multiple myeloma; and pegcrisantaspase plus venetoclax in relapsed/refractory acute myeloid leukemia</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">f692e264-5509-4e5e-949e-d2058e636b67</guid>
      <link>https://share.transistor.fm/s/1e93a7bc</link>
      <description>
        <![CDATA[<p>In this week's episode we’ll learn more about a phase 2 trial of first-line zanubrutinib, obinutuzumab, and venetoclax in TP53-mutated mantle cell lymphoma; early development of hyperdiploidy in multiple myeloma; and a phase 1 trial of the asparaginase pegcrisantaspase plus venetoclax in relapsed/refractory acute myeloid leukemia.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025563">Zanubrutinib, obinutuzumab, and venetoclax for first-line treatment of mantle cell lymphoma with a <em>TP53</em> mutation</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025250">Development of hyperdiploidy starts at an early age and takes a decade to complete</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024837">A phase 1 study of the amino acid modulator pegcrisantaspase and venetoclax for relapsed or refractory acute myeloid leukemia</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we’ll learn more about a phase 2 trial of first-line zanubrutinib, obinutuzumab, and venetoclax in TP53-mutated mantle cell lymphoma; early development of hyperdiploidy in multiple myeloma; and a phase 1 trial of the asparaginase pegcrisantaspase plus venetoclax in relapsed/refractory acute myeloid leukemia.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025563">Zanubrutinib, obinutuzumab, and venetoclax for first-line treatment of mantle cell lymphoma with a <em>TP53</em> mutation</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025250">Development of hyperdiploidy starts at an early age and takes a decade to complete</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024837">A phase 1 study of the amino acid modulator pegcrisantaspase and venetoclax for relapsed or refractory acute myeloid leukemia</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 30 Jan 2025 12:00:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/1e93a7bc/67b8e498.mp3" length="24753149" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1237</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we’ll learn more about a phase 2 trial of first-line zanubrutinib, obinutuzumab, and venetoclax in TP53-mutated mantle cell lymphoma; early development of hyperdiploidy in multiple myeloma; and a phase 1 trial of the asparaginase pegcrisantaspase plus venetoclax in relapsed/refractory acute myeloid leukemia.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025563">Zanubrutinib, obinutuzumab, and venetoclax for first-line treatment of mantle cell lymphoma with a <em>TP53</em> mutation</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025250">Development of hyperdiploidy starts at an early age and takes a decade to complete</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024837">A phase 1 study of the amino acid modulator pegcrisantaspase and venetoclax for relapsed or refractory acute myeloid leukemia</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Targeting C3 in autoimmune hemolytic anemias; venetoclax testing to predict AML response; an improved understanding of the structure of FXIII complex</title>
      <itunes:season>9</itunes:season>
      <podcast:season>9</podcast:season>
      <itunes:title>Targeting C3 in autoimmune hemolytic anemias; venetoclax testing to predict AML response; an improved understanding of the structure of FXIII complex</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">f0a8d98a-ac9b-4627-b8ea-6b4f9badc3b3</guid>
      <link>https://share.transistor.fm/s/0b8de8cb</link>
      <description>
        <![CDATA[<p>In this week's episode we'll learn about C3-targeted therapy in autoimmune hemolytic anemias. Based on results of an open-label, phase 2 study, pegcetacoplan was well-tolerated, with encouraging efficacy, particularly in patients with cold agglutinin disease. After that: Venetoclax sensitivity testing to predict AML response. In a significant step toward precision medicine, researchers have validated an assay capable of predicting response to the venetoclax-azacitidine regimen. Finally, an improved basic understanding of human coagulation factor XIII. Investigators present the cryo-electron microscopy structure of Factor XIII complex, providing new insights into etiology and the deleterious effects of certain specific mutations.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022549">Safety and efficacy of pegcetacoplan treatment for cold agglutinin disease and warm antibody autoimmune hemolytic anemia</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024968">Ex vivo venetoclax sensitivity predicts clinical response in acute myeloid leukemia in the prospective VenEx trial</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025369">Cryo-EM structure of the human native plasma coagulation factor XIII complex</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we'll learn about C3-targeted therapy in autoimmune hemolytic anemias. Based on results of an open-label, phase 2 study, pegcetacoplan was well-tolerated, with encouraging efficacy, particularly in patients with cold agglutinin disease. After that: Venetoclax sensitivity testing to predict AML response. In a significant step toward precision medicine, researchers have validated an assay capable of predicting response to the venetoclax-azacitidine regimen. Finally, an improved basic understanding of human coagulation factor XIII. Investigators present the cryo-electron microscopy structure of Factor XIII complex, providing new insights into etiology and the deleterious effects of certain specific mutations.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022549">Safety and efficacy of pegcetacoplan treatment for cold agglutinin disease and warm antibody autoimmune hemolytic anemia</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024968">Ex vivo venetoclax sensitivity predicts clinical response in acute myeloid leukemia in the prospective VenEx trial</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025369">Cryo-EM structure of the human native plasma coagulation factor XIII complex</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 23 Jan 2025 12:00:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/0b8de8cb/d743e97c.mp3" length="22858179" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1142</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we'll learn about C3-targeted therapy in autoimmune hemolytic anemias. Based on results of an open-label, phase 2 study, pegcetacoplan was well-tolerated, with encouraging efficacy, particularly in patients with cold agglutinin disease. After that: Venetoclax sensitivity testing to predict AML response. In a significant step toward precision medicine, researchers have validated an assay capable of predicting response to the venetoclax-azacitidine regimen. Finally, an improved basic understanding of human coagulation factor XIII. Investigators present the cryo-electron microscopy structure of Factor XIII complex, providing new insights into etiology and the deleterious effects of certain specific mutations.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022549">Safety and efficacy of pegcetacoplan treatment for cold agglutinin disease and warm antibody autoimmune hemolytic anemia</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024968">Ex vivo venetoclax sensitivity predicts clinical response in acute myeloid leukemia in the prospective VenEx trial</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025369">Cryo-EM structure of the human native plasma coagulation factor XIII complex</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Review Series on Globin Disorders</title>
      <itunes:season>9</itunes:season>
      <podcast:season>9</podcast:season>
      <itunes:title>Review Series on Globin Disorders</itunes:title>
      <itunes:episodeType>bonus</itunes:episodeType>
      <guid isPermaLink="false">e4d23108-a701-4b8b-bda9-28589ce0e83c</guid>
      <link>https://share.transistor.fm/s/39bb64e1</link>
      <description>
        <![CDATA[<p>In this Review Series episode on Globin Disorders introduced by Drs. Thomas Coates and Irene Roberts, we’ll hear from Dr. Douglas Higgs and Dr. Mitchell Weiss as they address advances in our understanding of globin gene biology.</p><p><a href="https://ashpublications.org/blood/article/144/8/797/517385/Introduction-to-a-review-series-on-globin">Click here to view the complete Review Series featured in Volume 144 Issue 8 of <em>Blood</em>.</a></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this Review Series episode on Globin Disorders introduced by Drs. Thomas Coates and Irene Roberts, we’ll hear from Dr. Douglas Higgs and Dr. Mitchell Weiss as they address advances in our understanding of globin gene biology.</p><p><a href="https://ashpublications.org/blood/article/144/8/797/517385/Introduction-to-a-review-series-on-globin">Click here to view the complete Review Series featured in Volume 144 Issue 8 of <em>Blood</em>.</a></p>]]>
      </content:encoded>
      <pubDate>Thu, 23 Jan 2025 11:55:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/39bb64e1/fc75b348.mp3" length="27970143" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/NEu1afZCod9T2iZ5A8XoGDV-GOcr9dc3MMvXSBnCK78/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS9kOGRj/OWY5NGZhOThmMjIw/MGUzYjE2YzI5Yjcy/OWE0NC5qcGc.jpg"/>
      <itunes:duration>1397</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this Review Series episode on Globin Disorders introduced by Drs. Thomas Coates and Irene Roberts, we’ll hear from Dr. Douglas Higgs and Dr. Mitchell Weiss as they address advances in our understanding of globin gene biology.</p><p><a href="https://ashpublications.org/blood/article/144/8/797/517385/Introduction-to-a-review-series-on-globin">Click here to view the complete Review Series featured in Volume 144 Issue 8 of <em>Blood</em>.</a></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Brentuximab vedotin, nivolumab, and chemotherapy in classical Hodgkin lymphoma; type 1 interferon signaling in sickle cell disease; and type 1 human leukocyte antigen gene mutations in cutaneous T-cell lymphoma</title>
      <itunes:season>9</itunes:season>
      <podcast:season>9</podcast:season>
      <itunes:title>Brentuximab vedotin, nivolumab, and chemotherapy in classical Hodgkin lymphoma; type 1 interferon signaling in sickle cell disease; and type 1 human leukocyte antigen gene mutations in cutaneous T-cell lymphoma</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">4f3aa8c4-2c84-4511-9da3-f199e4aeafb2</guid>
      <link>https://share.transistor.fm/s/cb32c21d</link>
      <description>
        <![CDATA[<p>In this week's episode we’ll learn more about an experimental regimen for classical Hodgkin lymphoma that combines brentuximab vedotin, nivolumab, and chemotherapy; a possible role for type 1 interferon signaling in developing autoantibodies to red blood cells in sickle cell disease; and how genomic alterations affecting class I human leukocyte antigen molecules may affect patients with cutaneous T-cell lymphoma. </p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024681">Brentuximab vedotin, nivolumab, doxorubicin, and dacarbazine for advanced-stage classical Hodgkin lymphoma</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025175">IFN-I promotes T-cell–independent immunity and RBC autoantibodies via modulation of B-1 cell subsets in murine SCD</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024817">Genetic alteration of class I HLA in cutaneous T-cell lymphoma</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we’ll learn more about an experimental regimen for classical Hodgkin lymphoma that combines brentuximab vedotin, nivolumab, and chemotherapy; a possible role for type 1 interferon signaling in developing autoantibodies to red blood cells in sickle cell disease; and how genomic alterations affecting class I human leukocyte antigen molecules may affect patients with cutaneous T-cell lymphoma. </p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024681">Brentuximab vedotin, nivolumab, doxorubicin, and dacarbazine for advanced-stage classical Hodgkin lymphoma</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025175">IFN-I promotes T-cell–independent immunity and RBC autoantibodies via modulation of B-1 cell subsets in murine SCD</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024817">Genetic alteration of class I HLA in cutaneous T-cell lymphoma</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 16 Jan 2025 12:00:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/cb32c21d/46a8a917.mp3" length="25912999" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1295</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we’ll learn more about an experimental regimen for classical Hodgkin lymphoma that combines brentuximab vedotin, nivolumab, and chemotherapy; a possible role for type 1 interferon signaling in developing autoantibodies to red blood cells in sickle cell disease; and how genomic alterations affecting class I human leukocyte antigen molecules may affect patients with cutaneous T-cell lymphoma. </p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024681">Brentuximab vedotin, nivolumab, doxorubicin, and dacarbazine for advanced-stage classical Hodgkin lymphoma</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025175">IFN-I promotes T-cell–independent immunity and RBC autoantibodies via modulation of B-1 cell subsets in murine SCD</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024817">Genetic alteration of class I HLA in cutaneous T-cell lymphoma</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Iron overload aggravates MDS pathophysiology; long-term outcomes after TPO-RA treatment in ITP; new insights into APL treatment outcomes by age and risk</title>
      <itunes:season>9</itunes:season>
      <podcast:season>9</podcast:season>
      <itunes:title>Iron overload aggravates MDS pathophysiology; long-term outcomes after TPO-RA treatment in ITP; new insights into APL treatment outcomes by age and risk</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">8af793d9-fea2-4136-b130-f6f72871570a</guid>
      <link>https://share.transistor.fm/s/0a4cacc5</link>
      <description>
        <![CDATA[<p>In this week's episode we'll learn about the role of iron in myelodysplastic syndromes, or MDS. After that: long-term treatment outcomes in immune thrombocytopenia from the STOPAGO study.  Finally, new insights into APL treatment outcomes and prognostic factors from the large-scale Harmony APL project which used ATRA-Arsenic combination therapy.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026135">Genetic iron overload aggravates, and pharmacological iron restriction improves, MDS pathophysiology in a preclinical study</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025707">Long-term follow-up of the STOPAGO study</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026186">Acute promyelocytic leukemia: long-term outcomes from the HARMONY project</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we'll learn about the role of iron in myelodysplastic syndromes, or MDS. After that: long-term treatment outcomes in immune thrombocytopenia from the STOPAGO study.  Finally, new insights into APL treatment outcomes and prognostic factors from the large-scale Harmony APL project which used ATRA-Arsenic combination therapy.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026135">Genetic iron overload aggravates, and pharmacological iron restriction improves, MDS pathophysiology in a preclinical study</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025707">Long-term follow-up of the STOPAGO study</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026186">Acute promyelocytic leukemia: long-term outcomes from the HARMONY project</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 09 Jan 2025 12:00:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/0a4cacc5/bf4a3f0e.mp3" length="20812794" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1040</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we'll learn about the role of iron in myelodysplastic syndromes, or MDS. After that: long-term treatment outcomes in immune thrombocytopenia from the STOPAGO study.  Finally, new insights into APL treatment outcomes and prognostic factors from the large-scale Harmony APL project which used ATRA-Arsenic combination therapy.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026135">Genetic iron overload aggravates, and pharmacological iron restriction improves, MDS pathophysiology in a preclinical study</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025707">Long-term follow-up of the STOPAGO study</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026186">Acute promyelocytic leukemia: long-term outcomes from the HARMONY project</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Dexamethasone dosing in newly diagnosed multiple myeloma, a new experimental model of X-linked sideroblastic anemia, and ciltacabtagene autoleucel in real-world myeloma treatment</title>
      <itunes:season>9</itunes:season>
      <podcast:season>9</podcast:season>
      <itunes:title>Dexamethasone dosing in newly diagnosed multiple myeloma, a new experimental model of X-linked sideroblastic anemia, and ciltacabtagene autoleucel in real-world myeloma treatment</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">5f1f15fb-43a7-4c47-a8eb-ef698a2597fb</guid>
      <link>https://share.transistor.fm/s/46e92fc2</link>
      <description>
        <![CDATA[<p>In this week's episode, we’ll learn about the prevalence and impact of dexamethasone dose reductions during triple or quadruple therapy for newly diagnosed multiple myeloma, a conditional knockout mouse model for testing gene therapy in X-linked sideroblastic anemia, and real-world efficacy and safety of ciltacabtagene autoleucel in patients with relapsed/refractory multiple myeloma.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025939">Dexamethasone dose intensity does not impact outcomes in newly diagnosed multiple myeloma: a secondary SWOG analysis</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025846">An erythroid-specific lentiviral vector improves anemia and iron metabolism in a new model of XLSA</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025945">Safety and efficacy of standard-of-care ciltacabtagene autoleucel for relapsed/refractory multiple myeloma</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, we’ll learn about the prevalence and impact of dexamethasone dose reductions during triple or quadruple therapy for newly diagnosed multiple myeloma, a conditional knockout mouse model for testing gene therapy in X-linked sideroblastic anemia, and real-world efficacy and safety of ciltacabtagene autoleucel in patients with relapsed/refractory multiple myeloma.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025939">Dexamethasone dose intensity does not impact outcomes in newly diagnosed multiple myeloma: a secondary SWOG analysis</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025846">An erythroid-specific lentiviral vector improves anemia and iron metabolism in a new model of XLSA</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025945">Safety and efficacy of standard-of-care ciltacabtagene autoleucel for relapsed/refractory multiple myeloma</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 02 Jan 2025 12:00:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/46e92fc2/c9aace72.mp3" length="24400477" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1219</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, we’ll learn about the prevalence and impact of dexamethasone dose reductions during triple or quadruple therapy for newly diagnosed multiple myeloma, a conditional knockout mouse model for testing gene therapy in X-linked sideroblastic anemia, and real-world efficacy and safety of ciltacabtagene autoleucel in patients with relapsed/refractory multiple myeloma.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025939">Dexamethasone dose intensity does not impact outcomes in newly diagnosed multiple myeloma: a secondary SWOG analysis</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025846">An erythroid-specific lentiviral vector improves anemia and iron metabolism in a new model of XLSA</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025945">Safety and efficacy of standard-of-care ciltacabtagene autoleucel for relapsed/refractory multiple myeloma</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Comparing BTK inhibitors in relapsed/refractory CLL; unraveling the genetic background of the AnWj-negative blood type; rapid adaptation of CLL cells to venetoclax  </title>
      <itunes:season>8</itunes:season>
      <podcast:season>8</podcast:season>
      <itunes:title>Comparing BTK inhibitors in relapsed/refractory CLL; unraveling the genetic background of the AnWj-negative blood type; rapid adaptation of CLL cells to venetoclax  </itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">4f945acd-96b3-457a-999a-2b113adb05a1</guid>
      <link>https://share.transistor.fm/s/bbb7b8e0</link>
      <description>
        <![CDATA[<p>In this week's episode, we'll be comparing BTK inhibitors in relapsed/refractory CLL. Then, we'll hear how researchers in the UK unraveled the genetic background of the AnWj blood group.  Finally we'll learn about the role of BCL-2 and BAFF in CLL cell survival following venetoclax therapy. </p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025099">Deletions in the MAL gene result in loss of Mal protein, defining the rare inherited AnWj-negative blood group phenotype</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024667">Sustained benefit of zanubrutinib vs ibrutinib in patients with R/R CLL/SLL: final comparative analysis of ALPINE</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024341">Venetoclax dose escalation rapidly activates a BAFF/BCL-2 survival axis in chronic lymphocytic leukemia</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, we'll be comparing BTK inhibitors in relapsed/refractory CLL. Then, we'll hear how researchers in the UK unraveled the genetic background of the AnWj blood group.  Finally we'll learn about the role of BCL-2 and BAFF in CLL cell survival following venetoclax therapy. </p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025099">Deletions in the MAL gene result in loss of Mal protein, defining the rare inherited AnWj-negative blood group phenotype</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024667">Sustained benefit of zanubrutinib vs ibrutinib in patients with R/R CLL/SLL: final comparative analysis of ALPINE</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024341">Venetoclax dose escalation rapidly activates a BAFF/BCL-2 survival axis in chronic lymphocytic leukemia</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 26 Dec 2024 12:00:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/bbb7b8e0/b88cc432.mp3" length="22832596" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1141</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, we'll be comparing BTK inhibitors in relapsed/refractory CLL. Then, we'll hear how researchers in the UK unraveled the genetic background of the AnWj blood group.  Finally we'll learn about the role of BCL-2 and BAFF in CLL cell survival following venetoclax therapy. </p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025099">Deletions in the MAL gene result in loss of Mal protein, defining the rare inherited AnWj-negative blood group phenotype</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024667">Sustained benefit of zanubrutinib vs ibrutinib in patients with R/R CLL/SLL: final comparative analysis of ALPINE</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024341">Venetoclax dose escalation rapidly activates a BAFF/BCL-2 survival axis in chronic lymphocytic leukemia</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Primary resistance to BCMA-targeted bispecifics in multiple myeloma, emapalumab therapy in hemophagocytic lymphohistiocytosis, and chemotherapy-induced pyroptosis as a mechanism of thrombus formation in patients with cancer</title>
      <itunes:season>8</itunes:season>
      <podcast:season>8</podcast:season>
      <itunes:title>Primary resistance to BCMA-targeted bispecifics in multiple myeloma, emapalumab therapy in hemophagocytic lymphohistiocytosis, and chemotherapy-induced pyroptosis as a mechanism of thrombus formation in patients with cancer</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">3eb6b8ac-6d36-4417-9144-5dbf123c06fc</guid>
      <link>https://share.transistor.fm/s/f7074fa7</link>
      <description>
        <![CDATA[<p>In this week's episode, we’ll learn more about mechanisms of primary resistance to BCMA-targeted bispecific T-cell engagers in relapsed/refractory multiple myeloma, the effects of emapalumab therapy on outcomes in patients with pediatric hemophagocytic lymphohistiocytosis who receive stem cell transplants, and a cell death process that may help account for increased thromboembolic risk in patients receiving cancer chemotherapy.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026212">Impact of soluble BCMA and non–T-cell factors on refractoriness to BCMA-targeting T-cell engagers in multiple myeloma</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025977">Emapalumab therapy for hemophagocytic lymphohistiocytosis before reduced-intensity transplantation improves chimerism</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023179">GSDME-mediated pyroptosis contributes to chemotherapy-induced platelet hyperactivity and thrombotic potential</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, we’ll learn more about mechanisms of primary resistance to BCMA-targeted bispecific T-cell engagers in relapsed/refractory multiple myeloma, the effects of emapalumab therapy on outcomes in patients with pediatric hemophagocytic lymphohistiocytosis who receive stem cell transplants, and a cell death process that may help account for increased thromboembolic risk in patients receiving cancer chemotherapy.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026212">Impact of soluble BCMA and non–T-cell factors on refractoriness to BCMA-targeting T-cell engagers in multiple myeloma</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025977">Emapalumab therapy for hemophagocytic lymphohistiocytosis before reduced-intensity transplantation improves chimerism</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023179">GSDME-mediated pyroptosis contributes to chemotherapy-induced platelet hyperactivity and thrombotic potential</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 19 Dec 2024 12:00:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/f7074fa7/0dee9e82.mp3" length="24118401" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1205</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, we’ll learn more about mechanisms of primary resistance to BCMA-targeted bispecific T-cell engagers in relapsed/refractory multiple myeloma, the effects of emapalumab therapy on outcomes in patients with pediatric hemophagocytic lymphohistiocytosis who receive stem cell transplants, and a cell death process that may help account for increased thromboembolic risk in patients receiving cancer chemotherapy.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024026212">Impact of soluble BCMA and non–T-cell factors on refractoriness to BCMA-targeting T-cell engagers in multiple myeloma</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025977">Emapalumab therapy for hemophagocytic lymphohistiocytosis before reduced-intensity transplantation improves chimerism</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023179">GSDME-mediated pyroptosis contributes to chemotherapy-induced platelet hyperactivity and thrombotic potential</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Unravelling follicular lymphoma subtypes; stroke rate trends in sickle cell disease; procoagulant platelet activation promotes venous thrombosis </title>
      <itunes:season>8</itunes:season>
      <podcast:season>8</podcast:season>
      <itunes:title>Unravelling follicular lymphoma subtypes; stroke rate trends in sickle cell disease; procoagulant platelet activation promotes venous thrombosis </itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">7ac9ee1b-f8a8-45a0-b9b8-1b4e1459bd92</guid>
      <link>https://share.transistor.fm/s/a096258f</link>
      <description>
        <![CDATA[<p>In this week's episode, unravelling follicular lymphoma subtypes. Researchers dissect the biological diversity of follicular lymphoma and introduce a new prognostic mode, that could change the way this B-cell neoplasm is subtyped and treated. Then, concerning stroke rate trends in sickle cell disease. A new report shows increasing rates of cerebrovascular events among people with SCD in California. Finally, procoagulant platelet activation promotes venous thrombosis. Investigators report finding procoagulant platelets in the circulation and in thrombi of patients and mice with DVT or PE. </p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024496">Follicular lymphoma comprises germinal center–like and memory-like molecular subtypes with prognostic significance</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023031">Rates of strokes in Californians with sickle cell disease in the post-STOP era</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025476">Procoagulant platelet activation promotes venous thrombosis</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, unravelling follicular lymphoma subtypes. Researchers dissect the biological diversity of follicular lymphoma and introduce a new prognostic mode, that could change the way this B-cell neoplasm is subtyped and treated. Then, concerning stroke rate trends in sickle cell disease. A new report shows increasing rates of cerebrovascular events among people with SCD in California. Finally, procoagulant platelet activation promotes venous thrombosis. Investigators report finding procoagulant platelets in the circulation and in thrombi of patients and mice with DVT or PE. </p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024496">Follicular lymphoma comprises germinal center–like and memory-like molecular subtypes with prognostic significance</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023031">Rates of strokes in Californians with sickle cell disease in the post-STOP era</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025476">Procoagulant platelet activation promotes venous thrombosis</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 12 Dec 2024 12:00:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/a096258f/544a5972.mp3" length="22391627" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1118</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, unravelling follicular lymphoma subtypes. Researchers dissect the biological diversity of follicular lymphoma and introduce a new prognostic mode, that could change the way this B-cell neoplasm is subtyped and treated. Then, concerning stroke rate trends in sickle cell disease. A new report shows increasing rates of cerebrovascular events among people with SCD in California. Finally, procoagulant platelet activation promotes venous thrombosis. Investigators report finding procoagulant platelets in the circulation and in thrombi of patients and mice with DVT or PE. </p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024496">Follicular lymphoma comprises germinal center–like and memory-like molecular subtypes with prognostic significance</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023031">Rates of strokes in Californians with sickle cell disease in the post-STOP era</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025476">Procoagulant platelet activation promotes venous thrombosis</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Clonal hematopoiesis in patients with telomere biology disorders, genomic alterations in extracutaneous juvenile xanthogranulomas, and the BCMA-CD3 bispecific antibody teclistamab in relapsed/refractory multiple myeloma</title>
      <itunes:season>8</itunes:season>
      <podcast:season>8</podcast:season>
      <itunes:title>Clonal hematopoiesis in patients with telomere biology disorders, genomic alterations in extracutaneous juvenile xanthogranulomas, and the BCMA-CD3 bispecific antibody teclistamab in relapsed/refractory multiple myeloma</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">aac69413-a78f-4fe1-b63f-77c4679fdd46</guid>
      <link>https://share.transistor.fm/s/6fae185c</link>
      <description>
        <![CDATA[<p>In this week's episode we’ll learn more about how clonal hematopoiesis affects prognosis in patients with telomere biology disorders, consider recently uncovered molecular subtypes of extracutaneous juvenile xanthogranulomas, and discuss a clinical trial of the BCMA-CD3 bispecific antibody teclistamab in patients with relapsed/refractory multiple myeloma who have received previous BCMA-targeted therapy.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025023">Clonal landscape and clinical outcomes of telomere biology disorders: somatic rescue and cancer mutations</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025127">Recurrent <em>CLTC::SYK</em> fusions and<em> CSF1R</em> mutations in juvenile xanthogranuloma of soft tissue</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023616">Efficacy and safety of teclistamab in patients with relapsed/refractory multiple myeloma after BCMA-targeting therapies</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we’ll learn more about how clonal hematopoiesis affects prognosis in patients with telomere biology disorders, consider recently uncovered molecular subtypes of extracutaneous juvenile xanthogranulomas, and discuss a clinical trial of the BCMA-CD3 bispecific antibody teclistamab in patients with relapsed/refractory multiple myeloma who have received previous BCMA-targeted therapy.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025023">Clonal landscape and clinical outcomes of telomere biology disorders: somatic rescue and cancer mutations</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025127">Recurrent <em>CLTC::SYK</em> fusions and<em> CSF1R</em> mutations in juvenile xanthogranuloma of soft tissue</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023616">Efficacy and safety of teclistamab in patients with relapsed/refractory multiple myeloma after BCMA-targeting therapies</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 05 Dec 2024 12:00:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/6fae185c/d7347400.mp3" length="24240126" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1211</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we’ll learn more about how clonal hematopoiesis affects prognosis in patients with telomere biology disorders, consider recently uncovered molecular subtypes of extracutaneous juvenile xanthogranulomas, and discuss a clinical trial of the BCMA-CD3 bispecific antibody teclistamab in patients with relapsed/refractory multiple myeloma who have received previous BCMA-targeted therapy.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025023">Clonal landscape and clinical outcomes of telomere biology disorders: somatic rescue and cancer mutations</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025127">Recurrent <em>CLTC::SYK</em> fusions and<em> CSF1R</em> mutations in juvenile xanthogranuloma of soft tissue</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023616">Efficacy and safety of teclistamab in patients with relapsed/refractory multiple myeloma after BCMA-targeting therapies</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Targeting mutant calreticulin in MPNs; focusing on bleeding risk in patients with cancer; revisiting diagnostic guidelines for familial HLH</title>
      <itunes:season>8</itunes:season>
      <podcast:season>8</podcast:season>
      <itunes:title>Targeting mutant calreticulin in MPNs; focusing on bleeding risk in patients with cancer; revisiting diagnostic guidelines for familial HLH</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">0c598cda-558b-47c2-84f0-fc99b446ff08</guid>
      <link>https://share.transistor.fm/s/6a85214a</link>
      <description>
        <![CDATA[<p>In this week's podcast, we'll learn about targeting mutant calreticulin in MPNs, or myeloproliferative neoplasms. Then, it’s time to address bleeding and clotting in cancer. Results of the prospective, observational CAT-BLED study provide much needed data on the high risk of clinically relevant bleeding, and its association with all-cause mortality, among cancer patients receiving systemic therapy. Finally, we'll revisit diagnostic guidelines for familial HLH, or hemophagocytic lymphohistiocytosis. The authors present new and improved diagnostic criteria with revised clinical criteria, and guidelines on cellular and genetic diagnostic assays.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024373">Selective targeting of mutated calreticulin by the monoclonal antibody INCA033989 inhibits oncogenic function of MPN</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025362">Bleeding events in patients with cancer: incidence, risk factors, and impact on prognosis in a prospective cohort study</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025077">Diagnostic guidelines for familial hemophagocytic lymphohistiocytosis revisited</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's podcast, we'll learn about targeting mutant calreticulin in MPNs, or myeloproliferative neoplasms. Then, it’s time to address bleeding and clotting in cancer. Results of the prospective, observational CAT-BLED study provide much needed data on the high risk of clinically relevant bleeding, and its association with all-cause mortality, among cancer patients receiving systemic therapy. Finally, we'll revisit diagnostic guidelines for familial HLH, or hemophagocytic lymphohistiocytosis. The authors present new and improved diagnostic criteria with revised clinical criteria, and guidelines on cellular and genetic diagnostic assays.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024373">Selective targeting of mutated calreticulin by the monoclonal antibody INCA033989 inhibits oncogenic function of MPN</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025362">Bleeding events in patients with cancer: incidence, risk factors, and impact on prognosis in a prospective cohort study</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025077">Diagnostic guidelines for familial hemophagocytic lymphohistiocytosis revisited</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 28 Nov 2024 12:00:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/6a85214a/866cb998.mp3" length="22705613" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1134</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's podcast, we'll learn about targeting mutant calreticulin in MPNs, or myeloproliferative neoplasms. Then, it’s time to address bleeding and clotting in cancer. Results of the prospective, observational CAT-BLED study provide much needed data on the high risk of clinically relevant bleeding, and its association with all-cause mortality, among cancer patients receiving systemic therapy. Finally, we'll revisit diagnostic guidelines for familial HLH, or hemophagocytic lymphohistiocytosis. The authors present new and improved diagnostic criteria with revised clinical criteria, and guidelines on cellular and genetic diagnostic assays.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024373">Selective targeting of mutated calreticulin by the monoclonal antibody INCA033989 inhibits oncogenic function of MPN</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025362">Bleeding events in patients with cancer: incidence, risk factors, and impact on prognosis in a prospective cohort study</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025077">Diagnostic guidelines for familial hemophagocytic lymphohistiocytosis revisited</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Review Series on T-Cell Lymphoma</title>
      <itunes:season>8</itunes:season>
      <podcast:season>8</podcast:season>
      <itunes:title>Review Series on T-Cell Lymphoma</itunes:title>
      <itunes:episodeType>bonus</itunes:episodeType>
      <guid isPermaLink="false">f4feb550-c55f-48df-b51e-d6b9e6f78186</guid>
      <link>https://share.transistor.fm/s/f349b026</link>
      <description>
        <![CDATA[<p>In this Review Series episode on T-Cell Lymphomas introduced by Dr. Philippe Armand we’ll hear from Drs. Laurence de Leval, Javeed Iqbal, and Enrica Marchi about their work concerning new treatment practices and insights to various t-cell lymphomas.</p><p><a href="https://ashpublications.org/blood/article/144/18/1847/518324/Introduction-to-a-review-series-on-peripheral-T">Click here to view the complete Review Series featured in Volume 144 Issue 18 of <em>Blood</em>.</a></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this Review Series episode on T-Cell Lymphomas introduced by Dr. Philippe Armand we’ll hear from Drs. Laurence de Leval, Javeed Iqbal, and Enrica Marchi about their work concerning new treatment practices and insights to various t-cell lymphomas.</p><p><a href="https://ashpublications.org/blood/article/144/18/1847/518324/Introduction-to-a-review-series-on-peripheral-T">Click here to view the complete Review Series featured in Volume 144 Issue 18 of <em>Blood</em>.</a></p>]]>
      </content:encoded>
      <pubDate>Thu, 21 Nov 2024 13:57:45 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/f349b026/9f1685ff.mp3" length="40039263" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/TVel8_VGd8n5in5VXl_rMZEVVEBU0M4NeXOZXMiZTuo/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS84MGU0/ZGEwMjk2OWVkNTM5/YzVmMGIyNGEyODUy/N2JmOC5qcGc.jpg"/>
      <itunes:duration>2001</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this Review Series episode on T-Cell Lymphomas introduced by Dr. Philippe Armand we’ll hear from Drs. Laurence de Leval, Javeed Iqbal, and Enrica Marchi about their work concerning new treatment practices and insights to various t-cell lymphomas.</p><p><a href="https://ashpublications.org/blood/article/144/18/1847/518324/Introduction-to-a-review-series-on-peripheral-T">Click here to view the complete Review Series featured in Volume 144 Issue 18 of <em>Blood</em>.</a></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Stratifying risk in acute myeloid leukemia, daratumumab plus chemotherapy in relapsed-refractory pediatric leukemias, and a method for creating genetically engineered platelets</title>
      <itunes:season>8</itunes:season>
      <podcast:season>8</podcast:season>
      <itunes:title>Stratifying risk in acute myeloid leukemia, daratumumab plus chemotherapy in relapsed-refractory pediatric leukemias, and a method for creating genetically engineered platelets</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">7516092c-ee5a-41c1-bd38-717c1ac627e5</guid>
      <link>https://share.transistor.fm/s/1f3d76aa</link>
      <description>
        <![CDATA[<p>In this week's episode we’ll learn more about a new risk classification scheme for use in patients with acute myeloid leukemia who are ineligible for intensive therapy, efficacy and safety of daratumumab plus chemotherapy in pediatric patients with acute lymphoblastic leukemia or lymphoblastic lymphoma, and a blood bank-compatible method for creating genetically engineered platelets with a wide range of potential uses.</p><p><strong>Featured Articles:</strong></p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025409">Genetic Risk Stratification and Outcomes Among Treatment-Naive Patients with AML Treated With Venetoclax and Azacitidine </a></li><li><a href="https://ashpublications.org/blood/article/doi/10.1182/blood.2024024493">Daratumumab in Pediatric Relapsed/Refractory Acute Lymphoblastic Leukemia or Lymphoblastic Lymphoma: DELPHINUS Study </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024405">Genetic Engineering of Transfusable Platelets with mRNA-Lipid Nanoparticles is Compatible with Blood Banking Practices </a></li></ul><p> </p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we’ll learn more about a new risk classification scheme for use in patients with acute myeloid leukemia who are ineligible for intensive therapy, efficacy and safety of daratumumab plus chemotherapy in pediatric patients with acute lymphoblastic leukemia or lymphoblastic lymphoma, and a blood bank-compatible method for creating genetically engineered platelets with a wide range of potential uses.</p><p><strong>Featured Articles:</strong></p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025409">Genetic Risk Stratification and Outcomes Among Treatment-Naive Patients with AML Treated With Venetoclax and Azacitidine </a></li><li><a href="https://ashpublications.org/blood/article/doi/10.1182/blood.2024024493">Daratumumab in Pediatric Relapsed/Refractory Acute Lymphoblastic Leukemia or Lymphoblastic Lymphoma: DELPHINUS Study </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024405">Genetic Engineering of Transfusable Platelets with mRNA-Lipid Nanoparticles is Compatible with Blood Banking Practices </a></li></ul><p> </p>]]>
      </content:encoded>
      <pubDate>Thu, 21 Nov 2024 12:00:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/1f3d76aa/3bd05e9f.mp3" length="21408409" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1069</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we’ll learn more about a new risk classification scheme for use in patients with acute myeloid leukemia who are ineligible for intensive therapy, efficacy and safety of daratumumab plus chemotherapy in pediatric patients with acute lymphoblastic leukemia or lymphoblastic lymphoma, and a blood bank-compatible method for creating genetically engineered platelets with a wide range of potential uses.</p><p><strong>Featured Articles:</strong></p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025409">Genetic Risk Stratification and Outcomes Among Treatment-Naive Patients with AML Treated With Venetoclax and Azacitidine </a></li><li><a href="https://ashpublications.org/blood/article/doi/10.1182/blood.2024024493">Daratumumab in Pediatric Relapsed/Refractory Acute Lymphoblastic Leukemia or Lymphoblastic Lymphoma: DELPHINUS Study </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024405">Genetic Engineering of Transfusable Platelets with mRNA-Lipid Nanoparticles is Compatible with Blood Banking Practices </a></li></ul><p> </p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Exploring the ecosystem of extramedullary myeloma; role of ruxolitinib for pediatric acute GvHD; “YAP”-ing about YAP1 and thrombopoiesis in ITP</title>
      <itunes:season>8</itunes:season>
      <podcast:season>8</podcast:season>
      <itunes:title>Exploring the ecosystem of extramedullary myeloma; role of ruxolitinib for pediatric acute GvHD; “YAP”-ing about YAP1 and thrombopoiesis in ITP</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">26c2b972-c12b-47c1-ab0b-84a6ef4f61a3</guid>
      <link>https://share.transistor.fm/s/e404ebdf</link>
      <description>
        <![CDATA[<p>In this week's episode we'll learn about new explorations in extramedullary myeloma. Then, we'll hear about the role of ruxolitinib in children with acute GvHD. Finally: yapping about YAP1 as a new treatment target in immune thrombocytopenia. </p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024590">Spatial transcriptomics reveals profound subclonal heterogeneity and T-cell dysfunction in extramedullary myeloma</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022565">Ruxolitinib for pediatric patients with treatment-naïve and steroid-refractory acute graft-versus-host disease: the REACH4 study</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023601">YAP1 regulates thrombopoiesis by binding to MYH9 in immune thrombocytopenia</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we'll learn about new explorations in extramedullary myeloma. Then, we'll hear about the role of ruxolitinib in children with acute GvHD. Finally: yapping about YAP1 as a new treatment target in immune thrombocytopenia. </p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024590">Spatial transcriptomics reveals profound subclonal heterogeneity and T-cell dysfunction in extramedullary myeloma</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022565">Ruxolitinib for pediatric patients with treatment-naïve and steroid-refractory acute graft-versus-host disease: the REACH4 study</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023601">YAP1 regulates thrombopoiesis by binding to MYH9 in immune thrombocytopenia</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 14 Nov 2024 12:00:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/e404ebdf/22f559f1.mp3" length="22358337" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1117</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we'll learn about new explorations in extramedullary myeloma. Then, we'll hear about the role of ruxolitinib in children with acute GvHD. Finally: yapping about YAP1 as a new treatment target in immune thrombocytopenia. </p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024590">Spatial transcriptomics reveals profound subclonal heterogeneity and T-cell dysfunction in extramedullary myeloma</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022565">Ruxolitinib for pediatric patients with treatment-naïve and steroid-refractory acute graft-versus-host disease: the REACH4 study</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023601">YAP1 regulates thrombopoiesis by binding to MYH9 in immune thrombocytopenia</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>First-line asciminib for chronic myeloid leukemia, a new risk score for clonal cytopenia, and genotyped D-positive blood transfusion in sickle cell anemia</title>
      <itunes:season>8</itunes:season>
      <podcast:season>8</podcast:season>
      <itunes:title>First-line asciminib for chronic myeloid leukemia, a new risk score for clonal cytopenia, and genotyped D-positive blood transfusion in sickle cell anemia</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">c9359cbe-229f-4035-a0ed-3049598cdaae</guid>
      <link>https://share.transistor.fm/s/481807a1</link>
      <description>
        <![CDATA[<p>In this week's episode we’ll learn more about the ASCEND study, which investigated first-line asciminib in chronic phase chronic myeloid leukemia; a new risk score for myeloid neoplasm transformation in patients with clonal cytopenia of undetermined significance; and use of <em>RHD</em> genotyped D-positive blood transfusions in patients with sickle cell and unexpected anti-D antibodies.</p><p>Featured Articles</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024657">Asciminib Monotherapy as Frontline Treatment of Chronic Phase Chronic Myeloid Leukaemia - Results from the ASCEND Study</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024756">Risk Prediction for Clonal Cytopenia: Multicenter Real-World Evidence </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025602">Genotyped RhD+ red cells for D-positive patients with sickle cell disease with conventional <em>RHD </em>and unexpected anti-D </a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we’ll learn more about the ASCEND study, which investigated first-line asciminib in chronic phase chronic myeloid leukemia; a new risk score for myeloid neoplasm transformation in patients with clonal cytopenia of undetermined significance; and use of <em>RHD</em> genotyped D-positive blood transfusions in patients with sickle cell and unexpected anti-D antibodies.</p><p>Featured Articles</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024657">Asciminib Monotherapy as Frontline Treatment of Chronic Phase Chronic Myeloid Leukaemia - Results from the ASCEND Study</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024756">Risk Prediction for Clonal Cytopenia: Multicenter Real-World Evidence </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025602">Genotyped RhD+ red cells for D-positive patients with sickle cell disease with conventional <em>RHD </em>and unexpected anti-D </a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 07 Nov 2024 12:00:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/481807a1/89809b2d.mp3" length="51191002" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1279</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we’ll learn more about the ASCEND study, which investigated first-line asciminib in chronic phase chronic myeloid leukemia; a new risk score for myeloid neoplasm transformation in patients with clonal cytopenia of undetermined significance; and use of <em>RHD</em> genotyped D-positive blood transfusions in patients with sickle cell and unexpected anti-D antibodies.</p><p>Featured Articles</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024657">Asciminib Monotherapy as Frontline Treatment of Chronic Phase Chronic Myeloid Leukaemia - Results from the ASCEND Study</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024756">Risk Prediction for Clonal Cytopenia: Multicenter Real-World Evidence </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025602">Genotyped RhD+ red cells for D-positive patients with sickle cell disease with conventional <em>RHD </em>and unexpected anti-D </a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Update on fixed-dose venetoclax-obinutuzumab in previously untreated CLL; dual epi-immunotherapy in cHL; predicting treatment failure in TKI-treated CML </title>
      <itunes:season>8</itunes:season>
      <podcast:season>8</podcast:season>
      <itunes:title>Update on fixed-dose venetoclax-obinutuzumab in previously untreated CLL; dual epi-immunotherapy in cHL; predicting treatment failure in TKI-treated CML </itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">6f5e88c1-7acb-49f1-bb33-c2c648f37a5c</guid>
      <link>https://share.transistor.fm/s/fbd72c68</link>
      <description>
        <![CDATA[<p>In this week's episode we'll learn about the updated phase 3 results on fixed-dose venetoclax plus obinutuzumab in previously untreated CLL. Then, we'll hear about dual epi-immunotherapy in classical Hodgkin lymphoma. Finally we'll explore redefining risk of treatment failure in CML.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024631">Venetoclax-obinutuzumab for previously untreated chronic lymphocytic leukemia: 6-year results of the randomized phase 3 CLL14 study</a></li><li><a href="https://ashpublications.org/blood/article/doi/10.1182/blood.2024024487/">Epigenetic agents plus anti-PD-1 reprogram the tumor microenvironment and restore antitumor efficacy in Hodgkin lymphoma</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024761">A predictive model for therapy failure in patients with chronic myeloid leukemia receiving tyrosine kinase inhibitor therapy</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we'll learn about the updated phase 3 results on fixed-dose venetoclax plus obinutuzumab in previously untreated CLL. Then, we'll hear about dual epi-immunotherapy in classical Hodgkin lymphoma. Finally we'll explore redefining risk of treatment failure in CML.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024631">Venetoclax-obinutuzumab for previously untreated chronic lymphocytic leukemia: 6-year results of the randomized phase 3 CLL14 study</a></li><li><a href="https://ashpublications.org/blood/article/doi/10.1182/blood.2024024487/">Epigenetic agents plus anti-PD-1 reprogram the tumor microenvironment and restore antitumor efficacy in Hodgkin lymphoma</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024761">A predictive model for therapy failure in patients with chronic myeloid leukemia receiving tyrosine kinase inhibitor therapy</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 31 Oct 2024 12:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/fbd72c68/9923943a.mp3" length="18307473" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1143</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we'll learn about the updated phase 3 results on fixed-dose venetoclax plus obinutuzumab in previously untreated CLL. Then, we'll hear about dual epi-immunotherapy in classical Hodgkin lymphoma. Finally we'll explore redefining risk of treatment failure in CML.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024631">Venetoclax-obinutuzumab for previously untreated chronic lymphocytic leukemia: 6-year results of the randomized phase 3 CLL14 study</a></li><li><a href="https://ashpublications.org/blood/article/doi/10.1182/blood.2024024487/">Epigenetic agents plus anti-PD-1 reprogram the tumor microenvironment and restore antitumor efficacy in Hodgkin lymphoma</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024761">A predictive model for therapy failure in patients with chronic myeloid leukemia receiving tyrosine kinase inhibitor therapy</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Bone marrow failure related to ERG insufficiency, factor 11 in vascular hyperpermeability, and new criteria for evaluating anemia in myelofibrosis</title>
      <itunes:season>8</itunes:season>
      <podcast:season>8</podcast:season>
      <itunes:title>Bone marrow failure related to ERG insufficiency, factor 11 in vascular hyperpermeability, and new criteria for evaluating anemia in myelofibrosis</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">54e55bd2-9625-47d3-9d01-a632e783bd25</guid>
      <link>https://share.transistor.fm/s/66d6a584</link>
      <description>
        <![CDATA[<p>In this week's episode we’ll learn more about the role of ERG loss-of-function variants in bone marrow failure and hematological malignancies, a proposed pathway linking factor 11 activation to increased vascular permeability during inflammation, and new clinical criteria for diagnosing anemia, defining transfusion-dependence, and evaluating anemia treatment responses in patients with myelofibrosis.</p><p><strong>Featured Articles:</strong></p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024607">Germ line ERG haploinsufficiency defines a new syndrome with cytopenia and hematological malignancy predisposition</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022257">Coagulation factor XI regulates endothelial cell permeability and barrier function in vitro and in vivo</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025802">Proposals for revised International Working Group–European LeukemiaNet criteria for anemia response in myelofibrosis</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we’ll learn more about the role of ERG loss-of-function variants in bone marrow failure and hematological malignancies, a proposed pathway linking factor 11 activation to increased vascular permeability during inflammation, and new clinical criteria for diagnosing anemia, defining transfusion-dependence, and evaluating anemia treatment responses in patients with myelofibrosis.</p><p><strong>Featured Articles:</strong></p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024607">Germ line ERG haploinsufficiency defines a new syndrome with cytopenia and hematological malignancy predisposition</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022257">Coagulation factor XI regulates endothelial cell permeability and barrier function in vitro and in vivo</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025802">Proposals for revised International Working Group–European LeukemiaNet criteria for anemia response in myelofibrosis</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 24 Oct 2024 12:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/66d6a584/c0582787.mp3" length="49273874" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1232</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we’ll learn more about the role of ERG loss-of-function variants in bone marrow failure and hematological malignancies, a proposed pathway linking factor 11 activation to increased vascular permeability during inflammation, and new clinical criteria for diagnosing anemia, defining transfusion-dependence, and evaluating anemia treatment responses in patients with myelofibrosis.</p><p><strong>Featured Articles:</strong></p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024607">Germ line ERG haploinsufficiency defines a new syndrome with cytopenia and hematological malignancy predisposition</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022257">Coagulation factor XI regulates endothelial cell permeability and barrier function in vitro and in vivo</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025802">Proposals for revised International Working Group–European LeukemiaNet criteria for anemia response in myelofibrosis</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Platelet glycoprotein receptor VI in abdominal aortic aneurysms, TP53 mutations in 5q-deleted myelodysplastic syndrome, and immunostimulatory cytokine plus CAR T-cell therapy in acute lymphoblastic leukemia</title>
      <itunes:season>8</itunes:season>
      <podcast:season>8</podcast:season>
      <itunes:title>Platelet glycoprotein receptor VI in abdominal aortic aneurysms, TP53 mutations in 5q-deleted myelodysplastic syndrome, and immunostimulatory cytokine plus CAR T-cell therapy in acute lymphoblastic leukemia</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">2ac0633d-80e7-4cb0-bf5f-63d2c7c1e5e6</guid>
      <link>https://share.transistor.fm/s/e3ae0cc6</link>
      <description>
        <![CDATA[<p>In this week's episode, we'll learn about the role of a platelet-specific glycoprotein receptor in abdominal aortic aneurysm formation, the influence of <em>TP53 </em>mutations on outcomes for patients with 5q-deleted myelodysplastic syndrome, and a rational combination treatment intended to produce more durable responses in patients with refractory B-cell acute lymphoblastic leukemia who are treated with CAR T-cell therapy.</p><p><strong>Featured Articles:</strong></p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023021655">Soluble glycoprotein VI predicts abdominal aortic aneurysm growth rate and is a novel therapeutic target</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024023840">Influence of TP53 gene mutations and their allelic status in myelodysplastic syndromes with isolated 5q deletion</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024952">A phase 1 clinical trial of NKTR-255 with CD19-22 CAR T-cell therapy for refractory B-cell acute lymphoblastic leukemia</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, we'll learn about the role of a platelet-specific glycoprotein receptor in abdominal aortic aneurysm formation, the influence of <em>TP53 </em>mutations on outcomes for patients with 5q-deleted myelodysplastic syndrome, and a rational combination treatment intended to produce more durable responses in patients with refractory B-cell acute lymphoblastic leukemia who are treated with CAR T-cell therapy.</p><p><strong>Featured Articles:</strong></p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023021655">Soluble glycoprotein VI predicts abdominal aortic aneurysm growth rate and is a novel therapeutic target</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024023840">Influence of TP53 gene mutations and their allelic status in myelodysplastic syndromes with isolated 5q deletion</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024952">A phase 1 clinical trial of NKTR-255 with CD19-22 CAR T-cell therapy for refractory B-cell acute lymphoblastic leukemia</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 17 Oct 2024 13:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/e3ae0cc6/872300dc.mp3" length="22804949" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1139</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, we'll learn about the role of a platelet-specific glycoprotein receptor in abdominal aortic aneurysm formation, the influence of <em>TP53 </em>mutations on outcomes for patients with 5q-deleted myelodysplastic syndrome, and a rational combination treatment intended to produce more durable responses in patients with refractory B-cell acute lymphoblastic leukemia who are treated with CAR T-cell therapy.</p><p><strong>Featured Articles:</strong></p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023021655">Soluble glycoprotein VI predicts abdominal aortic aneurysm growth rate and is a novel therapeutic target</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024023840">Influence of TP53 gene mutations and their allelic status in myelodysplastic syndromes with isolated 5q deletion</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024952">A phase 1 clinical trial of NKTR-255 with CD19-22 CAR T-cell therapy for refractory B-cell acute lymphoblastic leukemia</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Using NGS to refine risk stratification in T-ALL; a novel gene therapy approach in severe α-thalassemia; molecular taxonomy of MDS</title>
      <itunes:season>8</itunes:season>
      <podcast:season>8</podcast:season>
      <itunes:title>Using NGS to refine risk stratification in T-ALL; a novel gene therapy approach in severe α-thalassemia; molecular taxonomy of MDS</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">6d9df1c8-24b0-46d8-b8ca-b1592c69b8f9</guid>
      <link>https://share.transistor.fm/s/acbe72e9</link>
      <description>
        <![CDATA[<p>In this week's episode we'll learn about refining risk stratification in T-cell acute lymphoblastic leukemia, or ALL. After that, we'll discuss a novel gene therapy approach in severe alpha-thalassemia. Investigators describe an innovative mouse model and an effective gene therapy approach, renewing prospects for the development of novel strategies to treat this disease. Finally, we'll hear about how genomic profiling has helped identify subgroups associated with distinct clinical phenotypes and outcomes in the molecular taxonomy of myelodysplastic syndromes, or MDS. </p><p><strong>Featured Articles </strong></p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.%20">NGS-based stratification refines the risk stratification in T-ALL and identifies a very-high-risk subgroup of<br>patients</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023349">Use of HSC-targeted LNP to generate a mouse model of lethal α-thalassemia and treatment via lentiviral<br>gene therapy</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023727">Molecular taxonomy of myelodysplastic syndromes and its clinical implications</a></li></ul><p><br></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we'll learn about refining risk stratification in T-cell acute lymphoblastic leukemia, or ALL. After that, we'll discuss a novel gene therapy approach in severe alpha-thalassemia. Investigators describe an innovative mouse model and an effective gene therapy approach, renewing prospects for the development of novel strategies to treat this disease. Finally, we'll hear about how genomic profiling has helped identify subgroups associated with distinct clinical phenotypes and outcomes in the molecular taxonomy of myelodysplastic syndromes, or MDS. </p><p><strong>Featured Articles </strong></p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.%20">NGS-based stratification refines the risk stratification in T-ALL and identifies a very-high-risk subgroup of<br>patients</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023349">Use of HSC-targeted LNP to generate a mouse model of lethal α-thalassemia and treatment via lentiviral<br>gene therapy</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023727">Molecular taxonomy of myelodysplastic syndromes and its clinical implications</a></li></ul><p><br></p>]]>
      </content:encoded>
      <pubDate>Thu, 10 Oct 2024 12:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/acbe72e9/90a4fffa.mp3" length="26183160" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1308</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we'll learn about refining risk stratification in T-cell acute lymphoblastic leukemia, or ALL. After that, we'll discuss a novel gene therapy approach in severe alpha-thalassemia. Investigators describe an innovative mouse model and an effective gene therapy approach, renewing prospects for the development of novel strategies to treat this disease. Finally, we'll hear about how genomic profiling has helped identify subgroups associated with distinct clinical phenotypes and outcomes in the molecular taxonomy of myelodysplastic syndromes, or MDS. </p><p><strong>Featured Articles </strong></p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.%20">NGS-based stratification refines the risk stratification in T-ALL and identifies a very-high-risk subgroup of<br>patients</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023349">Use of HSC-targeted LNP to generate a mouse model of lethal α-thalassemia and treatment via lentiviral<br>gene therapy</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023727">Molecular taxonomy of myelodysplastic syndromes and its clinical implications</a></li></ul><p><br></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>A novel tripartite fusion drives treatment resistance in atypical APL; managing iTTP without TPE; hope for motherhood after allogeneic HCT</title>
      <itunes:season>8</itunes:season>
      <podcast:season>8</podcast:season>
      <itunes:title>A novel tripartite fusion drives treatment resistance in atypical APL; managing iTTP without TPE; hope for motherhood after allogeneic HCT</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">0e8c478b-38d1-441c-9293-030974e49abb</guid>
      <link>https://share.transistor.fm/s/93f9e4ee</link>
      <description>
        <![CDATA[<p>In this week's episode we’ll discuss a novel tripartite fusion drives treatment resistance in acute promyelocytic leukemia. In some patients with atypical APL, these novel retinoic acid receptor gene fusions result in truncation of the ligand binding domain of the retinoic acid receptor protein, resulting in non-responsiveness to treatment with all-trans retinoic acid. After that: managing immune thrombotic thrombocytopenia or iTTP without therapeutic plasma exchange, or TPE. Finally, hope for motherhood after allogeneic HCT.</p><p>Featured Articles: </p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024023883">Critical role of tripartite fusion and LBD truncation in certain RARA- and all RARG-related atypical APL</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023780">Management of immune thrombotic thrombocytopenic purpura without therapeutic plasma exchange</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024342">Hope for motherhood: pregnancy after allogeneic hematopoietic cell transplantation (a national multicenter study)</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we’ll discuss a novel tripartite fusion drives treatment resistance in acute promyelocytic leukemia. In some patients with atypical APL, these novel retinoic acid receptor gene fusions result in truncation of the ligand binding domain of the retinoic acid receptor protein, resulting in non-responsiveness to treatment with all-trans retinoic acid. After that: managing immune thrombotic thrombocytopenia or iTTP without therapeutic plasma exchange, or TPE. Finally, hope for motherhood after allogeneic HCT.</p><p>Featured Articles: </p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024023883">Critical role of tripartite fusion and LBD truncation in certain RARA- and all RARG-related atypical APL</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023780">Management of immune thrombotic thrombocytopenic purpura without therapeutic plasma exchange</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024342">Hope for motherhood: pregnancy after allogeneic hematopoietic cell transplantation (a national multicenter study)</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 03 Oct 2024 12:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/93f9e4ee/d9270d99.mp3" length="22222873" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1110</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we’ll discuss a novel tripartite fusion drives treatment resistance in acute promyelocytic leukemia. In some patients with atypical APL, these novel retinoic acid receptor gene fusions result in truncation of the ligand binding domain of the retinoic acid receptor protein, resulting in non-responsiveness to treatment with all-trans retinoic acid. After that: managing immune thrombotic thrombocytopenia or iTTP without therapeutic plasma exchange, or TPE. Finally, hope for motherhood after allogeneic HCT.</p><p>Featured Articles: </p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024023883">Critical role of tripartite fusion and LBD truncation in certain RARA- and all RARG-related atypical APL</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023780">Management of immune thrombotic thrombocytopenic purpura without therapeutic plasma exchange</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024342">Hope for motherhood: pregnancy after allogeneic hematopoietic cell transplantation (a national multicenter study)</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Pirtobrutinib plus venetoclax with or without rituximab in relapsed/refractory CLL; murine models of erythroid 5ALA synthesis disorders; targeting PKCa in diabetes and hemochromatosis</title>
      <itunes:season>8</itunes:season>
      <podcast:season>8</podcast:season>
      <itunes:title>Pirtobrutinib plus venetoclax with or without rituximab in relapsed/refractory CLL; murine models of erythroid 5ALA synthesis disorders; targeting PKCa in diabetes and hemochromatosis</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">5916ee73-923b-4ae3-a897-88ebecdd0ac5</guid>
      <link>https://share.transistor.fm/s/dda8e936</link>
      <description>
        <![CDATA[<p>In this week's episode we’ll discuss the safety and efficacy of pirtobrutinib with or without rituximab in relapsed/refractory CLL; learn more about erythroid 5ALA synthesis disorders and their conditional synthetic lethal dependency on pyridoxine; and discuss how targeting PKC alpha alleviates iron overload in diabetes and hemochromatosis through the inhibition of ferroportin.</p><p><strong>Featured Articles:</strong></p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024510">Fixed-duration pirtobrutinib plus venetoclax with or without rituximab in relapsed/refractory CLL: Phase 1b BRUIN trial</a></li><li><a href="https://ashpublications.org/blood/article/doi/10.1182/blood.2023023078/">Murine models of erythroid 5ALA synthesis disorders and their conditional synthetic lethal dependency on pyridoxine</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024023829">Targeting PKCα alleviates iron overload in diabetes and hemochromatosis through the inhibition of ferroportin</a></li></ul><p><br></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we’ll discuss the safety and efficacy of pirtobrutinib with or without rituximab in relapsed/refractory CLL; learn more about erythroid 5ALA synthesis disorders and their conditional synthetic lethal dependency on pyridoxine; and discuss how targeting PKC alpha alleviates iron overload in diabetes and hemochromatosis through the inhibition of ferroportin.</p><p><strong>Featured Articles:</strong></p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024510">Fixed-duration pirtobrutinib plus venetoclax with or without rituximab in relapsed/refractory CLL: Phase 1b BRUIN trial</a></li><li><a href="https://ashpublications.org/blood/article/doi/10.1182/blood.2023023078/">Murine models of erythroid 5ALA synthesis disorders and their conditional synthetic lethal dependency on pyridoxine</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024023829">Targeting PKCα alleviates iron overload in diabetes and hemochromatosis through the inhibition of ferroportin</a></li></ul><p><br></p>]]>
      </content:encoded>
      <pubDate>Thu, 26 Sep 2024 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/dda8e936/d4078b48.mp3" length="27956273" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1397</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we’ll discuss the safety and efficacy of pirtobrutinib with or without rituximab in relapsed/refractory CLL; learn more about erythroid 5ALA synthesis disorders and their conditional synthetic lethal dependency on pyridoxine; and discuss how targeting PKC alpha alleviates iron overload in diabetes and hemochromatosis through the inhibition of ferroportin.</p><p><strong>Featured Articles:</strong></p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024510">Fixed-duration pirtobrutinib plus venetoclax with or without rituximab in relapsed/refractory CLL: Phase 1b BRUIN trial</a></li><li><a href="https://ashpublications.org/blood/article/doi/10.1182/blood.2023023078/">Murine models of erythroid 5ALA synthesis disorders and their conditional synthetic lethal dependency on pyridoxine</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024023829">Targeting PKCα alleviates iron overload in diabetes and hemochromatosis through the inhibition of ferroportin</a></li></ul><p><br></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Transplant outcomes in pediatric Fanconi anemia; hepatic Foxo1 regulates iron homeostasis; clinical networks improve APL outcomes in Latin America</title>
      <itunes:season>8</itunes:season>
      <podcast:season>8</podcast:season>
      <itunes:title>Transplant outcomes in pediatric Fanconi anemia; hepatic Foxo1 regulates iron homeostasis; clinical networks improve APL outcomes in Latin America</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">f01e99df-a603-4a50-ae3a-d32aaebcdebe</guid>
      <link>https://share.transistor.fm/s/f6e98f80</link>
      <description>
        <![CDATA[<p>In this week's episode we'll discuss outcomes following hematopoietic stem cell transplantation in pediatric patients with Fanconi anemia. Then, we'll learn about how new research shows that the transcription factor Foxo1, commonly associated with glucose metabolism, regulates hepcidin expression and systemic iron homeostasis. Finally, in Latin America: using clinical networks to improve outcomes in patients with acute promyelocytic leukemia. After clinical networks were established, survival and relapse rates improved substantially, highlighting the effectiveness of this unique intervention strategy in low- and middle-income countries.</p><p><strong>Featured Articles: </strong></p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022751">Outcomes of hematopoietic stem cell transplantation in 813 pediatric patients with Fanconi anemia</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024293">Foxo1 is an iron-responsive transcriptional factor regulating systemic iron homeostasis</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024023890">Clinical networking results in continuous improvement of the outcome of patients with acute promyelocytic<br>leukemia</a></li></ul><p><br></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we'll discuss outcomes following hematopoietic stem cell transplantation in pediatric patients with Fanconi anemia. Then, we'll learn about how new research shows that the transcription factor Foxo1, commonly associated with glucose metabolism, regulates hepcidin expression and systemic iron homeostasis. Finally, in Latin America: using clinical networks to improve outcomes in patients with acute promyelocytic leukemia. After clinical networks were established, survival and relapse rates improved substantially, highlighting the effectiveness of this unique intervention strategy in low- and middle-income countries.</p><p><strong>Featured Articles: </strong></p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022751">Outcomes of hematopoietic stem cell transplantation in 813 pediatric patients with Fanconi anemia</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024293">Foxo1 is an iron-responsive transcriptional factor regulating systemic iron homeostasis</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024023890">Clinical networking results in continuous improvement of the outcome of patients with acute promyelocytic<br>leukemia</a></li></ul><p><br></p>]]>
      </content:encoded>
      <pubDate>Thu, 19 Sep 2024 12:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/f6e98f80/3c812413.mp3" length="22453281" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1122</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we'll discuss outcomes following hematopoietic stem cell transplantation in pediatric patients with Fanconi anemia. Then, we'll learn about how new research shows that the transcription factor Foxo1, commonly associated with glucose metabolism, regulates hepcidin expression and systemic iron homeostasis. Finally, in Latin America: using clinical networks to improve outcomes in patients with acute promyelocytic leukemia. After clinical networks were established, survival and relapse rates improved substantially, highlighting the effectiveness of this unique intervention strategy in low- and middle-income countries.</p><p><strong>Featured Articles: </strong></p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022751">Outcomes of hematopoietic stem cell transplantation in 813 pediatric patients with Fanconi anemia</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024293">Foxo1 is an iron-responsive transcriptional factor regulating systemic iron homeostasis</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024023890">Clinical networking results in continuous improvement of the outcome of patients with acute promyelocytic<br>leukemia</a></li></ul><p><br></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>CD8+ T-cell differentiation and treatment response in AML; ATM germline pathogenic variants affect cancer outcomes in ataxia-telangiectasia; efficacy of a selective menin-KMT2A inhibitor in KMT2A- and NPM1-altered leukemias</title>
      <itunes:season>8</itunes:season>
      <podcast:season>8</podcast:season>
      <itunes:title>CD8+ T-cell differentiation and treatment response in AML; ATM germline pathogenic variants affect cancer outcomes in ataxia-telangiectasia; efficacy of a selective menin-KMT2A inhibitor in KMT2A- and NPM1-altered leukemias</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">8f8b7276-80a2-4ef5-9265-2d53e1f2ae98</guid>
      <link>https://share.transistor.fm/s/00a1b829</link>
      <description>
        <![CDATA[<p>In this week's episode we’ll discuss how CD8+ T-cell differentiation and dysfunction inform treatment response in acute myeloid leukemia; learn more about the effect of ATM germline pathogenic variants on the outcomes in children with ataxia-telangiectasia and hematological malignancies; and discuss the preclinical efficacy of a potent, selective menin-KMT2A inhibitor JNJ-75276617 in <em>KMT2A</em>- and <em>NPM1</em>-altered leukemias.</p><p><strong>Featured Articles:</strong></p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023021680">CD8+ T-cell differentiation and dysfunction inform treatment response in acute myeloid leukemia</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024283"><em>ATM</em> germ line pathogenic variants affect outcomes in children with ataxia-telangiectasia and hematological<br>malignancies</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022480">Preclinical efficacy of the potent, selective menin-KMT2A inhibitor JNJ-75276617 (bleximenib) in<br><em>KMT2A</em>- and <em>NPM1</em>-altered leukemias</a></li></ul><p><br></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we’ll discuss how CD8+ T-cell differentiation and dysfunction inform treatment response in acute myeloid leukemia; learn more about the effect of ATM germline pathogenic variants on the outcomes in children with ataxia-telangiectasia and hematological malignancies; and discuss the preclinical efficacy of a potent, selective menin-KMT2A inhibitor JNJ-75276617 in <em>KMT2A</em>- and <em>NPM1</em>-altered leukemias.</p><p><strong>Featured Articles:</strong></p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023021680">CD8+ T-cell differentiation and dysfunction inform treatment response in acute myeloid leukemia</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024283"><em>ATM</em> germ line pathogenic variants affect outcomes in children with ataxia-telangiectasia and hematological<br>malignancies</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022480">Preclinical efficacy of the potent, selective menin-KMT2A inhibitor JNJ-75276617 (bleximenib) in<br><em>KMT2A</em>- and <em>NPM1</em>-altered leukemias</a></li></ul><p><br></p>]]>
      </content:encoded>
      <pubDate>Thu, 12 Sep 2024 14:07:17 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/00a1b829/7f27653f.mp3" length="54477151" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1362</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we’ll discuss how CD8+ T-cell differentiation and dysfunction inform treatment response in acute myeloid leukemia; learn more about the effect of ATM germline pathogenic variants on the outcomes in children with ataxia-telangiectasia and hematological malignancies; and discuss the preclinical efficacy of a potent, selective menin-KMT2A inhibitor JNJ-75276617 in <em>KMT2A</em>- and <em>NPM1</em>-altered leukemias.</p><p><strong>Featured Articles:</strong></p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023021680">CD8+ T-cell differentiation and dysfunction inform treatment response in acute myeloid leukemia</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024283"><em>ATM</em> germ line pathogenic variants affect outcomes in children with ataxia-telangiectasia and hematological<br>malignancies</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022480">Preclinical efficacy of the potent, selective menin-KMT2A inhibitor JNJ-75276617 (bleximenib) in<br><em>KMT2A</em>- and <em>NPM1</em>-altered leukemias</a></li></ul><p><br></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>TCR-T cells for post-HCT leukemia recurrence; platelets are the predominant source of procoagulant membranes in hemostasis; BR + R maintenance for MCL</title>
      <itunes:season>8</itunes:season>
      <podcast:season>8</podcast:season>
      <itunes:title>TCR-T cells for post-HCT leukemia recurrence; platelets are the predominant source of procoagulant membranes in hemostasis; BR + R maintenance for MCL</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">f4aa7046-e350-4c01-abe8-bc370a0a68b9</guid>
      <link>https://share.transistor.fm/s/642547af</link>
      <description>
        <![CDATA[<p>In this week's episode we'll discuss HA-1-targeted T-cell receptor T-cell therapy for recurrent leukemia after hematopoietic stem cell transplantation. Next, we'll learn about how 4D intravital imaging in mice reveals the key role of platelets as a source of procoagulant membranes in hemostasis. Finally, we'll hear about modifications to a common induction and maintenance treatment for treatment-naïve mantle-cell lymphoma.</p><p><strong>Featured Articles</strong></p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024105">HA-1–targeted T-cell receptor T-cell therapy for recurrent leukemia after hematopoietic stem cell<br>transplantation</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022608">4D intravital imaging studies identify platelets as the predominant cellular procoagulant surface in a mouse<br>hemostasis model</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024023962">Randomized study of induction with bendamustine-rituximab ± bortezomib and maintenance with<br>rituximab ± lenalidomide for MCL</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we'll discuss HA-1-targeted T-cell receptor T-cell therapy for recurrent leukemia after hematopoietic stem cell transplantation. Next, we'll learn about how 4D intravital imaging in mice reveals the key role of platelets as a source of procoagulant membranes in hemostasis. Finally, we'll hear about modifications to a common induction and maintenance treatment for treatment-naïve mantle-cell lymphoma.</p><p><strong>Featured Articles</strong></p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024105">HA-1–targeted T-cell receptor T-cell therapy for recurrent leukemia after hematopoietic stem cell<br>transplantation</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022608">4D intravital imaging studies identify platelets as the predominant cellular procoagulant surface in a mouse<br>hemostasis model</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024023962">Randomized study of induction with bendamustine-rituximab ± bortezomib and maintenance with<br>rituximab ± lenalidomide for MCL</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 05 Sep 2024 12:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/642547af/ed151887.mp3" length="21814330" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1090</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we'll discuss HA-1-targeted T-cell receptor T-cell therapy for recurrent leukemia after hematopoietic stem cell transplantation. Next, we'll learn about how 4D intravital imaging in mice reveals the key role of platelets as a source of procoagulant membranes in hemostasis. Finally, we'll hear about modifications to a common induction and maintenance treatment for treatment-naïve mantle-cell lymphoma.</p><p><strong>Featured Articles</strong></p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024105">HA-1–targeted T-cell receptor T-cell therapy for recurrent leukemia after hematopoietic stem cell<br>transplantation</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022608">4D intravital imaging studies identify platelets as the predominant cellular procoagulant surface in a mouse<br>hemostasis model</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024023962">Randomized study of induction with bendamustine-rituximab ± bortezomib and maintenance with<br>rituximab ± lenalidomide for MCL</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Outcomes of younger patients with mantle cell lymphoma; M-protein assessment during maintenance therapy in multiple myeloma; in vivo CAR T-cell generation using lentiviral vectors</title>
      <itunes:season>8</itunes:season>
      <podcast:season>8</podcast:season>
      <itunes:title>Outcomes of younger patients with mantle cell lymphoma; M-protein assessment during maintenance therapy in multiple myeloma; in vivo CAR T-cell generation using lentiviral vectors</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">f6b86890-a76b-454c-aea5-ec0806c29d2c</guid>
      <link>https://share.transistor.fm/s/0f9b6968</link>
      <description>
        <![CDATA[<p>In this week's episode we’ll discuss the outcomes of younger patients with mantle cell lymphoma experiencing late relapse; learn more about mass spectrometry-based assessment of M-protein in peripheral blood during maintenance therapy in multiple myeloma and discuss <em>in vivo </em>CAR T-cell generation in non-human primates using lentiviral vectors.</p><p><strong>Featured Articles: </strong></p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023525">Outcomes of younger patients with mantle cell lymphoma experiencing late relapse (&gt;24 months): the LATE-POD study</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024041">Mass spectrometry–based assessment of M protein in peripheral blood during maintenance therapy in<br>multiple myeloma</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024523">In vivo CAR T-cell generation in nonhuman primates using lentiviral vectors displaying a multidomain fusion ligand</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we’ll discuss the outcomes of younger patients with mantle cell lymphoma experiencing late relapse; learn more about mass spectrometry-based assessment of M-protein in peripheral blood during maintenance therapy in multiple myeloma and discuss <em>in vivo </em>CAR T-cell generation in non-human primates using lentiviral vectors.</p><p><strong>Featured Articles: </strong></p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023525">Outcomes of younger patients with mantle cell lymphoma experiencing late relapse (&gt;24 months): the LATE-POD study</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024041">Mass spectrometry–based assessment of M protein in peripheral blood during maintenance therapy in<br>multiple myeloma</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024523">In vivo CAR T-cell generation in nonhuman primates using lentiviral vectors displaying a multidomain fusion ligand</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 29 Aug 2024 13:02:09 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/0f9b6968/ae842f19.mp3" length="973624" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>59</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we’ll discuss the outcomes of younger patients with mantle cell lymphoma experiencing late relapse; learn more about mass spectrometry-based assessment of M-protein in peripheral blood during maintenance therapy in multiple myeloma and discuss <em>in vivo </em>CAR T-cell generation in non-human primates using lentiviral vectors.</p><p><strong>Featured Articles: </strong></p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023525">Outcomes of younger patients with mantle cell lymphoma experiencing late relapse (&gt;24 months): the LATE-POD study</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024041">Mass spectrometry–based assessment of M protein in peripheral blood during maintenance therapy in<br>multiple myeloma</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024523">In vivo CAR T-cell generation in nonhuman primates using lentiviral vectors displaying a multidomain fusion ligand</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Review Series on Factor XI</title>
      <itunes:season>8</itunes:season>
      <podcast:season>8</podcast:season>
      <itunes:title>Review Series on Factor XI</itunes:title>
      <itunes:episodeType>bonus</itunes:episodeType>
      <guid isPermaLink="false">e749678a-a2c6-4067-afa0-d8adae18be34</guid>
      <link>https://share.transistor.fm/s/97dca730</link>
      <description>
        <![CDATA[<p>Introduced by Associate Editor Dr. Thomas Ortel, this bonus episode discusses the Review Series on Factor XI, published in volume 143 issue 15 of <em>Blood</em> Journal. Dr. Ortel is joined by contributing authors Owen McCarty, PhD, Gili Kenet, MD, and David Gailani, MD. </p><p><strong>Review Series Articles: </strong></p><ul><li><a href="https://ashpublications.org/blood/article/143/15/1431/515584/Introduction-to-a-review-series-on-factor-XI">Introduction to a review series on factor XI</a></li><li><a href="https://ashpublications.org/blood/article/143/15/1445/498410/Biology-of-factor-XI">Biology of factor XI</a></li><li><a href="https://ashpublications.org/blood/article/143/15/1465/506712/Targeting-factor-XI-and-factor-XIa-to-prevent">Targeting factor XI and factor XIa to prevent thrombosis</a></li><li><a href="https://ashpublications.org/blood/article/143/15/1455/507070/Factor-XI-deficiency-phenotypic-age-related">Factor XI deficiency: phenotypic age-related considerations and clinical approach towards bleeding risk assessment</a></li></ul><p><br></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>Introduced by Associate Editor Dr. Thomas Ortel, this bonus episode discusses the Review Series on Factor XI, published in volume 143 issue 15 of <em>Blood</em> Journal. Dr. Ortel is joined by contributing authors Owen McCarty, PhD, Gili Kenet, MD, and David Gailani, MD. </p><p><strong>Review Series Articles: </strong></p><ul><li><a href="https://ashpublications.org/blood/article/143/15/1431/515584/Introduction-to-a-review-series-on-factor-XI">Introduction to a review series on factor XI</a></li><li><a href="https://ashpublications.org/blood/article/143/15/1445/498410/Biology-of-factor-XI">Biology of factor XI</a></li><li><a href="https://ashpublications.org/blood/article/143/15/1465/506712/Targeting-factor-XI-and-factor-XIa-to-prevent">Targeting factor XI and factor XIa to prevent thrombosis</a></li><li><a href="https://ashpublications.org/blood/article/143/15/1455/507070/Factor-XI-deficiency-phenotypic-age-related">Factor XI deficiency: phenotypic age-related considerations and clinical approach towards bleeding risk assessment</a></li></ul><p><br></p>]]>
      </content:encoded>
      <pubDate>Thu, 29 Aug 2024 13:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/97dca730/a4e8b7b3.mp3" length="53626140" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/fC_N5vWZyJYdFugW3Q8vR-43MuVJtP2Ye8UP--DV_RE/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS82M2Fm/MWNlMjBjNmE0YTVi/ZmQ4NmZlNjVkMDE5/MGMxNi5qcGc.jpg"/>
      <itunes:duration>2680</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>Introduced by Associate Editor Dr. Thomas Ortel, this bonus episode discusses the Review Series on Factor XI, published in volume 143 issue 15 of <em>Blood</em> Journal. Dr. Ortel is joined by contributing authors Owen McCarty, PhD, Gili Kenet, MD, and David Gailani, MD. </p><p><strong>Review Series Articles: </strong></p><ul><li><a href="https://ashpublications.org/blood/article/143/15/1431/515584/Introduction-to-a-review-series-on-factor-XI">Introduction to a review series on factor XI</a></li><li><a href="https://ashpublications.org/blood/article/143/15/1445/498410/Biology-of-factor-XI">Biology of factor XI</a></li><li><a href="https://ashpublications.org/blood/article/143/15/1465/506712/Targeting-factor-XI-and-factor-XIa-to-prevent">Targeting factor XI and factor XIa to prevent thrombosis</a></li><li><a href="https://ashpublications.org/blood/article/143/15/1455/507070/Factor-XI-deficiency-phenotypic-age-related">Factor XI deficiency: phenotypic age-related considerations and clinical approach towards bleeding risk assessment</a></li></ul><p><br></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Protective role of neonatal CMV infection in B-ALL; GVHD targets organoid-forming bile duct stem cells; seven-year outcomes for venetoclax-ibrutinib therapy in MCL</title>
      <itunes:season>8</itunes:season>
      <podcast:season>8</podcast:season>
      <itunes:title>Protective role of neonatal CMV infection in B-ALL; GVHD targets organoid-forming bile duct stem cells; seven-year outcomes for venetoclax-ibrutinib therapy in MCL</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">b8c3a858-f160-42e3-a54a-1367ebd02aef</guid>
      <link>https://share.transistor.fm/s/2d7d5918</link>
      <description>
        <![CDATA[<p>In this week's episode we'll learn how cytomegalovirus infection early in life depletes preleukemic cells in a mouse model of B-cell acute lymphoblastic leukemia. After that we'll discuss new research, where GVHD targets organoid-forming bile duct stem cells in a TGF-beta-dependent manner. Conversely, a TGF-beta inhibitor protects these stem cells against GVHD and mitigates biliary dysfunction. Finally, we'll hear about the seven-year outcomes for venetoclax-ibrutinib in relapsed or refractory mantle cell lymphoma. In addition to long-term survival benefits, researchers report durable treatment-free remissions and effective retreatment in patients with MRD-negative complete responses. </p><p><strong>Featured Articles: </strong></p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025038">Early-life infection depletes preleukemic cells in a mouse model of hyperdiploid B-cell acute lymphoblastic<br>leukemia</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023060">GVHD targets organoid-forming bile duct stem cells in a TGF-β–dependent manner</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023388">Seven-year outcomes of venetoclax-ibrutinib therapy in mantle cell lymphoma: durable responses and<br>treatment-free remissions</a></li></ul><p><br></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we'll learn how cytomegalovirus infection early in life depletes preleukemic cells in a mouse model of B-cell acute lymphoblastic leukemia. After that we'll discuss new research, where GVHD targets organoid-forming bile duct stem cells in a TGF-beta-dependent manner. Conversely, a TGF-beta inhibitor protects these stem cells against GVHD and mitigates biliary dysfunction. Finally, we'll hear about the seven-year outcomes for venetoclax-ibrutinib in relapsed or refractory mantle cell lymphoma. In addition to long-term survival benefits, researchers report durable treatment-free remissions and effective retreatment in patients with MRD-negative complete responses. </p><p><strong>Featured Articles: </strong></p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025038">Early-life infection depletes preleukemic cells in a mouse model of hyperdiploid B-cell acute lymphoblastic<br>leukemia</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023060">GVHD targets organoid-forming bile duct stem cells in a TGF-β–dependent manner</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023388">Seven-year outcomes of venetoclax-ibrutinib therapy in mantle cell lymphoma: durable responses and<br>treatment-free remissions</a></li></ul><p><br></p>]]>
      </content:encoded>
      <pubDate>Thu, 22 Aug 2024 12:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/2d7d5918/c55688ca.mp3" length="20338946" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1016</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we'll learn how cytomegalovirus infection early in life depletes preleukemic cells in a mouse model of B-cell acute lymphoblastic leukemia. After that we'll discuss new research, where GVHD targets organoid-forming bile duct stem cells in a TGF-beta-dependent manner. Conversely, a TGF-beta inhibitor protects these stem cells against GVHD and mitigates biliary dysfunction. Finally, we'll hear about the seven-year outcomes for venetoclax-ibrutinib in relapsed or refractory mantle cell lymphoma. In addition to long-term survival benefits, researchers report durable treatment-free remissions and effective retreatment in patients with MRD-negative complete responses. </p><p><strong>Featured Articles: </strong></p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024025038">Early-life infection depletes preleukemic cells in a mouse model of hyperdiploid B-cell acute lymphoblastic<br>leukemia</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023060">GVHD targets organoid-forming bile duct stem cells in a TGF-β–dependent manner</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023388">Seven-year outcomes of venetoclax-ibrutinib therapy in mantle cell lymphoma: durable responses and<br>treatment-free remissions</a></li></ul><p><br></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Iron, HFE haemochromatosis, and infections; bispecific antibodies improve CAR T-cell response; determinants of outcome in NPM1-mutated AML</title>
      <itunes:season>8</itunes:season>
      <podcast:season>8</podcast:season>
      <itunes:title>Iron, HFE haemochromatosis, and infections; bispecific antibodies improve CAR T-cell response; determinants of outcome in NPM1-mutated AML</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">85951897-6ea1-4621-a103-d48e339a186c</guid>
      <link>https://share.transistor.fm/s/e1804373</link>
      <description>
        <![CDATA[<p>In this week's episode we'll learn about iron, HFE hemochromatosis, and infections. In this large, population-based study, both high and low levels of plasma iron and transferrin saturation were associated with increased risks of infection. Then, we'll discuss how bispecific antibodies improve CAR T-cell response in B-cell malignancies. In-vitro and in-vivo data demonstrate enhanced therapeutic efficacy when a CD20-directed bispecific antibody is given in combination with CD19-directed CAR-T cells. Finally, we'll hear about determinants of outcome in NPM1-mutated AML. In a large series of patients with NPM1-mutated AML, investigators identified several variables beyond FLT3-ITD that adversely impacted outcomes. </p><p><strong>Featured Articles:</strong></p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022235">Iron, hemochromatosis genotypes, and risk of infections: a cohort study of 142 188 general population individuals</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024310">Molecular, clinical, and therapeutic determinants of outcome in NPM1-mutated AML</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022682">CD20-bispecific antibodies improve response to CD19-CAR T cells in lymphoma in vitro and CLL in vivo models</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we'll learn about iron, HFE hemochromatosis, and infections. In this large, population-based study, both high and low levels of plasma iron and transferrin saturation were associated with increased risks of infection. Then, we'll discuss how bispecific antibodies improve CAR T-cell response in B-cell malignancies. In-vitro and in-vivo data demonstrate enhanced therapeutic efficacy when a CD20-directed bispecific antibody is given in combination with CD19-directed CAR-T cells. Finally, we'll hear about determinants of outcome in NPM1-mutated AML. In a large series of patients with NPM1-mutated AML, investigators identified several variables beyond FLT3-ITD that adversely impacted outcomes. </p><p><strong>Featured Articles:</strong></p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022235">Iron, hemochromatosis genotypes, and risk of infections: a cohort study of 142 188 general population individuals</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024310">Molecular, clinical, and therapeutic determinants of outcome in NPM1-mutated AML</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022682">CD20-bispecific antibodies improve response to CD19-CAR T cells in lymphoma in vitro and CLL in vivo models</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 15 Aug 2024 12:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/e1804373/7df34ad5.mp3" length="28245664" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1411</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we'll learn about iron, HFE hemochromatosis, and infections. In this large, population-based study, both high and low levels of plasma iron and transferrin saturation were associated with increased risks of infection. Then, we'll discuss how bispecific antibodies improve CAR T-cell response in B-cell malignancies. In-vitro and in-vivo data demonstrate enhanced therapeutic efficacy when a CD20-directed bispecific antibody is given in combination with CD19-directed CAR-T cells. Finally, we'll hear about determinants of outcome in NPM1-mutated AML. In a large series of patients with NPM1-mutated AML, investigators identified several variables beyond FLT3-ITD that adversely impacted outcomes. </p><p><strong>Featured Articles:</strong></p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022235">Iron, hemochromatosis genotypes, and risk of infections: a cohort study of 142 188 general population individuals</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024310">Molecular, clinical, and therapeutic determinants of outcome in NPM1-mutated AML</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022682">CD20-bispecific antibodies improve response to CD19-CAR T cells in lymphoma in vitro and CLL in vivo models</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Immune fitness and response to taclistamab in R/R multiple myeloma; BCR::ABL1 M244V mutation causes resistance to asciminib; HSCT and myocardial fibrosis in young patients with SCD</title>
      <itunes:season>8</itunes:season>
      <podcast:season>8</podcast:season>
      <itunes:title>Immune fitness and response to taclistamab in R/R multiple myeloma; BCR::ABL1 M244V mutation causes resistance to asciminib; HSCT and myocardial fibrosis in young patients with SCD</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">21822132-2130-4efd-a4b9-638bf93a367d</guid>
      <link>https://share.transistor.fm/s/916194ab</link>
      <description>
        <![CDATA[<p>In this week's episode we’ll discuss how immune fitness impacts response to teclistamab in relapsed/refractory multiple myeloma; learn more about a new mechanism of resistance to asciminib conferred by the <em>BCR::ABL1 M244V</em> mutation, and discuss the impact of hematopoietic cell transplantation on myocardial fibrosis in young patients with sickle cell disease. </p><p><strong>Featured Articles:</strong></p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022823">Correlation of immune fitness with response to teclistamab in relapsed/refractory multiple myeloma in MajesTEC-1</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022538"><em>BCR::ABL1</em> kinase N-lobe mutants confer moderate to high degrees of resistance to asciminib</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023028">Impact of hematopoietic cell transplantation on myocardial fibrosis in young patients with sickle cell disease</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we’ll discuss how immune fitness impacts response to teclistamab in relapsed/refractory multiple myeloma; learn more about a new mechanism of resistance to asciminib conferred by the <em>BCR::ABL1 M244V</em> mutation, and discuss the impact of hematopoietic cell transplantation on myocardial fibrosis in young patients with sickle cell disease. </p><p><strong>Featured Articles:</strong></p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022823">Correlation of immune fitness with response to teclistamab in relapsed/refractory multiple myeloma in MajesTEC-1</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022538"><em>BCR::ABL1</em> kinase N-lobe mutants confer moderate to high degrees of resistance to asciminib</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023028">Impact of hematopoietic cell transplantation on myocardial fibrosis in young patients with sickle cell disease</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 08 Aug 2024 13:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/916194ab/50e2aa1b.mp3" length="16320939" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1019</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we’ll discuss how immune fitness impacts response to teclistamab in relapsed/refractory multiple myeloma; learn more about a new mechanism of resistance to asciminib conferred by the <em>BCR::ABL1 M244V</em> mutation, and discuss the impact of hematopoietic cell transplantation on myocardial fibrosis in young patients with sickle cell disease. </p><p><strong>Featured Articles:</strong></p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022823">Correlation of immune fitness with response to teclistamab in relapsed/refractory multiple myeloma in MajesTEC-1</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022538"><em>BCR::ABL1</em> kinase N-lobe mutants confer moderate to high degrees of resistance to asciminib</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023028">Impact of hematopoietic cell transplantation on myocardial fibrosis in young patients with sickle cell disease</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Decitabine in older patients with AML; EPCR and sickle chronic kidney disease; lymphocyte depletion versus post-transplant cyclophosphamide for mismatched donor transplant for inborn errors of immunity</title>
      <itunes:season>8</itunes:season>
      <podcast:season>8</podcast:season>
      <itunes:title>Decitabine in older patients with AML; EPCR and sickle chronic kidney disease; lymphocyte depletion versus post-transplant cyclophosphamide for mismatched donor transplant for inborn errors of immunity</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">6bfacba0-e49b-4185-8d40-dc30d6a2a8fc</guid>
      <link>https://share.transistor.fm/s/767807c6</link>
      <description>
        <![CDATA[<p>In this week's episode we’ll discuss the safety and efficacy of decitabine in older patients with AML; learn how heme-induced loss of renovascular endothelial protein C receptor promotes chronic kidney disease in sickle mice, and discuss the outcomes of treatment with HLA-mismatched HSCT with TCRab/CD19 lymphocyte depletion or post-HSCT cyclophosphamide for inborn errors of immunity. </p><p><strong>Featured Articles:</strong></p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023625">Decitabine in older patients with AML: Quality of life results of the EORTC-GIMEMA-GMDS-SG randomized phase III trial </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023528">Heme induced loss of renovascular endothelial protein C receptor promotes chronic kidney disease in sickle mice </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024038">Outcomes of HLA-mismatched HSCT with TCRab/CD19 depletion or post-HSCT cyclophosphamide for inborn errors or immunity </a></li></ul><p><br></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we’ll discuss the safety and efficacy of decitabine in older patients with AML; learn how heme-induced loss of renovascular endothelial protein C receptor promotes chronic kidney disease in sickle mice, and discuss the outcomes of treatment with HLA-mismatched HSCT with TCRab/CD19 lymphocyte depletion or post-HSCT cyclophosphamide for inborn errors of immunity. </p><p><strong>Featured Articles:</strong></p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023625">Decitabine in older patients with AML: Quality of life results of the EORTC-GIMEMA-GMDS-SG randomized phase III trial </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023528">Heme induced loss of renovascular endothelial protein C receptor promotes chronic kidney disease in sickle mice </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024038">Outcomes of HLA-mismatched HSCT with TCRab/CD19 depletion or post-HSCT cyclophosphamide for inborn errors or immunity </a></li></ul><p><br></p>]]>
      </content:encoded>
      <pubDate>Thu, 01 Aug 2024 12:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/767807c6/95ca699d.mp3" length="27487131" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1373</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we’ll discuss the safety and efficacy of decitabine in older patients with AML; learn how heme-induced loss of renovascular endothelial protein C receptor promotes chronic kidney disease in sickle mice, and discuss the outcomes of treatment with HLA-mismatched HSCT with TCRab/CD19 lymphocyte depletion or post-HSCT cyclophosphamide for inborn errors of immunity. </p><p><strong>Featured Articles:</strong></p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023625">Decitabine in older patients with AML: Quality of life results of the EORTC-GIMEMA-GMDS-SG randomized phase III trial </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023528">Heme induced loss of renovascular endothelial protein C receptor promotes chronic kidney disease in sickle mice </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024038">Outcomes of HLA-mismatched HSCT with TCRab/CD19 depletion or post-HSCT cyclophosphamide for inborn errors or immunity </a></li></ul><p><br></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Impact of MRD-negative on PFS in myeloma; IPSS-R down-staging before transplant in MDS; hereditary angioedema and venous thromboembolism </title>
      <itunes:season>8</itunes:season>
      <podcast:season>8</podcast:season>
      <itunes:title>Impact of MRD-negative on PFS in myeloma; IPSS-R down-staging before transplant in MDS; hereditary angioedema and venous thromboembolism </itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">5d9b337c-102b-41d3-9b28-9e75b3a40f95</guid>
      <link>https://share.transistor.fm/s/2e447d03</link>
      <description>
        <![CDATA[<p>In this week's episode we'll discuss minimal residual disease as an intermediate clinical endpoint for multiple myeloma. Then, we'll learn about IPSS-R downstaging before transplant in MDS. Finally we'll hear about the connection between hereditary angioedema and venous thromboembolism. </p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024371">EVIDENCE meta-analysis: evaluating minimal residual disease as an intermediate clinical endpoint for multiple myeloma </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022273">Does IPSS-R down-staging before transplantation improve the prognosis of patients with Myelodysplastic Neoplasms? </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022996">Increased risk of venous thromboembolism [or VTE] in young and middle-aged individuals with hereditary angioedema: a family study</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we'll discuss minimal residual disease as an intermediate clinical endpoint for multiple myeloma. Then, we'll learn about IPSS-R downstaging before transplant in MDS. Finally we'll hear about the connection between hereditary angioedema and venous thromboembolism. </p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024371">EVIDENCE meta-analysis: evaluating minimal residual disease as an intermediate clinical endpoint for multiple myeloma </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022273">Does IPSS-R down-staging before transplantation improve the prognosis of patients with Myelodysplastic Neoplasms? </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022996">Increased risk of venous thromboembolism [or VTE] in young and middle-aged individuals with hereditary angioedema: a family study</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 25 Jul 2024 12:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/2e447d03/eba31c5d.mp3" length="26223263" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1310</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we'll discuss minimal residual disease as an intermediate clinical endpoint for multiple myeloma. Then, we'll learn about IPSS-R downstaging before transplant in MDS. Finally we'll hear about the connection between hereditary angioedema and venous thromboembolism. </p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024371">EVIDENCE meta-analysis: evaluating minimal residual disease as an intermediate clinical endpoint for multiple myeloma </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022273">Does IPSS-R down-staging before transplantation improve the prognosis of patients with Myelodysplastic Neoplasms? </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022996">Increased risk of venous thromboembolism [or VTE] in young and middle-aged individuals with hereditary angioedema: a family study</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Acalabrutinib, venetoclax and obinutuzumab in relapsed/refractory CLL; alternative donor transplantation for severe aplastic anemia; clonal relapse dynamics in AML following allogeneic HCT</title>
      <itunes:season>8</itunes:season>
      <podcast:season>8</podcast:season>
      <itunes:title>Acalabrutinib, venetoclax and obinutuzumab in relapsed/refractory CLL; alternative donor transplantation for severe aplastic anemia; clonal relapse dynamics in AML following allogeneic HCT</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">2ca41478-6dd3-4ce6-a81a-2fb9ead26e85</guid>
      <link>https://share.transistor.fm/s/4d9aaf2e</link>
      <description>
        <![CDATA[<p>In this week's episode we’ll discuss the safety and efficacy of acalabrutinib, venetoclax and obinutuzumab in relapsed/refractory CLL; learn more about alternative donor transplantation for severe aplastic anemia and discuss clonal relapse dynamics in acute myeloid leukemia following allogeneic hematopoietic cell transplantation.</p><p><strong>Featured Articles: </strong></p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022730">Acalabrutinib, venetoclax and obinutuzumab in relapsed/refractory CLL: Final efficacy and ctDNA analysis of the CLL2-BAAG trial </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024173">Alternative donor transplantation for severe aplastic anemia: a comparative study of the SAAWP EBMT </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022697">Clonal relapse dynamics in acute myeloid leukemia following allogeneic hematopoietic cell transplantation </a></li></ul><p><br></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we’ll discuss the safety and efficacy of acalabrutinib, venetoclax and obinutuzumab in relapsed/refractory CLL; learn more about alternative donor transplantation for severe aplastic anemia and discuss clonal relapse dynamics in acute myeloid leukemia following allogeneic hematopoietic cell transplantation.</p><p><strong>Featured Articles: </strong></p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022730">Acalabrutinib, venetoclax and obinutuzumab in relapsed/refractory CLL: Final efficacy and ctDNA analysis of the CLL2-BAAG trial </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024173">Alternative donor transplantation for severe aplastic anemia: a comparative study of the SAAWP EBMT </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022697">Clonal relapse dynamics in acute myeloid leukemia following allogeneic hematopoietic cell transplantation </a></li></ul><p><br></p>]]>
      </content:encoded>
      <pubDate>Thu, 18 Jul 2024 12:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/4d9aaf2e/26d1cef0.mp3" length="28253028" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1412</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we’ll discuss the safety and efficacy of acalabrutinib, venetoclax and obinutuzumab in relapsed/refractory CLL; learn more about alternative donor transplantation for severe aplastic anemia and discuss clonal relapse dynamics in acute myeloid leukemia following allogeneic hematopoietic cell transplantation.</p><p><strong>Featured Articles: </strong></p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022730">Acalabrutinib, venetoclax and obinutuzumab in relapsed/refractory CLL: Final efficacy and ctDNA analysis of the CLL2-BAAG trial </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024173">Alternative donor transplantation for severe aplastic anemia: a comparative study of the SAAWP EBMT </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022697">Clonal relapse dynamics in acute myeloid leukemia following allogeneic hematopoietic cell transplantation </a></li></ul><p><br></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Clinical impact of CRh in AML; thrombosis features in a real-life PNH cohort; and restriction of SOX11 expression to EBV-negative Burkitt lymphomas  </title>
      <itunes:season>8</itunes:season>
      <podcast:season>8</podcast:season>
      <itunes:title>Clinical impact of CRh in AML; thrombosis features in a real-life PNH cohort; and restriction of SOX11 expression to EBV-negative Burkitt lymphomas  </itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">5c9cc3da-ed59-4b31-8e3c-5fff3a6d0e4d</guid>
      <link>https://share.transistor.fm/s/65c494a7</link>
      <description>
        <![CDATA[<p>In this week's episode we'll learn about the clinical benefit of complete remission with partial hematological recovery, or CRh, in patients with Acute Myeloid Leukemia (AML) treated with molecularly targeted drugs. Then we'll hear about a large cohort of patients with PNH were studied to detail PNH-related thrombotic events, unravel determinants of thrombosis, and evaluate anti-coagulation strategies. Finally, we'll see how new research shows that <em>SOX11 </em>expression is restricted to EBV-negative Burkitt lymphoma, and is associated with a specific genetic landscape. </p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023313">Complete Remission with Partial Hematological Recovery as a Palliative Endpoint for Treatment of Acute Myeloid Leukemia </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024023988">Paroxysmal nocturnal hemoglobinuria-related thrombosis in the era of novel therapies: a 2043 patient/years analysis </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023242"><em>SOX11 </em>expression is restricted to EBV-negative Burkitt lymphoma and associates with molecular genetic features </a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we'll learn about the clinical benefit of complete remission with partial hematological recovery, or CRh, in patients with Acute Myeloid Leukemia (AML) treated with molecularly targeted drugs. Then we'll hear about a large cohort of patients with PNH were studied to detail PNH-related thrombotic events, unravel determinants of thrombosis, and evaluate anti-coagulation strategies. Finally, we'll see how new research shows that <em>SOX11 </em>expression is restricted to EBV-negative Burkitt lymphoma, and is associated with a specific genetic landscape. </p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023313">Complete Remission with Partial Hematological Recovery as a Palliative Endpoint for Treatment of Acute Myeloid Leukemia </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024023988">Paroxysmal nocturnal hemoglobinuria-related thrombosis in the era of novel therapies: a 2043 patient/years analysis </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023242"><em>SOX11 </em>expression is restricted to EBV-negative Burkitt lymphoma and associates with molecular genetic features </a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 11 Jul 2024 14:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/65c494a7/1bcb58d1.mp3" length="28785896" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1198</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we'll learn about the clinical benefit of complete remission with partial hematological recovery, or CRh, in patients with Acute Myeloid Leukemia (AML) treated with molecularly targeted drugs. Then we'll hear about a large cohort of patients with PNH were studied to detail PNH-related thrombotic events, unravel determinants of thrombosis, and evaluate anti-coagulation strategies. Finally, we'll see how new research shows that <em>SOX11 </em>expression is restricted to EBV-negative Burkitt lymphoma, and is associated with a specific genetic landscape. </p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023313">Complete Remission with Partial Hematological Recovery as a Palliative Endpoint for Treatment of Acute Myeloid Leukemia </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024023988">Paroxysmal nocturnal hemoglobinuria-related thrombosis in the era of novel therapies: a 2043 patient/years analysis </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023242"><em>SOX11 </em>expression is restricted to EBV-negative Burkitt lymphoma and associates with molecular genetic features </a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Mutational and transcriptional landscape of pediatric BCP lymphoblastic lymphoma; the role of platelet-derived TGF-1 in immune thrombocytopenia; phase 3 trial of mavorixafor in WHIM syndrome</title>
      <itunes:season>8</itunes:season>
      <podcast:season>8</podcast:season>
      <itunes:title>Mutational and transcriptional landscape of pediatric BCP lymphoblastic lymphoma; the role of platelet-derived TGF-1 in immune thrombocytopenia; phase 3 trial of mavorixafor in WHIM syndrome</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">cf9fcd9e-0903-46b9-bb6e-7e0caf6ae6d2</guid>
      <link>https://share.transistor.fm/s/d526f448</link>
      <description>
        <![CDATA[<p>In this week's episode we’ll discuss the mutational and transcriptional landscape of pediatric BCP lymphoblastic leukemia; learn more about the role of platelet-derived TGF-β1 in immune thrombocytopenia; and discuss the findings from a phase 3 trial of mavorixafor in WHIM syndrome.</p><p><strong>Featured Articles:</strong></p><ul><li><a href="https://ashpublications.org/blood/article/144/1/74/516729/Mutational-and-transcriptional-landscape-of">Mutational and transcriptional landscape of pediatric B-cell precursor lymphoblastic lymphoma </a></li><li><a href="https://ashpublications.org/blood/article/144/1/99/516738/Platelet-derived-TGF-1-induces-functional">Platelet-derived TGF-β1 induces functional reprogramming of myeloid-derived suppressor cells in immune thrombocytopenia </a></li><li><a href="https://ashpublications.org/blood/article/144/1/35/516726/A-phase-3-randomized-trial-of-mavorixafor-a-CXCR4">Phase 3 randomized trial of mavorixafor, CXCR4 antagonist, in WHIM syndrome </a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we’ll discuss the mutational and transcriptional landscape of pediatric BCP lymphoblastic leukemia; learn more about the role of platelet-derived TGF-β1 in immune thrombocytopenia; and discuss the findings from a phase 3 trial of mavorixafor in WHIM syndrome.</p><p><strong>Featured Articles:</strong></p><ul><li><a href="https://ashpublications.org/blood/article/144/1/74/516729/Mutational-and-transcriptional-landscape-of">Mutational and transcriptional landscape of pediatric B-cell precursor lymphoblastic lymphoma </a></li><li><a href="https://ashpublications.org/blood/article/144/1/99/516738/Platelet-derived-TGF-1-induces-functional">Platelet-derived TGF-β1 induces functional reprogramming of myeloid-derived suppressor cells in immune thrombocytopenia </a></li><li><a href="https://ashpublications.org/blood/article/144/1/35/516726/A-phase-3-randomized-trial-of-mavorixafor-a-CXCR4">Phase 3 randomized trial of mavorixafor, CXCR4 antagonist, in WHIM syndrome </a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 04 Jul 2024 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/d526f448/65dbf893.mp3" length="33749712" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1405</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we’ll discuss the mutational and transcriptional landscape of pediatric BCP lymphoblastic leukemia; learn more about the role of platelet-derived TGF-β1 in immune thrombocytopenia; and discuss the findings from a phase 3 trial of mavorixafor in WHIM syndrome.</p><p><strong>Featured Articles:</strong></p><ul><li><a href="https://ashpublications.org/blood/article/144/1/74/516729/Mutational-and-transcriptional-landscape-of">Mutational and transcriptional landscape of pediatric B-cell precursor lymphoblastic lymphoma </a></li><li><a href="https://ashpublications.org/blood/article/144/1/99/516738/Platelet-derived-TGF-1-induces-functional">Platelet-derived TGF-β1 induces functional reprogramming of myeloid-derived suppressor cells in immune thrombocytopenia </a></li><li><a href="https://ashpublications.org/blood/article/144/1/35/516726/A-phase-3-randomized-trial-of-mavorixafor-a-CXCR4">Phase 3 randomized trial of mavorixafor, CXCR4 antagonist, in WHIM syndrome </a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Review Series on Oncogenic Signaling and Immune Evasion in Hematologic Malignancies</title>
      <itunes:season>7</itunes:season>
      <podcast:season>7</podcast:season>
      <itunes:title>Review Series on Oncogenic Signaling and Immune Evasion in Hematologic Malignancies</itunes:title>
      <itunes:episodeType>bonus</itunes:episodeType>
      <guid isPermaLink="false">772e5237-a824-42cf-b08b-d9a73275da3f</guid>
      <link>https://share.transistor.fm/s/c4809d5f</link>
      <description>
        <![CDATA[<p>Introduced by Associate Editor Robert Zeiser, this Review Series focuses on the problem of immune escape by acute myeloid leukemia (AML). The series opens with a review of how AML escapes T-cell–driven elimination and then focuses on how p53 function impinges on AML recognition by immune cells. The series finishes with a summary of new approaches to tackling this major problem.</p><p>Featured Series:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024023825">Introduction to a review series on oncogenic signaling and immune evasion in hematologic malignancies</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>Introduced by Associate Editor Robert Zeiser, this Review Series focuses on the problem of immune escape by acute myeloid leukemia (AML). The series opens with a review of how AML escapes T-cell–driven elimination and then focuses on how p53 function impinges on AML recognition by immune cells. The series finishes with a summary of new approaches to tackling this major problem.</p><p>Featured Series:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024023825">Introduction to a review series on oncogenic signaling and immune evasion in hematologic malignancies</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 27 Jun 2024 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/c4809d5f/7208333b.mp3" length="18849718" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/YptKvgP6BjX5M3KAgUhjH8xKEqBNrKYWSTYgYDAy0r0/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS8xMWNh/ZmE1ZGFmOTZhZjUz/MzZhNmU2YWNjMGQ4/YzI4ZC5qcGc.jpg"/>
      <itunes:duration>941</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>Introduced by Associate Editor Robert Zeiser, this Review Series focuses on the problem of immune escape by acute myeloid leukemia (AML). The series opens with a review of how AML escapes T-cell–driven elimination and then focuses on how p53 function impinges on AML recognition by immune cells. The series finishes with a summary of new approaches to tackling this major problem.</p><p>Featured Series:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024023825">Introduction to a review series on oncogenic signaling and immune evasion in hematologic malignancies</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>GM-CSF coordinates shelter in the cytokine storm; Interleukin-1 as a therapeutic target in TTP; CAR T-cell outcomes across race and ethnicity in LBCL</title>
      <itunes:season>7</itunes:season>
      <podcast:season>7</podcast:season>
      <itunes:title>GM-CSF coordinates shelter in the cytokine storm; Interleukin-1 as a therapeutic target in TTP; CAR T-cell outcomes across race and ethnicity in LBCL</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">f608aedd-b982-414e-bbd3-b22a9a472e7b</guid>
      <link>https://share.transistor.fm/s/2235502a</link>
      <description>
        <![CDATA[<p>In this week's episode we'll discuss new insights on the role of GM-CSF in establishing immune memory. The authors propose that the coordination of opposing immune memory programs, driven by GM-CSF, may be essential to efficient, yet controlled, innate immune responses. After that: Interleukin-1 inhibition in TTP. Researchers explore the potential of recombinant IL-1 receptor antagonist, anakinra, in a murine model of thrombotic thrombocytopenic purpura—an uncommon but potentially fatal disorder with limited therapeutic options. Finally, we'll learn about CAR T-cell therapy outcomes by race and ethnicity in large B-cell lymphoma. Non-Hispanic Black patients had lower rates of response and progression-free survival in axi-cel clinical trials and real-world data, raising awareness and giving further insights into potential inequitable access to care.<br><strong><br>Featured Articles:</strong></p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024330">GM-CSF receptor expression determines opposing innate memory phenotypes at different stages of myelopoiesis </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023021974">Mortality, cardiac and cerebral damage reduction by IL-1 inhibition in a murine model of TTP </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023024959">Real-World and Clinical Trial Outcomes in Large B-cell Lymphoma with Axicabtagene Ciloleucel Across Race and Ethnicity </a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we'll discuss new insights on the role of GM-CSF in establishing immune memory. The authors propose that the coordination of opposing immune memory programs, driven by GM-CSF, may be essential to efficient, yet controlled, innate immune responses. After that: Interleukin-1 inhibition in TTP. Researchers explore the potential of recombinant IL-1 receptor antagonist, anakinra, in a murine model of thrombotic thrombocytopenic purpura—an uncommon but potentially fatal disorder with limited therapeutic options. Finally, we'll learn about CAR T-cell therapy outcomes by race and ethnicity in large B-cell lymphoma. Non-Hispanic Black patients had lower rates of response and progression-free survival in axi-cel clinical trials and real-world data, raising awareness and giving further insights into potential inequitable access to care.<br><strong><br>Featured Articles:</strong></p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024330">GM-CSF receptor expression determines opposing innate memory phenotypes at different stages of myelopoiesis </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023021974">Mortality, cardiac and cerebral damage reduction by IL-1 inhibition in a murine model of TTP </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023024959">Real-World and Clinical Trial Outcomes in Large B-cell Lymphoma with Axicabtagene Ciloleucel Across Race and Ethnicity </a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 27 Jun 2024 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/2235502a/e4a40888.mp3" length="28774748" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1197</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we'll discuss new insights on the role of GM-CSF in establishing immune memory. The authors propose that the coordination of opposing immune memory programs, driven by GM-CSF, may be essential to efficient, yet controlled, innate immune responses. After that: Interleukin-1 inhibition in TTP. Researchers explore the potential of recombinant IL-1 receptor antagonist, anakinra, in a murine model of thrombotic thrombocytopenic purpura—an uncommon but potentially fatal disorder with limited therapeutic options. Finally, we'll learn about CAR T-cell therapy outcomes by race and ethnicity in large B-cell lymphoma. Non-Hispanic Black patients had lower rates of response and progression-free survival in axi-cel clinical trials and real-world data, raising awareness and giving further insights into potential inequitable access to care.<br><strong><br>Featured Articles:</strong></p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2024024330">GM-CSF receptor expression determines opposing innate memory phenotypes at different stages of myelopoiesis </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023021974">Mortality, cardiac and cerebral damage reduction by IL-1 inhibition in a murine model of TTP </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023024959">Real-World and Clinical Trial Outcomes in Large B-cell Lymphoma with Axicabtagene Ciloleucel Across Race and Ethnicity </a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Reassessing the CLL prognostic index; ADAMTS13 conformation and risk of relapse in immune-mediated TTP; haploidentical bone marrow transplant in sickle cell disease</title>
      <itunes:season>7</itunes:season>
      <podcast:season>7</podcast:season>
      <itunes:title>Reassessing the CLL prognostic index; ADAMTS13 conformation and risk of relapse in immune-mediated TTP; haploidentical bone marrow transplant in sickle cell disease</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">3680ae62-ed2e-4547-b012-1068c5698849</guid>
      <link>https://share.transistor.fm/s/b4fb830c</link>
      <description>
        <![CDATA[<p>In this week's episode we’ll discuss the prognostic value of the Chronic Lymphocytic Leukemia International Prognostic Index in the era of targeted therapies, learn how peak ADAMTS13 activity can be used to assess ADAMTS13 conformation and risk of relapse in immune-mediated thrombotic thrombocytopenic purpura, and discuss the findings from a phase 2 trial of haploidentical bone marrow transplant in sickle cell disease. </p><p><strong>Featured Articles</strong></p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022564">Reassessing the Chronic Lymphocytic Leukemia International Prognostic Index in the era of targeted therapies </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023269">Peak ADAMTS13 activity to assess ADAMTS13 conformation and risk of relapse in immune-mediated Thrombotic Thrombocytopenic Purpura </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023301">An international learning collaborative phase 2 trial for haploidentical bone marrow transplant in sickle cell disease </a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we’ll discuss the prognostic value of the Chronic Lymphocytic Leukemia International Prognostic Index in the era of targeted therapies, learn how peak ADAMTS13 activity can be used to assess ADAMTS13 conformation and risk of relapse in immune-mediated thrombotic thrombocytopenic purpura, and discuss the findings from a phase 2 trial of haploidentical bone marrow transplant in sickle cell disease. </p><p><strong>Featured Articles</strong></p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022564">Reassessing the Chronic Lymphocytic Leukemia International Prognostic Index in the era of targeted therapies </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023269">Peak ADAMTS13 activity to assess ADAMTS13 conformation and risk of relapse in immune-mediated Thrombotic Thrombocytopenic Purpura </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023301">An international learning collaborative phase 2 trial for haploidentical bone marrow transplant in sickle cell disease </a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 20 Jun 2024 12:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/b4fb830c/a5f6195d.mp3" length="34090594" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1419</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we’ll discuss the prognostic value of the Chronic Lymphocytic Leukemia International Prognostic Index in the era of targeted therapies, learn how peak ADAMTS13 activity can be used to assess ADAMTS13 conformation and risk of relapse in immune-mediated thrombotic thrombocytopenic purpura, and discuss the findings from a phase 2 trial of haploidentical bone marrow transplant in sickle cell disease. </p><p><strong>Featured Articles</strong></p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022564">Reassessing the Chronic Lymphocytic Leukemia International Prognostic Index in the era of targeted therapies </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023269">Peak ADAMTS13 activity to assess ADAMTS13 conformation and risk of relapse in immune-mediated Thrombotic Thrombocytopenic Purpura </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023301">An international learning collaborative phase 2 trial for haploidentical bone marrow transplant in sickle cell disease </a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>A biomarker for disease severity in Wiskott-Aldrich Syndrome; loss of Dnmt3a confers resistance to IFNα; unrelated donor selection in HSCT with PTCy</title>
      <itunes:season>7</itunes:season>
      <podcast:season>7</podcast:season>
      <itunes:title>A biomarker for disease severity in Wiskott-Aldrich Syndrome; loss of Dnmt3a confers resistance to IFNα; unrelated donor selection in HSCT with PTCy</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">caabefc1-60e2-44f4-9951-e606b85d23dd</guid>
      <link>https://share.transistor.fm/s/26807e89</link>
      <description>
        <![CDATA[<p>In this week's episode we'll discuss assessing risk profile in Wiskott-Aldrich Syndrome, or WAS. Then, we'll learn about how the loss of DNMT3A confers resistance to interferon-alpha in hematopoietic stem cells carrying the JAK2-V617F mutation. Finally, we'll explore unrelated donor selection for AML patients undergoing hematopoietic stem cell transplantation with post-transplant cyclophosphamide.</p><p>Featured Articles: </p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023021411">Wiskott-Aldrich Syndrome: A retrospective study on 577 patients defines the genotype as a predictive biomarker for disease severity and survival</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023020270">Loss of <em>Dnmt3a</em> increased self-renewal and resistance to pegylated interferon-alpha in </a><a href="http://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023020270"><em>JAK2-</em>V617F</a><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023020270">-positive myeloproliferative neoplasms </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023697">Younger unrelated donors may be preferable over HLA match in the PTCy era: A study from the Acute Leukemia Working Party of the European Society for Blood and Marrow Transplantation</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we'll discuss assessing risk profile in Wiskott-Aldrich Syndrome, or WAS. Then, we'll learn about how the loss of DNMT3A confers resistance to interferon-alpha in hematopoietic stem cells carrying the JAK2-V617F mutation. Finally, we'll explore unrelated donor selection for AML patients undergoing hematopoietic stem cell transplantation with post-transplant cyclophosphamide.</p><p>Featured Articles: </p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023021411">Wiskott-Aldrich Syndrome: A retrospective study on 577 patients defines the genotype as a predictive biomarker for disease severity and survival</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023020270">Loss of <em>Dnmt3a</em> increased self-renewal and resistance to pegylated interferon-alpha in </a><a href="http://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023020270"><em>JAK2-</em>V617F</a><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023020270">-positive myeloproliferative neoplasms </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023697">Younger unrelated donors may be preferable over HLA match in the PTCy era: A study from the Acute Leukemia Working Party of the European Society for Blood and Marrow Transplantation</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 13 Jun 2024 12:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/26807e89/01adc04c.mp3" length="27775708" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1156</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we'll discuss assessing risk profile in Wiskott-Aldrich Syndrome, or WAS. Then, we'll learn about how the loss of DNMT3A confers resistance to interferon-alpha in hematopoietic stem cells carrying the JAK2-V617F mutation. Finally, we'll explore unrelated donor selection for AML patients undergoing hematopoietic stem cell transplantation with post-transplant cyclophosphamide.</p><p>Featured Articles: </p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023021411">Wiskott-Aldrich Syndrome: A retrospective study on 577 patients defines the genotype as a predictive biomarker for disease severity and survival</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023020270">Loss of <em>Dnmt3a</em> increased self-renewal and resistance to pegylated interferon-alpha in </a><a href="http://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023020270"><em>JAK2-</em>V617F</a><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023020270">-positive myeloproliferative neoplasms </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023697">Younger unrelated donors may be preferable over HLA match in the PTCy era: A study from the Acute Leukemia Working Party of the European Society for Blood and Marrow Transplantation</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Nilotinib with or without cytarabine for Philadelphia-positive AML; thrombosis risk in Factor V Leiden and Prothrombin G20210A; ctDNA improves prognostic prediction in relapsed/refractory multiple myeloma</title>
      <itunes:season>7</itunes:season>
      <podcast:season>7</podcast:season>
      <itunes:title>Nilotinib with or without cytarabine for Philadelphia-positive AML; thrombosis risk in Factor V Leiden and Prothrombin G20210A; ctDNA improves prognostic prediction in relapsed/refractory multiple myeloma</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">c2337de4-dc9c-473d-a011-71ddafbc9767</guid>
      <link>https://share.transistor.fm/s/d02f9175</link>
      <description>
        <![CDATA[<p>In this week's episode we’ll discuss the safety and efficacy of nilotinib with or without cytarabine in Philadelphia-positive acute lymphoblastic leukemia; learn more about thrombosis risk in double heterozygous carriers of Factor V Leiden and prothrombin G20210A and discuss the utility of circulating cell-free tumor DNA in prognostic prediction in patients with relapsed/refractory multiple myeloma.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article/doi/10.1182/blood.2023023502/515222/Nilotinib-with-or-without-cytarabine-for">Nilotinib with or without cytarabine for Philadelphia positive acute lymphoblastic leukemia</a> </li><li><a href="https://ashpublications.org/blood/article/doi/10.1182/blood.2023023326/515331/Thrombosis-Risk-in-Double-Heterozygous-Carriers-of">Thrombosis risk in double heterozygous carriers of Factor V Leiden and Prothrombin G20210A in FinnGen and the UK Biobank </a></li><li><a href="https://ashpublications.org/blood/article/doi/10.1182/blood.2023022540/515164/ctDNA-improves-prognostic-prediction-in-relapsed">ctDNA improves prognostic prediction in relapsed/refractory multiple myeloma receiving ixazomib, lenalidomide, and dexamethasone </a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we’ll discuss the safety and efficacy of nilotinib with or without cytarabine in Philadelphia-positive acute lymphoblastic leukemia; learn more about thrombosis risk in double heterozygous carriers of Factor V Leiden and prothrombin G20210A and discuss the utility of circulating cell-free tumor DNA in prognostic prediction in patients with relapsed/refractory multiple myeloma.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article/doi/10.1182/blood.2023023502/515222/Nilotinib-with-or-without-cytarabine-for">Nilotinib with or without cytarabine for Philadelphia positive acute lymphoblastic leukemia</a> </li><li><a href="https://ashpublications.org/blood/article/doi/10.1182/blood.2023023326/515331/Thrombosis-Risk-in-Double-Heterozygous-Carriers-of">Thrombosis risk in double heterozygous carriers of Factor V Leiden and Prothrombin G20210A in FinnGen and the UK Biobank </a></li><li><a href="https://ashpublications.org/blood/article/doi/10.1182/blood.2023022540/515164/ctDNA-improves-prognostic-prediction-in-relapsed">ctDNA improves prognostic prediction in relapsed/refractory multiple myeloma receiving ixazomib, lenalidomide, and dexamethasone </a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 06 Jun 2024 12:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/d02f9175/7e32b23c.mp3" length="33278430" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1385</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we’ll discuss the safety and efficacy of nilotinib with or without cytarabine in Philadelphia-positive acute lymphoblastic leukemia; learn more about thrombosis risk in double heterozygous carriers of Factor V Leiden and prothrombin G20210A and discuss the utility of circulating cell-free tumor DNA in prognostic prediction in patients with relapsed/refractory multiple myeloma.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article/doi/10.1182/blood.2023023502/515222/Nilotinib-with-or-without-cytarabine-for">Nilotinib with or without cytarabine for Philadelphia positive acute lymphoblastic leukemia</a> </li><li><a href="https://ashpublications.org/blood/article/doi/10.1182/blood.2023023326/515331/Thrombosis-Risk-in-Double-Heterozygous-Carriers-of">Thrombosis risk in double heterozygous carriers of Factor V Leiden and Prothrombin G20210A in FinnGen and the UK Biobank </a></li><li><a href="https://ashpublications.org/blood/article/doi/10.1182/blood.2023022540/515164/ctDNA-improves-prognostic-prediction-in-relapsed">ctDNA improves prognostic prediction in relapsed/refractory multiple myeloma receiving ixazomib, lenalidomide, and dexamethasone </a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Hemophilia prophylaxis with fitusiran vs BPA/CFC; germline NBN variants in pediatric B-ALL; Histone demethylation and cell-intrinsic immune response in AML </title>
      <itunes:season>7</itunes:season>
      <podcast:season>7</podcast:season>
      <itunes:title>Hemophilia prophylaxis with fitusiran vs BPA/CFC; germline NBN variants in pediatric B-ALL; Histone demethylation and cell-intrinsic immune response in AML </itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">3ca1554c-97d3-44f2-884c-8b067e3ca6d4</guid>
      <link>https://share.transistor.fm/s/3cc26fae</link>
      <description>
        <![CDATA[<p>In this week's episode we'll learn about fitusiran prophylaxis in patients with hemophilia A or B, with or without inhibitors. Next we'll hear about new findings that heterozygous germline variants in the NBN gene that are linked to increased risk of B-cell acute lymphoblastic leukemia in children. Finally, we'll explore new insights on the histone demethylase PHF8, which has been identified as a master regulator of cell-intrinsic immune responses in acute myeloid leukemia. </p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023021864">Fitusiran prophylaxis in people with hemophilia A or B who switched from prior BPA/CFC prophylaxis: the ATLAS-PPX trial</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023336">Germline genetic <em>NBN </em>variation and predisposition to B-cell acute lymphoblastic leukemia in children </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023021640">Epigenetic control over the cell-intrinsic immune response antagonizes self-renewal in acute myeloid leukemia</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we'll learn about fitusiran prophylaxis in patients with hemophilia A or B, with or without inhibitors. Next we'll hear about new findings that heterozygous germline variants in the NBN gene that are linked to increased risk of B-cell acute lymphoblastic leukemia in children. Finally, we'll explore new insights on the histone demethylase PHF8, which has been identified as a master regulator of cell-intrinsic immune responses in acute myeloid leukemia. </p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023021864">Fitusiran prophylaxis in people with hemophilia A or B who switched from prior BPA/CFC prophylaxis: the ATLAS-PPX trial</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023336">Germline genetic <em>NBN </em>variation and predisposition to B-cell acute lymphoblastic leukemia in children </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023021640">Epigenetic control over the cell-intrinsic immune response antagonizes self-renewal in acute myeloid leukemia</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 30 May 2024 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/3cc26fae/951d7521.mp3" length="18227844" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1139</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we'll learn about fitusiran prophylaxis in patients with hemophilia A or B, with or without inhibitors. Next we'll hear about new findings that heterozygous germline variants in the NBN gene that are linked to increased risk of B-cell acute lymphoblastic leukemia in children. Finally, we'll explore new insights on the histone demethylase PHF8, which has been identified as a master regulator of cell-intrinsic immune responses in acute myeloid leukemia. </p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023021864">Fitusiran prophylaxis in people with hemophilia A or B who switched from prior BPA/CFC prophylaxis: the ATLAS-PPX trial</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023336">Germline genetic <em>NBN </em>variation and predisposition to B-cell acute lymphoblastic leukemia in children </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023021640">Epigenetic control over the cell-intrinsic immune response antagonizes self-renewal in acute myeloid leukemia</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Effects of voxelotor on cerebral blood flow in pediatric sickle cell disease; thrombosis in Vexas syndrome; response to tyrosine kinase inhibitors in ABL-class acute lymphoblastic leukemia</title>
      <itunes:season>7</itunes:season>
      <podcast:season>7</podcast:season>
      <itunes:title>Effects of voxelotor on cerebral blood flow in pediatric sickle cell disease; thrombosis in Vexas syndrome; response to tyrosine kinase inhibitors in ABL-class acute lymphoblastic leukemia</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">7ddede20-2f53-484b-b43d-dd78ee70f345</guid>
      <link>https://share.transistor.fm/s/93d64657</link>
      <description>
        <![CDATA[<p>In this week's episode we’ll discuss the effects of voxelotor on cerebral blood flow in pediatric sickle cell disease, learn more about venous and arterial thrombosis in patients with Vexas syndrome, and discuss differential sensitivity to tyrosine kinase inhibitors in ABL-class acute lymphoblastic leukemia. </p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022011">The influence of voxelotor on cerebral blood flow and oxygen extraction in pediatric sickle cell disease </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022329">Venous and arterial thrombosis in patients with VEXAS syndrome </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023120">Tyrosine kinase inhibitor response of ABL-class acute lymphoblastic leukemia: The role of kinase type and SH3 domain </a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we’ll discuss the effects of voxelotor on cerebral blood flow in pediatric sickle cell disease, learn more about venous and arterial thrombosis in patients with Vexas syndrome, and discuss differential sensitivity to tyrosine kinase inhibitors in ABL-class acute lymphoblastic leukemia. </p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022011">The influence of voxelotor on cerebral blood flow and oxygen extraction in pediatric sickle cell disease </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022329">Venous and arterial thrombosis in patients with VEXAS syndrome </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023120">Tyrosine kinase inhibitor response of ABL-class acute lymphoblastic leukemia: The role of kinase type and SH3 domain </a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 23 May 2024 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/93d64657/2522d7bb.mp3" length="32322219" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1346</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we’ll discuss the effects of voxelotor on cerebral blood flow in pediatric sickle cell disease, learn more about venous and arterial thrombosis in patients with Vexas syndrome, and discuss differential sensitivity to tyrosine kinase inhibitors in ABL-class acute lymphoblastic leukemia. </p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022011">The influence of voxelotor on cerebral blood flow and oxygen extraction in pediatric sickle cell disease </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022329">Venous and arterial thrombosis in patients with VEXAS syndrome </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023120">Tyrosine kinase inhibitor response of ABL-class acute lymphoblastic leukemia: The role of kinase type and SH3 domain </a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Stamping out high-risk myeloma with D-KRd and tandem transplant; plasmin-cleaved VWF in microthrombosis; SCD plasma sensitizes iPSC-derived sensory neurons </title>
      <itunes:season>7</itunes:season>
      <podcast:season>7</podcast:season>
      <itunes:title>Stamping out high-risk myeloma with D-KRd and tandem transplant; plasmin-cleaved VWF in microthrombosis; SCD plasma sensitizes iPSC-derived sensory neurons </itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">1e1b3d42-1292-480a-b09d-681acfdf7a4a</guid>
      <link>https://share.transistor.fm/s/2c8f0b7a</link>
      <description>
        <![CDATA[<p>In this week's podcast we'll discuss another step forward in stamping out high-risk myeloma. Then we'll hear about the plasmin-cleaved von Willebrand factor, or VWF, in microthrombosis. Finally we'll hear about new insights into the origins of sickle cell pain. </p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023597">Daratumumab, carfilzomib, lenalidomide, and dexamethasone with tandem transplant for high-risk newly<br>diagnosed myeloma</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023021265">Plasmin-cleaved von Willebrand factor as a biomarker for microvascular thrombosis</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022591">Sickle cell disease iPSC-derived sensory neurons exhibit increased excitability and sensitization to patient<br>plasma</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's podcast we'll discuss another step forward in stamping out high-risk myeloma. Then we'll hear about the plasmin-cleaved von Willebrand factor, or VWF, in microthrombosis. Finally we'll hear about new insights into the origins of sickle cell pain. </p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023597">Daratumumab, carfilzomib, lenalidomide, and dexamethasone with tandem transplant for high-risk newly<br>diagnosed myeloma</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023021265">Plasmin-cleaved von Willebrand factor as a biomarker for microvascular thrombosis</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022591">Sickle cell disease iPSC-derived sensory neurons exhibit increased excitability and sensitization to patient<br>plasma</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 16 May 2024 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/2c8f0b7a/b5b21e0e.mp3" length="28349159" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1180</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's podcast we'll discuss another step forward in stamping out high-risk myeloma. Then we'll hear about the plasmin-cleaved von Willebrand factor, or VWF, in microthrombosis. Finally we'll hear about new insights into the origins of sickle cell pain. </p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023597">Daratumumab, carfilzomib, lenalidomide, and dexamethasone with tandem transplant for high-risk newly<br>diagnosed myeloma</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023021265">Plasmin-cleaved von Willebrand factor as a biomarker for microvascular thrombosis</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022591">Sickle cell disease iPSC-derived sensory neurons exhibit increased excitability and sensitization to patient<br>plasma</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Allogeneic transplant in first remission for post-induction molecular MRD; circulating HSPCs actively participate in human hematopoiesis; let-7 miRNAs repress HIC2 to regulate BCL11A transcription and hemoglobin switching</title>
      <itunes:season>7</itunes:season>
      <podcast:season>7</podcast:season>
      <itunes:title>Allogeneic transplant in first remission for post-induction molecular MRD; circulating HSPCs actively participate in human hematopoiesis; let-7 miRNAs repress HIC2 to regulate BCL11A transcription and hemoglobin switching</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">f7b4f9df-baac-4204-a80a-023a509ed01e</guid>
      <link>https://share.transistor.fm/s/c5ec0164</link>
      <description>
        <![CDATA[<p>In this week's episode we’ll discuss the utility of MRD in identifying patients with <em>NPM1</em> AML who benefit from allogeneic transplant in first remission, learn more about the contribution of circulating hematopoietic stem/progenitor cell subsets to human hematopoietic hemostasis, and discuss the role of Let-7 miRNAs in regulation of BCL11A transcription and hemoglobin switching. </p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023096">Postinduction molecular MRD identifies patients with <em>NPM1 </em>AML who benefit from allogeneic transplant in first remission</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023399"><em>let-7 </em>miRNAs repress HIC2 to regulate BCL11A transcription and hemoglobin switching </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022666">Circulating Hematopoietic Stem/Progenitor Cell subsets contribute to human hematopoietic homeostasis</a></li></ul><p><br></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we’ll discuss the utility of MRD in identifying patients with <em>NPM1</em> AML who benefit from allogeneic transplant in first remission, learn more about the contribution of circulating hematopoietic stem/progenitor cell subsets to human hematopoietic hemostasis, and discuss the role of Let-7 miRNAs in regulation of BCL11A transcription and hemoglobin switching. </p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023096">Postinduction molecular MRD identifies patients with <em>NPM1 </em>AML who benefit from allogeneic transplant in first remission</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023399"><em>let-7 </em>miRNAs repress HIC2 to regulate BCL11A transcription and hemoglobin switching </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022666">Circulating Hematopoietic Stem/Progenitor Cell subsets contribute to human hematopoietic homeostasis</a></li></ul><p><br></p>]]>
      </content:encoded>
      <pubDate>Thu, 09 May 2024 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/c5ec0164/82fb2286.mp3" length="52159003" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1304</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we’ll discuss the utility of MRD in identifying patients with <em>NPM1</em> AML who benefit from allogeneic transplant in first remission, learn more about the contribution of circulating hematopoietic stem/progenitor cell subsets to human hematopoietic hemostasis, and discuss the role of Let-7 miRNAs in regulation of BCL11A transcription and hemoglobin switching. </p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023096">Postinduction molecular MRD identifies patients with <em>NPM1 </em>AML who benefit from allogeneic transplant in first remission</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023399"><em>let-7 </em>miRNAs repress HIC2 to regulate BCL11A transcription and hemoglobin switching </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022666">Circulating Hematopoietic Stem/Progenitor Cell subsets contribute to human hematopoietic homeostasis</a></li></ul><p><br></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>ADAMTS13 recovery in caplacizumab-treated TTP; inhibition of venetoclax-resistant BCL2 variants with sonrotoclax; genomic insights from Castleman disease in twins </title>
      <itunes:season>7</itunes:season>
      <podcast:season>7</podcast:season>
      <itunes:title>ADAMTS13 recovery in caplacizumab-treated TTP; inhibition of venetoclax-resistant BCL2 variants with sonrotoclax; genomic insights from Castleman disease in twins </itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">26b3a24f-5749-439e-a926-f1a84fb20add</guid>
      <link>https://share.transistor.fm/s/36aa1455</link>
      <description>
        <![CDATA[<p>In this week's epside we'll learn about ADAMTS recovery after caplacizumab therapy in patients with immune thrombotic thrombocytopenic purpura. Then, we'll hear about preclinical characterization of sonrotoclax, a potential second-generation BCL2 inhibitor. Finally we'll hear about new insights into the etiology of Castleman disease where researchers describe the unusual occurrence of idiopathic multicentric Castleman disease in identical twins. </p><p>Featured Articles: </p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022725">ADAMTS13 recovery in acute thrombotic thrombocytopenic purpura after caplacizumab therapy</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023019706">Sonrotoclax overcomes BCL2 G101V mutation–induced venetoclax resistance in preclinical models of<br>hematologic malignancy</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023021992">Single-cell landscape of idiopathic multicentric Castleman disease in identical twins</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's epside we'll learn about ADAMTS recovery after caplacizumab therapy in patients with immune thrombotic thrombocytopenic purpura. Then, we'll hear about preclinical characterization of sonrotoclax, a potential second-generation BCL2 inhibitor. Finally we'll hear about new insights into the etiology of Castleman disease where researchers describe the unusual occurrence of idiopathic multicentric Castleman disease in identical twins. </p><p>Featured Articles: </p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022725">ADAMTS13 recovery in acute thrombotic thrombocytopenic purpura after caplacizumab therapy</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023019706">Sonrotoclax overcomes BCL2 G101V mutation–induced venetoclax resistance in preclinical models of<br>hematologic malignancy</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023021992">Single-cell landscape of idiopathic multicentric Castleman disease in identical twins</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 02 May 2024 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/36aa1455/c925a565.mp3" length="27621154" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1150</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's epside we'll learn about ADAMTS recovery after caplacizumab therapy in patients with immune thrombotic thrombocytopenic purpura. Then, we'll hear about preclinical characterization of sonrotoclax, a potential second-generation BCL2 inhibitor. Finally we'll hear about new insights into the etiology of Castleman disease where researchers describe the unusual occurrence of idiopathic multicentric Castleman disease in identical twins. </p><p>Featured Articles: </p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022725">ADAMTS13 recovery in acute thrombotic thrombocytopenic purpura after caplacizumab therapy</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023019706">Sonrotoclax overcomes BCL2 G101V mutation–induced venetoclax resistance in preclinical models of<br>hematologic malignancy</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023021992">Single-cell landscape of idiopathic multicentric Castleman disease in identical twins</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Durable response after tisa-cel in adults with relapsed/refractory follicular lymphoma; high microRNA-145 plasma levels indicate decreased risk of VTE; epigenetic/immunogenetic signature in the prediction of outcomes for high-count monoclonal B lymphocytosis</title>
      <itunes:season>7</itunes:season>
      <podcast:season>7</podcast:season>
      <itunes:title>Durable response after tisa-cel in adults with relapsed/refractory follicular lymphoma; high microRNA-145 plasma levels indicate decreased risk of VTE; epigenetic/immunogenetic signature in the prediction of outcomes for high-count monoclonal B lymphocytosis</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">cae61e4a-5546-4dc7-bb7e-aa967bb9c56b</guid>
      <link>https://share.transistor.fm/s/96198224</link>
      <description>
        <![CDATA[<p>In this week's episode, we’ll discuss the findings from a study assessing responses after treatment with tisagenlecleucel <a href="#_msocom_1">[LM1]</a> in adults with relapsed/refractory follicular lymphoma, learn more about the association between high microRNA-145 plasma levels and decreased risk of future incident venous thromboembolism, and discuss how epigenetic and immunogenetic signatures can be used in the prediction of outcomes for high-count monoclonal B lymphocytosis.</p><p><br>Featured Articles: </p><ul><li><a href="http://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023021567">Durable Response After Tisagenlecleucel in Adults With Relapsed/Refractory Follicular Lymphoma: ELARA Trial Update </a></li><li><a href="http://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022180">Prediction of outcomes for high-count monoclonal B lymphocytosis using an epigenetic and immunogenetic signature </a></li><li><a href="http://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022285">High microRNA-145 plasma levels are associated with decreased risk of future incident venous thromboembolism: The HUNT study </a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, we’ll discuss the findings from a study assessing responses after treatment with tisagenlecleucel <a href="#_msocom_1">[LM1]</a> in adults with relapsed/refractory follicular lymphoma, learn more about the association between high microRNA-145 plasma levels and decreased risk of future incident venous thromboembolism, and discuss how epigenetic and immunogenetic signatures can be used in the prediction of outcomes for high-count monoclonal B lymphocytosis.</p><p><br>Featured Articles: </p><ul><li><a href="http://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023021567">Durable Response After Tisagenlecleucel in Adults With Relapsed/Refractory Follicular Lymphoma: ELARA Trial Update </a></li><li><a href="http://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022180">Prediction of outcomes for high-count monoclonal B lymphocytosis using an epigenetic and immunogenetic signature </a></li><li><a href="http://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022285">High microRNA-145 plasma levels are associated with decreased risk of future incident venous thromboembolism: The HUNT study </a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 25 Apr 2024 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/96198224/85baca93.mp3" length="34323162" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1429</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, we’ll discuss the findings from a study assessing responses after treatment with tisagenlecleucel <a href="#_msocom_1">[LM1]</a> in adults with relapsed/refractory follicular lymphoma, learn more about the association between high microRNA-145 plasma levels and decreased risk of future incident venous thromboembolism, and discuss how epigenetic and immunogenetic signatures can be used in the prediction of outcomes for high-count monoclonal B lymphocytosis.</p><p><br>Featured Articles: </p><ul><li><a href="http://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023021567">Durable Response After Tisagenlecleucel in Adults With Relapsed/Refractory Follicular Lymphoma: ELARA Trial Update </a></li><li><a href="http://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022180">Prediction of outcomes for high-count monoclonal B lymphocytosis using an epigenetic and immunogenetic signature </a></li><li><a href="http://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022285">High microRNA-145 plasma levels are associated with decreased risk of future incident venous thromboembolism: The HUNT study </a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Gut microbiota exploitation by CPX-351 in AML; optimizing anti-myeloma immunity for ASCT; which pediatric ITP patients will develop lupus? </title>
      <itunes:season>7</itunes:season>
      <podcast:season>7</podcast:season>
      <itunes:title>Gut microbiota exploitation by CPX-351 in AML; optimizing anti-myeloma immunity for ASCT; which pediatric ITP patients will develop lupus? </itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">c451aa70-065e-4f28-bd7d-be3ff296a217</guid>
      <link>https://share.transistor.fm/s/687f9c2e</link>
      <description>
        <![CDATA[<p>In this week's episode, we'll discuss gut microbiota exploitation by CPX-351 in acute myeloid leukemia. Then we'll learn about optimizing anti-myeloma immunity. New research shows that regulatory T cells suppress myeloma-specific immunity during autologous stem cell mobilization and transplantation. Finally we'll discuss among pediatric patients with ITP or other autoimmune cytopenias, which ones will go on to develop systemic lupus? </p><p>Featured Articles: </p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023021380">CPX-351 exploits the gut microbiota to promote mucosal barrier function, colonization resistance, and immune homeostasis</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022000">Regulatory T cells suppress myeloma-specific immunity during autologous stem cell mobilization and transplantation</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023021884">Antinuclear antibody–associated autoimmune cytopenia in childhood is a risk factor for systemic lupus erythematosus</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, we'll discuss gut microbiota exploitation by CPX-351 in acute myeloid leukemia. Then we'll learn about optimizing anti-myeloma immunity. New research shows that regulatory T cells suppress myeloma-specific immunity during autologous stem cell mobilization and transplantation. Finally we'll discuss among pediatric patients with ITP or other autoimmune cytopenias, which ones will go on to develop systemic lupus? </p><p>Featured Articles: </p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023021380">CPX-351 exploits the gut microbiota to promote mucosal barrier function, colonization resistance, and immune homeostasis</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022000">Regulatory T cells suppress myeloma-specific immunity during autologous stem cell mobilization and transplantation</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023021884">Antinuclear antibody–associated autoimmune cytopenia in childhood is a risk factor for systemic lupus erythematosus</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 18 Apr 2024 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/687f9c2e/d12f3250.mp3" length="27402468" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1140</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, we'll discuss gut microbiota exploitation by CPX-351 in acute myeloid leukemia. Then we'll learn about optimizing anti-myeloma immunity. New research shows that regulatory T cells suppress myeloma-specific immunity during autologous stem cell mobilization and transplantation. Finally we'll discuss among pediatric patients with ITP or other autoimmune cytopenias, which ones will go on to develop systemic lupus? </p><p>Featured Articles: </p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023021380">CPX-351 exploits the gut microbiota to promote mucosal barrier function, colonization resistance, and immune homeostasis</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022000">Regulatory T cells suppress myeloma-specific immunity during autologous stem cell mobilization and transplantation</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023021884">Antinuclear antibody–associated autoimmune cytopenia in childhood is a risk factor for systemic lupus erythematosus</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Jak2V617F clonal hematopoiesis promotes arterial thrombosis; Staphylococcus aureus infection in Sézary syndrome; clinical features of RAC2-related immunodeficiency</title>
      <itunes:season>7</itunes:season>
      <podcast:season>7</podcast:season>
      <itunes:title>Jak2V617F clonal hematopoiesis promotes arterial thrombosis; Staphylococcus aureus infection in Sézary syndrome; clinical features of RAC2-related immunodeficiency</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">2e2dc16c-5c48-4671-972f-d5980655db78</guid>
      <link>https://share.transistor.fm/s/7c026cfb</link>
      <description>
        <![CDATA[<p>In this week's episode we’ll discuss the mechanism by which Jak2V617F clonal hematopoiesis promotes arterial thrombosis, discuss how <em>Staphylococcus aureus</em> induces drug resistance in cancer T cells in Sézary syndrome, and learn more about the clinical and functional features of RAC2-related immunodeficiency.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article/143/15/1539/506721/Jak2V617F-clonal-hematopoiesis-promotes-arterial">Jak2V617F clonal hematopoiesis promotes arterial thrombosis via platelet activation and cross talk</a></li><li><a href="https://ashpublications.org/blood/article/doi/10.1182/blood.2023021671/506921/Staphylococcus-aureus-induce-drug-resistance-in"><em>Staphylococcus aureus</em> induces drug resistance in cancer T cells in Sézary syndrome</a></li><li><a href="https://ashpublications.org/blood/article/143/15/1476/507097/Clinical-and-functional-spectrum-of-RAC2-related">Clinical and functional spectrum of RAC2-related immunodeficiency<br></a><p><br></p></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we’ll discuss the mechanism by which Jak2V617F clonal hematopoiesis promotes arterial thrombosis, discuss how <em>Staphylococcus aureus</em> induces drug resistance in cancer T cells in Sézary syndrome, and learn more about the clinical and functional features of RAC2-related immunodeficiency.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article/143/15/1539/506721/Jak2V617F-clonal-hematopoiesis-promotes-arterial">Jak2V617F clonal hematopoiesis promotes arterial thrombosis via platelet activation and cross talk</a></li><li><a href="https://ashpublications.org/blood/article/doi/10.1182/blood.2023021671/506921/Staphylococcus-aureus-induce-drug-resistance-in"><em>Staphylococcus aureus</em> induces drug resistance in cancer T cells in Sézary syndrome</a></li><li><a href="https://ashpublications.org/blood/article/143/15/1476/507097/Clinical-and-functional-spectrum-of-RAC2-related">Clinical and functional spectrum of RAC2-related immunodeficiency<br></a><p><br></p></li></ul>]]>
      </content:encoded>
      <pubDate>Sat, 13 Apr 2024 00:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/7c026cfb/814fcef5.mp3" length="37895705" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1578</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we’ll discuss the mechanism by which Jak2V617F clonal hematopoiesis promotes arterial thrombosis, discuss how <em>Staphylococcus aureus</em> induces drug resistance in cancer T cells in Sézary syndrome, and learn more about the clinical and functional features of RAC2-related immunodeficiency.</p><p>Featured Articles:</p><ul><li><a href="https://ashpublications.org/blood/article/143/15/1539/506721/Jak2V617F-clonal-hematopoiesis-promotes-arterial">Jak2V617F clonal hematopoiesis promotes arterial thrombosis via platelet activation and cross talk</a></li><li><a href="https://ashpublications.org/blood/article/doi/10.1182/blood.2023021671/506921/Staphylococcus-aureus-induce-drug-resistance-in"><em>Staphylococcus aureus</em> induces drug resistance in cancer T cells in Sézary syndrome</a></li><li><a href="https://ashpublications.org/blood/article/143/15/1476/507097/Clinical-and-functional-spectrum-of-RAC2-related">Clinical and functional spectrum of RAC2-related immunodeficiency<br></a><p><br></p></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Molecular mimicry in aplastic anemia; emicizumab prophylaxis in infants with hemophilia; hydroxyurea reduces infections in SCA</title>
      <itunes:season>7</itunes:season>
      <podcast:season>7</podcast:season>
      <itunes:title>Molecular mimicry in aplastic anemia; emicizumab prophylaxis in infants with hemophilia; hydroxyurea reduces infections in SCA</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">bc3738c7-3b1e-4fc0-b570-d32a9795adf1</guid>
      <link>https://share.transistor.fm/s/d0fab387</link>
      <description>
        <![CDATA[<p>In this week's episode we'll discuss molecular mimicry in aplastic anemia, novel experiments show that antigens associated with viral infections can mimic epitopes presented on hematopoietic progenitor cells. Then, we'll learn about prophylaxis with subcutaneous emicizumab in infants with hemophilia. Finally we'll see how hydroxyurea is associated with a significant reduction in infections among children with sickle cell anemia in Uganda.</p><p>Articles featured this week:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023142">Virus-reactive T cells expanded in aplastic anemia eliminate hematopoietic progenitor cells by molecular<br>mimicry</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023021832">Emicizumab prophylaxis in infants with hemophilia A (HAVEN 7): primary analysis of a phase 3b open-label<br>trial</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023021575">Hydroxyurea reduces infections in children with sickle cell anemia in Uganda</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we'll discuss molecular mimicry in aplastic anemia, novel experiments show that antigens associated with viral infections can mimic epitopes presented on hematopoietic progenitor cells. Then, we'll learn about prophylaxis with subcutaneous emicizumab in infants with hemophilia. Finally we'll see how hydroxyurea is associated with a significant reduction in infections among children with sickle cell anemia in Uganda.</p><p>Articles featured this week:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023142">Virus-reactive T cells expanded in aplastic anemia eliminate hematopoietic progenitor cells by molecular<br>mimicry</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023021832">Emicizumab prophylaxis in infants with hemophilia A (HAVEN 7): primary analysis of a phase 3b open-label<br>trial</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023021575">Hydroxyurea reduces infections in children with sickle cell anemia in Uganda</a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 04 Apr 2024 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/d0fab387/12fbe233.mp3" length="28720424" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1194</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we'll discuss molecular mimicry in aplastic anemia, novel experiments show that antigens associated with viral infections can mimic epitopes presented on hematopoietic progenitor cells. Then, we'll learn about prophylaxis with subcutaneous emicizumab in infants with hemophilia. Finally we'll see how hydroxyurea is associated with a significant reduction in infections among children with sickle cell anemia in Uganda.</p><p>Articles featured this week:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023023142">Virus-reactive T cells expanded in aplastic anemia eliminate hematopoietic progenitor cells by molecular<br>mimicry</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023021832">Emicizumab prophylaxis in infants with hemophilia A (HAVEN 7): primary analysis of a phase 3b open-label<br>trial</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023021575">Hydroxyurea reduces infections in children with sickle cell anemia in Uganda</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Review Series on the Influence of the Tumor Microenvironment on the Pathogenesis of B-Cell Lymphomas</title>
      <itunes:season>7</itunes:season>
      <podcast:season>7</podcast:season>
      <itunes:title>Review Series on the Influence of the Tumor Microenvironment on the Pathogenesis of B-Cell Lymphomas</itunes:title>
      <itunes:episodeType>bonus</itunes:episodeType>
      <guid isPermaLink="false">bc959a56-18f0-42cb-ad56-92d603925166</guid>
      <link>https://share.transistor.fm/s/b83321f9</link>
      <description>
        <![CDATA[<p>In this bonus episode of Blood Podcast, Associate Editor, Dr. Freda Stevenson is joined by Drs. Karin Tarte, Andrea Radtke, and Leandro Cerchietti to discuss the Review Series on the influence of the tumor microenvironment on the pathogenesis of B-cell lymphomas. </p><p>Find the <a href="https://ashpublications.org/blood/article/143/12/1091/498854/">full review series</a> in <em>Blood Journal</em> volume 143 issue 12. </p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this bonus episode of Blood Podcast, Associate Editor, Dr. Freda Stevenson is joined by Drs. Karin Tarte, Andrea Radtke, and Leandro Cerchietti to discuss the Review Series on the influence of the tumor microenvironment on the pathogenesis of B-cell lymphomas. </p><p>Find the <a href="https://ashpublications.org/blood/article/143/12/1091/498854/">full review series</a> in <em>Blood Journal</em> volume 143 issue 12. </p>]]>
      </content:encoded>
      <pubDate>Thu, 28 Mar 2024 14:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/b83321f9/14a3b070.mp3" length="38522012" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/z8WLAgrbahA_U-zpdGAXTkubKxTASnlrYsbV-JFZnok/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS9lYmM4/ZGVhMmZjYjVmY2Nk/ZTQ2OTM3NTRjNmZh/ZTNhNS5qcGc.jpg"/>
      <itunes:duration>1925</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this bonus episode of Blood Podcast, Associate Editor, Dr. Freda Stevenson is joined by Drs. Karin Tarte, Andrea Radtke, and Leandro Cerchietti to discuss the Review Series on the influence of the tumor microenvironment on the pathogenesis of B-cell lymphomas. </p><p>Find the <a href="https://ashpublications.org/blood/article/143/12/1091/498854/">full review series</a> in <em>Blood Journal</em> volume 143 issue 12. </p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Free light chain mass spectrometry in diagnosis and monitoring of AL amyloidosis; T cells of AML patients in remission have distinct RNA signatures; and protective effect of ADAMTS13 in sickle cell mice depends on von Willebrand factor clearance</title>
      <itunes:season>7</itunes:season>
      <podcast:season>7</podcast:season>
      <itunes:title>Free light chain mass spectrometry in diagnosis and monitoring of AL amyloidosis; T cells of AML patients in remission have distinct RNA signatures; and protective effect of ADAMTS13 in sickle cell mice depends on von Willebrand factor clearance</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">78daab00-2e4a-45b0-87d3-67a217e2066f</guid>
      <link>https://share.transistor.fm/s/ec605345</link>
      <description>
        <![CDATA[<p>In this week's episode we’ll discuss the findings from a study assessing the utility of free light chain mass spectrometry in AL amyloidosis, learn more about distinct single-cell RNA-sequencing signatures of bone marrow T cells of AML patients in remission after an allogeneic stem cell transplant, and discuss why von Willebrand factor clearance is critical for the protective effect of ADAMTS13 in mice with sickle cell anemia.</p><p>Articles featured in this episode: </p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023021583">Clearance of VWF by hepatic macrophages is critical for the protective effect of ADAMTS13 in sickle cell anemia mice </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022399">Complete responses in AL amyloidosis are unequal: the impact of free light chain mass spectrometry in AL amyloidosis</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023021815">The remission status of patients with AML post-alloSCT is associated with a distinct single-cell bone marrow T-cell signature </a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we’ll discuss the findings from a study assessing the utility of free light chain mass spectrometry in AL amyloidosis, learn more about distinct single-cell RNA-sequencing signatures of bone marrow T cells of AML patients in remission after an allogeneic stem cell transplant, and discuss why von Willebrand factor clearance is critical for the protective effect of ADAMTS13 in mice with sickle cell anemia.</p><p>Articles featured in this episode: </p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023021583">Clearance of VWF by hepatic macrophages is critical for the protective effect of ADAMTS13 in sickle cell anemia mice </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022399">Complete responses in AL amyloidosis are unequal: the impact of free light chain mass spectrometry in AL amyloidosis</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023021815">The remission status of patients with AML post-alloSCT is associated with a distinct single-cell bone marrow T-cell signature </a></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 28 Mar 2024 13:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/ec605345/87f6378d.mp3" length="32538210" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1354</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we’ll discuss the findings from a study assessing the utility of free light chain mass spectrometry in AL amyloidosis, learn more about distinct single-cell RNA-sequencing signatures of bone marrow T cells of AML patients in remission after an allogeneic stem cell transplant, and discuss why von Willebrand factor clearance is critical for the protective effect of ADAMTS13 in mice with sickle cell anemia.</p><p>Articles featured in this episode: </p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023021583">Clearance of VWF by hepatic macrophages is critical for the protective effect of ADAMTS13 in sickle cell anemia mice </a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022399">Complete responses in AL amyloidosis are unequal: the impact of free light chain mass spectrometry in AL amyloidosis</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023021815">The remission status of patients with AML post-alloSCT is associated with a distinct single-cell bone marrow T-cell signature </a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Eculizumab in transplant-associated thrombotic microangiopathy; reclassifying malignant monocytosis; targeting tissue factor in antiphospholipid syndrome</title>
      <itunes:season>7</itunes:season>
      <podcast:season>7</podcast:season>
      <itunes:title>Eculizumab in transplant-associated thrombotic microangiopathy; reclassifying malignant monocytosis; targeting tissue factor in antiphospholipid syndrome</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">9d8035e8-f72f-49a7-b02c-f859059864db</guid>
      <link>https://share.transistor.fm/s/bdcee2bf</link>
      <description>
        <![CDATA[<p>In this week's episode we'll discuss eculizumab in stem cell transplant-associated thrombotic microangiopathy. Then, we'll learn about reclassifying malignant monocytosis, these newly classified cases have distinct mutational and transcriptional profiles. Finally, we'll hear about targeting the tissue factor coagulation initiation complex prevents antiphospholipid antibody development.</p><p>Articles featured in this episode:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022526"> A prospective multi-institutional study of eculizumab to treat high-risk stem cell transplantation–associated TMA</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023021199"> Comparing malignant monocytosis across the updated WHO and ICC classifications of 2022</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022276"> Treatment outcomes of complement protein C5 inhibition in 509 UK patients with paroxysmal nocturnal hemoglobinuria<br></a><br></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we'll discuss eculizumab in stem cell transplant-associated thrombotic microangiopathy. Then, we'll learn about reclassifying malignant monocytosis, these newly classified cases have distinct mutational and transcriptional profiles. Finally, we'll hear about targeting the tissue factor coagulation initiation complex prevents antiphospholipid antibody development.</p><p>Articles featured in this episode:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022526"> A prospective multi-institutional study of eculizumab to treat high-risk stem cell transplantation–associated TMA</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023021199"> Comparing malignant monocytosis across the updated WHO and ICC classifications of 2022</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022276"> Treatment outcomes of complement protein C5 inhibition in 509 UK patients with paroxysmal nocturnal hemoglobinuria<br></a><br></li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 21 Mar 2024 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/bdcee2bf/4ec541b6.mp3" length="30065305" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1250</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we'll discuss eculizumab in stem cell transplant-associated thrombotic microangiopathy. Then, we'll learn about reclassifying malignant monocytosis, these newly classified cases have distinct mutational and transcriptional profiles. Finally, we'll hear about targeting the tissue factor coagulation initiation complex prevents antiphospholipid antibody development.</p><p>Articles featured in this episode:</p><ul><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022526"> A prospective multi-institutional study of eculizumab to treat high-risk stem cell transplantation–associated TMA</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023021199"> Comparing malignant monocytosis across the updated WHO and ICC classifications of 2022</a></li><li><a href="https://ashpublications.org/blood/article-lookup/DOI/10.1182/blood.2023022276"> Treatment outcomes of complement protein C5 inhibition in 509 UK patients with paroxysmal nocturnal hemoglobinuria<br></a><br></li></ul>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Identification of rare relapse-initiating stem cells post-transplantation; interferon α impairs erythropoiesis in sickle cell disease; TNFα promotes clonal dominance of KIT D816V+ cells in mastocytosis</title>
      <itunes:season>7</itunes:season>
      <podcast:season>7</podcast:season>
      <itunes:title>Identification of rare relapse-initiating stem cells post-transplantation; interferon α impairs erythropoiesis in sickle cell disease; TNFα promotes clonal dominance of KIT D816V+ cells in mastocytosis</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">827f9235-278a-4bd2-b32b-6e1468b7e289</guid>
      <link>https://share.transistor.fm/s/77314f45</link>
      <description>
        <![CDATA[<p>In this week's episode we’ll learn more about rare relapse-initiating stem cells in patients with MDS or AML in complete remission post-transplantation, discuss the role of interferon α in erythropoiesis in sickle cell disease, and learn more about how TNFα promotes clonal dominance of KIT D816V+ cells in mastocytosis.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we’ll learn more about rare relapse-initiating stem cells in patients with MDS or AML in complete remission post-transplantation, discuss the role of interferon α in erythropoiesis in sickle cell disease, and learn more about how TNFα promotes clonal dominance of KIT D816V+ cells in mastocytosis.</p>]]>
      </content:encoded>
      <pubDate>Thu, 14 Mar 2024 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/77314f45/615d9370.mp3" length="32892214" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1368</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we’ll learn more about rare relapse-initiating stem cells in patients with MDS or AML in complete remission post-transplantation, discuss the role of interferon α in erythropoiesis in sickle cell disease, and learn more about how TNFα promotes clonal dominance of KIT D816V+ cells in mastocytosis.</p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>How PAR2 signaling drives thrombo-inflammation; pretransfusion hemoglobin levels linked to survival in beta-thalassemia; etoposide is better than its reputation in primary HLH </title>
      <itunes:season>7</itunes:season>
      <podcast:season>7</podcast:season>
      <itunes:title>How PAR2 signaling drives thrombo-inflammation; pretransfusion hemoglobin levels linked to survival in beta-thalassemia; etoposide is better than its reputation in primary HLH </itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">94e4fd46-d964-494c-ada8-cf7f9adfc38d</guid>
      <link>https://share.transistor.fm/s/0625a5ca</link>
      <description>
        <![CDATA[<p>In this week's episode we'll discuss PAR2-biased signaling in thrombo-inflammation. Then, we'll learn about how hemoglobin levels are linked to survival in transfusion-dependent beta-thalassemia. Finally we'll hear about how etoposide is better than its reputation in primary HLH—hemophagocytic lymphohistiocytosis. Symptomatic patients treated with etoposide have substantially better outcomes as compared to the historical experience.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we'll discuss PAR2-biased signaling in thrombo-inflammation. Then, we'll learn about how hemoglobin levels are linked to survival in transfusion-dependent beta-thalassemia. Finally we'll hear about how etoposide is better than its reputation in primary HLH—hemophagocytic lymphohistiocytosis. Symptomatic patients treated with etoposide have substantially better outcomes as compared to the historical experience.</p>]]>
      </content:encoded>
      <pubDate>Thu, 07 Mar 2024 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/0625a5ca/bd0ba1b4.mp3" length="25691797" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1068</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we'll discuss PAR2-biased signaling in thrombo-inflammation. Then, we'll learn about how hemoglobin levels are linked to survival in transfusion-dependent beta-thalassemia. Finally we'll hear about how etoposide is better than its reputation in primary HLH—hemophagocytic lymphohistiocytosis. Symptomatic patients treated with etoposide have substantially better outcomes as compared to the historical experience.</p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Brentuximab vedotin plus dacarbazine or nivolumab in classical Hodgkin lymphoma; loss of CD20 causes resistance to mosunetuzumab in r/r B-cell lymphomas; trogocytosis as a driver of RBC antigen loss</title>
      <itunes:season>7</itunes:season>
      <podcast:season>7</podcast:season>
      <itunes:title>Brentuximab vedotin plus dacarbazine or nivolumab in classical Hodgkin lymphoma; loss of CD20 causes resistance to mosunetuzumab in r/r B-cell lymphomas; trogocytosis as a driver of RBC antigen loss</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">67577eb1-5ea4-4003-be73-31709f3c9774</guid>
      <link>https://share.transistor.fm/s/7e38be12</link>
      <description>
        <![CDATA[<p>In this week's episode we’ll discuss the findings from a prospective trial of brentuximab vedotin with dacarbazine or nivolumab in older patients with classical Hodgkin lymphoma, learn more about CD20 antigen loss as a mechanism of resistance to mosunetuzumab in relapsed/refractory B-cell lymphomas, and discuss the role of trogocytosis in red blood cell antigen loss.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we’ll discuss the findings from a prospective trial of brentuximab vedotin with dacarbazine or nivolumab in older patients with classical Hodgkin lymphoma, learn more about CD20 antigen loss as a mechanism of resistance to mosunetuzumab in relapsed/refractory B-cell lymphomas, and discuss the role of trogocytosis in red blood cell antigen loss.</p>]]>
      </content:encoded>
      <pubDate>Thu, 29 Feb 2024 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/7e38be12/f5dde191.mp3" length="33219848" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1382</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we’ll discuss the findings from a prospective trial of brentuximab vedotin with dacarbazine or nivolumab in older patients with classical Hodgkin lymphoma, learn more about CD20 antigen loss as a mechanism of resistance to mosunetuzumab in relapsed/refractory B-cell lymphomas, and discuss the role of trogocytosis in red blood cell antigen loss.</p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>CAR T cells plus ibrutinib in relapsed/refractory MCL; targeting SGF29 in AML; diffusion-limited oxygen release from stored blood </title>
      <itunes:season>7</itunes:season>
      <podcast:season>7</podcast:season>
      <itunes:title>CAR T cells plus ibrutinib in relapsed/refractory MCL; targeting SGF29 in AML; diffusion-limited oxygen release from stored blood </itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">d637dbbf-fe98-42f6-a8a2-b3a13e45b2b9</guid>
      <link>https://share.transistor.fm/s/31b5baf3</link>
      <description>
        <![CDATA[<p>In this week's episode we'll discuss CAR T cells plus ibrutinib for the treatment of relapsed/refractory mantle cell lymphoma. Next, we'll learn about a new SAGA for acute myeloid leukemia. Finally, we'll hear about new evidence that oxygen delivery to tissues can become diffusion-limited during perfusion with stored blood.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we'll discuss CAR T cells plus ibrutinib for the treatment of relapsed/refractory mantle cell lymphoma. Next, we'll learn about a new SAGA for acute myeloid leukemia. Finally, we'll hear about new evidence that oxygen delivery to tissues can become diffusion-limited during perfusion with stored blood.</p>]]>
      </content:encoded>
      <pubDate>Thu, 22 Feb 2024 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/31b5baf3/c357015a.mp3" length="27188066" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1130</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we'll discuss CAR T cells plus ibrutinib for the treatment of relapsed/refractory mantle cell lymphoma. Next, we'll learn about a new SAGA for acute myeloid leukemia. Finally, we'll hear about new evidence that oxygen delivery to tissues can become diffusion-limited during perfusion with stored blood.</p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Long-term outcomes of pulmonary embolism in children and adolescents; hereditary angioedema caused by a methionine-379 to lysine substitution in kininogens; predictors of loss of MRD negativity in multiple myeloma</title>
      <itunes:season>7</itunes:season>
      <podcast:season>7</podcast:season>
      <itunes:title>Long-term outcomes of pulmonary embolism in children and adolescents; hereditary angioedema caused by a methionine-379 to lysine substitution in kininogens; predictors of loss of MRD negativity in multiple myeloma</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">40c53116-05a4-4553-833e-19ca971437e2</guid>
      <link>https://share.transistor.fm/s/980c02c7</link>
      <description>
        <![CDATA[<p>In this week's episode we’ll report on the findings from a study evaluating the long-term outcomes of pulmonary embolism in children and adolescents, discuss a new mechanism for hereditary angioedema caused by a methionine-379 to lysine substitution in kininogens, and learn more about predictors of unsustained minimal residual disease negativity in multiple myeloma patients.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we’ll report on the findings from a study evaluating the long-term outcomes of pulmonary embolism in children and adolescents, discuss a new mechanism for hereditary angioedema caused by a methionine-379 to lysine substitution in kininogens, and learn more about predictors of unsustained minimal residual disease negativity in multiple myeloma patients.</p>]]>
      </content:encoded>
      <pubDate>Thu, 15 Feb 2024 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/980c02c7/e423f928.mp3" length="36210612" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1507</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we’ll report on the findings from a study evaluating the long-term outcomes of pulmonary embolism in children and adolescents, discuss a new mechanism for hereditary angioedema caused by a methionine-379 to lysine substitution in kininogens, and learn more about predictors of unsustained minimal residual disease negativity in multiple myeloma patients.</p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Extended follow-up of axi-cel in indolent NHL; platelets help clear senescent RBCs; novel risk stratification strategy for CNS lymphoma</title>
      <itunes:season>7</itunes:season>
      <podcast:season>7</podcast:season>
      <itunes:title>Extended follow-up of axi-cel in indolent NHL; platelets help clear senescent RBCs; novel risk stratification strategy for CNS lymphoma</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">06773305-b5ab-4ea9-8e3e-4d6ac6dc0ecb</guid>
      <link>https://share.transistor.fm/s/014abfe0</link>
      <description>
        <![CDATA[<p>In this week's episode we'll discuss extended follow-up from the ZUMA-5 trial of axicabtagene ciloleucel, or axi-cel. Then we'll learn about the role of platelets in binding and clearing senescent red blood cells. Finally, we'll hear about a new risk stratification strategy for lymphomas of the central nervous system, or CNS. </p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we'll discuss extended follow-up from the ZUMA-5 trial of axicabtagene ciloleucel, or axi-cel. Then we'll learn about the role of platelets in binding and clearing senescent red blood cells. Finally, we'll hear about a new risk stratification strategy for lymphomas of the central nervous system, or CNS. </p>]]>
      </content:encoded>
      <pubDate>Thu, 08 Feb 2024 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/014abfe0/681b1fe1.mp3" length="27361163" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1138</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we'll discuss extended follow-up from the ZUMA-5 trial of axicabtagene ciloleucel, or axi-cel. Then we'll learn about the role of platelets in binding and clearing senescent red blood cells. Finally, we'll hear about a new risk stratification strategy for lymphomas of the central nervous system, or CNS. </p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Lisocabtagene maraleucel in relapsed or refractory large B-cell lymphoma; reciprocal stabilization of coagulation factor XIII-A and -B subunits; inotuzumab ozogamicin for MRD in ALL</title>
      <itunes:season>7</itunes:season>
      <podcast:season>7</podcast:season>
      <itunes:title>Lisocabtagene maraleucel in relapsed or refractory large B-cell lymphoma; reciprocal stabilization of coagulation factor XIII-A and -B subunits; inotuzumab ozogamicin for MRD in ALL</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">98e32632-fdc6-42e7-aa31-123a221a9ab3</guid>
      <link>https://share.transistor.fm/s/1364e5bd</link>
      <description>
        <![CDATA[<p>In this week's episode we’ll discuss the findings from a two-year follow-up study of lisocabtagene maraleucel in relapsed or refractory large B-cell lymphoma, learn more about how reciprocal stabilization of coagulation factor XIII-A and -B subunits influences plasma FXIII concentration, and discuss the findings from a phase 2 study of inotuzumab ozogamicin for measurable residual disease in acute lymphoblastic leukemia in remission.</p><p><br></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we’ll discuss the findings from a two-year follow-up study of lisocabtagene maraleucel in relapsed or refractory large B-cell lymphoma, learn more about how reciprocal stabilization of coagulation factor XIII-A and -B subunits influences plasma FXIII concentration, and discuss the findings from a phase 2 study of inotuzumab ozogamicin for measurable residual disease in acute lymphoblastic leukemia in remission.</p><p><br></p>]]>
      </content:encoded>
      <pubDate>Thu, 01 Feb 2024 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/1364e5bd/48bd2f9a.mp3" length="32347089" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1346</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we’ll discuss the findings from a two-year follow-up study of lisocabtagene maraleucel in relapsed or refractory large B-cell lymphoma, learn more about how reciprocal stabilization of coagulation factor XIII-A and -B subunits influences plasma FXIII concentration, and discuss the findings from a phase 2 study of inotuzumab ozogamicin for measurable residual disease in acute lymphoblastic leukemia in remission.</p><p><br></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Maternal anticancer drug exposure and leukemia; PIEZO1-TMEM16F coupling in hereditary xerocytosis; NPM1 MRD during venetoclax therapy in NPM1-mutated AML</title>
      <itunes:season>7</itunes:season>
      <podcast:season>7</podcast:season>
      <itunes:title>Maternal anticancer drug exposure and leukemia; PIEZO1-TMEM16F coupling in hereditary xerocytosis; NPM1 MRD during venetoclax therapy in NPM1-mutated AML</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">f366a968-0209-464c-a8d8-9bad991b4f40</guid>
      <link>https://share.transistor.fm/s/472e1acd</link>
      <description>
        <![CDATA[<p>In this week’s episode, we’ll discuss the association between occupational exposure to anticancer agents in a parent and subsequent cancer in a child. Then we’ll learn about deciphering and disrupting the activation of PIEZO1 in hereditary xerocytosis. Finally, we’ll hear about the assessment of measurable residual disease, or MRD, in patients with NPM1-mutated AML, or acute myeloid leukemia, receiving venetoclax-based NON-intensive therapy.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week’s episode, we’ll discuss the association between occupational exposure to anticancer agents in a parent and subsequent cancer in a child. Then we’ll learn about deciphering and disrupting the activation of PIEZO1 in hereditary xerocytosis. Finally, we’ll hear about the assessment of measurable residual disease, or MRD, in patients with NPM1-mutated AML, or acute myeloid leukemia, receiving venetoclax-based NON-intensive therapy.</p>]]>
      </content:encoded>
      <pubDate>Thu, 25 Jan 2024 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/472e1acd/d59ff2e3.mp3" length="26267465" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1092</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week’s episode, we’ll discuss the association between occupational exposure to anticancer agents in a parent and subsequent cancer in a child. Then we’ll learn about deciphering and disrupting the activation of PIEZO1 in hereditary xerocytosis. Finally, we’ll hear about the assessment of measurable residual disease, or MRD, in patients with NPM1-mutated AML, or acute myeloid leukemia, receiving venetoclax-based NON-intensive therapy.</p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>TCRαβ/CD19-cell depleted haploHSCT for pediatric leukemia; malignancy-associated hemophagocytic lymphohistiocytosis in Sweden; the bone marrow as the primary site of thrombopoiesis</title>
      <itunes:season>7</itunes:season>
      <podcast:season>7</podcast:season>
      <itunes:title>TCRαβ/CD19-cell depleted haploHSCT for pediatric leukemia; malignancy-associated hemophagocytic lymphohistiocytosis in Sweden; the bone marrow as the primary site of thrombopoiesis</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">1d47a6d9-58b4-446b-998a-bae1cda9a7e6</guid>
      <link>https://share.transistor.fm/s/865a706a</link>
      <description>
        <![CDATA[<p>In this week's episode we’ll discuss the findings from a prospective trial of TCRαβ/CD19-cell depleted HLA-haploidentical transplantation to treat pediatric acute leukemia, learn more about the incidence, clinical characteristics, and survival of malignancy-associated hemophagocytic lymphohistiocytosis in Sweden, and discuss the bone marrow as the primary site of thrombopoiesis. </p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we’ll discuss the findings from a prospective trial of TCRαβ/CD19-cell depleted HLA-haploidentical transplantation to treat pediatric acute leukemia, learn more about the incidence, clinical characteristics, and survival of malignancy-associated hemophagocytic lymphohistiocytosis in Sweden, and discuss the bone marrow as the primary site of thrombopoiesis. </p>]]>
      </content:encoded>
      <pubDate>Thu, 18 Jan 2024 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/865a706a/594a6595.mp3" length="31604226" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1315</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we’ll discuss the findings from a prospective trial of TCRαβ/CD19-cell depleted HLA-haploidentical transplantation to treat pediatric acute leukemia, learn more about the incidence, clinical characteristics, and survival of malignancy-associated hemophagocytic lymphohistiocytosis in Sweden, and discuss the bone marrow as the primary site of thrombopoiesis. </p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Fibrin polymerization and thrombosis; preventing CD19-negative relapse after CAR T-cell therapy in ALL; and impact of aberrant FUS condensates on HSC aging</title>
      <itunes:season>7</itunes:season>
      <podcast:season>7</podcast:season>
      <itunes:title>Fibrin polymerization and thrombosis; preventing CD19-negative relapse after CAR T-cell therapy in ALL; and impact of aberrant FUS condensates on HSC aging</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">2d1dd742-6997-4ed0-b8a0-05a356c484f2</guid>
      <link>https://share.transistor.fm/s/fb0dc98f</link>
      <description>
        <![CDATA[<p>In this week's episode we’ll explore the role of fibrinogen polymerization in thrombosis. Then, we’ll discuss preventing CD19-negative relapse after CAR T-cell therapy in acute lymphoblastic leukemia. Finally, we’ll learn how increased levels of the RNA-binding protein FUS has been identified as an effector of hematopoietic stem cell aging. </p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we’ll explore the role of fibrinogen polymerization in thrombosis. Then, we’ll discuss preventing CD19-negative relapse after CAR T-cell therapy in acute lymphoblastic leukemia. Finally, we’ll learn how increased levels of the RNA-binding protein FUS has been identified as an effector of hematopoietic stem cell aging. </p>]]>
      </content:encoded>
      <pubDate>Thu, 11 Jan 2024 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/fb0dc98f/b647ef8b.mp3" length="25985014" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1080</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we’ll explore the role of fibrinogen polymerization in thrombosis. Then, we’ll discuss preventing CD19-negative relapse after CAR T-cell therapy in acute lymphoblastic leukemia. Finally, we’ll learn how increased levels of the RNA-binding protein FUS has been identified as an effector of hematopoietic stem cell aging. </p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>CD24Fc for prevention of GVHD; origins of active EBV disease; the role of PF4 in platelet activation</title>
      <itunes:season>7</itunes:season>
      <podcast:season>7</podcast:season>
      <itunes:title>CD24Fc for prevention of GVHD; origins of active EBV disease; the role of PF4 in platelet activation</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">017fd99f-3614-4802-a925-0f91ed6a381e</guid>
      <link>https://share.transistor.fm/s/b12c8d02</link>
      <description>
        <![CDATA[<p>In this week's episode we’ll discuss the findings from a phase 2 study of CD24Fc for prevention of graft-versus-host disease, learn more about the origins of chronic active Epstein-Barr virus disease, and discuss the role of PF4 in platelet activation.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we’ll discuss the findings from a phase 2 study of CD24Fc for prevention of graft-versus-host disease, learn more about the origins of chronic active Epstein-Barr virus disease, and discuss the role of PF4 in platelet activation.</p>]]>
      </content:encoded>
      <pubDate>Thu, 04 Jan 2024 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/b12c8d02/9428fcfc.mp3" length="31382600" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1305</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we’ll discuss the findings from a phase 2 study of CD24Fc for prevention of graft-versus-host disease, learn more about the origins of chronic active Epstein-Barr virus disease, and discuss the role of PF4 in platelet activation.</p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Profiling a new VITT-like disorder; real-world outcomes of tafasitamab and lenalidomide in LBCL; and spatial mapping of human hematopoiesis</title>
      <itunes:season>6</itunes:season>
      <podcast:season>6</podcast:season>
      <itunes:title>Profiling a new VITT-like disorder; real-world outcomes of tafasitamab and lenalidomide in LBCL; and spatial mapping of human hematopoiesis</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">5f220262-b938-4a5e-9e7c-1018a94ea121</guid>
      <link>https://share.transistor.fm/s/d077aa4c</link>
      <description>
        <![CDATA[<p>In this week's episode we'll uncover the clinical and pathological profile of a new disorder similar to VITT, or vaccine-induced thrombocytopenia and thrombosis. Then, we'll discuss real-world outcomes in patients with large B-cell lymphoma treated with tafasitamab and lenalidomide. Finally we'll learn about how advances in technology help unravel the spatial biology of bone marrow. </p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we'll uncover the clinical and pathological profile of a new disorder similar to VITT, or vaccine-induced thrombocytopenia and thrombosis. Then, we'll discuss real-world outcomes in patients with large B-cell lymphoma treated with tafasitamab and lenalidomide. Finally we'll learn about how advances in technology help unravel the spatial biology of bone marrow. </p>]]>
      </content:encoded>
      <pubDate>Thu, 28 Dec 2023 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/d077aa4c/54795f11.mp3" length="26911214" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1119</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we'll uncover the clinical and pathological profile of a new disorder similar to VITT, or vaccine-induced thrombocytopenia and thrombosis. Then, we'll discuss real-world outcomes in patients with large B-cell lymphoma treated with tafasitamab and lenalidomide. Finally we'll learn about how advances in technology help unravel the spatial biology of bone marrow. </p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>A natural history of familial platelet disorder with myeloid malignancy; HEXIM1 as an essential transcription regulator in erythropoiesis; residual disease predicts relapse in CML patients</title>
      <itunes:season>6</itunes:season>
      <podcast:season>6</podcast:season>
      <itunes:title>A natural history of familial platelet disorder with myeloid malignancy; HEXIM1 as an essential transcription regulator in erythropoiesis; residual disease predicts relapse in CML patients</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">a6f262f0-6084-42ed-9fc4-c460c1496bae</guid>
      <link>https://share.transistor.fm/s/c74a3d43</link>
      <description>
        <![CDATA[<p>In this week's episode we’ll discuss the findings from a natural history study of patients with familial platelet disorder with myeloid malignancy, learn more about the role of HEXIM1 as an essential transcription regulator in human erythropoiesis, and discuss the utility of residual disease as a predictor of relapse in CML patients stopping TKI therapy.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we’ll discuss the findings from a natural history study of patients with familial platelet disorder with myeloid malignancy, learn more about the role of HEXIM1 as an essential transcription regulator in human erythropoiesis, and discuss the utility of residual disease as a predictor of relapse in CML patients stopping TKI therapy.</p>]]>
      </content:encoded>
      <pubDate>Thu, 21 Dec 2023 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/c74a3d43/eb5391fb.mp3" length="31562788" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1313</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we’ll discuss the findings from a natural history study of patients with familial platelet disorder with myeloid malignancy, learn more about the role of HEXIM1 as an essential transcription regulator in human erythropoiesis, and discuss the utility of residual disease as a predictor of relapse in CML patients stopping TKI therapy.</p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>ETP and MRD for risk assessment in T-ALL; allogeneic HCT outcomes in CGD; effects of pathogenic/likely pathogenic variants in inherited hemostasis disorders</title>
      <itunes:season>6</itunes:season>
      <podcast:season>6</podcast:season>
      <itunes:title>ETP and MRD for risk assessment in T-ALL; allogeneic HCT outcomes in CGD; effects of pathogenic/likely pathogenic variants in inherited hemostasis disorders</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">316e9f24-304d-4fc9-8230-c2d366502c03</guid>
      <link>https://share.transistor.fm/s/fe2f9dd2</link>
      <description>
        <![CDATA[<p>On today's episode we’ll discuss the prognostic significance of the ETP phenotype in children with T-cell ALL, address knowledge gaps in the management of chronic granulomatous disease and learn about the effects of pathogenic and likely pathogenic variants for inherited hemostasis disorders.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>On today's episode we’ll discuss the prognostic significance of the ETP phenotype in children with T-cell ALL, address knowledge gaps in the management of chronic granulomatous disease and learn about the effects of pathogenic and likely pathogenic variants for inherited hemostasis disorders.</p>]]>
      </content:encoded>
      <pubDate>Thu, 14 Dec 2023 12:55:33 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/fe2f9dd2/4283160c.mp3" length="29470979" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1226</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>On today's episode we’ll discuss the prognostic significance of the ETP phenotype in children with T-cell ALL, address knowledge gaps in the management of chronic granulomatous disease and learn about the effects of pathogenic and likely pathogenic variants for inherited hemostasis disorders.</p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Sorafenib plus intensive chemotherapy in newly diagnosed FLT3-ITD AML; inhibition of PLK4 in TP53-mutated AML; the role of CD44 in Plasmodium falciparum infection</title>
      <itunes:season>6</itunes:season>
      <podcast:season>6</podcast:season>
      <itunes:title>Sorafenib plus intensive chemotherapy in newly diagnosed FLT3-ITD AML; inhibition of PLK4 in TP53-mutated AML; the role of CD44 in Plasmodium falciparum infection</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">c02e17bd-ce69-40c6-9cb9-803671959747</guid>
      <link>https://share.transistor.fm/s/338b288d</link>
      <description>
        <![CDATA[<p>On today's episode we’ll discuss the findings from a phase 2 study of sorafenib plus intensive chemotherapy in newly diagnosed <em>FLT3</em>-ITD AML, learn more about the inhibition of PLK4 in <em>TP53</em>-mutated AML, and discuss the role of CD44 in <em>Plasmodium falciparum</em> infection.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>On today's episode we’ll discuss the findings from a phase 2 study of sorafenib plus intensive chemotherapy in newly diagnosed <em>FLT3</em>-ITD AML, learn more about the inhibition of PLK4 in <em>TP53</em>-mutated AML, and discuss the role of CD44 in <em>Plasmodium falciparum</em> infection.</p>]]>
      </content:encoded>
      <pubDate>Thu, 07 Dec 2023 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/338b288d/f161f3e4.mp3" length="32539452" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1354</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>On today's episode we’ll discuss the findings from a phase 2 study of sorafenib plus intensive chemotherapy in newly diagnosed <em>FLT3</em>-ITD AML, learn more about the inhibition of PLK4 in <em>TP53</em>-mutated AML, and discuss the role of CD44 in <em>Plasmodium falciparum</em> infection.</p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>High-risk cytogenetics in solitary bone plasmacytomas; complement activation in vaso-occlusive pain episodes; platelet reactivity to predict thrombotic disease risk</title>
      <itunes:season>6</itunes:season>
      <podcast:season>6</podcast:season>
      <itunes:title>High-risk cytogenetics in solitary bone plasmacytomas; complement activation in vaso-occlusive pain episodes; platelet reactivity to predict thrombotic disease risk</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">71726bce-7ec5-42fb-9d92-9ccb0e266cb3</guid>
      <link>https://share.transistor.fm/s/e0112f40</link>
      <description>
        <![CDATA[<p>On today’s podcast we'll discuss high-risk cytogenetic abnormalities in solitary bone plasmacytomas. Then, we'll consider complement activation in vaso-occlusive pain episodes and how targeting C5a generation inhibited those effects. Finally we'll explore the genetics of platelet reactivity and how researchers used this data to develop a genetic score that was associated with risk of thrombotic diseases.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>On today’s podcast we'll discuss high-risk cytogenetic abnormalities in solitary bone plasmacytomas. Then, we'll consider complement activation in vaso-occlusive pain episodes and how targeting C5a generation inhibited those effects. Finally we'll explore the genetics of platelet reactivity and how researchers used this data to develop a genetic score that was associated with risk of thrombotic diseases.</p>]]>
      </content:encoded>
      <pubDate>Thu, 30 Nov 2023 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/e0112f40/0d2a818b.mp3" length="26757147" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1112</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>On today’s podcast we'll discuss high-risk cytogenetic abnormalities in solitary bone plasmacytomas. Then, we'll consider complement activation in vaso-occlusive pain episodes and how targeting C5a generation inhibited those effects. Finally we'll explore the genetics of platelet reactivity and how researchers used this data to develop a genetic score that was associated with risk of thrombotic diseases.</p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Very long-term follow-up of FCR therapy for CLL, risk assessment of KMT2A-rearranged B-cell precursor ALL in adults; anti-myeloma therapy using antibodies armed with B-BiTEs</title>
      <itunes:season>6</itunes:season>
      <podcast:season>6</podcast:season>
      <itunes:title>Very long-term follow-up of FCR therapy for CLL, risk assessment of KMT2A-rearranged B-cell precursor ALL in adults; anti-myeloma therapy using antibodies armed with B-BiTEs</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">817623d6-443e-4b10-9851-42ef968e0ca0</guid>
      <link>https://share.transistor.fm/s/027038f4</link>
      <description>
        <![CDATA[<p>On this week's episode we’ll discuss the findings from a long-term follow up study of fludarabine, cyclophosphamide, and rituximab in <em>IGHV-</em>mutated CLL, learn more about the impact of genetic alterations and minimal residual disease in adults with KMT2A-rearranged B-cell precursor ALL, and discuss a pre-clinical study of reinforced immunotherapy for myeloma using a new bispecific antibody-based approach.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>On this week's episode we’ll discuss the findings from a long-term follow up study of fludarabine, cyclophosphamide, and rituximab in <em>IGHV-</em>mutated CLL, learn more about the impact of genetic alterations and minimal residual disease in adults with KMT2A-rearranged B-cell precursor ALL, and discuss a pre-clinical study of reinforced immunotherapy for myeloma using a new bispecific antibody-based approach.</p>]]>
      </content:encoded>
      <pubDate>Thu, 23 Nov 2023 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/027038f4/4c0eedb8.mp3" length="35535818" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1478</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>On this week's episode we’ll discuss the findings from a long-term follow up study of fludarabine, cyclophosphamide, and rituximab in <em>IGHV-</em>mutated CLL, learn more about the impact of genetic alterations and minimal residual disease in adults with KMT2A-rearranged B-cell precursor ALL, and discuss a pre-clinical study of reinforced immunotherapy for myeloma using a new bispecific antibody-based approach.</p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Fractionated gemtuzumab ozagamicin Dosing in Elderly AML Patients; Loss-of-function of ENT3 drives histiocytosis; Alternative splicing of CD20 5’-UTR in B-lymphomas</title>
      <itunes:season>6</itunes:season>
      <podcast:season>6</podcast:season>
      <itunes:title>Fractionated gemtuzumab ozagamicin Dosing in Elderly AML Patients; Loss-of-function of ENT3 drives histiocytosis; Alternative splicing of CD20 5’-UTR in B-lymphomas</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">193614e4-aca1-48f2-bd8c-47b1c0a94044</guid>
      <link>https://share.transistor.fm/s/08c876ca</link>
      <description>
        <![CDATA[<p>In this week's episode we'll discuss if fractionated dosing of gemtuzumab ozogamicin provide additional benefit over a single dose in older adults with AML. Then, we'll consider how the loss-of-function of ENT3 drives histiocytosis. Researchers describe a novel pathway leading to histiocytosis that involves hyperactivation of TLR-MAPKinase signaling. This suggests a potential benefit of MAPKinase -directed targeted therapy in a range of histocytoses. Finally we'll discuss unraveling resistance mechanisms to anti-CD20 treatments in B-cell malignancies. Through alternative splicing, the MS4A1 gene encoding human CD20 generates multiple mRNA isoforms with distinct 5’ untranslated regions. </p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we'll discuss if fractionated dosing of gemtuzumab ozogamicin provide additional benefit over a single dose in older adults with AML. Then, we'll consider how the loss-of-function of ENT3 drives histiocytosis. Researchers describe a novel pathway leading to histiocytosis that involves hyperactivation of TLR-MAPKinase signaling. This suggests a potential benefit of MAPKinase -directed targeted therapy in a range of histocytoses. Finally we'll discuss unraveling resistance mechanisms to anti-CD20 treatments in B-cell malignancies. Through alternative splicing, the MS4A1 gene encoding human CD20 generates multiple mRNA isoforms with distinct 5’ untranslated regions. </p>]]>
      </content:encoded>
      <pubDate>Thu, 16 Nov 2023 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/08c876ca/bf11e0d0.mp3" length="28554952" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1187</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we'll discuss if fractionated dosing of gemtuzumab ozogamicin provide additional benefit over a single dose in older adults with AML. Then, we'll consider how the loss-of-function of ENT3 drives histiocytosis. Researchers describe a novel pathway leading to histiocytosis that involves hyperactivation of TLR-MAPKinase signaling. This suggests a potential benefit of MAPKinase -directed targeted therapy in a range of histocytoses. Finally we'll discuss unraveling resistance mechanisms to anti-CD20 treatments in B-cell malignancies. Through alternative splicing, the MS4A1 gene encoding human CD20 generates multiple mRNA isoforms with distinct 5’ untranslated regions. </p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Review Series on RNA Therapeutics in Hematology</title>
      <itunes:season>6</itunes:season>
      <podcast:season>6</podcast:season>
      <itunes:title>Review Series on RNA Therapeutics in Hematology</itunes:title>
      <itunes:episodeType>bonus</itunes:episodeType>
      <guid isPermaLink="false">a6adb056-29ea-49f6-87a9-0c62d16f6de2</guid>
      <link>https://share.transistor.fm/s/920065c9</link>
      <description>
        <![CDATA[<p>In this bonus episode of Blood Podcast, Coordinating Editor, Dr. Jason Gotlib is joined by Drs. Sioban Keel, Margaret Ragni, and Andoni Echaniz-Laguna to discuss the Review Series on RNA Therapeutics in Hematology. The series highlights areas in which RNA therapeutics are most advanced: acute hepatic porphyria, transthyretin amyloidosis, and hemophilia.</p><p><a href="https://ashpublications.org/blood/article/142/19/1577/498624/Introduction-to-a-review-series-on-RNA?searchresult=1">Review Series on RNA Therapeutics in Hematology</a></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this bonus episode of Blood Podcast, Coordinating Editor, Dr. Jason Gotlib is joined by Drs. Sioban Keel, Margaret Ragni, and Andoni Echaniz-Laguna to discuss the Review Series on RNA Therapeutics in Hematology. The series highlights areas in which RNA therapeutics are most advanced: acute hepatic porphyria, transthyretin amyloidosis, and hemophilia.</p><p><a href="https://ashpublications.org/blood/article/142/19/1577/498624/Introduction-to-a-review-series-on-RNA?searchresult=1">Review Series on RNA Therapeutics in Hematology</a></p>]]>
      </content:encoded>
      <pubDate>Tue, 14 Nov 2023 14:00:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/920065c9/494817e6.mp3" length="46047483" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/fDxQ7Q86ptAc8Zt_42C5AgaFRpXQNxfbx-WNLPLUhMk/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS82MDk2/MzFjZjFiNjEzZDIw/OWU2MjljMmVjMzUz/ZDk1Ny5qcGc.jpg"/>
      <itunes:duration>2301</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this bonus episode of Blood Podcast, Coordinating Editor, Dr. Jason Gotlib is joined by Drs. Sioban Keel, Margaret Ragni, and Andoni Echaniz-Laguna to discuss the Review Series on RNA Therapeutics in Hematology. The series highlights areas in which RNA therapeutics are most advanced: acute hepatic porphyria, transthyretin amyloidosis, and hemophilia.</p><p><a href="https://ashpublications.org/blood/article/142/19/1577/498624/Introduction-to-a-review-series-on-RNA?searchresult=1">Review Series on RNA Therapeutics in Hematology</a></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Prognostic significance of splicing factor gene mutations in AML; therapy resistance in multiple myeloma; the effects of KIT ligand deletion on HSC homeostasis</title>
      <itunes:season>6</itunes:season>
      <podcast:season>6</podcast:season>
      <itunes:title>Prognostic significance of splicing factor gene mutations in AML; therapy resistance in multiple myeloma; the effects of KIT ligand deletion on HSC homeostasis</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">6dfa2d81-9c57-4d42-ba90-9e3a52266274</guid>
      <link>https://share.transistor.fm/s/642a7027</link>
      <description>
        <![CDATA[<p>In this week's episode we’ll discuss the prognostic significance of splicing factor gene mutations in newly diagnosed AML, learn more about the findings from a multi-omics study of therapy resistance in multiple myeloma, and discuss the effects of KIT ligand deletion on systemic KIT levels and hematopoietic stem cell homeostasis. </p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we’ll discuss the prognostic significance of splicing factor gene mutations in newly diagnosed AML, learn more about the findings from a multi-omics study of therapy resistance in multiple myeloma, and discuss the effects of KIT ligand deletion on systemic KIT levels and hematopoietic stem cell homeostasis. </p>]]>
      </content:encoded>
      <pubDate>Thu, 09 Nov 2023 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/642a7027/92d9e3ab.mp3" length="28675408" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1193</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we’ll discuss the prognostic significance of splicing factor gene mutations in newly diagnosed AML, learn more about the findings from a multi-omics study of therapy resistance in multiple myeloma, and discuss the effects of KIT ligand deletion on systemic KIT levels and hematopoietic stem cell homeostasis. </p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Targeting prostacyclin to inhibit platelet activation; MRD-tailored myeloma maintenance; AREG and HSC function in DNA damage repair deficiency and aging</title>
      <itunes:season>6</itunes:season>
      <podcast:season>6</podcast:season>
      <itunes:title>Targeting prostacyclin to inhibit platelet activation; MRD-tailored myeloma maintenance; AREG and HSC function in DNA damage repair deficiency and aging</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">bd1a7c74-48f2-445d-9f33-6f2e869a000a</guid>
      <link>https://share.transistor.fm/s/b149c73b</link>
      <description>
        <![CDATA[<p>In this week's episode we'll see how targeting the prostacyclin receptor is a promising strategy for regulating hemostasis and thrombosis. Then, we'll learn how new evidence indicates that the progression rate is low in MRD-negative myeloma patients who discontinue post-transplant lenalidomide and dexamethasone maintenance therapy after 2 years. Finally we'll discuss how amphiregulin from leptin receptor-positive niche cells in the bone marrow mediates crosstalk between the niche and hematopoietic stem cells under conditions of DNA repair deficiency and aging.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode we'll see how targeting the prostacyclin receptor is a promising strategy for regulating hemostasis and thrombosis. Then, we'll learn how new evidence indicates that the progression rate is low in MRD-negative myeloma patients who discontinue post-transplant lenalidomide and dexamethasone maintenance therapy after 2 years. Finally we'll discuss how amphiregulin from leptin receptor-positive niche cells in the bone marrow mediates crosstalk between the niche and hematopoietic stem cells under conditions of DNA repair deficiency and aging.</p>]]>
      </content:encoded>
      <pubDate>Thu, 02 Nov 2023 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/b149c73b/31f417c9.mp3" length="28704015" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1194</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode we'll see how targeting the prostacyclin receptor is a promising strategy for regulating hemostasis and thrombosis. Then, we'll learn how new evidence indicates that the progression rate is low in MRD-negative myeloma patients who discontinue post-transplant lenalidomide and dexamethasone maintenance therapy after 2 years. Finally we'll discuss how amphiregulin from leptin receptor-positive niche cells in the bone marrow mediates crosstalk between the niche and hematopoietic stem cells under conditions of DNA repair deficiency and aging.</p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Lenalinomide plus rituximab for elderly patients with DLBCL, platelet GP6-mediated neutrophil recruitment in acute lung injury, and the role of AXL3 in mantle cell lymphoma.</title>
      <itunes:season>6</itunes:season>
      <podcast:season>6</podcast:season>
      <itunes:title>Lenalinomide plus rituximab for elderly patients with DLBCL, platelet GP6-mediated neutrophil recruitment in acute lung injury, and the role of AXL3 in mantle cell lymphoma.</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">ce8505b9-5e0e-4d3b-8358-ad8ad5178a87</guid>
      <link>https://share.transistor.fm/s/89ee4370</link>
      <description>
        <![CDATA[<p>In this week's episode, we discuss the findings from a phase 2 study of lenalinomide plus rituximab in elderly frail patients with DLBCL, learn more about platelet GP6-mediated neutrophil recruitment in early stages of acute lung injury, and discuss a newly identified isoform of the tyrosine kinase AXL, termed AXL3, in mantle cell lymphoma.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, we discuss the findings from a phase 2 study of lenalinomide plus rituximab in elderly frail patients with DLBCL, learn more about platelet GP6-mediated neutrophil recruitment in early stages of acute lung injury, and discuss a newly identified isoform of the tyrosine kinase AXL, termed AXL3, in mantle cell lymphoma.</p>]]>
      </content:encoded>
      <pubDate>Thu, 26 Oct 2023 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/89ee4370/7fe4fee4.mp3" length="28024792" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1165</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, we discuss the findings from a phase 2 study of lenalinomide plus rituximab in elderly frail patients with DLBCL, learn more about platelet GP6-mediated neutrophil recruitment in early stages of acute lung injury, and discuss a newly identified isoform of the tyrosine kinase AXL, termed AXL3, in mantle cell lymphoma.</p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Gut microbiota diversity and mortality in pediatric allo-HSCT; C5 inhibition in atypical HUS; and pembrolizumab plus vorinostat in PD-1-refractory Hodgkin lymphoma</title>
      <itunes:season>6</itunes:season>
      <podcast:season>6</podcast:season>
      <itunes:title>Gut microbiota diversity and mortality in pediatric allo-HSCT; C5 inhibition in atypical HUS; and pembrolizumab plus vorinostat in PD-1-refractory Hodgkin lymphoma</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">15d5c26c-d917-483b-9467-3c5bec5d71cf</guid>
      <link>https://share.transistor.fm/s/8a0f13e7</link>
      <description>
        <![CDATA[<p>In this week's episode, we'll learn how the diversity of gut microbiota predicts mortality and acute graft-versus-host disease in pediatric allogeneic transplant recipients. Then we'll discuss complement inhibition in patients with complement-mediated atypical hemolytic uremic syndrome. Finally we'll learn how PD-1 plus HDAC equals responses in previously treated Hodgkin lymphoma, specifically that response rates were encouraging in a heavily pretreated cohort, even among patients with PD-1 refractory disease.  </p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, we'll learn how the diversity of gut microbiota predicts mortality and acute graft-versus-host disease in pediatric allogeneic transplant recipients. Then we'll discuss complement inhibition in patients with complement-mediated atypical hemolytic uremic syndrome. Finally we'll learn how PD-1 plus HDAC equals responses in previously treated Hodgkin lymphoma, specifically that response rates were encouraging in a heavily pretreated cohort, even among patients with PD-1 refractory disease.  </p>]]>
      </content:encoded>
      <pubDate>Thu, 19 Oct 2023 15:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/8a0f13e7/2d1ccf37.mp3" length="28152309" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1170</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, we'll learn how the diversity of gut microbiota predicts mortality and acute graft-versus-host disease in pediatric allogeneic transplant recipients. Then we'll discuss complement inhibition in patients with complement-mediated atypical hemolytic uremic syndrome. Finally we'll learn how PD-1 plus HDAC equals responses in previously treated Hodgkin lymphoma, specifically that response rates were encouraging in a heavily pretreated cohort, even among patients with PD-1 refractory disease.  </p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>IL-15 inhibitor BNZ-1 is safe and effective in T-cell LGLL, gene therapy trial for Wiskott-Aldrich syndrome, and ethical framework to select patients for CAR T-cell therapy</title>
      <itunes:season>6</itunes:season>
      <podcast:season>6</podcast:season>
      <itunes:title>IL-15 inhibitor BNZ-1 is safe and effective in T-cell LGLL, gene therapy trial for Wiskott-Aldrich syndrome, and ethical framework to select patients for CAR T-cell therapy</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">632b851b-dcc4-4cb3-bb15-aca0cd71c65f</guid>
      <link>https://share.transistor.fm/s/9de44987</link>
      <description>
        <![CDATA[<p>In this week's episode, we’ll discuss a phase two trial in patients with T-cell large granular lymphocytic leukemia treated with the inhibitor BNZ-1 to block receptor binding of IL-15, learn more about the outcomes of gene therapy for Wiskott-Aldrich syndrome, and discuss ways to mitigate inequity when prioritizing patients for CAR T-cell therapy. </p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, we’ll discuss a phase two trial in patients with T-cell large granular lymphocytic leukemia treated with the inhibitor BNZ-1 to block receptor binding of IL-15, learn more about the outcomes of gene therapy for Wiskott-Aldrich syndrome, and discuss ways to mitigate inequity when prioritizing patients for CAR T-cell therapy. </p>]]>
      </content:encoded>
      <pubDate>Thu, 12 Oct 2023 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/9de44987/3af4ac79.mp3" length="32679403" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1360</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, we’ll discuss a phase two trial in patients with T-cell large granular lymphocytic leukemia treated with the inhibitor BNZ-1 to block receptor binding of IL-15, learn more about the outcomes of gene therapy for Wiskott-Aldrich syndrome, and discuss ways to mitigate inequity when prioritizing patients for CAR T-cell therapy. </p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>DDX41 gene variant prevalence and AML/MDS risk, VITAL mAb treatment of light chain amyloidosis, and movement/neurocognitive toxicities after BCMA CAR T cell treatment </title>
      <itunes:season>6</itunes:season>
      <podcast:season>6</podcast:season>
      <itunes:title>DDX41 gene variant prevalence and AML/MDS risk, VITAL mAb treatment of light chain amyloidosis, and movement/neurocognitive toxicities after BCMA CAR T cell treatment </itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">bb7c9f99-1d74-48ba-ada2-1b5466d2561f</guid>
      <link>https://share.transistor.fm/s/697dc3a9</link>
      <description>
        <![CDATA[<p>In this week’s episode, we’ll learn that Germline pathogenic variants of the DDX41 gene are relatively common in the general population and linked to higher risk of AML and MDS, discuss the birtamimab plus standard of care in light chain amyloidosis, and review new insights on rare movement and neurocognitive toxicities that are observed after BCMA-directed CAR T cell treatment. </p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week’s episode, we’ll learn that Germline pathogenic variants of the DDX41 gene are relatively common in the general population and linked to higher risk of AML and MDS, discuss the birtamimab plus standard of care in light chain amyloidosis, and review new insights on rare movement and neurocognitive toxicities that are observed after BCMA-directed CAR T cell treatment. </p>]]>
      </content:encoded>
      <pubDate>Thu, 05 Oct 2023 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/697dc3a9/7ac120cf.mp3" length="26986552" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1122</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week’s episode, we’ll learn that Germline pathogenic variants of the DDX41 gene are relatively common in the general population and linked to higher risk of AML and MDS, discuss the birtamimab plus standard of care in light chain amyloidosis, and review new insights on rare movement and neurocognitive toxicities that are observed after BCMA-directed CAR T cell treatment. </p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>IL-7 receptor signaling in B-cell differentiation, venetoclax plus obinutuzumab in older patients with CLL, LDL promotes microvascular thrombosis via von Willebrand Factor</title>
      <itunes:season>6</itunes:season>
      <podcast:season>6</podcast:season>
      <itunes:title>IL-7 receptor signaling in B-cell differentiation, venetoclax plus obinutuzumab in older patients with CLL, LDL promotes microvascular thrombosis via von Willebrand Factor</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">31355f93-c13b-4e90-b8fa-966b35f20dd5</guid>
      <link>https://share.transistor.fm/s/dc84d302</link>
      <description>
        <![CDATA[<p>In this weeks episode, we’ll learn more about the role of IL-7 receptor signaling in the differentiation and expansion of human B-cell progenitors, discuss the use of fixed-duration venetoclax plus obinutuzumab in older patients with chronic lymphocytic leukemia, and learn how low-density lipoprotein promotes microvascular thrombosis by enhancing von Willebrand Factor self-association </p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this weeks episode, we’ll learn more about the role of IL-7 receptor signaling in the differentiation and expansion of human B-cell progenitors, discuss the use of fixed-duration venetoclax plus obinutuzumab in older patients with chronic lymphocytic leukemia, and learn how low-density lipoprotein promotes microvascular thrombosis by enhancing von Willebrand Factor self-association </p>]]>
      </content:encoded>
      <pubDate>Thu, 28 Sep 2023 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/dc84d302/a7c2f84d.mp3" length="28913712" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1203</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this weeks episode, we’ll learn more about the role of IL-7 receptor signaling in the differentiation and expansion of human B-cell progenitors, discuss the use of fixed-duration venetoclax plus obinutuzumab in older patients with chronic lymphocytic leukemia, and learn how low-density lipoprotein promotes microvascular thrombosis by enhancing von Willebrand Factor self-association </p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Real-world CAR T therapy in older DLBCL patients, monoclonal antibody blocking APC for hemophilia therapy, and  targeting the epichaperome in AML </title>
      <itunes:season>6</itunes:season>
      <podcast:season>6</podcast:season>
      <itunes:title>Real-world CAR T therapy in older DLBCL patients, monoclonal antibody blocking APC for hemophilia therapy, and  targeting the epichaperome in AML </itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">b7dd5ba6-b093-4759-9a19-b5e6fb3c01b5</guid>
      <link>https://share.transistor.fm/s/d1acc69e</link>
      <description>
        <![CDATA[<p>In this week’s episode, we discuss real-world evidence for CAR T cell therapy in older patients with diffuse large B-cell lymphoma, inhibiting endogenous anticoagulant pathways in congenital factor deficiencies, and finally targeting the HSP90 epichaperome in acute myeloid leukemia. </p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week’s episode, we discuss real-world evidence for CAR T cell therapy in older patients with diffuse large B-cell lymphoma, inhibiting endogenous anticoagulant pathways in congenital factor deficiencies, and finally targeting the HSP90 epichaperome in acute myeloid leukemia. </p>]]>
      </content:encoded>
      <pubDate>Thu, 21 Sep 2023 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/d1acc69e/65f3a1a4.mp3" length="26315109" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1094</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week’s episode, we discuss real-world evidence for CAR T cell therapy in older patients with diffuse large B-cell lymphoma, inhibiting endogenous anticoagulant pathways in congenital factor deficiencies, and finally targeting the HSP90 epichaperome in acute myeloid leukemia. </p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Obinutuzumab, ibrutinib, and venetoclax in untreated CLL with deletion(17p)/TP53 mutation; NOTCH2 mutants promote chemo-resistance in DLBCL; and the role of DBY/HLA class II complexes in chronic GVHD</title>
      <itunes:season>6</itunes:season>
      <podcast:season>6</podcast:season>
      <itunes:title>Obinutuzumab, ibrutinib, and venetoclax in untreated CLL with deletion(17p)/TP53 mutation; NOTCH2 mutants promote chemo-resistance in DLBCL; and the role of DBY/HLA class II complexes in chronic GVHD</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">1bb95b28-45cd-4218-a423-8b732575f685</guid>
      <link>https://share.transistor.fm/s/d55f112b</link>
      <description>
        <![CDATA[<p>In this week's episode, we'll discuss the findings from the final analysis of the CLL2-GIVe trial, learn how <em>NOTCH2</em> mutants promote resistance to chemotherapy in diffuse large B-cell lymphoma, and discuss the role of DBY/HLA class II<em> </em>complexes<em> </em>in chronic graft-versus-host disease.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, we'll discuss the findings from the final analysis of the CLL2-GIVe trial, learn how <em>NOTCH2</em> mutants promote resistance to chemotherapy in diffuse large B-cell lymphoma, and discuss the role of DBY/HLA class II<em> </em>complexes<em> </em>in chronic graft-versus-host disease.</p>]]>
      </content:encoded>
      <pubDate>Thu, 14 Sep 2023 12:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/d55f112b/baa7fc0e.mp3" length="31892240" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1327</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, we'll discuss the findings from the final analysis of the CLL2-GIVe trial, learn how <em>NOTCH2</em> mutants promote resistance to chemotherapy in diffuse large B-cell lymphoma, and discuss the role of DBY/HLA class II<em> </em>complexes<em> </em>in chronic graft-versus-host disease.</p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Long-term outcomes with pembrolizumab in Hodgkin lymphoma, the “incredible ULK” alleviates β-thalassemia, and recommendations for managing CAR T hematotoxicity</title>
      <itunes:season>6</itunes:season>
      <podcast:season>6</podcast:season>
      <itunes:title>Long-term outcomes with pembrolizumab in Hodgkin lymphoma, the “incredible ULK” alleviates β-thalassemia, and recommendations for managing CAR T hematotoxicity</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">36882dfe-15a3-4b2b-be2b-06aa4be6d15c</guid>
      <link>https://share.transistor.fm/s/6b61cd51</link>
      <description>
        <![CDATA[<p>In this week's episode, we’ll learn about long-term outcomes with pembrolizumab in relapsed/refractory classical Hodgkin lymphoma. Next, what’s behind the accumulation of toxic free alpha-globin in beta-thalassemia? Finally, a road map for managing CAR T cell hematologic toxicity. </p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, we’ll learn about long-term outcomes with pembrolizumab in relapsed/refractory classical Hodgkin lymphoma. Next, what’s behind the accumulation of toxic free alpha-globin in beta-thalassemia? Finally, a road map for managing CAR T cell hematologic toxicity. </p>]]>
      </content:encoded>
      <pubDate>Thu, 07 Sep 2023 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/6b61cd51/6c0cc4c1.mp3" length="27883927" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1159</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, we’ll learn about long-term outcomes with pembrolizumab in relapsed/refractory classical Hodgkin lymphoma. Next, what’s behind the accumulation of toxic free alpha-globin in beta-thalassemia? Finally, a road map for managing CAR T cell hematologic toxicity. </p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>How I Manage Inpatient Consultations for Quantitative Neutrophil Abnormalities in Adults</title>
      <itunes:season>6</itunes:season>
      <podcast:season>6</podcast:season>
      <itunes:title>How I Manage Inpatient Consultations for Quantitative Neutrophil Abnormalities in Adults</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">a2e0593c-7424-47db-920e-ad48d24883a9</guid>
      <link>https://share.transistor.fm/s/2e7237fc</link>
      <description>
        <![CDATA[<p><em>Blood</em> associate editors Jeanne Hendrickson and Thomas Ortel edited a How I Treat series on inpatient consultative hematology. In this timely series of articles, the authors present an approach to bleeding, thrombosis, anemia, and quantitative neutrophil abnormalities.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p><em>Blood</em> associate editors Jeanne Hendrickson and Thomas Ortel edited a How I Treat series on inpatient consultative hematology. In this timely series of articles, the authors present an approach to bleeding, thrombosis, anemia, and quantitative neutrophil abnormalities.</p>]]>
      </content:encoded>
      <pubDate>Thu, 31 Aug 2023 14:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/2e7237fc/870a2c27.mp3" length="32463046" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1622</itunes:duration>
      <itunes:summary>
        <![CDATA[<p><em>Blood</em> associate editors Jeanne Hendrickson and Thomas Ortel edited a How I Treat series on inpatient consultative hematology. In this timely series of articles, the authors present an approach to bleeding, thrombosis, anemia, and quantitative neutrophil abnormalities.</p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Dimethyl fumarate in cutaneous T-cell lymphoma, lipid nanoparticles for editing of human hematopoietic cells, and racial and geographic disparities in lymphoma trials</title>
      <itunes:season>6</itunes:season>
      <podcast:season>6</podcast:season>
      <itunes:title>Dimethyl fumarate in cutaneous T-cell lymphoma, lipid nanoparticles for editing of human hematopoietic cells, and racial and geographic disparities in lymphoma trials</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">d5ed4cc4-0253-45bc-8038-0c03cbe00aa0</guid>
      <link>https://share.transistor.fm/s/7c167444</link>
      <description>
        <![CDATA[<p>In this week's episode, we’ll learn more about the treatment of relapsed and refractory cutaneous T-cell lymphoma with dimethyl fumarate, discuss the use of lipid nanoparticles for <em>ex vivo </em>editing of human hematopoietic cells, and learn more about racial and geographic disparities in lymphoma clinical trials.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, we’ll learn more about the treatment of relapsed and refractory cutaneous T-cell lymphoma with dimethyl fumarate, discuss the use of lipid nanoparticles for <em>ex vivo </em>editing of human hematopoietic cells, and learn more about racial and geographic disparities in lymphoma clinical trials.</p>]]>
      </content:encoded>
      <pubDate>Thu, 31 Aug 2023 12:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/7c167444/859d6c56.mp3" length="34092136" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1418</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, we’ll learn more about the treatment of relapsed and refractory cutaneous T-cell lymphoma with dimethyl fumarate, discuss the use of lipid nanoparticles for <em>ex vivo </em>editing of human hematopoietic cells, and learn more about racial and geographic disparities in lymphoma clinical trials.</p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Detailed safety profile of acalabrutinib vs ibrutinib in CLL, inflammation in trauma-induced coagulopathy, abatacept exposure and acute GVHD risk</title>
      <itunes:season>6</itunes:season>
      <podcast:season>6</podcast:season>
      <itunes:title>Detailed safety profile of acalabrutinib vs ibrutinib in CLL, inflammation in trauma-induced coagulopathy, abatacept exposure and acute GVHD risk</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">a7d621c3-4f00-4d08-8bbf-74aecccee1d2</guid>
      <link>https://share.transistor.fm/s/bd6ec6a2</link>
      <description>
        <![CDATA[<p>In this week’s episode, we’ll review a detailed safety profile of acalabrutinib versus ibrutinib in patients with previously treated chronic lymphocytic leukemia, discuss a report that leukocyte inflammation contributes to trauma-induced coagulopathy by oxidation and degradation of fibrinogen, and finally, discuss a pharmacokinetic-pharmacodynamic analysis that shows higher abatacept exposure decreases occurrence of acute graft versus host disease (GVHD) after allogeneic hematopoietic stem cell transplantation (HSCT) from an unrelated donor. </p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week’s episode, we’ll review a detailed safety profile of acalabrutinib versus ibrutinib in patients with previously treated chronic lymphocytic leukemia, discuss a report that leukocyte inflammation contributes to trauma-induced coagulopathy by oxidation and degradation of fibrinogen, and finally, discuss a pharmacokinetic-pharmacodynamic analysis that shows higher abatacept exposure decreases occurrence of acute graft versus host disease (GVHD) after allogeneic hematopoietic stem cell transplantation (HSCT) from an unrelated donor. </p>]]>
      </content:encoded>
      <pubDate>Thu, 24 Aug 2023 12:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/bd6ec6a2/0cdbaeb8.mp3" length="30191539" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1256</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week’s episode, we’ll review a detailed safety profile of acalabrutinib versus ibrutinib in patients with previously treated chronic lymphocytic leukemia, discuss a report that leukocyte inflammation contributes to trauma-induced coagulopathy by oxidation and degradation of fibrinogen, and finally, discuss a pharmacokinetic-pharmacodynamic analysis that shows higher abatacept exposure decreases occurrence of acute graft versus host disease (GVHD) after allogeneic hematopoietic stem cell transplantation (HSCT) from an unrelated donor. </p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Pembrolizumab after ASCT in PTCL, germline predisposition to myeloid neoplasms  in patients with hypoplastic bone marrow, and limited plasticity of monocyte fate and function</title>
      <itunes:season>6</itunes:season>
      <podcast:season>6</podcast:season>
      <itunes:title>Pembrolizumab after ASCT in PTCL, germline predisposition to myeloid neoplasms  in patients with hypoplastic bone marrow, and limited plasticity of monocyte fate and function</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">e51fa39f-ecad-4729-bd23-3a0766725365</guid>
      <link>https://share.transistor.fm/s/fcaf7fc2</link>
      <description>
        <![CDATA[<p>In this week’s episode, we’ll discuss pembrolizumab after autologous stem cell transplantation in patients with peripheral T-cell lymphoma. Newly reported phase 2 study results show that blocking PD-1 with pembrolizumab had a favorable safety profile and demonstrated promising activity, supporting further confirmatory studies in this setting; germline genetic predisposition to myeloid neoplasms in patients with hypoplastic bone marrow. Researchers report mutations that are significantly associated with cytopenias in adulthood in these patients. And pathogenic or likely pathogenic variants were linked to severe cytopenias and advanced myeloid malignancies; and finally, if monocytes and their descendants are less plastic than previously thought. Investigators have identified four functionally specialized monocyte subsets that derive from specific myeloid progenitor lineages. They show that the fate of these monocyte subsets is epigenetically scripted, with little flexibility after differentiation begins, even under conditions of stress.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week’s episode, we’ll discuss pembrolizumab after autologous stem cell transplantation in patients with peripheral T-cell lymphoma. Newly reported phase 2 study results show that blocking PD-1 with pembrolizumab had a favorable safety profile and demonstrated promising activity, supporting further confirmatory studies in this setting; germline genetic predisposition to myeloid neoplasms in patients with hypoplastic bone marrow. Researchers report mutations that are significantly associated with cytopenias in adulthood in these patients. And pathogenic or likely pathogenic variants were linked to severe cytopenias and advanced myeloid malignancies; and finally, if monocytes and their descendants are less plastic than previously thought. Investigators have identified four functionally specialized monocyte subsets that derive from specific myeloid progenitor lineages. They show that the fate of these monocyte subsets is epigenetically scripted, with little flexibility after differentiation begins, even under conditions of stress.</p>]]>
      </content:encoded>
      <pubDate>Thu, 17 Aug 2023 12:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/fcaf7fc2/86463bca.mp3" length="30744315" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1278</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week’s episode, we’ll discuss pembrolizumab after autologous stem cell transplantation in patients with peripheral T-cell lymphoma. Newly reported phase 2 study results show that blocking PD-1 with pembrolizumab had a favorable safety profile and demonstrated promising activity, supporting further confirmatory studies in this setting; germline genetic predisposition to myeloid neoplasms in patients with hypoplastic bone marrow. Researchers report mutations that are significantly associated with cytopenias in adulthood in these patients. And pathogenic or likely pathogenic variants were linked to severe cytopenias and advanced myeloid malignancies; and finally, if monocytes and their descendants are less plastic than previously thought. Investigators have identified four functionally specialized monocyte subsets that derive from specific myeloid progenitor lineages. They show that the fate of these monocyte subsets is epigenetically scripted, with little flexibility after differentiation begins, even under conditions of stress.</p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Review Series on Hematopoietic Stem Cells</title>
      <itunes:season>6</itunes:season>
      <podcast:season>6</podcast:season>
      <itunes:title>Review Series on Hematopoietic Stem Cells</itunes:title>
      <itunes:episodeType>bonus</itunes:episodeType>
      <guid isPermaLink="false">b0e2ac78-3bd0-483e-b9c2-d65b1259899e</guid>
      <link>https://share.transistor.fm/s/3041b007</link>
      <description>
        <![CDATA[<p>In this week’s bonus episode of Blood Podcast, Associate Editor, Dr. John Crispino discusses the Review Series on Hematopoietic Stem Cells with authors, Dr. David Kent and Dr. Jennifer Trowbridge.    </p><p><a href="https://ashpublications.org/blood/article/142/6/497/497285/Introduction-to-a-review-series-on-hematopoietic?searchresult=1">Review Series on Hematopoietic Stem Cells</a></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week’s bonus episode of Blood Podcast, Associate Editor, Dr. John Crispino discusses the Review Series on Hematopoietic Stem Cells with authors, Dr. David Kent and Dr. Jennifer Trowbridge.    </p><p><a href="https://ashpublications.org/blood/article/142/6/497/497285/Introduction-to-a-review-series-on-hematopoietic?searchresult=1">Review Series on Hematopoietic Stem Cells</a></p>]]>
      </content:encoded>
      <pubDate>Thu, 10 Aug 2023 14:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/3041b007/14c61631.mp3" length="21662998" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/Lq3vBDvuj2J3r_nl5vmU_nTZZsVlwhvtaRlphyuCISE/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS84ZjZm/NDFiMTJjZGQzNzEy/NWVlMGExZTJjY2E5/ZWI0OS5qcGc.jpg"/>
      <itunes:duration>1082</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week’s bonus episode of Blood Podcast, Associate Editor, Dr. John Crispino discusses the Review Series on Hematopoietic Stem Cells with authors, Dr. David Kent and Dr. Jennifer Trowbridge.    </p><p><a href="https://ashpublications.org/blood/article/142/6/497/497285/Introduction-to-a-review-series-on-hematopoietic?searchresult=1">Review Series on Hematopoietic Stem Cells</a></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>WGS informs risk of follicular lymphoma transformation; resolvin D4 regulates neutrophil deployment; Hodgkin lymphoma-directed treatment for early-stage NLPHL</title>
      <itunes:season>6</itunes:season>
      <podcast:season>6</podcast:season>
      <itunes:title>WGS informs risk of follicular lymphoma transformation; resolvin D4 regulates neutrophil deployment; Hodgkin lymphoma-directed treatment for early-stage NLPHL</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">1f4d0c45-4ba1-4010-80ab-31cef21fa706</guid>
      <link>https://share.transistor.fm/s/7376a8c7</link>
      <description>
        <![CDATA[<p>In this week's episode, we’ll learn more about what whole genome sequencing reveals about genetic subtypes of follicular lymphoma and risk of transformation, discuss the role of the lipid mediator, resolvin D4, in infectious neutrophil deployment and emergency granulopoiesis, and learn more about Hodgkin lymphoma-directed therapy and the role of PET in early-stage nodular lymphocyte-predominant Hodgkin lymphoma. </p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, we’ll learn more about what whole genome sequencing reveals about genetic subtypes of follicular lymphoma and risk of transformation, discuss the role of the lipid mediator, resolvin D4, in infectious neutrophil deployment and emergency granulopoiesis, and learn more about Hodgkin lymphoma-directed therapy and the role of PET in early-stage nodular lymphocyte-predominant Hodgkin lymphoma. </p>]]>
      </content:encoded>
      <pubDate>Thu, 10 Aug 2023 12:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/7376a8c7/1ac81c37.mp3" length="29758948" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1238</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, we’ll learn more about what whole genome sequencing reveals about genetic subtypes of follicular lymphoma and risk of transformation, discuss the role of the lipid mediator, resolvin D4, in infectious neutrophil deployment and emergency granulopoiesis, and learn more about Hodgkin lymphoma-directed therapy and the role of PET in early-stage nodular lymphocyte-predominant Hodgkin lymphoma. </p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Ventricular arrhythmias in sickle cell anemia, molecular heterogeneity of pediatric lymphoproliferative disorders, the role of the bone marrow microenvironment in myeloid disorders</title>
      <itunes:season>6</itunes:season>
      <podcast:season>6</podcast:season>
      <itunes:title>Ventricular arrhythmias in sickle cell anemia, molecular heterogeneity of pediatric lymphoproliferative disorders, the role of the bone marrow microenvironment in myeloid disorders</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">72d73464-5cb3-4864-8d76-f10c908fa259</guid>
      <link>https://share.transistor.fm/s/afa5b2c8</link>
      <description>
        <![CDATA[<p>In this week's episode, we'll learn more about ventricular arrhythmias in sickle cell anemia, discuss the molecular heterogeneity of pediatric monomorphic post–solid organ transplant lymphoproliferative disorders, and uncover the role of the bone marrow microenvironment as a driver of myeloid disorders.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, we'll learn more about ventricular arrhythmias in sickle cell anemia, discuss the molecular heterogeneity of pediatric monomorphic post–solid organ transplant lymphoproliferative disorders, and uncover the role of the bone marrow microenvironment as a driver of myeloid disorders.</p>]]>
      </content:encoded>
      <pubDate>Thu, 03 Aug 2023 12:34:10 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/afa5b2c8/b5776f50.mp3" length="31430568" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1307</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, we'll learn more about ventricular arrhythmias in sickle cell anemia, discuss the molecular heterogeneity of pediatric monomorphic post–solid organ transplant lymphoproliferative disorders, and uncover the role of the bone marrow microenvironment as a driver of myeloid disorders.</p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Silent infarcts in iTTP remission, a ZDHHC palmitoyltransferase regulates oxidative phosphorylation in AML, and  hepatic sinusoid as a niche for ANKL</title>
      <itunes:season>6</itunes:season>
      <podcast:season>6</podcast:season>
      <itunes:title>Silent infarcts in iTTP remission, a ZDHHC palmitoyltransferase regulates oxidative phosphorylation in AML, and  hepatic sinusoid as a niche for ANKL</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">4966387d-302b-465b-a727-b7569a044f03</guid>
      <link>https://share.transistor.fm/s/b399dad4</link>
      <description>
        <![CDATA[<p>In this week’s episode, we discuss the impact of silent cerebral infarction in patients with immune mediated thrombotic thrombocytopenic purpura (or iTTP) in clinical remission, how the survival of leukemia stem cells is highly dependent on oxidative phosphorylation in the mitochondria, and targeting iron import as a potential therapeutic approach in aggressive natural killer cell leukemia (or ANKL).</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week’s episode, we discuss the impact of silent cerebral infarction in patients with immune mediated thrombotic thrombocytopenic purpura (or iTTP) in clinical remission, how the survival of leukemia stem cells is highly dependent on oxidative phosphorylation in the mitochondria, and targeting iron import as a potential therapeutic approach in aggressive natural killer cell leukemia (or ANKL).</p>]]>
      </content:encoded>
      <pubDate>Thu, 27 Jul 2023 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/b399dad4/bd0deab0.mp3" length="26967695" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1121</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week’s episode, we discuss the impact of silent cerebral infarction in patients with immune mediated thrombotic thrombocytopenic purpura (or iTTP) in clinical remission, how the survival of leukemia stem cells is highly dependent on oxidative phosphorylation in the mitochondria, and targeting iron import as a potential therapeutic approach in aggressive natural killer cell leukemia (or ANKL).</p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Poverty and relapse risk in children with ALL, eligibility and enrollment of diverse populations in myeloma trials, and clonal hematopoiesis in VEXAS syndrome</title>
      <itunes:season>6</itunes:season>
      <podcast:season>6</podcast:season>
      <itunes:title>Poverty and relapse risk in children with ALL, eligibility and enrollment of diverse populations in myeloma trials, and clonal hematopoiesis in VEXAS syndrome</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">dd6d6914-4fb5-4991-a758-945b4dfe5493</guid>
      <link>https://share.transistor.fm/s/07ca62ff</link>
      <description>
        <![CDATA[<p>In this week's episode, we’ll learn more about poverty and relapse risk in children with ALL, discuss eligibility criteria and enrollment of diverse racial and ethnic populations in multiple myeloma clinical trials, and learn more about clonal hematopoiesis in VEXAS syndrome.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, we’ll learn more about poverty and relapse risk in children with ALL, discuss eligibility criteria and enrollment of diverse racial and ethnic populations in multiple myeloma clinical trials, and learn more about clonal hematopoiesis in VEXAS syndrome.</p>]]>
      </content:encoded>
      <pubDate>Thu, 20 Jul 2023 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/07ca62ff/6aae0c28.mp3" length="33157531" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1379</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, we’ll learn more about poverty and relapse risk in children with ALL, discuss eligibility criteria and enrollment of diverse racial and ethnic populations in multiple myeloma clinical trials, and learn more about clonal hematopoiesis in VEXAS syndrome.</p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Pembrolizumab in PMBCL, allogeneic CD19 CAR T cells for pediatric B-cell ALL, and fetal iron overload in β-thalassemia </title>
      <itunes:season>6</itunes:season>
      <podcast:season>6</podcast:season>
      <itunes:title>Pembrolizumab in PMBCL, allogeneic CD19 CAR T cells for pediatric B-cell ALL, and fetal iron overload in β-thalassemia </itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">fbe27b46-9ab8-49ab-b81a-c186f1f903ce</guid>
      <link>https://share.transistor.fm/s/77e2cf50</link>
      <description>
        <![CDATA[<p>In this week's episode, we'll discuss if some patients with relapsed or refractory primary mediastinal B-cell lymphoma can be cured by checkpoint blockade alone. Next, autologous CAR T cells are highly effective, yet not always feasible in children with relapsed or refractory B-cell precursor acute lymphoblastic leukemia. Lastly, we'll discuss ironing out beta-thalassemia during pregnancy.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, we'll discuss if some patients with relapsed or refractory primary mediastinal B-cell lymphoma can be cured by checkpoint blockade alone. Next, autologous CAR T cells are highly effective, yet not always feasible in children with relapsed or refractory B-cell precursor acute lymphoblastic leukemia. Lastly, we'll discuss ironing out beta-thalassemia during pregnancy.</p>]]>
      </content:encoded>
      <pubDate>Thu, 13 Jul 2023 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/77e2cf50/bc319e51.mp3" length="27287330" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1134</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, we'll discuss if some patients with relapsed or refractory primary mediastinal B-cell lymphoma can be cured by checkpoint blockade alone. Next, autologous CAR T cells are highly effective, yet not always feasible in children with relapsed or refractory B-cell precursor acute lymphoblastic leukemia. Lastly, we'll discuss ironing out beta-thalassemia during pregnancy.</p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Gene therapy for WHIM syndrome, fate of hematopoietic stem cells after transplantation, and the role of C-terminal FGF23 peptides in iron conservation</title>
      <itunes:season>6</itunes:season>
      <podcast:season>6</podcast:season>
      <itunes:title>Gene therapy for WHIM syndrome, fate of hematopoietic stem cells after transplantation, and the role of C-terminal FGF23 peptides in iron conservation</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">66914d28-d041-4326-9a29-a266c6db76d1</guid>
      <link>https://share.transistor.fm/s/75adaa18</link>
      <description>
        <![CDATA[<p>In this week's episode, we’ll discuss the findings from a study attempting gene therapy for WHIM syndrome for the first time, learn more about the fate of hematopoietic stem cells after transplantation, and discuss the role of C-terminal FGF23 peptides in iron conservation.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, we’ll discuss the findings from a study attempting gene therapy for WHIM syndrome for the first time, learn more about the fate of hematopoietic stem cells after transplantation, and discuss the role of C-terminal FGF23 peptides in iron conservation.</p>]]>
      </content:encoded>
      <pubDate>Thu, 06 Jul 2023 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/75adaa18/61a42c11.mp3" length="28234414" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1174</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, we’ll discuss the findings from a study attempting gene therapy for WHIM syndrome for the first time, learn more about the fate of hematopoietic stem cells after transplantation, and discuss the role of C-terminal FGF23 peptides in iron conservation.</p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Key role of hepcidin in polycythemia vera, signatures of CAR T cell dysfunction, and IL-34 as a novel AML therapy?</title>
      <itunes:season>5</itunes:season>
      <podcast:season>5</podcast:season>
      <itunes:title>Key role of hepcidin in polycythemia vera, signatures of CAR T cell dysfunction, and IL-34 as a novel AML therapy?</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">efc2e61c-e0a7-4701-a5e4-3889a703c906</guid>
      <link>https://share.transistor.fm/s/362272f3</link>
      <description>
        <![CDATA[<p>In this week's episode, we'll discuss new evidence on the critical role of hepcidin, the master regulator of iron metabolism, in the pathogenesis of polycythemia vera. Next, costimulatory molecules regulate mechanisms of CAR T cell dysfunction. Finally, we'll discuss how TREM2 is a novel receptor for IL-34, promoting differentiation of normal and leukemic myeloid cells. </p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, we'll discuss new evidence on the critical role of hepcidin, the master regulator of iron metabolism, in the pathogenesis of polycythemia vera. Next, costimulatory molecules regulate mechanisms of CAR T cell dysfunction. Finally, we'll discuss how TREM2 is a novel receptor for IL-34, promoting differentiation of normal and leukemic myeloid cells. </p>]]>
      </content:encoded>
      <pubDate>Thu, 29 Jun 2023 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/362272f3/261b0639.mp3" length="28041864" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1166</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, we'll discuss new evidence on the critical role of hepcidin, the master regulator of iron metabolism, in the pathogenesis of polycythemia vera. Next, costimulatory molecules regulate mechanisms of CAR T cell dysfunction. Finally, we'll discuss how TREM2 is a novel receptor for IL-34, promoting differentiation of normal and leukemic myeloid cells. </p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>BMT as initial treatment for severe aplastic anemia, macrophage metabolic rewiring in sickle cell disease, and predicting outcomes using PET radiomics in diffuse large B cell lymphoma</title>
      <itunes:season>5</itunes:season>
      <podcast:season>5</podcast:season>
      <itunes:title>BMT as initial treatment for severe aplastic anemia, macrophage metabolic rewiring in sickle cell disease, and predicting outcomes using PET radiomics in diffuse large B cell lymphoma</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">3bf86ea5-3d4d-4ff9-8252-68728aa3e0b7</guid>
      <link>https://share.transistor.fm/s/79906cd6</link>
      <description>
        <![CDATA[<p>In this week’s episode we’ll report on the findings from a phase 2 trial of bone marrow transplantation as initial therapy for patients with severe aplastic anemia, discuss the utility of a PET radiomics-based model in predicting outcomes in diffuse large B-cell lymphoma, and learn more about macrophage metabolic rewiring in sickle cell disease.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week’s episode we’ll report on the findings from a phase 2 trial of bone marrow transplantation as initial therapy for patients with severe aplastic anemia, discuss the utility of a PET radiomics-based model in predicting outcomes in diffuse large B-cell lymphoma, and learn more about macrophage metabolic rewiring in sickle cell disease.</p>]]>
      </content:encoded>
      <pubDate>Thu, 22 Jun 2023 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/79906cd6/285f1980.mp3" length="28018627" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1165</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week’s episode we’ll report on the findings from a phase 2 trial of bone marrow transplantation as initial therapy for patients with severe aplastic anemia, discuss the utility of a PET radiomics-based model in predicting outcomes in diffuse large B-cell lymphoma, and learn more about macrophage metabolic rewiring in sickle cell disease.</p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>End of the vincristine/steroid pulse era in pediatric ALL?, “trial and error” with abatacept in GVHD, and hemorrhage risk with dasatinib therapy</title>
      <itunes:season>5</itunes:season>
      <podcast:season>5</podcast:season>
      <itunes:title>End of the vincristine/steroid pulse era in pediatric ALL?, “trial and error” with abatacept in GVHD, and hemorrhage risk with dasatinib therapy</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">fab1bdd8-d338-4b64-88e3-c8fbe9c99968</guid>
      <link>https://share.transistor.fm/s/8bd6fd8d</link>
      <description>
        <![CDATA[<p>In this week’s episode we will review no survival benefit for vincristine/steroid pulses in contemporary studies of childhood acute lymphoblastic leukemia (or ALL). Next, the rheumatology drug abatacept may be a promising strategy for the treatment of acute graft-versus-host disease (or GVHD). Finally, we'll discuss the hemorrhage risk of dasatinib therapy.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week’s episode we will review no survival benefit for vincristine/steroid pulses in contemporary studies of childhood acute lymphoblastic leukemia (or ALL). Next, the rheumatology drug abatacept may be a promising strategy for the treatment of acute graft-versus-host disease (or GVHD). Finally, we'll discuss the hemorrhage risk of dasatinib therapy.</p>]]>
      </content:encoded>
      <pubDate>Thu, 15 Jun 2023 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/8bd6fd8d/abae09b5.mp3" length="26048148" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1083</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week’s episode we will review no survival benefit for vincristine/steroid pulses in contemporary studies of childhood acute lymphoblastic leukemia (or ALL). Next, the rheumatology drug abatacept may be a promising strategy for the treatment of acute graft-versus-host disease (or GVHD). Finally, we'll discuss the hemorrhage risk of dasatinib therapy.</p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Prolonged response after stopping TPO-RA in ITP, TP53 mutations and myelofibrosis outcomes, clinical picture of ERCC6L2 disease, where variants predispose to marrow failure and malignancy</title>
      <itunes:season>5</itunes:season>
      <podcast:season>5</podcast:season>
      <itunes:title>Prolonged response after stopping TPO-RA in ITP, TP53 mutations and myelofibrosis outcomes, clinical picture of ERCC6L2 disease, where variants predispose to marrow failure and malignancy</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">ee12a7a1-8004-4fc9-8c94-dd89083fd5c6</guid>
      <link>https://share.transistor.fm/s/4458d604</link>
      <description>
        <![CDATA[]]>
      </description>
      <content:encoded>
        <![CDATA[]]>
      </content:encoded>
      <pubDate>Thu, 08 Jun 2023 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/4458d604/4038f60a.mp3" length="32980512" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1372</itunes:duration>
      <itunes:summary>
        <![CDATA[]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Hodgkin lymphoma outcomes in the novel agent era, genomic safe harbors for precision T cell engineering, and a transcriptomic atlas to map imatinib resistance in CML </title>
      <itunes:season>5</itunes:season>
      <podcast:season>5</podcast:season>
      <itunes:title>Hodgkin lymphoma outcomes in the novel agent era, genomic safe harbors for precision T cell engineering, and a transcriptomic atlas to map imatinib resistance in CML </itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">89f93769-d88a-4f58-87d5-fd24f35a8254</guid>
      <link>https://share.transistor.fm/s/39dadf97</link>
      <description>
        <![CDATA[<p>In this week’s episode, we'll discuss how patients with relapsed or refractory Hodgkin lymphoma survival outcomes have improved after development of several novel agents. Next, precision engineering of therapeutic T cells through extragenic safe harbors. Finally, using a single-cell atlas to map features of imatinib resistance in diagnostic CML bone marrow, investigators present gene expression signatures predictive of response to TKI therapy.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week’s episode, we'll discuss how patients with relapsed or refractory Hodgkin lymphoma survival outcomes have improved after development of several novel agents. Next, precision engineering of therapeutic T cells through extragenic safe harbors. Finally, using a single-cell atlas to map features of imatinib resistance in diagnostic CML bone marrow, investigators present gene expression signatures predictive of response to TKI therapy.</p>]]>
      </content:encoded>
      <pubDate>Thu, 01 Jun 2023 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/39dadf97/f47635f7.mp3" length="17145192" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1069</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week’s episode, we'll discuss how patients with relapsed or refractory Hodgkin lymphoma survival outcomes have improved after development of several novel agents. Next, precision engineering of therapeutic T cells through extragenic safe harbors. Finally, using a single-cell atlas to map features of imatinib resistance in diagnostic CML bone marrow, investigators present gene expression signatures predictive of response to TKI therapy.</p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Pembrolizumab plus AVD for classical Hodgkin lymphoma, targeting the CD40/CD40-ligand axis in Waldenström Macroglobulinemia, and CXCR4-expressing CAR-cytokine induced killer cells in AML</title>
      <itunes:season>5</itunes:season>
      <podcast:season>5</podcast:season>
      <itunes:title>Pembrolizumab plus AVD for classical Hodgkin lymphoma, targeting the CD40/CD40-ligand axis in Waldenström Macroglobulinemia, and CXCR4-expressing CAR-cytokine induced killer cells in AML</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">d988dcf3-662e-4bb0-bf11-f6c8ed6be3d2</guid>
      <link>https://share.transistor.fm/s/57e52260</link>
      <description>
        <![CDATA[<p>In this week’s episode we’ll discuss the findings from a study exploring the combination of concurrent pembrolizumab, adriamycin, vinblastine, and dacarbazine in newly diagnosed classical Hodgkin lymphoma, learn more about the effects of targeting the CD40/CD40-ligand axis in Waldenström Macroglobulinemia, and review the findings from a study aimed at improving the bone marrow homing of CAR-cytokine induced killer cells in AML.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week’s episode we’ll discuss the findings from a study exploring the combination of concurrent pembrolizumab, adriamycin, vinblastine, and dacarbazine in newly diagnosed classical Hodgkin lymphoma, learn more about the effects of targeting the CD40/CD40-ligand axis in Waldenström Macroglobulinemia, and review the findings from a study aimed at improving the bone marrow homing of CAR-cytokine induced killer cells in AML.</p>]]>
      </content:encoded>
      <pubDate>Thu, 25 May 2023 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/57e52260/094ad0ea.mp3" length="20275309" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1265</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week’s episode we’ll discuss the findings from a study exploring the combination of concurrent pembrolizumab, adriamycin, vinblastine, and dacarbazine in newly diagnosed classical Hodgkin lymphoma, learn more about the effects of targeting the CD40/CD40-ligand axis in Waldenström Macroglobulinemia, and review the findings from a study aimed at improving the bone marrow homing of CAR-cytokine induced killer cells in AML.</p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>How I Treat Series: Emergent CAR T-Cell Toxicities</title>
      <itunes:season>5</itunes:season>
      <podcast:season>5</podcast:season>
      <itunes:title>How I Treat Series: Emergent CAR T-Cell Toxicities</itunes:title>
      <itunes:episodeType>bonus</itunes:episodeType>
      <guid isPermaLink="false">579d96e6-a8f2-472b-9b65-b103d5822a37</guid>
      <link>https://share.transistor.fm/s/ac35bd76</link>
      <description>
        <![CDATA[<p>In this bonus episode, Associate Editor, Dr. Helen Heslop discusses the How I Treat series on Emergent CAR-T cell toxicities with authors Dr. Fabiana Perna, Dr. Natalie Grover and Dr. Nirali Shah.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this bonus episode, Associate Editor, Dr. Helen Heslop discusses the How I Treat series on Emergent CAR-T cell toxicities with authors Dr. Fabiana Perna, Dr. Natalie Grover and Dr. Nirali Shah.</p>]]>
      </content:encoded>
      <pubDate>Thu, 18 May 2023 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/ac35bd76/9701cdcd.mp3" length="30970688" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1547</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this bonus episode, Associate Editor, Dr. Helen Heslop discusses the How I Treat series on Emergent CAR-T cell toxicities with authors Dr. Fabiana Perna, Dr. Natalie Grover and Dr. Nirali Shah.</p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Specific CD8+ T cell clones in ITP, Refining DLBCL prognosis with the “dark-zone signature”, and rethinking the regenerative role of HSCs in acute hematopoietic emergencies</title>
      <itunes:season>5</itunes:season>
      <podcast:season>5</podcast:season>
      <itunes:title>Specific CD8+ T cell clones in ITP, Refining DLBCL prognosis with the “dark-zone signature”, and rethinking the regenerative role of HSCs in acute hematopoietic emergencies</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">ff1377af-fb98-49f7-9a9a-999b6152ad58</guid>
      <link>https://share.transistor.fm/s/97711387</link>
      <description>
        <![CDATA[<p>In this week’s episode, we will review patients with chronic ITP having clonal expansions of a specific subset of CD8 T cells, called terminally differentiated effector memory T cells, or TEMRA. Next, for patients with diffuse large B-cell lymphomas, use of a so-called dark-zone signature, previously referred to as the double-hit signature, could help refine prognosis. Finally on today's podcast we'll discuss rethinking the role of hematopoietic stem cells following physiologic emergencies such as acute inflammation and blood loss.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week’s episode, we will review patients with chronic ITP having clonal expansions of a specific subset of CD8 T cells, called terminally differentiated effector memory T cells, or TEMRA. Next, for patients with diffuse large B-cell lymphomas, use of a so-called dark-zone signature, previously referred to as the double-hit signature, could help refine prognosis. Finally on today's podcast we'll discuss rethinking the role of hematopoietic stem cells following physiologic emergencies such as acute inflammation and blood loss.</p>]]>
      </content:encoded>
      <pubDate>Thu, 18 May 2023 12:20:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/97711387/846744c5.mp3" length="17603040" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1098</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week’s episode, we will review patients with chronic ITP having clonal expansions of a specific subset of CD8 T cells, called terminally differentiated effector memory T cells, or TEMRA. Next, for patients with diffuse large B-cell lymphomas, use of a so-called dark-zone signature, previously referred to as the double-hit signature, could help refine prognosis. Finally on today's podcast we'll discuss rethinking the role of hematopoietic stem cells following physiologic emergencies such as acute inflammation and blood loss.</p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Tips for Trainees for a Career in Publishing with Drs. Nancy Berliner and Andrew Roberts</title>
      <itunes:season>5</itunes:season>
      <podcast:season>5</podcast:season>
      <itunes:title>Tips for Trainees for a Career in Publishing with Drs. Nancy Berliner and Andrew Roberts</itunes:title>
      <itunes:episodeType>bonus</itunes:episodeType>
      <guid isPermaLink="false">d3555118-1b44-4e86-823e-249c92fed0a8</guid>
      <link>https://share.transistor.fm/s/c529d485</link>
      <description>
        <![CDATA[<p>In this special episode, Trainee Council Chairs, Drs. Becky Zon and Ajay Major, interview Dr. Nancy Berliner, Blood Editor-in Chief and Dr. Andrew Roberts, Blood Deputy Editor, on their careers in academic editing and publishing, including career development tips for trainees who are interested in a career in publishing.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this special episode, Trainee Council Chairs, Drs. Becky Zon and Ajay Major, interview Dr. Nancy Berliner, Blood Editor-in Chief and Dr. Andrew Roberts, Blood Deputy Editor, on their careers in academic editing and publishing, including career development tips for trainees who are interested in a career in publishing.</p>]]>
      </content:encoded>
      <pubDate>Mon, 15 May 2023 14:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/c529d485/bbac73fc.mp3" length="35670643" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1784</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this special episode, Trainee Council Chairs, Drs. Becky Zon and Ajay Major, interview Dr. Nancy Berliner, Blood Editor-in Chief and Dr. Andrew Roberts, Blood Deputy Editor, on their careers in academic editing and publishing, including career development tips for trainees who are interested in a career in publishing.</p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Axi-cel in refractory large B-cell lymphoma, effects of C1 inhibitor deficiency on coagulation, and the evolution of therapy-related myeloid neoplasms</title>
      <itunes:season>5</itunes:season>
      <podcast:season>5</podcast:season>
      <itunes:title>Axi-cel in refractory large B-cell lymphoma, effects of C1 inhibitor deficiency on coagulation, and the evolution of therapy-related myeloid neoplasms</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">260e005e-244b-49bf-8003-2d17d85094d3</guid>
      <link>https://share.transistor.fm/s/334b525e</link>
      <description>
        <![CDATA[<p>In this week’s episode we’ll report on the findings from a 5-year follow-up study of axicabtagene ciloleucel in refractory large B-cell lymphoma, discuss the role of C1 inhibitor deficiency in coagulation and venous thrombosis, and learn how chemotherapy signatures can be used to track the evolution of therapy-related myeloid neoplasms.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week’s episode we’ll report on the findings from a 5-year follow-up study of axicabtagene ciloleucel in refractory large B-cell lymphoma, discuss the role of C1 inhibitor deficiency in coagulation and venous thrombosis, and learn how chemotherapy signatures can be used to track the evolution of therapy-related myeloid neoplasms.</p>]]>
      </content:encoded>
      <pubDate>Thu, 11 May 2023 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/334b525e/53a98e49.mp3" length="18516918" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1155</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week’s episode we’ll report on the findings from a 5-year follow-up study of axicabtagene ciloleucel in refractory large B-cell lymphoma, discuss the role of C1 inhibitor deficiency in coagulation and venous thrombosis, and learn how chemotherapy signatures can be used to track the evolution of therapy-related myeloid neoplasms.</p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Gut microbiota and outcomes in DLBCL, NFIA-ETO2 fusion cooperates with TP53 in leukemogenesis, and the impact of nirmatrelvir + ritonavir on CLL patient outcomes during the Omicron surge</title>
      <itunes:season>5</itunes:season>
      <podcast:season>5</podcast:season>
      <itunes:title>Gut microbiota and outcomes in DLBCL, NFIA-ETO2 fusion cooperates with TP53 in leukemogenesis, and the impact of nirmatrelvir + ritonavir on CLL patient outcomes during the Omicron surge</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">37670ca3-8ba3-485f-8c5d-fd19fffe07a3</guid>
      <link>https://share.transistor.fm/s/276e67f2</link>
      <description>
        <![CDATA[<p>In this week’s episode we'll review imbalances in gut microbiota may impact the efficacy and safety of immunochemotherapy in patients with diffuse large B-cell lymphoma. Next, the<em> NFIA-ETO2</em> fusion, found exclusively in pediatric patients with pure erythroid leukemia, impairs the normal process of erythroid differentiation. Finally, we'll look at the effectiveness of nirmatrelvir plus ritonavir in patients with CLL infected with SARS-CoV-2 during the Omicron surge.  </p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week’s episode we'll review imbalances in gut microbiota may impact the efficacy and safety of immunochemotherapy in patients with diffuse large B-cell lymphoma. Next, the<em> NFIA-ETO2</em> fusion, found exclusively in pediatric patients with pure erythroid leukemia, impairs the normal process of erythroid differentiation. Finally, we'll look at the effectiveness of nirmatrelvir plus ritonavir in patients with CLL infected with SARS-CoV-2 during the Omicron surge.  </p>]]>
      </content:encoded>
      <pubDate>Thu, 04 May 2023 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/276e67f2/960b927a.mp3" length="17822724" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1112</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week’s episode we'll review imbalances in gut microbiota may impact the efficacy and safety of immunochemotherapy in patients with diffuse large B-cell lymphoma. Next, the<em> NFIA-ETO2</em> fusion, found exclusively in pediatric patients with pure erythroid leukemia, impairs the normal process of erythroid differentiation. Finally, we'll look at the effectiveness of nirmatrelvir plus ritonavir in patients with CLL infected with SARS-CoV-2 during the Omicron surge.  </p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Revised response criteria for high-risk MDS, machine learning guides diagnosis of bone marrow failure syndromes, and RhD-positive transfusions for Asian-type DEL patients with serologic RhD-negative typing</title>
      <itunes:season>5</itunes:season>
      <podcast:season>5</podcast:season>
      <itunes:title>Revised response criteria for high-risk MDS, machine learning guides diagnosis of bone marrow failure syndromes, and RhD-positive transfusions for Asian-type DEL patients with serologic RhD-negative typing</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">ec721238-dcc3-4d0b-8a49-ed21ec776cba</guid>
      <link>https://share.transistor.fm/s/1d69dd1e</link>
      <description>
        <![CDATA[<p>In this week’s episode, we’ll discuss the newly revised International Working Group response criteria for patients with higher-risk MDS, learn more about the utility of machine learning in the differential diagnosis of bone marrow failure, and discuss whether patients with the Asian-type DEL allele, who type as serologic Rh-D-negative, can be safely transfused with RhD-positive blood.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week’s episode, we’ll discuss the newly revised International Working Group response criteria for patients with higher-risk MDS, learn more about the utility of machine learning in the differential diagnosis of bone marrow failure, and discuss whether patients with the Asian-type DEL allele, who type as serologic Rh-D-negative, can be safely transfused with RhD-positive blood.</p>]]>
      </content:encoded>
      <pubDate>Thu, 27 Apr 2023 12:45:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/1d69dd1e/887a3dc3.mp3" length="21110828" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1317</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week’s episode, we’ll discuss the newly revised International Working Group response criteria for patients with higher-risk MDS, learn more about the utility of machine learning in the differential diagnosis of bone marrow failure, and discuss whether patients with the Asian-type DEL allele, who type as serologic Rh-D-negative, can be safely transfused with RhD-positive blood.</p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>AIHA during pregnancy, rapid immune tolerance induction in severe hemophilia A, and aging changes control of HSC proliferation</title>
      <itunes:season>5</itunes:season>
      <podcast:season>5</podcast:season>
      <itunes:title>AIHA during pregnancy, rapid immune tolerance induction in severe hemophilia A, and aging changes control of HSC proliferation</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">01745f05-62c8-4a9d-89d6-e9135b6aeae1</guid>
      <link>https://share.transistor.fm/s/0021cd6f</link>
      <description>
        <![CDATA[<p>In this week’s episode we will review treatment and outcomes for patients with autoimmune hemolytic anemia during pregnancy. Next, rapid immune tolerance induction in patients with hemophilia A and high-titer inhibitors. Finally, researchers compare kinetics and cell cycle progression in hematopoietic stem cells from cord blood, young adults, and aged healthy donors.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week’s episode we will review treatment and outcomes for patients with autoimmune hemolytic anemia during pregnancy. Next, rapid immune tolerance induction in patients with hemophilia A and high-titer inhibitors. Finally, researchers compare kinetics and cell cycle progression in hematopoietic stem cells from cord blood, young adults, and aged healthy donors.</p>]]>
      </content:encoded>
      <pubDate>Thu, 20 Apr 2023 13:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/0021cd6f/4331b665.mp3" length="16372688" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1021</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week’s episode we will review treatment and outcomes for patients with autoimmune hemolytic anemia during pregnancy. Next, rapid immune tolerance induction in patients with hemophilia A and high-titer inhibitors. Finally, researchers compare kinetics and cell cycle progression in hematopoietic stem cells from cord blood, young adults, and aged healthy donors.</p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Review Series on Classical Myeloproliferative Neoplasms</title>
      <itunes:season>5</itunes:season>
      <podcast:season>5</podcast:season>
      <itunes:title>Review Series on Classical Myeloproliferative Neoplasms</itunes:title>
      <itunes:episodeType>bonus</itunes:episodeType>
      <guid isPermaLink="false">1647f5e1-f6db-44d0-8410-2b0ca3d6d68b</guid>
      <link>https://share.transistor.fm/s/7e5bd9b7</link>
      <description>
        <![CDATA[<p>In this episode Associate Editor, Dr. Mario Cazzola discusses the review series on Classical Myeloproliferative Neoplasms, with authors, Dr. Ann Mullaly and Dr. Alison Moliterno.  </p><p><a href="https://ashpublications.org/blood/article/141/16/1897/494808/Introduction-to-a-review-series-on-classic?searchresult=1">Review Series on Classical Myeloproliferative Neoplasms</a></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this episode Associate Editor, Dr. Mario Cazzola discusses the review series on Classical Myeloproliferative Neoplasms, with authors, Dr. Ann Mullaly and Dr. Alison Moliterno.  </p><p><a href="https://ashpublications.org/blood/article/141/16/1897/494808/Introduction-to-a-review-series-on-classic?searchresult=1">Review Series on Classical Myeloproliferative Neoplasms</a></p>]]>
      </content:encoded>
      <pubDate>Thu, 20 Apr 2023 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/7e5bd9b7/0dbe8d26.mp3" length="27592926" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/AMmDX31mymuicrZlX1ZWunIavGKA-XGJ5GHts8Cd5H8/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS9iYzJk/MzQ5YjNjYmE2Njhl/M2Y4OGE4ZjIxZTM5/YjhmOC5qcGc.jpg"/>
      <itunes:duration>1378</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this episode Associate Editor, Dr. Mario Cazzola discusses the review series on Classical Myeloproliferative Neoplasms, with authors, Dr. Ann Mullaly and Dr. Alison Moliterno.  </p><p><a href="https://ashpublications.org/blood/article/141/16/1897/494808/Introduction-to-a-review-series-on-classic?searchresult=1">Review Series on Classical Myeloproliferative Neoplasms</a></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Factor H variants in paroxysmal nocturnal hemoglobinuria, the role of factor XII in SCD-related thrombosis, and clinical features of therapy-related NPM1-mutated AML</title>
      <itunes:season>5</itunes:season>
      <podcast:season>5</podcast:season>
      <itunes:title>Factor H variants in paroxysmal nocturnal hemoglobinuria, the role of factor XII in SCD-related thrombosis, and clinical features of therapy-related NPM1-mutated AML</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">fbccd2c5-ec44-4262-ad49-f03eed66625a</guid>
      <link>https://share.transistor.fm/s/49d1ca9b</link>
      <description>
        <![CDATA[<p>In this week’s episode, we’ll learn how rare germline genetic variants in complement factor H (CFH) affect the course of paroxysmal nocturnal hemoglobinuria, discuss the role of coagulation factor XII in thrombotic complications and vaso-occlusion associated with sickle cell disease, and learn more about the overlapping features of therapy-related and de novo <em>NPM1</em>-mutated AML.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week’s episode, we’ll learn how rare germline genetic variants in complement factor H (CFH) affect the course of paroxysmal nocturnal hemoglobinuria, discuss the role of coagulation factor XII in thrombotic complications and vaso-occlusion associated with sickle cell disease, and learn more about the overlapping features of therapy-related and de novo <em>NPM1</em>-mutated AML.</p>]]>
      </content:encoded>
      <pubDate>Fri, 14 Apr 2023 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/49d1ca9b/2d2d3375.mp3" length="21935763" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1369</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week’s episode, we’ll learn how rare germline genetic variants in complement factor H (CFH) affect the course of paroxysmal nocturnal hemoglobinuria, discuss the role of coagulation factor XII in thrombotic complications and vaso-occlusion associated with sickle cell disease, and learn more about the overlapping features of therapy-related and de novo <em>NPM1</em>-mutated AML.</p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Lenalidomide and genetic profiling in myeloma, T-cell immunotherapy upregulates AML cell MHC-class II, and young fecal microbiota rejuvenate HSCs</title>
      <itunes:season>5</itunes:season>
      <podcast:season>5</podcast:season>
      <itunes:title>Lenalidomide and genetic profiling in myeloma, T-cell immunotherapy upregulates AML cell MHC-class II, and young fecal microbiota rejuvenate HSCs</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">fdfeae7e-af35-4862-856b-912d2c32dbe6</guid>
      <link>https://share.transistor.fm/s/78bef358</link>
      <description>
        <![CDATA[<p>In this week’s episode we will review optimizing the value of post-transplant lenalidomide maintenance in multiple myeloma. Next, T-cell immunotherapies targeting AML antigens upregulate MHC Class II expression on AML cells. Finally, young bugs rejuvenate old blood: transplanting fecal microbiota from younger mice into older mice improved hematopoietic stem cell function and restored lymphoid differentiation potential.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week’s episode we will review optimizing the value of post-transplant lenalidomide maintenance in multiple myeloma. Next, T-cell immunotherapies targeting AML antigens upregulate MHC Class II expression on AML cells. Finally, young bugs rejuvenate old blood: transplanting fecal microbiota from younger mice into older mice improved hematopoietic stem cell function and restored lymphoid differentiation potential.</p>]]>
      </content:encoded>
      <pubDate>Thu, 06 Apr 2023 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/78bef358/55c4d302.mp3" length="16285987" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1016</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week’s episode we will review optimizing the value of post-transplant lenalidomide maintenance in multiple myeloma. Next, T-cell immunotherapies targeting AML antigens upregulate MHC Class II expression on AML cells. Finally, young bugs rejuvenate old blood: transplanting fecal microbiota from younger mice into older mice improved hematopoietic stem cell function and restored lymphoid differentiation potential.</p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>HLA-E-restricted immune response in EBV infection, the role of NRX-0492 in CLL, and NSAIDs for bone marrow failure in Ghosal Hematodiaphyseal Dysplasia</title>
      <itunes:season>5</itunes:season>
      <podcast:season>5</podcast:season>
      <itunes:title>HLA-E-restricted immune response in EBV infection, the role of NRX-0492 in CLL, and NSAIDs for bone marrow failure in Ghosal Hematodiaphyseal Dysplasia</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">4d94f323-1782-43ec-bd06-db4124a98872</guid>
      <link>https://share.transistor.fm/s/8f7a418b</link>
      <description>
        <![CDATA[<p>In this week’s episode we’ll learn how HLA-E-restricted immune responses help control Epstein-Barr virus infection, discuss the activity of NRX-0492 in chronic lymphoblastic leukemia, and learn more about the efficacy of non-steroid inflammatory drugs in the treatment of bone marrow failure associated with Ghosal Hematodiaphyseal Dysplasia.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week’s episode we’ll learn how HLA-E-restricted immune responses help control Epstein-Barr virus infection, discuss the activity of NRX-0492 in chronic lymphoblastic leukemia, and learn more about the efficacy of non-steroid inflammatory drugs in the treatment of bone marrow failure associated with Ghosal Hematodiaphyseal Dysplasia.</p>]]>
      </content:encoded>
      <pubDate>Thu, 30 Mar 2023 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/8f7a418b/4c4a6749.mp3" length="22364220" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1396</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week’s episode we’ll learn how HLA-E-restricted immune responses help control Epstein-Barr virus infection, discuss the activity of NRX-0492 in chronic lymphoblastic leukemia, and learn more about the efficacy of non-steroid inflammatory drugs in the treatment of bone marrow failure associated with Ghosal Hematodiaphyseal Dysplasia.</p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Review Series on Germ Line Predisposition to Hematologic Malignancy</title>
      <itunes:season>5</itunes:season>
      <podcast:season>5</podcast:season>
      <itunes:title>Review Series on Germ Line Predisposition to Hematologic Malignancy</itunes:title>
      <itunes:episodeType>bonus</itunes:episodeType>
      <guid isPermaLink="false">6220aed7-1d3a-44e1-8e75-62e5e90e85a8</guid>
      <link>https://share.transistor.fm/s/9acd2996</link>
      <description>
        <![CDATA[<p>In this bonus episode Associate Editor, Dr. Mario Cazzola discusses the review series on Germline predisposition to hematologic malignancies with authors, Dr. Lucy Godley, Dr. Anna Brown, and Dr. Dennis Hickstein.   </p><p><a href="https://ashpublications.org/blood/article/141/13/1509/494487/Introduction-to-a-review-series-on-germ-line?searchresult=1">Review Series on Germ Line Predisposition to Hematologic Malignancy</a></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this bonus episode Associate Editor, Dr. Mario Cazzola discusses the review series on Germline predisposition to hematologic malignancies with authors, Dr. Lucy Godley, Dr. Anna Brown, and Dr. Dennis Hickstein.   </p><p><a href="https://ashpublications.org/blood/article/141/13/1509/494487/Introduction-to-a-review-series-on-germ-line?searchresult=1">Review Series on Germ Line Predisposition to Hematologic Malignancy</a></p>]]>
      </content:encoded>
      <pubDate>Thu, 30 Mar 2023 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/9acd2996/d4280310.mp3" length="40153162" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/D0Vk7s2IpolzA3Hdxg6d2Ip6ryY9-OX3HMw0gKIxYzA/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS9kZTAy/ODJhMmM4OTE1OWQ0/MzlkMGVkODkxNDgz/YjBkNy5qcGc.jpg"/>
      <itunes:duration>2006</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this bonus episode Associate Editor, Dr. Mario Cazzola discusses the review series on Germline predisposition to hematologic malignancies with authors, Dr. Lucy Godley, Dr. Anna Brown, and Dr. Dennis Hickstein.   </p><p><a href="https://ashpublications.org/blood/article/141/13/1509/494487/Introduction-to-a-review-series-on-germ-line?searchresult=1">Review Series on Germ Line Predisposition to Hematologic Malignancy</a></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title> Anti-malaria benefit of hydroxyurea in SCA, IL-22 in the treatment in lower GI acute GVHD, and FLT3-ITD changes depend on context in AML</title>
      <itunes:season>5</itunes:season>
      <podcast:season>5</podcast:season>
      <itunes:title> Anti-malaria benefit of hydroxyurea in SCA, IL-22 in the treatment in lower GI acute GVHD, and FLT3-ITD changes depend on context in AML</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">2677988a-02ca-442d-9401-8b668689e3a7</guid>
      <link>https://share.transistor.fm/s/0673d7ab</link>
      <description>
        <![CDATA[<p>In this week’s episode we will review a study in sub-Saharan Africa where treatment of sickle cell anemia with hydroxyurea is associated with a lower incidence of malaria. New research suggests mild myelosuppression associated with hydroxyurea treatment may actually have a salutary effect. Next, a potential new treatment approach in lower GI acute GVHD. Adding an interleukin-22 therapy to corticosteroid treatment was well tolerated with a high rate of response in this very challenging patient population. Finally, common AML driver mutations such as<em> FLT3ITD</em> (or internal tandem duplications) orchestrate distinct transcriptional and epigenetic programs based on different genetic contexts. In the context of a common pediatric AML mutation, <em>FLT3ITD</em> selectively activated type I interferon signaling, suggesting a distinct therapeutic vulnerability.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week’s episode we will review a study in sub-Saharan Africa where treatment of sickle cell anemia with hydroxyurea is associated with a lower incidence of malaria. New research suggests mild myelosuppression associated with hydroxyurea treatment may actually have a salutary effect. Next, a potential new treatment approach in lower GI acute GVHD. Adding an interleukin-22 therapy to corticosteroid treatment was well tolerated with a high rate of response in this very challenging patient population. Finally, common AML driver mutations such as<em> FLT3ITD</em> (or internal tandem duplications) orchestrate distinct transcriptional and epigenetic programs based on different genetic contexts. In the context of a common pediatric AML mutation, <em>FLT3ITD</em> selectively activated type I interferon signaling, suggesting a distinct therapeutic vulnerability.</p>]]>
      </content:encoded>
      <pubDate>Thu, 23 Mar 2023 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/0673d7ab/c887c1c9.mp3" length="17364750" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1083</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week’s episode we will review a study in sub-Saharan Africa where treatment of sickle cell anemia with hydroxyurea is associated with a lower incidence of malaria. New research suggests mild myelosuppression associated with hydroxyurea treatment may actually have a salutary effect. Next, a potential new treatment approach in lower GI acute GVHD. Adding an interleukin-22 therapy to corticosteroid treatment was well tolerated with a high rate of response in this very challenging patient population. Finally, common AML driver mutations such as<em> FLT3ITD</em> (or internal tandem duplications) orchestrate distinct transcriptional and epigenetic programs based on different genetic contexts. In the context of a common pediatric AML mutation, <em>FLT3ITD</em> selectively activated type I interferon signaling, suggesting a distinct therapeutic vulnerability.</p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Single-cell genotyping of MDS/CMML clonal output, VTE risk in diffuse glioma, and Del(1p32) is an adverse prognostic factor in myeloma</title>
      <itunes:season>5</itunes:season>
      <podcast:season>5</podcast:season>
      <itunes:title>Single-cell genotyping of MDS/CMML clonal output, VTE risk in diffuse glioma, and Del(1p32) is an adverse prognostic factor in myeloma</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">1c96a875-1e9b-41ac-9ffb-8a6c4eb5e39f</guid>
      <link>https://share.transistor.fm/s/f817d7df</link>
      <description>
        <![CDATA[<p>In this week’s episode we’ll discuss how azacytidine therapy influences the contributions of mutated HSC clones to hematopoiesis in MDS and CMML, learn more about the risk of venous thromboembolism in patients with adult-type diffuse glioma, and discuss the importance of 1p32 deletions as an independent and adverse prognostic factor in myeloma.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week’s episode we’ll discuss how azacytidine therapy influences the contributions of mutated HSC clones to hematopoiesis in MDS and CMML, learn more about the risk of venous thromboembolism in patients with adult-type diffuse glioma, and discuss the importance of 1p32 deletions as an independent and adverse prognostic factor in myeloma.</p>]]>
      </content:encoded>
      <pubDate>Thu, 16 Mar 2023 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/f817d7df/bf7ed3f6.mp3" length="20077957" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1253</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week’s episode we’ll discuss how azacytidine therapy influences the contributions of mutated HSC clones to hematopoiesis in MDS and CMML, learn more about the risk of venous thromboembolism in patients with adult-type diffuse glioma, and discuss the importance of 1p32 deletions as an independent and adverse prognostic factor in myeloma.</p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>RUNX1 isoform imbalance drives ML-DS, VWF-binding RNA aptamer for hemophilia A treatment, and EZH1/2 inhibitor valemetostat in relapsed/refractory ATL</title>
      <itunes:season>5</itunes:season>
      <podcast:season>5</podcast:season>
      <itunes:title>RUNX1 isoform imbalance drives ML-DS, VWF-binding RNA aptamer for hemophilia A treatment, and EZH1/2 inhibitor valemetostat in relapsed/refractory ATL</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">e3d103fa-ee3e-44a5-ae9f-51c5eb1bcc0d</guid>
      <link>https://share.transistor.fm/s/1a06af33</link>
      <description>
        <![CDATA[<p>In this week’s episode we will review an imbalance among RUNX1 isoforms is key to the pathogenesis of trisomy 21-associated myeloid leukemia, raising the possibility that equilibrium could be restored genetically or pharmacologically. Next, an RNA aptamer demonstrating promising results in patients with hemophilia A. Lastly, phase 2 data on valemetostat, a selective inhibitor of EZH1 and 2, in relapsed or refractory adult T-cell leukemia/lymphoma.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week’s episode we will review an imbalance among RUNX1 isoforms is key to the pathogenesis of trisomy 21-associated myeloid leukemia, raising the possibility that equilibrium could be restored genetically or pharmacologically. Next, an RNA aptamer demonstrating promising results in patients with hemophilia A. Lastly, phase 2 data on valemetostat, a selective inhibitor of EZH1 and 2, in relapsed or refractory adult T-cell leukemia/lymphoma.</p>]]>
      </content:encoded>
      <pubDate>Thu, 09 Mar 2023 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/1a06af33/0baf84f7.mp3" length="16642574" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1038</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week’s episode we will review an imbalance among RUNX1 isoforms is key to the pathogenesis of trisomy 21-associated myeloid leukemia, raising the possibility that equilibrium could be restored genetically or pharmacologically. Next, an RNA aptamer demonstrating promising results in patients with hemophilia A. Lastly, phase 2 data on valemetostat, a selective inhibitor of EZH1 and 2, in relapsed or refractory adult T-cell leukemia/lymphoma.</p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Phase 3 trial of leniolisib in activated PI3Kδ syndrome, dabrafenib plus trametinib in relapsed/refractory hairy cell leukemia, and TγδLGL leukemia as a more symptomatic subset of leukemia</title>
      <itunes:season>5</itunes:season>
      <podcast:season>5</podcast:season>
      <itunes:title>Phase 3 trial of leniolisib in activated PI3Kδ syndrome, dabrafenib plus trametinib in relapsed/refractory hairy cell leukemia, and TγδLGL leukemia as a more symptomatic subset of leukemia</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">df6552d3-612d-46c8-83a3-c70626298ca5</guid>
      <link>https://share.transistor.fm/s/2c90855d</link>
      <description>
        <![CDATA[<p>In this week’s episode, we’ll discuss the findings from a phase 3 trial of PI3Kδ inhibitor leniolisib in activated PI3Kd syndrome, learn more about the efficacy and safety of dabrafenib plus trametinib in relapsed/refractory <em>BRAF V600E</em> mutation-positive hairy cell leukemia, and review the findings from a study conducted in an international cohort of patients with Tγδ LGL leukemia.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week’s episode, we’ll discuss the findings from a phase 3 trial of PI3Kδ inhibitor leniolisib in activated PI3Kd syndrome, learn more about the efficacy and safety of dabrafenib plus trametinib in relapsed/refractory <em>BRAF V600E</em> mutation-positive hairy cell leukemia, and review the findings from a study conducted in an international cohort of patients with Tγδ LGL leukemia.</p>]]>
      </content:encoded>
      <pubDate>Thu, 02 Mar 2023 13:00:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/2c90855d/0c0cb85f.mp3" length="21104227" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1317</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week’s episode, we’ll discuss the findings from a phase 3 trial of PI3Kδ inhibitor leniolisib in activated PI3Kd syndrome, learn more about the efficacy and safety of dabrafenib plus trametinib in relapsed/refractory <em>BRAF V600E</em> mutation-positive hairy cell leukemia, and review the findings from a study conducted in an international cohort of patients with Tγδ LGL leukemia.</p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Review Series on Banked Allogeneic Immune Effector Cells</title>
      <itunes:season>5</itunes:season>
      <podcast:season>5</podcast:season>
      <itunes:title>Review Series on Banked Allogeneic Immune Effector Cells</itunes:title>
      <itunes:episodeType>bonus</itunes:episodeType>
      <guid isPermaLink="false">5bf67cce-61ba-437f-8595-f381a96373d0</guid>
      <link>https://share.transistor.fm/s/328654a5</link>
      <description>
        <![CDATA[<p>In this bonus episode Associate Editor, Dr. Helen Heslop discusses Banked Allogeneic Immune Effector Cells with <em>Blood </em>author Dr. Jeffrey Miller.  </p><p><a href="https://ashpublications.org/blood/article/141/8/811/494021/Introduction-to-a-review-series-on-banked?searchresult=1">Review Series on Banked Allogeneic Immune Effector Cells</a></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this bonus episode Associate Editor, Dr. Helen Heslop discusses Banked Allogeneic Immune Effector Cells with <em>Blood </em>author Dr. Jeffrey Miller.  </p><p><a href="https://ashpublications.org/blood/article/141/8/811/494021/Introduction-to-a-review-series-on-banked?searchresult=1">Review Series on Banked Allogeneic Immune Effector Cells</a></p>]]>
      </content:encoded>
      <pubDate>Thu, 23 Feb 2023 12:35:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/328654a5/22835fdf.mp3" length="26120678" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/NAI8VyiX85ggZfz0I1asdFgO_dOP3N4PFpukRrzH4Vw/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS9jZTg2/ZTUxOTY2Y2VjN2Qz/NTczOTk3MDM2ODIx/YWE4ZC5qcGc.jpg"/>
      <itunes:duration>1304</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this bonus episode Associate Editor, Dr. Helen Heslop discusses Banked Allogeneic Immune Effector Cells with <em>Blood </em>author Dr. Jeffrey Miller.  </p><p><a href="https://ashpublications.org/blood/article/141/8/811/494021/Introduction-to-a-review-series-on-banked?searchresult=1">Review Series on Banked Allogeneic Immune Effector Cells</a></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Hydroxyurea for secondary stroke prevention in SCD, mutant CALR as a rogue cytokine in MPNs, and parsing pathobiology in Burkitt lymphoma</title>
      <itunes:season>5</itunes:season>
      <podcast:season>5</podcast:season>
      <itunes:title>Hydroxyurea for secondary stroke prevention in SCD, mutant CALR as a rogue cytokine in MPNs, and parsing pathobiology in Burkitt lymphoma</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">cbf99457-c88c-4f2c-be2d-d866122c4f22</guid>
      <link>https://share.transistor.fm/s/c74b4858</link>
      <description>
        <![CDATA[<p>In this week’s episode we will first review a new clinical trial evidence that for patients with sickle cell anemia in resource limited settings, both low and moderate dose hydroxyurea are effective for secondary stroke prevention. Next, a research article showing how secreted mutant calreticulin functions as a “rogue cytokine” in myeloproliferative neoplasms, acting in a paracrine manner to promote growth of nearby tumor cells. Finally, we’ll review new research on the pathobiology of adult and pediatric Burkitt lymphoma. With the help of whole-genome sequencing, investigators unraveled distinct subgroups, which may provide a new framework for epidemiology, diagnosis, and treatment of these lymphomas.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week’s episode we will first review a new clinical trial evidence that for patients with sickle cell anemia in resource limited settings, both low and moderate dose hydroxyurea are effective for secondary stroke prevention. Next, a research article showing how secreted mutant calreticulin functions as a “rogue cytokine” in myeloproliferative neoplasms, acting in a paracrine manner to promote growth of nearby tumor cells. Finally, we’ll review new research on the pathobiology of adult and pediatric Burkitt lymphoma. With the help of whole-genome sequencing, investigators unraveled distinct subgroups, which may provide a new framework for epidemiology, diagnosis, and treatment of these lymphomas.</p>]]>
      </content:encoded>
      <pubDate>Thu, 23 Feb 2023 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/c74b4858/23716910.mp3" length="16067537" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1002</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week’s episode we will first review a new clinical trial evidence that for patients with sickle cell anemia in resource limited settings, both low and moderate dose hydroxyurea are effective for secondary stroke prevention. Next, a research article showing how secreted mutant calreticulin functions as a “rogue cytokine” in myeloproliferative neoplasms, acting in a paracrine manner to promote growth of nearby tumor cells. Finally, we’ll review new research on the pathobiology of adult and pediatric Burkitt lymphoma. With the help of whole-genome sequencing, investigators unraveled distinct subgroups, which may provide a new framework for epidemiology, diagnosis, and treatment of these lymphomas.</p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>HSCT for hypomorphic RAG deficiency, EBV-driven lymphoid neoplasms in pediatric ALL, and clonal hematopoiesis and recurrent vascular events in stroke patients</title>
      <itunes:season>5</itunes:season>
      <podcast:season>5</podcast:season>
      <itunes:title>HSCT for hypomorphic RAG deficiency, EBV-driven lymphoid neoplasms in pediatric ALL, and clonal hematopoiesis and recurrent vascular events in stroke patients</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">a0e06902-f65c-415a-90ad-75459091fc29</guid>
      <link>https://share.transistor.fm/s/911eadbe</link>
      <description>
        <![CDATA[<p>In this week’s episode we’ll discuss the benefits of early diagnosis and hematopoietic stem cell transplant in patients with hypomorphic RAG deficiency, learn more about EBV-driven lymphoid neoplasms associated with pediatric ALL maintenance therapy, and analyze the associations between clonal hematopoiesis and recurrent vascular events and death in patients with ischemic stroke. </p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week’s episode we’ll discuss the benefits of early diagnosis and hematopoietic stem cell transplant in patients with hypomorphic RAG deficiency, learn more about EBV-driven lymphoid neoplasms associated with pediatric ALL maintenance therapy, and analyze the associations between clonal hematopoiesis and recurrent vascular events and death in patients with ischemic stroke. </p>]]>
      </content:encoded>
      <pubDate>Thu, 16 Feb 2023 12:50:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/911eadbe/078bd9d4.mp3" length="19490008" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1216</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week’s episode we’ll discuss the benefits of early diagnosis and hematopoietic stem cell transplant in patients with hypomorphic RAG deficiency, learn more about EBV-driven lymphoid neoplasms associated with pediatric ALL maintenance therapy, and analyze the associations between clonal hematopoiesis and recurrent vascular events and death in patients with ischemic stroke. </p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>MRD dynamics during ixazomib maintenance in MM, disparities in CAR T-cell therapy for ALL, and BAX variants and resistance to BH3-mimetics in AML </title>
      <itunes:season>5</itunes:season>
      <podcast:season>5</podcast:season>
      <itunes:title>MRD dynamics during ixazomib maintenance in MM, disparities in CAR T-cell therapy for ALL, and BAX variants and resistance to BH3-mimetics in AML </itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">3b23edc7-8a8d-48e9-8862-3ed89cdcbda8</guid>
      <link>https://share.transistor.fm/s/75a2850f</link>
      <description>
        <![CDATA[<p>In this week's episode, we’ll discuss the dynamics of measurable residual disease, or MRD, over time in myeloma patients undergoing ixazomib maintenance. Serial measurements were feasible and provided more detailed risk stratification than single timepoint measurements—findings that could have implications for the use of MRD to guide treatment duration. Up next, a research article exploring the relationships between poverty, and lack of neighborhood opportunity, with outcomes of CAR T -cell therapy in children with acute lymphoblastic leukemia. The findings suggest opportunities for interventions to improve access for less socioeconomically advantaged children. Finally, we’ll review a report demonstrating that acquired mutations in the pro-apoptotic effector protein BAX are common in patients with AML treated with venetoclax. These and other research observations reveal BAX variants as a hurdle to the long-term success of BCL2-targeted therapy in this disease.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this week's episode, we’ll discuss the dynamics of measurable residual disease, or MRD, over time in myeloma patients undergoing ixazomib maintenance. Serial measurements were feasible and provided more detailed risk stratification than single timepoint measurements—findings that could have implications for the use of MRD to guide treatment duration. Up next, a research article exploring the relationships between poverty, and lack of neighborhood opportunity, with outcomes of CAR T -cell therapy in children with acute lymphoblastic leukemia. The findings suggest opportunities for interventions to improve access for less socioeconomically advantaged children. Finally, we’ll review a report demonstrating that acquired mutations in the pro-apoptotic effector protein BAX are common in patients with AML treated with venetoclax. These and other research observations reveal BAX variants as a hurdle to the long-term success of BCL2-targeted therapy in this disease.</p>]]>
      </content:encoded>
      <pubDate>Thu, 09 Feb 2023 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/75a2850f/40d59fdd.mp3" length="18626409" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1162</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this week's episode, we’ll discuss the dynamics of measurable residual disease, or MRD, over time in myeloma patients undergoing ixazomib maintenance. Serial measurements were feasible and provided more detailed risk stratification than single timepoint measurements—findings that could have implications for the use of MRD to guide treatment duration. Up next, a research article exploring the relationships between poverty, and lack of neighborhood opportunity, with outcomes of CAR T -cell therapy in children with acute lymphoblastic leukemia. The findings suggest opportunities for interventions to improve access for less socioeconomically advantaged children. Finally, we’ll review a report demonstrating that acquired mutations in the pro-apoptotic effector protein BAX are common in patients with AML treated with venetoclax. These and other research observations reveal BAX variants as a hurdle to the long-term success of BCL2-targeted therapy in this disease.</p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Itacitinib monotherapy for GVHD, the role of ERG in EVI1-driven AML, and germline DDX41 mutations in myeloid neoplasms</title>
      <itunes:season>5</itunes:season>
      <podcast:season>5</podcast:season>
      <itunes:title>Itacitinib monotherapy for GVHD, the role of ERG in EVI1-driven AML, and germline DDX41 mutations in myeloid neoplasms</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">0e9b0091-7254-40fa-8d1b-538ca985f31b</guid>
      <link>https://share.transistor.fm/s/95462b60</link>
      <description>
        <![CDATA[In this week's episode, we’ll discuss the safety and efficacy of itacitinib monotherapy in low-risk acute GVHD, learn how ERG was discovered to be a key transcriptional target in EVI1-driven AML, and define a unique subtype of myeloid neoplasms characterized by germline DDX41 mutations.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week's episode, we’ll discuss the safety and efficacy of itacitinib monotherapy in low-risk acute GVHD, learn how ERG was discovered to be a key transcriptional target in EVI1-driven AML, and define a unique subtype of myeloid neoplasms characterized by germline DDX41 mutations.]]>
      </content:encoded>
      <pubDate>Thu, 02 Feb 2023 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/95462b60/6a6160d7.mp3" length="21443694" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1338</itunes:duration>
      <itunes:summary>In this week's episode, we’ll discuss the safety and efficacy of itacitinib monotherapy in low-risk acute GVHD, learn how ERG was discovered to be a key transcriptional target in EVI1-driven AML, and define a unique subtype of myeloid neoplasms characterized by germline DDX41 mutations.</itunes:summary>
      <itunes:subtitle>In this week's episode, we’ll discuss the safety and efficacy of itacitinib monotherapy in low-risk acute GVHD, learn how ERG was discovered to be a key transcriptional target in EVI1-driven AML, and define a unique subtype of myeloid neoplasms characteri</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Stem cell transplant for SCD normalizes brain blood flow, novel GALE variants disrupt platelet development, and revisiting risk classification in NPM1-mutant AML </title>
      <itunes:season>5</itunes:season>
      <podcast:season>5</podcast:season>
      <itunes:title>Stem cell transplant for SCD normalizes brain blood flow, novel GALE variants disrupt platelet development, and revisiting risk classification in NPM1-mutant AML </itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">7d931167-c8da-4dc8-8e6a-e6d4312e59a3</guid>
      <link>https://share.transistor.fm/s/b1f8b342</link>
      <description>
        <![CDATA[In this week’s episode, new research shows that in children with sickle cell disease, stem cell transplantation normalizes blood flow in the brain. The improvements in cerebral hemodynamics seen in this study may help explain the stroke protection seen following transplant in this high-risk patient population. Next up, a research article providing new insights on thrombocytopenia related to the GALE gene, including the identification of several previously unreported variants. The findings highlight the importance of GALE in the glycosylation of proteins that play a role in the production and function of platelets. Finally, we’ll review a brief report on NPM1-mutated AML with adverse cytogenetics in light of the updated ELN 2022 classification. In short, adverse-risk cytogenetics remain significantly associated with unfavorable prognosis under the refined definitions, supporting the recent categorization of this entity as adverse-risk.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, new research shows that in children with sickle cell disease, stem cell transplantation normalizes blood flow in the brain. The improvements in cerebral hemodynamics seen in this study may help explain the stroke protection seen following transplant in this high-risk patient population. Next up, a research article providing new insights on thrombocytopenia related to the GALE gene, including the identification of several previously unreported variants. The findings highlight the importance of GALE in the glycosylation of proteins that play a role in the production and function of platelets. Finally, we’ll review a brief report on NPM1-mutated AML with adverse cytogenetics in light of the updated ELN 2022 classification. In short, adverse-risk cytogenetics remain significantly associated with unfavorable prognosis under the refined definitions, supporting the recent categorization of this entity as adverse-risk.]]>
      </content:encoded>
      <pubDate>Thu, 26 Jan 2023 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/b1f8b342/d811c254.mp3" length="16705030" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1042</itunes:duration>
      <itunes:summary>In this week’s episode, new research shows that in children with sickle cell disease, stem cell transplantation normalizes blood flow in the brain. The improvements in cerebral hemodynamics seen in this study may help explain the stroke protection seen following transplant in this high-risk patient population. Next up, a research article providing new insights on thrombocytopenia related to the GALE gene, including the identification of several previously unreported variants. The findings highlight the importance of GALE in the glycosylation of proteins that play a role in the production and function of platelets. Finally, we’ll review a brief report on NPM1-mutated AML with adverse cytogenetics in light of the updated ELN 2022 classification. In short, adverse-risk cytogenetics remain significantly associated with unfavorable prognosis under the refined definitions, supporting the recent categorization of this entity as adverse-risk.</itunes:summary>
      <itunes:subtitle>In this week’s episode, new research shows that in children with sickle cell disease, stem cell transplantation normalizes blood flow in the brain. The improvements in cerebral hemodynamics seen in this study may help explain the stroke protection seen fo</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Review Series on Single-Cell Genomics</title>
      <itunes:season>5</itunes:season>
      <podcast:season>5</podcast:season>
      <itunes:title>Review Series on Single-Cell Genomics</itunes:title>
      <itunes:episodeType>bonus</itunes:episodeType>
      <guid isPermaLink="false">a845825a-d126-480c-9ff2-a8482c5838cb</guid>
      <link>https://share.transistor.fm/s/a9ea1b29</link>
      <description>
        <![CDATA[<p>In this bonus episode Associate Editor, Dr. Bertie Göttgens and Dr. Ravi Majeti discuss the series on Single Cell Genomics and Heme Malignancies-Leukemia/MPNs.   </p><p><a href="https://ashpublications.org/blood/article/141/4/323/486597/Introduction-to-a-review-series-on-single-cell?searchresult=1">Blood Review Series on Single-Cell Genomics</a></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this bonus episode Associate Editor, Dr. Bertie Göttgens and Dr. Ravi Majeti discuss the series on Single Cell Genomics and Heme Malignancies-Leukemia/MPNs.   </p><p><a href="https://ashpublications.org/blood/article/141/4/323/486597/Introduction-to-a-review-series-on-single-cell?searchresult=1">Blood Review Series on Single-Cell Genomics</a></p>]]>
      </content:encoded>
      <pubDate>Thu, 26 Jan 2023 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/a9ea1b29/4329fcd6.mp3" length="15912524" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/a4KltHgGCFhoWiB-IrTUCw5w-NiTGUrzdkxSf--Q8kI/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS82MWM0/MmU1MzNkZGU4YzM3/ODBjODYyOGY3OGYy/MTdhMC5qcGc.jpg"/>
      <itunes:duration>794</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this bonus episode Associate Editor, Dr. Bertie Göttgens and Dr. Ravi Majeti discuss the series on Single Cell Genomics and Heme Malignancies-Leukemia/MPNs.   </p><p><a href="https://ashpublications.org/blood/article/141/4/323/486597/Introduction-to-a-review-series-on-single-cell?searchresult=1">Blood Review Series on Single-Cell Genomics</a></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Allogeneic transplantation in older and infirm AML patients, cilta-cel in progressive multiple myeloma, and anti-CD20 therapy in relapsed TTP</title>
      <itunes:season>5</itunes:season>
      <podcast:season>5</podcast:season>
      <itunes:title>Allogeneic transplantation in older and infirm AML patients, cilta-cel in progressive multiple myeloma, and anti-CD20 therapy in relapsed TTP</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">9196c8c1-f3ad-4173-a077-649a0ccefbd5</guid>
      <link>https://share.transistor.fm/s/c9def917</link>
      <description>
        <![CDATA[In this week’s episode we’ll discuss the benefits of allogeneic hematopoietic stem cell transplantation in older and medically infirm patients with AML, learn more about the efficacy and safety of cilta-cel in patients with progressive multiple myeloma after exposure to other BCMA-targeting agents, and review the role of anti-CD20 therapy in relapsed immune-mediated thrombotic thrombocytopenic purpura.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode we’ll discuss the benefits of allogeneic hematopoietic stem cell transplantation in older and medically infirm patients with AML, learn more about the efficacy and safety of cilta-cel in patients with progressive multiple myeloma after exposure to other BCMA-targeting agents, and review the role of anti-CD20 therapy in relapsed immune-mediated thrombotic thrombocytopenic purpura.]]>
      </content:encoded>
      <pubDate>Thu, 19 Jan 2023 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/c9def917/188e47a0.mp3" length="20490195" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1278</itunes:duration>
      <itunes:summary>In this week’s episode we’ll discuss the benefits of allogeneic hematopoietic stem cell transplantation in older and medically infirm patients with AML, learn more about the efficacy and safety of cilta-cel in patients with progressive multiple myeloma after exposure to other BCMA-targeting agents, and review the role of anti-CD20 therapy in relapsed immune-mediated thrombotic thrombocytopenic purpura.</itunes:summary>
      <itunes:subtitle>In this week’s episode we’ll discuss the benefits of allogeneic hematopoietic stem cell transplantation in older and medically infirm patients with AML, learn more about the efficacy and safety of cilta-cel in patients with progressive multiple myeloma af</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Piezo antigens define a new blood group system, enasidenib in mutant-IDH2 relapsed/refractory AML, and breakthrough COVID-19 despite prophylaxis in B-cell malignancies</title>
      <itunes:season>5</itunes:season>
      <podcast:season>5</podcast:season>
      <itunes:title>Piezo antigens define a new blood group system, enasidenib in mutant-IDH2 relapsed/refractory AML, and breakthrough COVID-19 despite prophylaxis in B-cell malignancies</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">06f406bf-5c29-4402-87b8-9439e33ac923</guid>
      <link>https://share.transistor.fm/s/f8670cf7</link>
      <description>
        <![CDATA[In this week’s episode, we’ll discuss new research revealing that the mechanosensory ion channel Piezo1 is the elusive carrier molecule of the Er blood group antigens, thus establishing a new blood group system. Next, we review results of a randomized phase 3 trial of enasidenib versus conventional treatment in late-stage mutant-IDH2 relapsed or refractory AML. Although the primary endpoint of overall survival was not met, investigators say the risk benefit ratio remains positive. Finally, we’ll review a study showing a clinically significant risk of breakthrough COVID-19 infections in patients with B-cell malignancies despite vaccination and pre-exposure prophylaxis with tixagevimab-cilgavimab during the Omicron era. However, hospitalization rates in the study were low and no deaths were reported.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we’ll discuss new research revealing that the mechanosensory ion channel Piezo1 is the elusive carrier molecule of the Er blood group antigens, thus establishing a new blood group system. Next, we review results of a randomized phase 3 trial of enasidenib versus conventional treatment in late-stage mutant-IDH2 relapsed or refractory AML. Although the primary endpoint of overall survival was not met, investigators say the risk benefit ratio remains positive. Finally, we’ll review a study showing a clinically significant risk of breakthrough COVID-19 infections in patients with B-cell malignancies despite vaccination and pre-exposure prophylaxis with tixagevimab-cilgavimab during the Omicron era. However, hospitalization rates in the study were low and no deaths were reported.]]>
      </content:encoded>
      <pubDate>Thu, 12 Jan 2023 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/f8670cf7/93154045.mp3" length="16579375" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1034</itunes:duration>
      <itunes:summary>In this week’s episode, we’ll discuss new research revealing that the mechanosensory ion channel Piezo1 is the elusive carrier molecule of the Er blood group antigens, thus establishing a new blood group system. Next, we review results of a randomized phase 3 trial of enasidenib versus conventional treatment in late-stage mutant-IDH2 relapsed or refractory AML. Although the primary endpoint of overall survival was not met, investigators say the risk benefit ratio remains positive. Finally, we’ll review a study showing a clinically significant risk of breakthrough COVID-19 infections in patients with B-cell malignancies despite vaccination and pre-exposure prophylaxis with tixagevimab-cilgavimab during the Omicron era. However, hospitalization rates in the study were low and no deaths were reported.</itunes:summary>
      <itunes:subtitle>In this week’s episode, we’ll discuss new research revealing that the mechanosensory ion channel Piezo1 is the elusive carrier molecule of the Er blood group antigens, thus establishing a new blood group system. Next, we review results of a randomized pha</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Immune thrombocytopenia in pregnancy, ASCT in adults with inborn errors of immunity, and long-term health outcomes of childhood AML survivors</title>
      <itunes:season>5</itunes:season>
      <podcast:season>5</podcast:season>
      <itunes:title>Immune thrombocytopenia in pregnancy, ASCT in adults with inborn errors of immunity, and long-term health outcomes of childhood AML survivors</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">2fce0190-2731-4307-875d-0dcb5ac7abb7</guid>
      <link>https://share.transistor.fm/s/4428cca7</link>
      <description>
        <![CDATA[In this week’s episode we’ll discuss whether pregnancy increases the risk of bleeding in women with immune thrombocytopenia, compare the outcomes of allogeneic stem cell transplantation versus conservative management in adults with inborn errors of immunity, and learn more about the long-term health outcomes and late mortality in childhood AML survivors.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode we’ll discuss whether pregnancy increases the risk of bleeding in women with immune thrombocytopenia, compare the outcomes of allogeneic stem cell transplantation versus conservative management in adults with inborn errors of immunity, and learn more about the long-term health outcomes and late mortality in childhood AML survivors.]]>
      </content:encoded>
      <pubDate>Thu, 05 Jan 2023 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/4428cca7/47872e29.mp3" length="18617222" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1161</itunes:duration>
      <itunes:summary>In this week’s episode we’ll discuss whether pregnancy increases the risk of bleeding in women with immune thrombocytopenia, compare the outcomes of allogeneic stem cell transplantation versus conservative management in adults with inborn errors of immunity, and learn more about the long-term health outcomes and late mortality in childhood AML survivors.</itunes:summary>
      <itunes:subtitle>In this week’s episode we’ll discuss whether pregnancy increases the risk of bleeding in women with immune thrombocytopenia, compare the outcomes of allogeneic stem cell transplantation versus conservative management in adults with inborn errors of immuni</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>How I Treat Series: Management of High-risk Patients Following Allogeneic Transplant</title>
      <itunes:season>5</itunes:season>
      <podcast:season>5</podcast:season>
      <itunes:title>How I Treat Series: Management of High-risk Patients Following Allogeneic Transplant</itunes:title>
      <itunes:episodeType>bonus</itunes:episodeType>
      <guid isPermaLink="false">f28fc382-b2a9-4124-8a66-f323ac07eb01</guid>
      <link>https://share.transistor.fm/s/38886710</link>
      <description>
        <![CDATA[In this episode, Associate Editor, Dr. Robert Zeiser and Dr. Yi-Bin Chen discuss the series on How I Manage High-Risk Patients Following Allogeneic Hematopoietic Cell Transplantation.]]>
      </description>
      <content:encoded>
        <![CDATA[In this episode, Associate Editor, Dr. Robert Zeiser and Dr. Yi-Bin Chen discuss the series on How I Manage High-Risk Patients Following Allogeneic Hematopoietic Cell Transplantation.]]>
      </content:encoded>
      <pubDate>Thu, 05 Jan 2023 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/38886710/fe041102.mp3" length="25262598" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1262</itunes:duration>
      <itunes:summary>In this episode, Associate Editor, Dr. Robert Zeiser and Dr. Yi-Bin Chen discuss the series on How I Manage High-Risk Patients Following Allogeneic Hematopoietic Cell Transplantation.</itunes:summary>
      <itunes:subtitle>In this episode, Associate Editor, Dr. Robert Zeiser and Dr. Yi-Bin Chen discuss the series on How I Manage High-Risk Patients Following Allogeneic Hematopoietic Cell Transplantation.</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>IL-13/IL-4 signaling and fibrotic progression in myelofibrosis, VWF-targeted thrombolysis in acute ischemic stroke, and NK cell dysfunction in relapsed AML</title>
      <itunes:season>4</itunes:season>
      <podcast:season>4</podcast:season>
      <itunes:title>IL-13/IL-4 signaling and fibrotic progression in myelofibrosis, VWF-targeted thrombolysis in acute ischemic stroke, and NK cell dysfunction in relapsed AML</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">471f896e-22ca-416c-a8e9-a9836716ff0d</guid>
      <link>https://share.transistor.fm/s/6236f31a</link>
      <description>
        <![CDATA[In this week’s episode, we'll discuss involvement of IL-13 and IL-4 signaling in fibrotic progression of myelofibrosis; next, we review results on a novel agent using vWF-dependent mechanisms to lyse pathological thrombi in acute ischemic stroke. Finally, we’ll shed new light on findings that implicate the GARP-TGF-beta-1 pathway in the loss of natural killer cell cytotoxicity in relapsed AML. ]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we'll discuss involvement of IL-13 and IL-4 signaling in fibrotic progression of myelofibrosis; next, we review results on a novel agent using vWF-dependent mechanisms to lyse pathological thrombi in acute ischemic stroke. Finally, we’ll shed new light on findings that implicate the GARP-TGF-beta-1 pathway in the loss of natural killer cell cytotoxicity in relapsed AML. ]]>
      </content:encoded>
      <pubDate>Thu, 29 Dec 2022 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/6236f31a/896479c5.mp3" length="15436668" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>963</itunes:duration>
      <itunes:summary>In this week’s episode, we'll discuss involvement of IL-13 and IL-4 signaling in fibrotic progression of myelofibrosis; next, we review results on a novel agent using vWF-dependent mechanisms to lyse pathological thrombi in acute ischemic stroke. Finally, we’ll shed new light on findings that implicate the GARP-TGF-beta-1 pathway in the loss of natural killer cell cytotoxicity in relapsed AML. </itunes:summary>
      <itunes:subtitle>In this week’s episode, we'll discuss involvement of IL-13 and IL-4 signaling in fibrotic progression of myelofibrosis; next, we review results on a novel agent using vWF-dependent mechanisms to lyse pathological thrombi in acute ischemic stroke. Finally,</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Effects of iron repletion on donor RBC quality, long-term outcomes in relapsed/refractory hairy cell leukemia after vemurafenib, and off-the-shelf cryopreserved platelets for detecting HIT</title>
      <itunes:season>4</itunes:season>
      <podcast:season>4</podcast:season>
      <itunes:title>Effects of iron repletion on donor RBC quality, long-term outcomes in relapsed/refractory hairy cell leukemia after vemurafenib, and off-the-shelf cryopreserved platelets for detecting HIT</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">b6b88798-f30d-4749-9f81-6c2112937bb4</guid>
      <link>https://share.transistor.fm/s/9bcc9f00</link>
      <description>
        <![CDATA[In this week’s episode, we’ll discuss the effects of iron repletion on the quality of donated red blood cells and donor well-being, learn more about the long-term outcomes of patients with relapsed/refractory hairy cell leukemia after vemurafenib monotherapy, and discuss the use of off-the-shelf cryopreserved platelets for detecting heparin-induced thrombocytopenia and vaccine-induced immune thrombotic thrombocytopenia.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we’ll discuss the effects of iron repletion on the quality of donated red blood cells and donor well-being, learn more about the long-term outcomes of patients with relapsed/refractory hairy cell leukemia after vemurafenib monotherapy, and discuss the use of off-the-shelf cryopreserved platelets for detecting heparin-induced thrombocytopenia and vaccine-induced immune thrombotic thrombocytopenia.]]>
      </content:encoded>
      <pubDate>Thu, 22 Dec 2022 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/9bcc9f00/4a01dc10.mp3" length="20385001" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1272</itunes:duration>
      <itunes:summary>In this week’s episode, we’ll discuss the effects of iron repletion on the quality of donated red blood cells and donor well-being, learn more about the long-term outcomes of patients with relapsed/refractory hairy cell leukemia after vemurafenib monotherapy, and discuss the use of off-the-shelf cryopreserved platelets for detecting heparin-induced thrombocytopenia and vaccine-induced immune thrombotic thrombocytopenia.</itunes:summary>
      <itunes:subtitle>In this week’s episode, we’ll discuss the effects of iron repletion on the quality of donated red blood cells and donor well-being, learn more about the long-term outcomes of patients with relapsed/refractory hairy cell leukemia after vemurafenib monother</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Germline predisposition variants occur in all age groups in MDS, αβ-haplo-HCT excels in children with acute leukemias/MDS, and poor outcomes after CAR T cell failure in B-cell lymphomas</title>
      <itunes:season>4</itunes:season>
      <podcast:season>4</podcast:season>
      <itunes:title>Germline predisposition variants occur in all age groups in MDS, αβ-haplo-HCT excels in children with acute leukemias/MDS, and poor outcomes after CAR T cell failure in B-cell lymphomas</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">9e2ededf-d9d0-4cb6-b454-39b91efca692</guid>
      <link>https://share.transistor.fm/s/f4127efd</link>
      <description>
        <![CDATA[In this week’s episode, research shows that in patients with myelodysplastic syndromes, or MDS, the frequency of pathogenic or likely pathogenic germline variants is relatively high across all age groups, not just younger patients. Based on these results, it may be time to expand genetic testing to all patients.  Next, we'll review primary results of a prospective, multicenter study of children with acute leukemias or MDS who underwent T-cell receptor αβ+ and CD19+ cell-depleted haploidentical HCT with reduced-toxicity conditioning. Finally, an emerging unmet need related to CAR T cell therapy: patients who progress after receiving CAR T cells have poor outcomes and no agreed upon standard of care. We’ll review findings from a large registry study demonstrating infrequent responses to post-CAR T cell treatment and short survival times, highlighting a need for novel strategies. ]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, research shows that in patients with myelodysplastic syndromes, or MDS, the frequency of pathogenic or likely pathogenic germline variants is relatively high across all age groups, not just younger patients. Based on these results, it may be time to expand genetic testing to all patients.  Next, we'll review primary results of a prospective, multicenter study of children with acute leukemias or MDS who underwent T-cell receptor αβ+ and CD19+ cell-depleted haploidentical HCT with reduced-toxicity conditioning. Finally, an emerging unmet need related to CAR T cell therapy: patients who progress after receiving CAR T cells have poor outcomes and no agreed upon standard of care. We’ll review findings from a large registry study demonstrating infrequent responses to post-CAR T cell treatment and short survival times, highlighting a need for novel strategies. ]]>
      </content:encoded>
      <pubDate>Thu, 15 Dec 2022 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/f4127efd/cd7a2918.mp3" length="19706745" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1229</itunes:duration>
      <itunes:summary>In this week’s episode, research shows that in patients with myelodysplastic syndromes, or MDS, the frequency of pathogenic or likely pathogenic germline variants is relatively high across all age groups, not just younger patients. Based on these results, it may be time to expand genetic testing to all patients.  Next, we'll review primary results of a prospective, multicenter study of children with acute leukemias or MDS who underwent T-cell receptor αβ+ and CD19+ cell-depleted haploidentical HCT with reduced-toxicity conditioning. Finally, an emerging unmet need related to CAR T cell therapy: patients who progress after receiving CAR T cells have poor outcomes and no agreed upon standard of care. We’ll review findings from a large registry study demonstrating infrequent responses to post-CAR T cell treatment and short survival times, highlighting a need for novel strategies. </itunes:summary>
      <itunes:subtitle>In this week’s episode, research shows that in patients with myelodysplastic syndromes, or MDS, the frequency of pathogenic or likely pathogenic germline variants is relatively high across all age groups, not just younger patients. Based on these results,</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Predicting VTE in multiple myeloma, azithromycin promotes relapse after HSCT, and dual antigen targeted NK cells in B cell malignancies</title>
      <itunes:season>4</itunes:season>
      <podcast:season>4</podcast:season>
      <itunes:title>Predicting VTE in multiple myeloma, azithromycin promotes relapse after HSCT, and dual antigen targeted NK cells in B cell malignancies</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">bfe2f203-8cda-4a06-acc3-e183ceafb43c</guid>
      <link>https://share.transistor.fm/s/3e176b4a</link>
      <description>
        <![CDATA[In this week’s episode we’ll discuss the newly developed PRISM score for risk prediction of venous thromboembolism in multiple myeloma, learn more about relapse-promoting effects of azithromycin after allogeneic stem cell transplantation, and discuss the efficacy of off-the-shelf natural killer cells in preventing antigen escape in lymphoma and leukemia.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode we’ll discuss the newly developed PRISM score for risk prediction of venous thromboembolism in multiple myeloma, learn more about relapse-promoting effects of azithromycin after allogeneic stem cell transplantation, and discuss the efficacy of off-the-shelf natural killer cells in preventing antigen escape in lymphoma and leukemia.]]>
      </content:encoded>
      <pubDate>Thu, 08 Dec 2022 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/3e176b4a/850d373a.mp3" length="19368702" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1208</itunes:duration>
      <itunes:summary>In this week’s episode we’ll discuss the newly developed PRISM score for risk prediction of venous thromboembolism in multiple myeloma, learn more about relapse-promoting effects of azithromycin after allogeneic stem cell transplantation, and discuss the efficacy of off-the-shelf natural killer cells in preventing antigen escape in lymphoma and leukemia.</itunes:summary>
      <itunes:subtitle>In this week’s episode we’ll discuss the newly developed PRISM score for risk prediction of venous thromboembolism in multiple myeloma, learn more about relapse-promoting effects of azithromycin after allogeneic stem cell transplantation, and discuss the </itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Using MRD to guide CLL treatment intensity, donor NK cells boost immune reconstitution after haplo-BMT, and  EZH2 drives retinoic acid resistance in variant APL</title>
      <itunes:season>4</itunes:season>
      <podcast:season>4</podcast:season>
      <itunes:title>Using MRD to guide CLL treatment intensity, donor NK cells boost immune reconstitution after haplo-BMT, and  EZH2 drives retinoic acid resistance in variant APL</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">3a8505f6-d3c5-414a-868f-5f3e1310d21a</guid>
      <link>https://share.transistor.fm/s/54d9d1b3</link>
      <description>
        <![CDATA[In this week’s episode we discuss encouraging results of a phase 2 study using a sequential ibrutinib-venetoclax treatment approach driven by MRD findings in individual patients with chronic lymphocytic leukemia, or CLL. Next, we examine new research demonstrating that donor natural killer cells trigger release of beta-2 microglobulin by host dendritic cells, greatly accelerating donor-derived immune reconstitution after allogeneic bone marrow transplant in mice. We’ll look at the therapeutic implications of this as well. Lastly, we review a study of retinoic acid resistance in a mouse model of variant acute promyelocytic leukemia. Resistance was driven by the epigenetic regulator EZH2, which suggests the potential for an EZH2-targeted therapeutic approach.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode we discuss encouraging results of a phase 2 study using a sequential ibrutinib-venetoclax treatment approach driven by MRD findings in individual patients with chronic lymphocytic leukemia, or CLL. Next, we examine new research demonstrating that donor natural killer cells trigger release of beta-2 microglobulin by host dendritic cells, greatly accelerating donor-derived immune reconstitution after allogeneic bone marrow transplant in mice. We’ll look at the therapeutic implications of this as well. Lastly, we review a study of retinoic acid resistance in a mouse model of variant acute promyelocytic leukemia. Resistance was driven by the epigenetic regulator EZH2, which suggests the potential for an EZH2-targeted therapeutic approach.]]>
      </content:encoded>
      <pubDate>Thu, 01 Dec 2022 13:15:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/54d9d1b3/44fab11b.mp3" length="17533062" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1094</itunes:duration>
      <itunes:summary>In this week’s episode we discuss encouraging results of a phase 2 study using a sequential ibrutinib-venetoclax treatment approach driven by MRD findings in individual patients with chronic lymphocytic leukemia, or CLL. Next, we examine new research demonstrating that donor natural killer cells trigger release of beta-2 microglobulin by host dendritic cells, greatly accelerating donor-derived immune reconstitution after allogeneic bone marrow transplant in mice. We’ll look at the therapeutic implications of this as well. Lastly, we review a study of retinoic acid resistance in a mouse model of variant acute promyelocytic leukemia. Resistance was driven by the epigenetic regulator EZH2, which suggests the potential for an EZH2-targeted therapeutic approach.</itunes:summary>
      <itunes:subtitle>In this week’s episode we discuss encouraging results of a phase 2 study using a sequential ibrutinib-venetoclax treatment approach driven by MRD findings in individual patients with chronic lymphocytic leukemia, or CLL. Next, we examine new research demo</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Tolerability of CD19 CAR T cells in lymphoma, causes of platelet spherocytosis, and using prebiotics to reduce GVHD</title>
      <itunes:season>4</itunes:season>
      <podcast:season>4</podcast:season>
      <itunes:title>Tolerability of CD19 CAR T cells in lymphoma, causes of platelet spherocytosis, and using prebiotics to reduce GVHD</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">cb0f77f1-005e-4473-8cdf-b8f6f21416b9</guid>
      <link>https://share.transistor.fm/s/cd6b2faa</link>
      <description>
        <![CDATA[In this week’s episode, we’ll discuss patient-reported outcomes in the phase 3 ZUMA-7 trial of CAR T-cell therapy in second-line relapsed/refractory large B-cell lymphoma, learn more about the association between the loss of α4A- and β1-tubulin and severe platelet spherocytosis, and discuss the interaction between prebiotic galactooligosaccharides and mouse gut microbiota in graft-versus-host disease.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we’ll discuss patient-reported outcomes in the phase 3 ZUMA-7 trial of CAR T-cell therapy in second-line relapsed/refractory large B-cell lymphoma, learn more about the association between the loss of α4A- and β1-tubulin and severe platelet spherocytosis, and discuss the interaction between prebiotic galactooligosaccharides and mouse gut microbiota in graft-versus-host disease.]]>
      </content:encoded>
      <pubDate>Thu, 24 Nov 2022 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/cd6b2faa/9b0da1a6.mp3" length="18873477" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1177</itunes:duration>
      <itunes:summary>In this week’s episode, we’ll discuss patient-reported outcomes in the phase 3 ZUMA-7 trial of CAR T-cell therapy in second-line relapsed/refractory large B-cell lymphoma, learn more about the association between the loss of α4A- and β1-tubulin and severe platelet spherocytosis, and discuss the interaction between prebiotic galactooligosaccharides and mouse gut microbiota in graft-versus-host disease.</itunes:summary>
      <itunes:subtitle>In this week’s episode, we’ll discuss patient-reported outcomes in the phase 3 ZUMA-7 trial of CAR T-cell therapy in second-line relapsed/refractory large B-cell lymphoma, learn more about the association between the loss of α4A- and β1-tubulin and severe</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Transplant in adult Ph+ ALL, acalabrutinib and ventricular arrythmias, and antibody prevention of fetal/neonatal alloimmune thrombocytopenia </title>
      <itunes:season>4</itunes:season>
      <podcast:season>4</podcast:season>
      <itunes:title>Transplant in adult Ph+ ALL, acalabrutinib and ventricular arrythmias, and antibody prevention of fetal/neonatal alloimmune thrombocytopenia </itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">8d02162e-e403-45ea-aa6d-e0399af3e7ee</guid>
      <link>https://share.transistor.fm/s/5c5b6dad</link>
      <description>
        <![CDATA[In this week’s episode we discuss the role of allogeneic transplant in adult patients with Philadelphia chromosome-positive acute lymphoblastic leukemia. In a retrospective study, transplant provided no survival benefit in patients with rapid and deep responses to induction therapy that included BCR-ABL1 inhibitors. Up next, we discuss the evidence for an increased risk of ventricular arrythmias with use of acalabrutinib, which has emerged as a class effect of Bruton tyrosine kinase inhibitors. Lastly, we examine a novel, alloantigen-specific model to test the efficacy of a prophylactic treatment strategy for preventing fetal/neonatal alloimmune thrombocytopenia.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode we discuss the role of allogeneic transplant in adult patients with Philadelphia chromosome-positive acute lymphoblastic leukemia. In a retrospective study, transplant provided no survival benefit in patients with rapid and deep responses to induction therapy that included BCR-ABL1 inhibitors. Up next, we discuss the evidence for an increased risk of ventricular arrythmias with use of acalabrutinib, which has emerged as a class effect of Bruton tyrosine kinase inhibitors. Lastly, we examine a novel, alloantigen-specific model to test the efficacy of a prophylactic treatment strategy for preventing fetal/neonatal alloimmune thrombocytopenia.]]>
      </content:encoded>
      <pubDate>Thu, 17 Nov 2022 12:45:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/5c5b6dad/83f203e5.mp3" length="18031457" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1125</itunes:duration>
      <itunes:summary>In this week’s episode we discuss the role of allogeneic transplant in adult patients with Philadelphia chromosome-positive acute lymphoblastic leukemia. In a retrospective study, transplant provided no survival benefit in patients with rapid and deep responses to induction therapy that included BCR-ABL1 inhibitors. Up next, we discuss the evidence for an increased risk of ventricular arrythmias with use of acalabrutinib, which has emerged as a class effect of Bruton tyrosine kinase inhibitors. Lastly, we examine a novel, alloantigen-specific model to test the efficacy of a prophylactic treatment strategy for preventing fetal/neonatal alloimmune thrombocytopenia.</itunes:summary>
      <itunes:subtitle>In this week’s episode we discuss the role of allogeneic transplant in adult patients with Philadelphia chromosome-positive acute lymphoblastic leukemia. In a retrospective study, transplant provided no survival benefit in patients with rapid and deep res</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Restricting dietary methionine in AML, transferrin in high altitude-induced hypercoagulability, and LIF as protection against GVHD</title>
      <itunes:season>4</itunes:season>
      <podcast:season>4</podcast:season>
      <itunes:title>Restricting dietary methionine in AML, transferrin in high altitude-induced hypercoagulability, and LIF as protection against GVHD</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">51a4437e-905e-402b-a5b8-dfba6f8a94cd</guid>
      <link>https://share.transistor.fm/s/d12a768d</link>
      <description>
        <![CDATA[In this week’s episode, we’ll learn more about the impact of dietary methionine restriction on the progression of AML, discuss transferrin upregulation as a cause of high-altitude-induced hypercoagulability, and learn more about the protective effects of leukemia inhibitory factor against graft-versus-host disease. ]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we’ll learn more about the impact of dietary methionine restriction on the progression of AML, discuss transferrin upregulation as a cause of high-altitude-induced hypercoagulability, and learn more about the protective effects of leukemia inhibitory factor against graft-versus-host disease. ]]>
      </content:encoded>
      <pubDate>Thu, 10 Nov 2022 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/d12a768d/4a479149.mp3" length="18218391" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1137</itunes:duration>
      <itunes:summary>In this week’s episode, we’ll learn more about the impact of dietary methionine restriction on the progression of AML, discuss transferrin upregulation as a cause of high-altitude-induced hypercoagulability, and learn more about the protective effects of leukemia inhibitory factor against graft-versus-host disease. </itunes:summary>
      <itunes:subtitle>In this week’s episode, we’ll learn more about the impact of dietary methionine restriction on the progression of AML, discuss transferrin upregulation as a cause of high-altitude-induced hypercoagulability, and learn more about the protective effects of </itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Sickle hemoglobin activates monocytes via TLR4, germinal center B cells provide a niche for T-cell lymphoma, and a combination immunosuppression regimen for acquired hemophilia A</title>
      <itunes:season>4</itunes:season>
      <podcast:season>4</podcast:season>
      <itunes:title>Sickle hemoglobin activates monocytes via TLR4, germinal center B cells provide a niche for T-cell lymphoma, and a combination immunosuppression regimen for acquired hemophilia A</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">67c0457b-1ff0-4ace-8204-823e1a6a759f</guid>
      <link>https://share.transistor.fm/s/a58c88d6</link>
      <description>
        <![CDATA[In this week’s episode, we will review a study that cell-free hemoglobin S was found to induce high levels of pro-inflammatory cytokine production in monocytes. The effect is mediated by Toll-like receptor 4, or TLR4, suggesting intriguing therapeutic possibilities for sickle cell disease.  Secondly, germinal center B cells with aberrant expression profiles undergo independent clonal evolution in the microenvironment of angioimmunoblastic T-cell lymphoma. New findings published in Blood elucidate mechanisms of disease pathogenesis and uncover a new potential target for treatment. Finally, an upfront combination of three immunosuppressive agents was highly effective and well tolerated in patients with acquired hemophilia A. Although prospective studies are needed, the triple regimen could be an attractive treatment option, particularly for elderly and frail patients.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we will review a study that cell-free hemoglobin S was found to induce high levels of pro-inflammatory cytokine production in monocytes. The effect is mediated by Toll-like receptor 4, or TLR4, suggesting intriguing therapeutic possibilities for sickle cell disease.  Secondly, germinal center B cells with aberrant expression profiles undergo independent clonal evolution in the microenvironment of angioimmunoblastic T-cell lymphoma. New findings published in Blood elucidate mechanisms of disease pathogenesis and uncover a new potential target for treatment. Finally, an upfront combination of three immunosuppressive agents was highly effective and well tolerated in patients with acquired hemophilia A. Although prospective studies are needed, the triple regimen could be an attractive treatment option, particularly for elderly and frail patients.]]>
      </content:encoded>
      <pubDate>Thu, 03 Nov 2022 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/a58c88d6/db400e6b.mp3" length="16943579" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1057</itunes:duration>
      <itunes:summary>In this week’s episode, we will review a study that cell-free hemoglobin S was found to induce high levels of pro-inflammatory cytokine production in monocytes. The effect is mediated by Toll-like receptor 4, or TLR4, suggesting intriguing therapeutic possibilities for sickle cell disease.  Secondly, germinal center B cells with aberrant expression profiles undergo independent clonal evolution in the microenvironment of angioimmunoblastic T-cell lymphoma. New findings published in Blood elucidate mechanisms of disease pathogenesis and uncover a new potential target for treatment. Finally, an upfront combination of three immunosuppressive agents was highly effective and well tolerated in patients with acquired hemophilia A. Although prospective studies are needed, the triple regimen could be an attractive treatment option, particularly for elderly and frail patients.</itunes:summary>
      <itunes:subtitle>In this week’s episode, we will review a study that cell-free hemoglobin S was found to induce high levels of pro-inflammatory cytokine production in monocytes. The effect is mediated by Toll-like receptor 4, or TLR4, suggesting intriguing therapeutic pos</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Lineage switching in MLL/AF4 leukemia, ibrutinib in mantle cell lymphoma with CNS relapse, and gilteritinib plus azacitidine in newly diagnosed FLT3-mutated AML</title>
      <itunes:season>4</itunes:season>
      <podcast:season>4</podcast:season>
      <itunes:title>Lineage switching in MLL/AF4 leukemia, ibrutinib in mantle cell lymphoma with CNS relapse, and gilteritinib plus azacitidine in newly diagnosed FLT3-mutated AML</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">debbd1fa-5beb-4e69-a596-a7dd4815ea5e</guid>
      <link>https://share.transistor.fm/s/684251a2</link>
      <description>
        <![CDATA[In this week’s episode we’ll discuss the role of epigenetic regulator genes in lineage switching in MLL/AF4 leukemia, learn more about the efficacy of ibrutinib in mantle cell lymphoma with central nervous system relapse, and discuss the findings from a phase 3 trial of gilteritinib plus azacitidine in patients with newly diagnosed FLT3-mutated AML.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode we’ll discuss the role of epigenetic regulator genes in lineage switching in MLL/AF4 leukemia, learn more about the efficacy of ibrutinib in mantle cell lymphoma with central nervous system relapse, and discuss the findings from a phase 3 trial of gilteritinib plus azacitidine in patients with newly diagnosed FLT3-mutated AML.]]>
      </content:encoded>
      <pubDate>Thu, 27 Oct 2022 12:45:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/684251a2/6f005589.mp3" length="22077954" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1378</itunes:duration>
      <itunes:summary>In this week’s episode we’ll discuss the role of epigenetic regulator genes in lineage switching in MLL/AF4 leukemia, learn more about the efficacy of ibrutinib in mantle cell lymphoma with central nervous system relapse, and discuss the findings from a phase 3 trial of gilteritinib plus azacitidine in patients with newly diagnosed FLT3-mutated AML.</itunes:summary>
      <itunes:subtitle>In this week’s episode we’ll discuss the role of epigenetic regulator genes in lineage switching in MLL/AF4 leukemia, learn more about the efficacy of ibrutinib in mantle cell lymphoma with central nervous system relapse, and discuss the findings from a p</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Lenalidomide and subsequent TP53-mutated myeloid neoplasms, abnormal uterine bleeding after VTE, and novel tri-specific antibody for B-ALL</title>
      <itunes:season>4</itunes:season>
      <podcast:season>4</podcast:season>
      <itunes:title>Lenalidomide and subsequent TP53-mutated myeloid neoplasms, abnormal uterine bleeding after VTE, and novel tri-specific antibody for B-ALL</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">28708f12-39bb-4ca2-a53c-572ff8050411</guid>
      <link>https://share.transistor.fm/s/a3ff594a</link>
      <description>
        <![CDATA[In this week’s episode we will review data showing that lenalidomide promotes development of TP53-mutated, therapy-related myeloid neoplasms. Next, we'll discuss the first prospective study to evaluate abnormal uterine bleeding in women starting anticoagulation for venous thromboembolism. Lastly, we'll review an optimized tri-specific antibody that overcomes immune escape and enhances therapeutic efficacy in a patient-derived xenograft model of B-cell ALL.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode we will review data showing that lenalidomide promotes development of TP53-mutated, therapy-related myeloid neoplasms. Next, we'll discuss the first prospective study to evaluate abnormal uterine bleeding in women starting anticoagulation for venous thromboembolism. Lastly, we'll review an optimized tri-specific antibody that overcomes immune escape and enhances therapeutic efficacy in a patient-derived xenograft model of B-cell ALL.]]>
      </content:encoded>
      <pubDate>Thu, 20 Oct 2022 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/a3ff594a/a5b5e058.mp3" length="17204306" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1073</itunes:duration>
      <itunes:summary>In this week’s episode we will review data showing that lenalidomide promotes development of TP53-mutated, therapy-related myeloid neoplasms. Next, we'll discuss the first prospective study to evaluate abnormal uterine bleeding in women starting anticoagulation for venous thromboembolism. Lastly, we'll review an optimized tri-specific antibody that overcomes immune escape and enhances therapeutic efficacy in a patient-derived xenograft model of B-cell ALL.</itunes:summary>
      <itunes:subtitle>In this week’s episode we will review data showing that lenalidomide promotes development of TP53-mutated, therapy-related myeloid neoplasms. Next, we'll discuss the first prospective study to evaluate abnormal uterine bleeding in women starting anticoagu</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Review Series on Megakaryopoiesis and Platelet Production</title>
      <itunes:season>4</itunes:season>
      <podcast:season>4</podcast:season>
      <itunes:title>Review Series on Megakaryopoiesis and Platelet Production</itunes:title>
      <itunes:episodeType>bonus</itunes:episodeType>
      <guid isPermaLink="false">622d8002-2715-43c4-a1c5-1f37f8184c53</guid>
      <link>https://share.transistor.fm/s/78634d5b</link>
      <description>
        <![CDATA[<p>Megakaryocytes contribute to multiple processes in the body, including platelet production and regulation of hematopoietic stem cells. Therefore, it is not surprising that alterations in this lineage not only affect platelets but also impact hematopoiesis in other ways. Fortunately, our understanding of megakaryocyte biology has increased significantly with the advent of advanced technologies such as next-generation sequencing and sophisticated microscopy.</p><p><a href="https://ashpublications.org/blood/article/139/22/3227/484188/Introduction-to-a-review-series-on?searchresult=1">Blood Review Series on Megakaryopoiesis and Platelet Production</a></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>Megakaryocytes contribute to multiple processes in the body, including platelet production and regulation of hematopoietic stem cells. Therefore, it is not surprising that alterations in this lineage not only affect platelets but also impact hematopoiesis in other ways. Fortunately, our understanding of megakaryocyte biology has increased significantly with the advent of advanced technologies such as next-generation sequencing and sophisticated microscopy.</p><p><a href="https://ashpublications.org/blood/article/139/22/3227/484188/Introduction-to-a-review-series-on?searchresult=1">Blood Review Series on Megakaryopoiesis and Platelet Production</a></p>]]>
      </content:encoded>
      <pubDate>Thu, 20 Oct 2022 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/78634d5b/38b240ae.mp3" length="25923022" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/3AwqSMtqMyJ0ecNKGuAYjMHu64H2RfV35dE7zbJJ5qY/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS9iZDNm/MzRjZjgxMDNlZjE0/MzEyNTRjM2JmOTM2/Yjk1Yi5qcGc.jpg"/>
      <itunes:duration>1295</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>Megakaryocytes contribute to multiple processes in the body, including platelet production and regulation of hematopoietic stem cells. Therefore, it is not surprising that alterations in this lineage not only affect platelets but also impact hematopoiesis in other ways. Fortunately, our understanding of megakaryocyte biology has increased significantly with the advent of advanced technologies such as next-generation sequencing and sophisticated microscopy.</p><p><a href="https://ashpublications.org/blood/article/139/22/3227/484188/Introduction-to-a-review-series-on?searchresult=1">Blood Review Series on Megakaryopoiesis and Platelet Production</a></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Prognostic impact of NPM1 and FLT3 mutations in AML, progression of monoclonal B cell lymphocytosis, and creating RBCs with rare blood types in the laboratory</title>
      <itunes:season>4</itunes:season>
      <podcast:season>4</podcast:season>
      <itunes:title>Prognostic impact of NPM1 and FLT3 mutations in AML, progression of monoclonal B cell lymphocytosis, and creating RBCs with rare blood types in the laboratory</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">31ae5536-5c2f-4d30-a4e9-021616f6bc24</guid>
      <link>https://share.transistor.fm/s/f798472b</link>
      <description>
        <![CDATA[In this week’s episode we’ll learn more about the prognostic impact of NPM1 and FLT3 mutations in AML, discuss the progression and survival of monoclonal B-cell lymphocytosis, and learn more about the use of red blood cells derived from pluripotent stem cells in transfusion medicine.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode we’ll learn more about the prognostic impact of NPM1 and FLT3 mutations in AML, discuss the progression and survival of monoclonal B-cell lymphocytosis, and learn more about the use of red blood cells derived from pluripotent stem cells in transfusion medicine.]]>
      </content:encoded>
      <pubDate>Thu, 13 Oct 2022 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/f798472b/4daed19e.mp3" length="20510887" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1280</itunes:duration>
      <itunes:summary>In this week’s episode we’ll learn more about the prognostic impact of NPM1 and FLT3 mutations in AML, discuss the progression and survival of monoclonal B-cell lymphocytosis, and learn more about the use of red blood cells derived from pluripotent stem cells in transfusion medicine.</itunes:summary>
      <itunes:subtitle>In this week’s episode we’ll learn more about the prognostic impact of NPM1 and FLT3 mutations in AML, discuss the progression and survival of monoclonal B-cell lymphocytosis, and learn more about the use of red blood cells derived from pluripotent stem c</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Transplant outcomes in adults with immunodeficiencies and erythroblastic islands as niches for terminal erythropoiesis and granulopoiesis</title>
      <itunes:season>4</itunes:season>
      <podcast:season>4</podcast:season>
      <itunes:title>Transplant outcomes in adults with immunodeficiencies and erythroblastic islands as niches for terminal erythropoiesis and granulopoiesis</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">7256a7a2-ae75-47cc-9213-ab7fb2f27ef0</guid>
      <link>https://share.transistor.fm/s/787a1e46</link>
      <description>
        <![CDATA[In this week’s episode we'll review results of the largest retrospective study to date of allogeneic transplantation in adult patients with inborn errors of immunity. We’ll then discuss intriguing new research demonstrating that erythroblastic islands in the bone marrow foster granulopoiesis alongside terminal erythropoiesis—which lays a foundation for better understanding how blood cell production is regulated within these niches.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode we'll review results of the largest retrospective study to date of allogeneic transplantation in adult patients with inborn errors of immunity. We’ll then discuss intriguing new research demonstrating that erythroblastic islands in the bone marrow foster granulopoiesis alongside terminal erythropoiesis—which lays a foundation for better understanding how blood cell production is regulated within these niches.]]>
      </content:encoded>
      <pubDate>Fri, 07 Oct 2022 00:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/787a1e46/f17f8834.mp3" length="13493194" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>841</itunes:duration>
      <itunes:summary>In this week’s episode we'll review results of the largest retrospective study to date of allogeneic transplantation in adult patients with inborn errors of immunity. We’ll then discuss intriguing new research demonstrating that erythroblastic islands in the bone marrow foster granulopoiesis alongside terminal erythropoiesis—which lays a foundation for better understanding how blood cell production is regulated within these niches.</itunes:summary>
      <itunes:subtitle>In this week’s episode we'll review results of the largest retrospective study to date of allogeneic transplantation in adult patients with inborn errors of immunity. We’ll then discuss intriguing new research demonstrating that erythroblastic islands in </itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Ticagrelor in pediatric sickle cell disease, UBA1 translation impacts severity of VEXAS syndrome, and T-cell immunity and chemotherapy response in ALL</title>
      <itunes:season>4</itunes:season>
      <podcast:season>4</podcast:season>
      <itunes:title>Ticagrelor in pediatric sickle cell disease, UBA1 translation impacts severity of VEXAS syndrome, and T-cell immunity and chemotherapy response in ALL</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">6607daee-f83c-4091-9506-d75396432de0</guid>
      <link>https://share.transistor.fm/s/314b76f6</link>
      <description>
        <![CDATA[In this week’s episode we’ll learn more about the negative findings from the phase three trial of ticagrelor for preventing vaso-occlusive crises in children with sickle cell disease, discuss how residual cytoplasmic UBA1 contributes to the pathogenesis of VEXAS syndrome, and learn more about the impact of host T-cell immunity in the response to chemotherapy in pediatric ALL. ]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode we’ll learn more about the negative findings from the phase three trial of ticagrelor for preventing vaso-occlusive crises in children with sickle cell disease, discuss how residual cytoplasmic UBA1 contributes to the pathogenesis of VEXAS syndrome, and learn more about the impact of host T-cell immunity in the response to chemotherapy in pediatric ALL. ]]>
      </content:encoded>
      <pubDate>Thu, 29 Sep 2022 12:35:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/314b76f6/763437df.mp3" length="20814081" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1299</itunes:duration>
      <itunes:summary>In this week’s episode we’ll learn more about the negative findings from the phase three trial of ticagrelor for preventing vaso-occlusive crises in children with sickle cell disease, discuss how residual cytoplasmic UBA1 contributes to the pathogenesis of VEXAS syndrome, and learn more about the impact of host T-cell immunity in the response to chemotherapy in pediatric ALL. </itunes:summary>
      <itunes:subtitle>In this week’s episode we’ll learn more about the negative findings from the phase three trial of ticagrelor for preventing vaso-occlusive crises in children with sickle cell disease, discuss how residual cytoplasmic UBA1 contributes to the pathogenesis o</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Race affects treatment outcomes in iTTP, 2022 ELN AML recommendations, and a comprehensive MRD assessment in MCL</title>
      <itunes:season>4</itunes:season>
      <podcast:season>4</podcast:season>
      <itunes:title>Race affects treatment outcomes in iTTP, 2022 ELN AML recommendations, and a comprehensive MRD assessment in MCL</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">1f8bcea1-65ae-45ed-801b-118a6337555c</guid>
      <link>https://share.transistor.fm/s/654f56e1</link>
      <description>
        <![CDATA[In this week’s episode we’ll take a quick look at the latest European Leukemia Net recommendations for the diagnosis and management of acute myeloid leukemia. We’ll also describe a comprehensive analysis of a phase 3 trial indicating that MRD is a strong outcome predictor over the entire natural history of mantle cell lymphoma, setting the stage for potential risk stratification tools that may be suitable for MRD-guided treatment. We'll also look at a large US registry study demonstrating that black patients with idiopathic thrombotic thrombocytopenic purpura had a shorter time to relapse and less response to rituximab compared to white patients. These findings suggest a potential need for closer monitoring, early retreatment, and alternative treatments.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode we’ll take a quick look at the latest European Leukemia Net recommendations for the diagnosis and management of acute myeloid leukemia. We’ll also describe a comprehensive analysis of a phase 3 trial indicating that MRD is a strong outcome predictor over the entire natural history of mantle cell lymphoma, setting the stage for potential risk stratification tools that may be suitable for MRD-guided treatment. We'll also look at a large US registry study demonstrating that black patients with idiopathic thrombotic thrombocytopenic purpura had a shorter time to relapse and less response to rituximab compared to white patients. These findings suggest a potential need for closer monitoring, early retreatment, and alternative treatments.]]>
      </content:encoded>
      <pubDate>Thu, 22 Sep 2022 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/654f56e1/12175c6c.mp3" length="19626935" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1224</itunes:duration>
      <itunes:summary>In this week’s episode we’ll take a quick look at the latest European Leukemia Net recommendations for the diagnosis and management of acute myeloid leukemia. We’ll also describe a comprehensive analysis of a phase 3 trial indicating that MRD is a strong outcome predictor over the entire natural history of mantle cell lymphoma, setting the stage for potential risk stratification tools that may be suitable for MRD-guided treatment. We'll also look at a large US registry study demonstrating that black patients with idiopathic thrombotic thrombocytopenic purpura had a shorter time to relapse and less response to rituximab compared to white patients. These findings suggest a potential need for closer monitoring, early retreatment, and alternative treatments.</itunes:summary>
      <itunes:subtitle>In this week’s episode we’ll take a quick look at the latest European Leukemia Net recommendations for the diagnosis and management of acute myeloid leukemia. We’ll also describe a comprehensive analysis of a phase 3 trial indicating that MRD is a strong </itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>The International Consensus Classification:  An interview with Drs. Daniel Arber and Elias Campo</title>
      <itunes:season>4</itunes:season>
      <podcast:season>4</podcast:season>
      <itunes:title>The International Consensus Classification:  An interview with Drs. Daniel Arber and Elias Campo</itunes:title>
      <itunes:episodeType>bonus</itunes:episodeType>
      <guid isPermaLink="false">524b82c7-147b-47d3-a3e2-a5496df1c607</guid>
      <link>https://share.transistor.fm/s/9d8f30c1</link>
      <description>
        <![CDATA[In this bonus episode, we’re delighted to have Dr. Dan Arber from the University of Chicago and Dr. Elias Campo from the University of Barcelona. With members of the Clinical Advisory Committee, Drs. Arber and Campo led efforts to develop the new International Consensus Classification for what we refer to as the ICC.]]>
      </description>
      <content:encoded>
        <![CDATA[In this bonus episode, we’re delighted to have Dr. Dan Arber from the University of Chicago and Dr. Elias Campo from the University of Barcelona. With members of the Clinical Advisory Committee, Drs. Arber and Campo led efforts to develop the new International Consensus Classification for what we refer to as the ICC.]]>
      </content:encoded>
      <pubDate>Thu, 15 Sep 2022 14:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/9d8f30c1/190b62ec.mp3" length="27502055" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1144</itunes:duration>
      <itunes:summary>In this bonus episode, we’re delighted to have Dr. Dan Arber from the University of Chicago and Dr. Elias Campo from the University of Barcelona. With members of the Clinical Advisory Committee, Drs. Arber and Campo led efforts to develop the new International Consensus Classification for what we refer to as the ICC.</itunes:summary>
      <itunes:subtitle>In this bonus episode, we’re delighted to have Dr. Dan Arber from the University of Chicago and Dr. Elias Campo from the University of Barcelona. With members of the Clinical Advisory Committee, Drs. Arber and Campo led efforts to develop the new Internat</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Tranexamic acid prophylaxis in heme malignancies, N-glycosylation as a therapeutic vulnerability in CALR-mutant MPN, and myocardial fibrosis in sickle cell anemia</title>
      <itunes:season>4</itunes:season>
      <podcast:season>4</podcast:season>
      <itunes:title>Tranexamic acid prophylaxis in heme malignancies, N-glycosylation as a therapeutic vulnerability in CALR-mutant MPN, and myocardial fibrosis in sickle cell anemia</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">b0d1fcd9-b340-440e-9a72-3fa71dcab670</guid>
      <link>https://share.transistor.fm/s/73cf4ca6</link>
      <description>
        <![CDATA[In this week’s episode we’ll discuss the efficacy of tranexamic acid prophylaxis in patients with hematological malignancies, learn more about N-glycosylation as a therapeutic vulnerability in CALR-mutant MPN, and discuss how early initiation of disease-modifying therapy may be able to reduce myocardial fibrosis in sickle cell anemia.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode we’ll discuss the efficacy of tranexamic acid prophylaxis in patients with hematological malignancies, learn more about N-glycosylation as a therapeutic vulnerability in CALR-mutant MPN, and discuss how early initiation of disease-modifying therapy may be able to reduce myocardial fibrosis in sickle cell anemia.]]>
      </content:encoded>
      <pubDate>Thu, 15 Sep 2022 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/73cf4ca6/ebe1d1d0.mp3" length="20210904" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1261</itunes:duration>
      <itunes:summary>In this week’s episode we’ll discuss the efficacy of tranexamic acid prophylaxis in patients with hematological malignancies, learn more about N-glycosylation as a therapeutic vulnerability in CALR-mutant MPN, and discuss how early initiation of disease-modifying therapy may be able to reduce myocardial fibrosis in sickle cell anemia.</itunes:summary>
      <itunes:subtitle>In this week’s episode we’ll discuss the efficacy of tranexamic acid prophylaxis in patients with hematological malignancies, learn more about N-glycosylation as a therapeutic vulnerability in CALR-mutant MPN, and discuss how early initiation of disease-m</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Rest alleviates T-cell exhaustion by bispecific antibodies, exercise vs desmopressin in mild hemophilia A, and targeting MDM2 to enhance antileukemia immunity after transplant</title>
      <itunes:season>4</itunes:season>
      <podcast:season>4</podcast:season>
      <itunes:title>Rest alleviates T-cell exhaustion by bispecific antibodies, exercise vs desmopressin in mild hemophilia A, and targeting MDM2 to enhance antileukemia immunity after transplant</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">00eea2e3-e2bc-47da-97e1-7232f380901e</guid>
      <link>https://share.transistor.fm/s/a4e8810b</link>
      <description>
        <![CDATA[]]>
      </description>
      <content:encoded>
        <![CDATA[]]>
      </content:encoded>
      <pubDate>Thu, 08 Sep 2022 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/a4e8810b/b9194b9b.mp3" length="17558294" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1095</itunes:duration>
      <itunes:summary>
        <![CDATA[]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Sutimlimab vs placebo in cold agglutinin disease, the impact of etoposide versus auto-transplant in PTCL, and the role of pulmonary NETs in sickle cell disease</title>
      <itunes:season>4</itunes:season>
      <podcast:season>4</podcast:season>
      <itunes:title>Sutimlimab vs placebo in cold agglutinin disease, the impact of etoposide versus auto-transplant in PTCL, and the role of pulmonary NETs in sickle cell disease</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">62c01c1f-2987-4900-ac4f-9ad4cefb0ffa</guid>
      <link>https://share.transistor.fm/s/0864c530</link>
      <description>
        <![CDATA[In this week’s episode, we review results of a randomized, placebo-controlled phase 3 trial demonstrating that targeted inhibition of C1s with the monoclonal antibody sutimlimab is effective and well tolerated in non-transfusion-dependent patients with cold agglutinin disease. We’ll also review a population-based study evaluating the impact of adding either etoposide or autologous stem cell transplantation to CHOP in young and fit patients with peripheral T cell lymphomas. Finally, we’ll review a paper that elucidates a mechanism of lung injury in sickle cell disease. It involves gasdermin-D-dependent production of neutrophil extracellular traps in the liver, which travel intravascularly to the lung, where they promote occlusion of the pulmonary microcirculation.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we review results of a randomized, placebo-controlled phase 3 trial demonstrating that targeted inhibition of C1s with the monoclonal antibody sutimlimab is effective and well tolerated in non-transfusion-dependent patients with cold agglutinin disease. We’ll also review a population-based study evaluating the impact of adding either etoposide or autologous stem cell transplantation to CHOP in young and fit patients with peripheral T cell lymphomas. Finally, we’ll review a paper that elucidates a mechanism of lung injury in sickle cell disease. It involves gasdermin-D-dependent production of neutrophil extracellular traps in the liver, which travel intravascularly to the lung, where they promote occlusion of the pulmonary microcirculation.]]>
      </content:encoded>
      <pubDate>Thu, 01 Sep 2022 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/0864c530/1fd56a8c.mp3" length="19829755" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1237</itunes:duration>
      <itunes:summary>In this week’s episode, we review results of a randomized, placebo-controlled phase 3 trial demonstrating that targeted inhibition of C1s with the monoclonal antibody sutimlimab is effective and well tolerated in non-transfusion-dependent patients with cold agglutinin disease. We’ll also review a population-based study evaluating the impact of adding either etoposide or autologous stem cell transplantation to CHOP in young and fit patients with peripheral T cell lymphomas. Finally, we’ll review a paper that elucidates a mechanism of lung injury in sickle cell disease. It involves gasdermin-D-dependent production of neutrophil extracellular traps in the liver, which travel intravascularly to the lung, where they promote occlusion of the pulmonary microcirculation.</itunes:summary>
      <itunes:subtitle>In this week’s episode, we review results of a randomized, placebo-controlled phase 3 trial demonstrating that targeted inhibition of C1s with the monoclonal antibody sutimlimab is effective and well tolerated in non-transfusion-dependent patients with co</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Rivaroxaban after cancer surgery, genetics and survival in severe aplastic anemia, and a 5-year follow up of rituximab-venetoclax in relapsed/refractory CLL</title>
      <itunes:season>4</itunes:season>
      <podcast:season>4</podcast:season>
      <itunes:title>Rivaroxaban after cancer surgery, genetics and survival in severe aplastic anemia, and a 5-year follow up of rituximab-venetoclax in relapsed/refractory CLL</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">b675d0e3-f7e4-458e-953c-096ae7e1ec85</guid>
      <link>https://share.transistor.fm/s/2cc9ebc1</link>
      <description>
        <![CDATA[In this week’s episode discuss the efficacy of rivaroxaban as antithrombotic prophylaxis after laparoscopic surgery for colorectal cancer, learn more about the association between genomic variants and survival outcomes after hematopoietic cell transplantation in severe aplastic anemia, and discuss the long-term safety and efficacy of fixed-duration venetoclax plus rituximab in relapsed/refractory CLL.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode discuss the efficacy of rivaroxaban as antithrombotic prophylaxis after laparoscopic surgery for colorectal cancer, learn more about the association between genomic variants and survival outcomes after hematopoietic cell transplantation in severe aplastic anemia, and discuss the long-term safety and efficacy of fixed-duration venetoclax plus rituximab in relapsed/refractory CLL.]]>
      </content:encoded>
      <pubDate>Thu, 25 Aug 2022 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/2cc9ebc1/8ff4d8b6.mp3" length="19064146" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1188</itunes:duration>
      <itunes:summary>In this week’s episode discuss the efficacy of rivaroxaban as antithrombotic prophylaxis after laparoscopic surgery for colorectal cancer, learn more about the association between genomic variants and survival outcomes after hematopoietic cell transplantation in severe aplastic anemia, and discuss the long-term safety and efficacy of fixed-duration venetoclax plus rituximab in relapsed/refractory CLL.</itunes:summary>
      <itunes:subtitle>In this week’s episode discuss the efficacy of rivaroxaban as antithrombotic prophylaxis after laparoscopic surgery for colorectal cancer, learn more about the association between genomic variants and survival outcomes after hematopoietic cell transplanta</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Stroke in hereditary TTP, and germline DDX41 variants as risk factors and prognostic markers in myeloid neoplasms</title>
      <itunes:season>4</itunes:season>
      <podcast:season>4</podcast:season>
      <itunes:title>Stroke in hereditary TTP, and germline DDX41 variants as risk factors and prognostic markers in myeloid neoplasms</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">15dbf5b4-47c3-4c83-a957-fa9eb8c56e82</guid>
      <link>https://share.transistor.fm/s/2ad44cd9</link>
      <description>
        <![CDATA[In this week’s episode, we’ll learn more about neuropsychiatric manifestations and stroke risk in hereditary TTP, discuss germline DDX41 variants as predisposing factors to myeloid neoplasms, and learn more about the prognostic impact of DDX41 mutations in adults with intensively treated AML. ]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we’ll learn more about neuropsychiatric manifestations and stroke risk in hereditary TTP, discuss germline DDX41 variants as predisposing factors to myeloid neoplasms, and learn more about the prognostic impact of DDX41 mutations in adults with intensively treated AML. ]]>
      </content:encoded>
      <pubDate>Thu, 18 Aug 2022 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/2ad44cd9/688b55c9.mp3" length="20425133" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1273</itunes:duration>
      <itunes:summary>In this week’s episode, we’ll learn more about neuropsychiatric manifestations and stroke risk in hereditary TTP, discuss germline DDX41 variants as predisposing factors to myeloid neoplasms, and learn more about the prognostic impact of DDX41 mutations in adults with intensively treated AML. </itunes:summary>
      <itunes:subtitle>In this week’s episode, we’ll learn more about neuropsychiatric manifestations and stroke risk in hereditary TTP, discuss germline DDX41 variants as predisposing factors to myeloid neoplasms, and learn more about the prognostic impact of DDX41 mutations i</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Cost effectiveness of first-line daratumumab in MM, base-edited CAR T cells for T-ALL, and the role of SETBP1 mutations in chronic neutrophilic leukemia</title>
      <itunes:season>4</itunes:season>
      <podcast:season>4</podcast:season>
      <itunes:title>Cost effectiveness of first-line daratumumab in MM, base-edited CAR T cells for T-ALL, and the role of SETBP1 mutations in chronic neutrophilic leukemia</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">2bbd3889-7ab1-459a-9048-deae7a599e22</guid>
      <link>https://share.transistor.fm/s/1b19b72a</link>
      <description>
        <![CDATA[In this week’s episode new research suggesting that, in patients with transplant-eligible multiple myeloma, adding daratumumab to first-line combination regimens may be a more cost effective strategy than saving it for second-line use. We’ll also review the work of researchers who applied base-editing technology to develop a complex and potent CAR T cell product for potential “off-the-shelf” use in patients with T-cell leukemias and other CD7-positive malignancies. Finally, we’ll review a paper that elucidates the role of SETBP1 mutations in chronic neutrophilic leukemia, pointing the way toward a potential multi-pronged therapeutic approach to this rare myeloproliferative neoplasm.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode new research suggesting that, in patients with transplant-eligible multiple myeloma, adding daratumumab to first-line combination regimens may be a more cost effective strategy than saving it for second-line use. We’ll also review the work of researchers who applied base-editing technology to develop a complex and potent CAR T cell product for potential “off-the-shelf” use in patients with T-cell leukemias and other CD7-positive malignancies. Finally, we’ll review a paper that elucidates the role of SETBP1 mutations in chronic neutrophilic leukemia, pointing the way toward a potential multi-pronged therapeutic approach to this rare myeloproliferative neoplasm.]]>
      </content:encoded>
      <pubDate>Thu, 11 Aug 2022 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/1b19b72a/027d19b2.mp3" length="18607883" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1160</itunes:duration>
      <itunes:summary>In this week’s episode new research suggesting that, in patients with transplant-eligible multiple myeloma, adding daratumumab to first-line combination regimens may be a more cost effective strategy than saving it for second-line use. We’ll also review the work of researchers who applied base-editing technology to develop a complex and potent CAR T cell product for potential “off-the-shelf” use in patients with T-cell leukemias and other CD7-positive malignancies. Finally, we’ll review a paper that elucidates the role of SETBP1 mutations in chronic neutrophilic leukemia, pointing the way toward a potential multi-pronged therapeutic approach to this rare myeloproliferative neoplasm.</itunes:summary>
      <itunes:subtitle>In this week’s episode new research suggesting that, in patients with transplant-eligible multiple myeloma, adding daratumumab to first-line combination regimens may be a more cost effective strategy than saving it for second-line use. We’ll also review t</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Immune thrombocytopenia and adenoviral SARS-COV2 vaccines, genomics, and a risk assessment model of anti-CD19 CAR T-cell treatment outcomes in lymphoma</title>
      <itunes:season>4</itunes:season>
      <podcast:season>4</podcast:season>
      <itunes:title>Immune thrombocytopenia and adenoviral SARS-COV2 vaccines, genomics, and a risk assessment model of anti-CD19 CAR T-cell treatment outcomes in lymphoma</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">0ca9bc84-fb00-400c-99d4-8dde414daf5a</guid>
      <link>https://share.transistor.fm/s/b70e8b64</link>
      <description>
        <![CDATA[In this week’s episode we’ll discuss the factors influencing the development of immune thrombocytopenia after administration of the ChAdOx1 nCov-19 vaccine, learn about the genomic features underlying anti-CD19 CAR T-cell treatment failure in lymphoma, and introduce a new predictive model for risk assessment before CAR T-cell therapy for large B-cell lymphoma.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode we’ll discuss the factors influencing the development of immune thrombocytopenia after administration of the ChAdOx1 nCov-19 vaccine, learn about the genomic features underlying anti-CD19 CAR T-cell treatment failure in lymphoma, and introduce a new predictive model for risk assessment before CAR T-cell therapy for large B-cell lymphoma.]]>
      </content:encoded>
      <pubDate>Thu, 04 Aug 2022 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/b70e8b64/8ade8649.mp3" length="19785449" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1233</itunes:duration>
      <itunes:summary>In this week’s episode we’ll discuss the factors influencing the development of immune thrombocytopenia after administration of the ChAdOx1 nCov-19 vaccine, learn about the genomic features underlying anti-CD19 CAR T-cell treatment failure in lymphoma, and introduce a new predictive model for risk assessment before CAR T-cell therapy for large B-cell lymphoma.</itunes:summary>
      <itunes:subtitle>In this week’s episode we’ll discuss the factors influencing the development of immune thrombocytopenia after administration of the ChAdOx1 nCov-19 vaccine, learn about the genomic features underlying anti-CD19 CAR T-cell treatment failure in lymphoma, an</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Naturally selected CD7 CAR T cell therapy for T-lineage malignancies, CD4+ T cell exhaustion and PD-L1 inhibition in B-ALL, and tPA-induced phosphorylation of occludin in stroke</title>
      <itunes:season>4</itunes:season>
      <podcast:season>4</podcast:season>
      <itunes:title>Naturally selected CD7 CAR T cell therapy for T-lineage malignancies, CD4+ T cell exhaustion and PD-L1 inhibition in B-ALL, and tPA-induced phosphorylation of occludin in stroke</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">47248391-c7d6-4259-a233-f61b44c796d4</guid>
      <link>https://share.transistor.fm/s/767d1f12</link>
      <description>
        <![CDATA[In this week’s episode we review a novel approach to generating autologous CD7-specific CAR T therapy for patients with T-cell malignancies that overcomes a key limitation: target-driven fratricide. We’ll also learn about new research pinpointing a key subset of exhausted CD4+ T cells in B- ALL, which also provides a rationale for combining tyrosine kinase inhibitors and PD-L1 blockers to reverse exhaustion and enhance leukemia clearance. Finally, we’ll discuss studies in a mouse model of acute ischemic stroke, showing that inhibiting phosphorylation of a tight junction protein in endothelial cells reduces risk of intracranial hemorrhage after treatment with recombinant tissue plasminogen activator.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode we review a novel approach to generating autologous CD7-specific CAR T therapy for patients with T-cell malignancies that overcomes a key limitation: target-driven fratricide. We’ll also learn about new research pinpointing a key subset of exhausted CD4+ T cells in B- ALL, which also provides a rationale for combining tyrosine kinase inhibitors and PD-L1 blockers to reverse exhaustion and enhance leukemia clearance. Finally, we’ll discuss studies in a mouse model of acute ischemic stroke, showing that inhibiting phosphorylation of a tight junction protein in endothelial cells reduces risk of intracranial hemorrhage after treatment with recombinant tissue plasminogen activator.]]>
      </content:encoded>
      <pubDate>Thu, 28 Jul 2022 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/767d1f12/e37ea420.mp3" length="17064861" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1063</itunes:duration>
      <itunes:summary>In this week’s episode we review a novel approach to generating autologous CD7-specific CAR T therapy for patients with T-cell malignancies that overcomes a key limitation: target-driven fratricide. We’ll also learn about new research pinpointing a key subset of exhausted CD4+ T cells in B- ALL, which also provides a rationale for combining tyrosine kinase inhibitors and PD-L1 blockers to reverse exhaustion and enhance leukemia clearance. Finally, we’ll discuss studies in a mouse model of acute ischemic stroke, showing that inhibiting phosphorylation of a tight junction protein in endothelial cells reduces risk of intracranial hemorrhage after treatment with recombinant tissue plasminogen activator.</itunes:summary>
      <itunes:subtitle>In this week’s episode we review a novel approach to generating autologous CD7-specific CAR T therapy for patients with T-cell malignancies that overcomes a key limitation: target-driven fratricide. We’ll also learn about new research pinpointing a key su</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Role of PIEZO1 in leukocyte extravasation, CD8+ T-cell activation in macrophage activation syndrome, and ABO O blood group as a novel risk factor for HIT</title>
      <itunes:season>4</itunes:season>
      <podcast:season>4</podcast:season>
      <itunes:title>Role of PIEZO1 in leukocyte extravasation, CD8+ T-cell activation in macrophage activation syndrome, and ABO O blood group as a novel risk factor for HIT</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">74790fac-940c-4ed2-9bb1-4fd2799e852f</guid>
      <link>https://share.transistor.fm/s/8e9da76b</link>
      <description>
        <![CDATA[In this week’s episode we first review new work revealing the critical role of the tension-sensitive cation channel PIEZO1 in the transendothelial migration of leukocytes. We’ll also review new research suggesting that CD8+ T-cells dimly expressing the CD4 antigen are increased in patients with various forms of secondary HLH, a finding that may have diagnostic, prognostic, and therapeutic significance. Finally, we’ll review a large, genome-wide association study identifying the ABO O blood group as a novel risk factor for heparin-induced thrombocytopenia—a finding that could have implications for prediction of this syndrome and for the management of related conditions.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode we first review new work revealing the critical role of the tension-sensitive cation channel PIEZO1 in the transendothelial migration of leukocytes. We’ll also review new research suggesting that CD8+ T-cells dimly expressing the CD4 antigen are increased in patients with various forms of secondary HLH, a finding that may have diagnostic, prognostic, and therapeutic significance. Finally, we’ll review a large, genome-wide association study identifying the ABO O blood group as a novel risk factor for heparin-induced thrombocytopenia—a finding that could have implications for prediction of this syndrome and for the management of related conditions.]]>
      </content:encoded>
      <pubDate>Thu, 21 Jul 2022 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/8e9da76b/6087479f.mp3" length="20369137" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1270</itunes:duration>
      <itunes:summary>In this week’s episode we first review new work revealing the critical role of the tension-sensitive cation channel PIEZO1 in the transendothelial migration of leukocytes. We’ll also review new research suggesting that CD8+ T-cells dimly expressing the CD4 antigen are increased in patients with various forms of secondary HLH, a finding that may have diagnostic, prognostic, and therapeutic significance. Finally, we’ll review a large, genome-wide association study identifying the ABO O blood group as a novel risk factor for heparin-induced thrombocytopenia—a finding that could have implications for prediction of this syndrome and for the management of related conditions.</itunes:summary>
      <itunes:subtitle>In this week’s episode we first review new work revealing the critical role of the tension-sensitive cation channel PIEZO1 in the transendothelial migration of leukocytes. We’ll also review new research suggesting that CD8+ T-cells dimly expressing the CD</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Long-term ibrutinib-rituximab vs FCR in CLL, procoagulant platelet sentinels in prevention of inflammatory bleeding, and new SERPINC1 variants in thrombophilia</title>
      <itunes:season>4</itunes:season>
      <podcast:season>4</podcast:season>
      <itunes:title>Long-term ibrutinib-rituximab vs FCR in CLL, procoagulant platelet sentinels in prevention of inflammatory bleeding, and new SERPINC1 variants in thrombophilia</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">dae4dd0d-70b9-479f-a9ba-d876aa82212e</guid>
      <link>https://share.transistor.fm/s/5c464742</link>
      <description>
        <![CDATA[In this week’s episode we’ll compare the long-term outcomes of ibrutinib-rituximab combination therapy versus FCR chemoimmunotherapy in chronic lymphocytic leukemia, discuss the role of procoagulant platelet sentinels in inflammatory bleeding, and learn more about variants in the SERPINC1 gene encoding antithrombin that cause severe thrombophilia.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode we’ll compare the long-term outcomes of ibrutinib-rituximab combination therapy versus FCR chemoimmunotherapy in chronic lymphocytic leukemia, discuss the role of procoagulant platelet sentinels in inflammatory bleeding, and learn more about variants in the SERPINC1 gene encoding antithrombin that cause severe thrombophilia.]]>
      </content:encoded>
      <pubDate>Thu, 14 Jul 2022 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/5c464742/43b63af4.mp3" length="17804313" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1110</itunes:duration>
      <itunes:summary>In this week’s episode we’ll compare the long-term outcomes of ibrutinib-rituximab combination therapy versus FCR chemoimmunotherapy in chronic lymphocytic leukemia, discuss the role of procoagulant platelet sentinels in inflammatory bleeding, and learn more about variants in the SERPINC1 gene encoding antithrombin that cause severe thrombophilia.</itunes:summary>
      <itunes:subtitle>In this week’s episode we’ll compare the long-term outcomes of ibrutinib-rituximab combination therapy versus FCR chemoimmunotherapy in chronic lymphocytic leukemia, discuss the role of procoagulant platelet sentinels in inflammatory bleeding, and learn m</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Malignancy risk from genetically modified immune effector cells, p53 immunohistochemistry as a new tool in AML, and phenotypic escape from CD19-directed immunotherapies.</title>
      <itunes:season>4</itunes:season>
      <podcast:season>4</podcast:season>
      <itunes:title>Malignancy risk from genetically modified immune effector cells, p53 immunohistochemistry as a new tool in AML, and phenotypic escape from CD19-directed immunotherapies.</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">ae870e6f-5de4-4415-bebc-14f044fc001a</guid>
      <link>https://share.transistor.fm/s/10aba56e</link>
      <description>
        <![CDATA[Today we’ll learn more about the risk of subsequent malignancies in patients treated with genetically modified immune effector cells, discuss how p53 immunohistochemistry can be a global readout for TP53 alterations in AML, and uncover the role of CD19-negative CD22-positive B-cell progenitors in immune escape from CD19-directed therapies. ]]>
      </description>
      <content:encoded>
        <![CDATA[Today we’ll learn more about the risk of subsequent malignancies in patients treated with genetically modified immune effector cells, discuss how p53 immunohistochemistry can be a global readout for TP53 alterations in AML, and uncover the role of CD19-negative CD22-positive B-cell progenitors in immune escape from CD19-directed therapies. ]]>
      </content:encoded>
      <pubDate>Thu, 07 Jul 2022 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/10aba56e/56e7bbf7.mp3" length="21165965" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1320</itunes:duration>
      <itunes:summary>Today we’ll learn more about the risk of subsequent malignancies in patients treated with genetically modified immune effector cells, discuss how p53 immunohistochemistry can be a global readout for TP53 alterations in AML, and uncover the role of CD19-negative CD22-positive B-cell progenitors in immune escape from CD19-directed therapies. </itunes:summary>
      <itunes:subtitle>Today we’ll learn more about the risk of subsequent malignancies in patients treated with genetically modified immune effector cells, discuss how p53 immunohistochemistry can be a global readout for TP53 alterations in AML, and uncover the role of CD19-ne</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Overcoming CAR T cell resistance in myeloma, why anti-CCR4 antibody therapy in CTCL sometimes fails, and corticosteroids increase risk of VOE in sickle disease</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:title>Overcoming CAR T cell resistance in myeloma, why anti-CCR4 antibody therapy in CTCL sometimes fails, and corticosteroids increase risk of VOE in sickle disease</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">df78ba4b-da21-44c6-bf33-26b788baeba6</guid>
      <link>https://share.transistor.fm/s/975a99a7</link>
      <description>
        <![CDATA[In this week’s episode we review a novel strategy for overcoming resistance to CAR T cell therapy that involves the dual targeting of myeloma cells and cancer-associated fibroblasts. We’ll also explore a recent report demonstrating that loss of CCR4 expression is common after treatment of CTCL with the anti-CCR4 antibody mogamulizumab. Finally, we’ll review real-world data demonstrating an association between corticosteroid exposure and risk of vaso-occlusive episodes in patients with sickle cell disease, providing further evidence that steroids should be avoided in this setting.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode we review a novel strategy for overcoming resistance to CAR T cell therapy that involves the dual targeting of myeloma cells and cancer-associated fibroblasts. We’ll also explore a recent report demonstrating that loss of CCR4 expression is common after treatment of CTCL with the anti-CCR4 antibody mogamulizumab. Finally, we’ll review real-world data demonstrating an association between corticosteroid exposure and risk of vaso-occlusive episodes in patients with sickle cell disease, providing further evidence that steroids should be avoided in this setting.]]>
      </content:encoded>
      <pubDate>Thu, 30 Jun 2022 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/975a99a7/0b83b116.mp3" length="18397037" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1147</itunes:duration>
      <itunes:summary>In this week’s episode we review a novel strategy for overcoming resistance to CAR T cell therapy that involves the dual targeting of myeloma cells and cancer-associated fibroblasts. We’ll also explore a recent report demonstrating that loss of CCR4 expression is common after treatment of CTCL with the anti-CCR4 antibody mogamulizumab. Finally, we’ll review real-world data demonstrating an association between corticosteroid exposure and risk of vaso-occlusive episodes in patients with sickle cell disease, providing further evidence that steroids should be avoided in this setting.</itunes:summary>
      <itunes:subtitle>In this week’s episode we review a novel strategy for overcoming resistance to CAR T cell therapy that involves the dual targeting of myeloma cells and cancer-associated fibroblasts. We’ll also explore a recent report demonstrating that loss of CCR4 expre</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Salvage therapy with NICE for Hodgkin lymphoma, BMP2/SMAD pathway activation in leukemic transformation, and the role of zinc in T-cell reconstitution after HSCT</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:title>Salvage therapy with NICE for Hodgkin lymphoma, BMP2/SMAD pathway activation in leukemic transformation, and the role of zinc in T-cell reconstitution after HSCT</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">1f6eb446-51ec-47ca-8891-d7f53b3e998a</guid>
      <link>https://share.transistor.fm/s/8b1e8b80</link>
      <description>
        <![CDATA[In this week’s episode we’ll learn more about salvage therapy with nivolumab plus or minus ICE (or NICE) for Hodgkin lymphoma, discuss the role of BMP2/SMAD pathway activation in leukemic transformation, and learn more about the role of zinc in T-cell reconstitution after transplantation. ]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode we’ll learn more about salvage therapy with nivolumab plus or minus ICE (or NICE) for Hodgkin lymphoma, discuss the role of BMP2/SMAD pathway activation in leukemic transformation, and learn more about the role of zinc in T-cell reconstitution after transplantation. ]]>
      </content:encoded>
      <pubDate>Thu, 23 Jun 2022 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/8b1e8b80/f5ecfabe.mp3" length="17919140" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1117</itunes:duration>
      <itunes:summary>In this week’s episode we’ll learn more about salvage therapy with nivolumab plus or minus ICE (or NICE) for Hodgkin lymphoma, discuss the role of BMP2/SMAD pathway activation in leukemic transformation, and learn more about the role of zinc in T-cell reconstitution after transplantation. </itunes:summary>
      <itunes:subtitle>In this week’s episode we’ll learn more about salvage therapy with nivolumab plus or minus ICE (or NICE) for Hodgkin lymphoma, discuss the role of BMP2/SMAD pathway activation in leukemic transformation, and learn more about the role of zinc in T-cell rec</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>MRD and post-transplant outcomes in older AML patients, enhancer hijacking in a novel high-risk B-other ALL subtype, and ruxolitinib in pediatric HLH </title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:title>MRD and post-transplant outcomes in older AML patients, enhancer hijacking in a novel high-risk B-other ALL subtype, and ruxolitinib in pediatric HLH </itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">982f1954-0475-4c13-8eaa-9a6cf8373d46</guid>
      <link>https://share.transistor.fm/s/3f7943ff</link>
      <description>
        <![CDATA[In this week’s episode we will discuss new data demonstrating that, in older patients with AML, post-transplant relapse risk is driven by clinical and molecular features present at diagnosis, but not remission MRD.  We’ll also explore two studies that characterize a novel high-risk B-ALL subtype, defined by two unique genomic alterations that includes a deletion resulting in enhancer hijacking that deregulates expression of the CDX2 homeobox transcription factor. Finally, we’ll review results of a large, single-arm phase 2 trial providing encouraging clinical evidence for the use of ruxolitinib as a front-line treatment for pediatric hemophagocytic lymphohistiocytosis.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode we will discuss new data demonstrating that, in older patients with AML, post-transplant relapse risk is driven by clinical and molecular features present at diagnosis, but not remission MRD.  We’ll also explore two studies that characterize a novel high-risk B-ALL subtype, defined by two unique genomic alterations that includes a deletion resulting in enhancer hijacking that deregulates expression of the CDX2 homeobox transcription factor. Finally, we’ll review results of a large, single-arm phase 2 trial providing encouraging clinical evidence for the use of ruxolitinib as a front-line treatment for pediatric hemophagocytic lymphohistiocytosis.]]>
      </content:encoded>
      <pubDate>Thu, 16 Jun 2022 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/3f7943ff/319ca3c5.mp3" length="19258615" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1201</itunes:duration>
      <itunes:summary>In this week’s episode we will discuss new data demonstrating that, in older patients with AML, post-transplant relapse risk is driven by clinical and molecular features present at diagnosis, but not remission MRD.  We’ll also explore two studies that characterize a novel high-risk B-ALL subtype, defined by two unique genomic alterations that includes a deletion resulting in enhancer hijacking that deregulates expression of the CDX2 homeobox transcription factor. Finally, we’ll review results of a large, single-arm phase 2 trial providing encouraging clinical evidence for the use of ruxolitinib as a front-line treatment for pediatric hemophagocytic lymphohistiocytosis.</itunes:summary>
      <itunes:subtitle>In this week’s episode we will discuss new data demonstrating that, in older patients with AML, post-transplant relapse risk is driven by clinical and molecular features present at diagnosis, but not remission MRD.  We’ll also explore two studies that cha</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Anti-PF4 antibodies after Covid vaccination, CAR T-cell therapy for CNS leukemia, and advances in Diamond-Blackfan anemia</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:title>Anti-PF4 antibodies after Covid vaccination, CAR T-cell therapy for CNS leukemia, and advances in Diamond-Blackfan anemia</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">e57ca121-837f-4fac-b7c4-ac9bbabc2fbf</guid>
      <link>https://share.transistor.fm/s/1936d2b0</link>
      <description>
        <![CDATA[In this week's episode, we’ll learn more about the interaction between anti-PF4 antibodies and anticoagulants in vaccine-induced thrombotic thrombocytopenia, discuss the efficacy and safety of CD19-specific CAR T-cell-based therapy in B-cell ALL patients with central nervous system leukemia, and learn more about erythroid cell-extrinsic factors that can inhibit erythropoiesis in adjacent cells. ]]>
      </description>
      <content:encoded>
        <![CDATA[In this week's episode, we’ll learn more about the interaction between anti-PF4 antibodies and anticoagulants in vaccine-induced thrombotic thrombocytopenia, discuss the efficacy and safety of CD19-specific CAR T-cell-based therapy in B-cell ALL patients with central nervous system leukemia, and learn more about erythroid cell-extrinsic factors that can inhibit erythropoiesis in adjacent cells. ]]>
      </content:encoded>
      <pubDate>Thu, 09 Jun 2022 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/1936d2b0/a3314ec1.mp3" length="19780030" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1233</itunes:duration>
      <itunes:summary>In this week's episode, we’ll learn more about the interaction between anti-PF4 antibodies and anticoagulants in vaccine-induced thrombotic thrombocytopenia, discuss the efficacy and safety of CD19-specific CAR T-cell-based therapy in B-cell ALL patients with central nervous system leukemia, and learn more about erythroid cell-extrinsic factors that can inhibit erythropoiesis in adjacent cells. </itunes:summary>
      <itunes:subtitle>In this week's episode, we’ll learn more about the interaction between anti-PF4 antibodies and anticoagulants in vaccine-induced thrombotic thrombocytopenia, discuss the efficacy and safety of CD19-specific CAR T-cell-based therapy in B-cell ALL patients </itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Fixed-duration ibrutinib + venetoclax for CLL, aryl hydrocarbon receptor in idiopathic pneumonia syndrome, and VWF propeptide and multimerization </title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:title>Fixed-duration ibrutinib + venetoclax for CLL, aryl hydrocarbon receptor in idiopathic pneumonia syndrome, and VWF propeptide and multimerization </itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">d62be047-48ea-4ae4-bd5c-725eebced323</guid>
      <link>https://share.transistor.fm/s/ff4499f8</link>
      <description>
        <![CDATA[In this week's episode, we discuss results from the international phase 2 CAPTIVATE study showing that in patients with treatment-naive CLL, fixed-dose ibrutinib plus venetoclax yields deep and durable responses and promising progression-free survival. We’ll also explore data that show that aryl hydrocarbon receptor is a critical inflammation checkpoint in the lung epithelium—a finding that may have therapeutic implications for idiopathic pneumonia syndrome. Lastly, we’ll review new insights into the role of von Willebrand Factor propeptide in facilitating multimer formation, shedding light on a potential novel treatment approach for type 2a von Willebrand disease. ]]>
      </description>
      <content:encoded>
        <![CDATA[In this week's episode, we discuss results from the international phase 2 CAPTIVATE study showing that in patients with treatment-naive CLL, fixed-dose ibrutinib plus venetoclax yields deep and durable responses and promising progression-free survival. We’ll also explore data that show that aryl hydrocarbon receptor is a critical inflammation checkpoint in the lung epithelium—a finding that may have therapeutic implications for idiopathic pneumonia syndrome. Lastly, we’ll review new insights into the role of von Willebrand Factor propeptide in facilitating multimer formation, shedding light on a potential novel treatment approach for type 2a von Willebrand disease. ]]>
      </content:encoded>
      <pubDate>Thu, 02 Jun 2022 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/ff4499f8/38411de1.mp3" length="21574931" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1345</itunes:duration>
      <itunes:summary>In this week's episode, we discuss results from the international phase 2 CAPTIVATE study showing that in patients with treatment-naive CLL, fixed-dose ibrutinib plus venetoclax yields deep and durable responses and promising progression-free survival. We’ll also explore data that show that aryl hydrocarbon receptor is a critical inflammation checkpoint in the lung epithelium—a finding that may have therapeutic implications for idiopathic pneumonia syndrome. Lastly, we’ll review new insights into the role of von Willebrand Factor propeptide in facilitating multimer formation, shedding light on a potential novel treatment approach for type 2a von Willebrand disease. </itunes:summary>
      <itunes:subtitle>In this week's episode, we discuss results from the international phase 2 CAPTIVATE study showing that in patients with treatment-naive CLL, fixed-dose ibrutinib plus venetoclax yields deep and durable responses and promising progression-free survival. We</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>HEATR3 variants as a new cause of Diamond-Blackfan anemia, zanubrutinib in mantle cell lymphoma, and HMGB1 inhibits Epo signaling in anemia of inflammation</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:title>HEATR3 variants as a new cause of Diamond-Blackfan anemia, zanubrutinib in mantle cell lymphoma, and HMGB1 inhibits Epo signaling in anemia of inflammation</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">1dccc466-e2f9-4429-aeb8-60bb4949dc1f</guid>
      <link>https://share.transistor.fm/s/091132ce</link>
      <description>
        <![CDATA[In this week's episode we discuss the role of HEATR3 variants as a new cause of Diamond-Blackfan anemia, learn more about the long-term efficacy and safety of zanubrutinib in relapsed or refractory mantle cell lymphoma, and uncover an unexpected role for HMGB1 in anemia of inflammation by inhibiting erythropoietin signaling.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week's episode we discuss the role of HEATR3 variants as a new cause of Diamond-Blackfan anemia, learn more about the long-term efficacy and safety of zanubrutinib in relapsed or refractory mantle cell lymphoma, and uncover an unexpected role for HMGB1 in anemia of inflammation by inhibiting erythropoietin signaling.]]>
      </content:encoded>
      <pubDate>Thu, 26 May 2022 12:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/091132ce/55e9930d.mp3" length="18964098" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1182</itunes:duration>
      <itunes:summary>In this week's episode we discuss the role of HEATR3 variants as a new cause of Diamond-Blackfan anemia, learn more about the long-term efficacy and safety of zanubrutinib in relapsed or refractory mantle cell lymphoma, and uncover an unexpected role for HMGB1 in anemia of inflammation by inhibiting erythropoietin signaling.</itunes:summary>
      <itunes:subtitle>In this week's episode we discuss the role of HEATR3 variants as a new cause of Diamond-Blackfan anemia, learn more about the long-term efficacy and safety of zanubrutinib in relapsed or refractory mantle cell lymphoma, and uncover an unexpected role for </itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>HLA-DQ heterodimers and transplantation, the genomic landscape of LGL leukemia, and an updated classification of hemochromatosis</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:title>HLA-DQ heterodimers and transplantation, the genomic landscape of LGL leukemia, and an updated classification of hemochromatosis</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">a80bc311-fdd5-46fa-98b8-d5f1786192f9</guid>
      <link>https://share.transistor.fm/s/3f06419f</link>
      <description>
        <![CDATA[In this week’s episode we’ll feature new research demonstrating that certain HLA-DQ heterodimers can help predict clinical outcome following hematopoietic cell transplantation. Next, we’ll review a recent integrated and comprehensive genomic analysis that sheds new light on the molecular characteristics of large granular lymphocyte leukemia and its subtypes. Finally, we’ll review the work of a group that proposes a new and more accessible hemochromatosis classification system based on clinical characteristics and genetic features. ]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode we’ll feature new research demonstrating that certain HLA-DQ heterodimers can help predict clinical outcome following hematopoietic cell transplantation. Next, we’ll review a recent integrated and comprehensive genomic analysis that sheds new light on the molecular characteristics of large granular lymphocyte leukemia and its subtypes. Finally, we’ll review the work of a group that proposes a new and more accessible hemochromatosis classification system based on clinical characteristics and genetic features. ]]>
      </content:encoded>
      <pubDate>Thu, 19 May 2022 13:00:52 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/3f06419f/5c236e9c.mp3" length="21101491" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1316</itunes:duration>
      <itunes:summary>In this week’s episode we’ll feature new research demonstrating that certain HLA-DQ heterodimers can help predict clinical outcome following hematopoietic cell transplantation. Next, we’ll review a recent integrated and comprehensive genomic analysis that sheds new light on the molecular characteristics of large granular lymphocyte leukemia and its subtypes. Finally, we’ll review the work of a group that proposes a new and more accessible hemochromatosis classification system based on clinical characteristics and genetic features. </itunes:summary>
      <itunes:subtitle>In this week’s episode we’ll feature new research demonstrating that certain HLA-DQ heterodimers can help predict clinical outcome following hematopoietic cell transplantation. Next, we’ll review a recent integrated and comprehensive genomic analysis that</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Role of macrophage NOX2 in alveolar homeostasis, hydroxyurea versus peginterferon alfa-2a in high-risk PV and ET, and the emerging PV treatment landscape </title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:title>Role of macrophage NOX2 in alveolar homeostasis, hydroxyurea versus peginterferon alfa-2a in high-risk PV and ET, and the emerging PV treatment landscape </itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">eb3ae8a4-76bb-44e2-81a2-099712440407</guid>
      <link>https://share.transistor.fm/s/48307572</link>
      <description>
        <![CDATA[In this week’s episode we’ll discuss an undescribed role for NOX2 in maintaining lung homeostasis through suppression of alveolar macrophage activation. We’ll also cover results of a phase 3 randomized trial that compares the safety and efficacy of hydroxyurea and peginterferon alfa-2a in patients with high-risk polycythemia vera and essential thrombocythemia (or PV and ET, respectively). Finally, we’ll go more in depth on the emerging treatment landscape for PV, and the limits of current clinical trial endpoints.  ]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode we’ll discuss an undescribed role for NOX2 in maintaining lung homeostasis through suppression of alveolar macrophage activation. We’ll also cover results of a phase 3 randomized trial that compares the safety and efficacy of hydroxyurea and peginterferon alfa-2a in patients with high-risk polycythemia vera and essential thrombocythemia (or PV and ET, respectively). Finally, we’ll go more in depth on the emerging treatment landscape for PV, and the limits of current clinical trial endpoints.  ]]>
      </content:encoded>
      <pubDate>Thu, 12 May 2022 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/48307572/f38e92f8.mp3" length="20146056" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1256</itunes:duration>
      <itunes:summary>In this week’s episode we’ll discuss an undescribed role for NOX2 in maintaining lung homeostasis through suppression of alveolar macrophage activation. We’ll also cover results of a phase 3 randomized trial that compares the safety and efficacy of hydroxyurea and peginterferon alfa-2a in patients with high-risk polycythemia vera and essential thrombocythemia (or PV and ET, respectively). Finally, we’ll go more in depth on the emerging treatment landscape for PV, and the limits of current clinical trial endpoints.  </itunes:summary>
      <itunes:subtitle>In this week’s episode we’ll discuss an undescribed role for NOX2 in maintaining lung homeostasis through suppression of alveolar macrophage activation. We’ll also cover results of a phase 3 randomized trial that compares the safety and efficacy of hydrox</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Microbiome and CD4 T-cell recovery after allogeneic HCT, and a paradigm shift to CAR T-cells in the second line for large B-cell lymphoma?</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:title>Microbiome and CD4 T-cell recovery after allogeneic HCT, and a paradigm shift to CAR T-cells in the second line for large B-cell lymphoma?</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">388d1710-3369-4882-b939-798f479c1069</guid>
      <link>https://share.transistor.fm/s/950023d6</link>
      <description>
        <![CDATA[In this week’s episode we’ll discuss the effects of intestinal microbial diversity on patient outcomes following allogeneic hematopoietic cell transplant and review the results of three different phase 3 trials comparing CAR T-cells to autologous stem cell transplant in patients with refractory or early relapsing large B cell lymphoma, which have the potential to result in a paradigm shift in the standard of care for second-line therapy. ]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode we’ll discuss the effects of intestinal microbial diversity on patient outcomes following allogeneic hematopoietic cell transplant and review the results of three different phase 3 trials comparing CAR T-cells to autologous stem cell transplant in patients with refractory or early relapsing large B cell lymphoma, which have the potential to result in a paradigm shift in the standard of care for second-line therapy. ]]>
      </content:encoded>
      <pubDate>Thu, 05 May 2022 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/950023d6/da43d136.mp3" length="19583293" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1221</itunes:duration>
      <itunes:summary>In this week’s episode we’ll discuss the effects of intestinal microbial diversity on patient outcomes following allogeneic hematopoietic cell transplant and review the results of three different phase 3 trials comparing CAR T-cells to autologous stem cell transplant in patients with refractory or early relapsing large B cell lymphoma, which have the potential to result in a paradigm shift in the standard of care for second-line therapy. </itunes:summary>
      <itunes:subtitle>In this week’s episode we’ll discuss the effects of intestinal microbial diversity on patient outcomes following allogeneic hematopoietic cell transplant and review the results of three different phase 3 trials comparing CAR T-cells to autologous stem cel</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Canakinumab in SCA, antigen-specific donor T-cells to prevent post-transplant relapse in ALL, and nasopharyngeal mucosal immunity defects in transplanted SCID patients</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:title>Canakinumab in SCA, antigen-specific donor T-cells to prevent post-transplant relapse in ALL, and nasopharyngeal mucosal immunity defects in transplanted SCID patients</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">17a92394-1c36-4622-9d32-97253ff97b58</guid>
      <link>https://share.transistor.fm/s/62dcd9a6</link>
      <description>
        <![CDATA[In this week’s episode, we’ll discuss the efficacy of canakinumab in children and young adults with sickle cell anemia, learn more about the use of donor-derived multiple leukemia antigen specific T-cell therapy to prevent relapse in post-transplant patients with ALL, and discuss the defects in nasopharyngeal mucosal immunity in patients with severe combined immunodeficiency after hematopoietic stem cell transplantation.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we’ll discuss the efficacy of canakinumab in children and young adults with sickle cell anemia, learn more about the use of donor-derived multiple leukemia antigen specific T-cell therapy to prevent relapse in post-transplant patients with ALL, and discuss the defects in nasopharyngeal mucosal immunity in patients with severe combined immunodeficiency after hematopoietic stem cell transplantation.]]>
      </content:encoded>
      <pubDate>Thu, 28 Apr 2022 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/62dcd9a6/3fdb8471.mp3" length="19372248" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1208</itunes:duration>
      <itunes:summary>In this week’s episode, we’ll discuss the efficacy of canakinumab in children and young adults with sickle cell anemia, learn more about the use of donor-derived multiple leukemia antigen specific T-cell therapy to prevent relapse in post-transplant patients with ALL, and discuss the defects in nasopharyngeal mucosal immunity in patients with severe combined immunodeficiency after hematopoietic stem cell transplantation.</itunes:summary>
      <itunes:subtitle>In this week’s episode, we’ll discuss the efficacy of canakinumab in children and young adults with sickle cell anemia, learn more about the use of donor-derived multiple leukemia antigen specific T-cell therapy to prevent relapse in post-transplant patie</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Timing (and utility) of CNS prophylaxis in DLBCL, Apollo deficiency in a bone marrow failure syndrome, and GATA1 mutants in congenital anemia </title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:title>Timing (and utility) of CNS prophylaxis in DLBCL, Apollo deficiency in a bone marrow failure syndrome, and GATA1 mutants in congenital anemia </itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">2f0c3fd9-cc69-4b30-91a9-c6b750134f2d</guid>
      <link>https://share.transistor.fm/s/501b3f65</link>
      <description>
        <![CDATA[In this week’s episode we’ll cover a retrospective study on the timing of high-dose methotrexate CNS prophylaxis in diffuse large B-cell lymphoma, results of which suggest end-of-treatment delivery might be preferred to earlier administration. The second research article describes how biallelic Apollo variants lead to an inherited bone marrow failure syndrome that resembles dyskeratosis congenita, albeit with normal telomere length. We’ll conclude with research revealing how a rare form of congenital anemia is caused by novel missense mutations in GATA1.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode we’ll cover a retrospective study on the timing of high-dose methotrexate CNS prophylaxis in diffuse large B-cell lymphoma, results of which suggest end-of-treatment delivery might be preferred to earlier administration. The second research article describes how biallelic Apollo variants lead to an inherited bone marrow failure syndrome that resembles dyskeratosis congenita, albeit with normal telomere length. We’ll conclude with research revealing how a rare form of congenital anemia is caused by novel missense mutations in GATA1.]]>
      </content:encoded>
      <pubDate>Thu, 21 Apr 2022 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/501b3f65/82c367c8.mp3" length="16813304" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1048</itunes:duration>
      <itunes:summary>In this week’s episode we’ll cover a retrospective study on the timing of high-dose methotrexate CNS prophylaxis in diffuse large B-cell lymphoma, results of which suggest end-of-treatment delivery might be preferred to earlier administration. The second research article describes how biallelic Apollo variants lead to an inherited bone marrow failure syndrome that resembles dyskeratosis congenita, albeit with normal telomere length. We’ll conclude with research revealing how a rare form of congenital anemia is caused by novel missense mutations in GATA1.</itunes:summary>
      <itunes:subtitle>In this week’s episode we’ll cover a retrospective study on the timing of high-dose methotrexate CNS prophylaxis in diffuse large B-cell lymphoma, results of which suggest end-of-treatment delivery might be preferred to earlier administration. The second </itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Obinutuzumab plus lenalidomide in advanced follicular lymphoma, mechanisms of anemia in children with malaria, and  granulocyte microvesicles for septic shock</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:title>Obinutuzumab plus lenalidomide in advanced follicular lymphoma, mechanisms of anemia in children with malaria, and  granulocyte microvesicles for septic shock</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">06a93c37-c1f0-4c61-abb3-3fa1e3749b89</guid>
      <link>https://share.transistor.fm/s/a49d8f45</link>
      <description>
        <![CDATA[In this week’s episode we’ll discuss the efficacy of the obinutuzumab-lenalinomide combination in advanced follicular lymphoma, learn more about the underlying mechanisms of anemia in children infected with Plasmodium falciparum, and discuss how granulocyte microvesicles could improve outcomes in septic shock.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode we’ll discuss the efficacy of the obinutuzumab-lenalinomide combination in advanced follicular lymphoma, learn more about the underlying mechanisms of anemia in children infected with Plasmodium falciparum, and discuss how granulocyte microvesicles could improve outcomes in septic shock.]]>
      </content:encoded>
      <pubDate>Thu, 14 Apr 2022 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/a49d8f45/2678d930.mp3" length="18396067" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1147</itunes:duration>
      <itunes:summary>In this week’s episode we’ll discuss the efficacy of the obinutuzumab-lenalinomide combination in advanced follicular lymphoma, learn more about the underlying mechanisms of anemia in children infected with Plasmodium falciparum, and discuss how granulocyte microvesicles could improve outcomes in septic shock.</itunes:summary>
      <itunes:subtitle>In this week’s episode we’ll discuss the efficacy of the obinutuzumab-lenalinomide combination in advanced follicular lymphoma, learn more about the underlying mechanisms of anemia in children infected with Plasmodium falciparum, and discuss how granulocy</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Structural racism and AML survival, promoter competition and hemoglobin switching, and CAR T-cell therapy and high-risk cytogenetics in ALL</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:title>Structural racism and AML survival, promoter competition and hemoglobin switching, and CAR T-cell therapy and high-risk cytogenetics in ALL</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">6dbceb7e-5914-499b-86de-f3a84142eadf</guid>
      <link>https://share.transistor.fm/s/bfb74323</link>
      <description>
        <![CDATA[In this week’s episode we’ll first cover a research article demonstrating the striking contribution of neighborhood disadvantage to racial and ethnic disparities in survival in patients with acute myeloid leukemia. The second research article provides a model for understanding how disruption of the adult-globin promoter may alleviate promoter competition, thereby reactivating fetal gamma-globin gene expression. We will close with a research article showing that CD19-directed CAR T-cell therapy provides durable remissions in patients with relapsed or refractory ALL across cytogenetic categories, including those patients with high-risk cytogenetics.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode we’ll first cover a research article demonstrating the striking contribution of neighborhood disadvantage to racial and ethnic disparities in survival in patients with acute myeloid leukemia. The second research article provides a model for understanding how disruption of the adult-globin promoter may alleviate promoter competition, thereby reactivating fetal gamma-globin gene expression. We will close with a research article showing that CD19-directed CAR T-cell therapy provides durable remissions in patients with relapsed or refractory ALL across cytogenetic categories, including those patients with high-risk cytogenetics.]]>
      </content:encoded>
      <pubDate>Thu, 07 Apr 2022 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/bfb74323/08819d35.mp3" length="17254853" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1075</itunes:duration>
      <itunes:summary>In this week’s episode we’ll first cover a research article demonstrating the striking contribution of neighborhood disadvantage to racial and ethnic disparities in survival in patients with acute myeloid leukemia. The second research article provides a model for understanding how disruption of the adult-globin promoter may alleviate promoter competition, thereby reactivating fetal gamma-globin gene expression. We will close with a research article showing that CD19-directed CAR T-cell therapy provides durable remissions in patients with relapsed or refractory ALL across cytogenetic categories, including those patients with high-risk cytogenetics.</itunes:summary>
      <itunes:subtitle>In this week’s episode we’ll first cover a research article demonstrating the striking contribution of neighborhood disadvantage to racial and ethnic disparities in survival in patients with acute myeloid leukemia. The second research article provides a m</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Targeting the PBX1-FOXM1 axis in myeloma, SF3B1 mutations in MDS, and pulmonary artery hypertension-associated mortality in β-thalassemia patients</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:title>Targeting the PBX1-FOXM1 axis in myeloma, SF3B1 mutations in MDS, and pulmonary artery hypertension-associated mortality in β-thalassemia patients</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">d99ab03e-d073-4609-9f4d-9e1480868f77</guid>
      <link>https://share.transistor.fm/s/ae1640f2</link>
      <description>
        <![CDATA[In this week's podcast, we’ll discuss the role of the PBX1-FOXM1 axis in multiple myeloma, learn more about the pathobiology of SF3B1 splicing factor mutations in myelodysplastic syndromes with ring sideroblasts, and discuss mortality rates due to pulmonary arterial hypertension in patients with β-thalassemia.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week's podcast, we’ll discuss the role of the PBX1-FOXM1 axis in multiple myeloma, learn more about the pathobiology of SF3B1 splicing factor mutations in myelodysplastic syndromes with ring sideroblasts, and discuss mortality rates due to pulmonary arterial hypertension in patients with β-thalassemia.]]>
      </content:encoded>
      <pubDate>Thu, 31 Mar 2022 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/ae1640f2/67e61251.mp3" length="18611710" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1160</itunes:duration>
      <itunes:summary>In this week's podcast, we’ll discuss the role of the PBX1-FOXM1 axis in multiple myeloma, learn more about the pathobiology of SF3B1 splicing factor mutations in myelodysplastic syndromes with ring sideroblasts, and discuss mortality rates due to pulmonary arterial hypertension in patients with β-thalassemia.</itunes:summary>
      <itunes:subtitle>In this week's podcast, we’ll discuss the role of the PBX1-FOXM1 axis in multiple myeloma, learn more about the pathobiology of SF3B1 splicing factor mutations in myelodysplastic syndromes with ring sideroblasts, and discuss mortality rates due to pulmona</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Novel high-risk subtypes in adult B-ALL, Liso-cel CAR-T therapy in CLL, and liquid biopsies in large B-cell lymphomas</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:title>Novel high-risk subtypes in adult B-ALL, Liso-cel CAR-T therapy in CLL, and liquid biopsies in large B-cell lymphomas</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">57333dfa-c320-47e7-92c5-0bcf43d87120</guid>
      <link>https://share.transistor.fm/s/84fe2ae8</link>
      <description>
        <![CDATA[In this week's podcast, we’ll cover a research article that describes two novel subgroups of adult B-cell ALL with high expression of CDX2 and IDH mutations that are linked to poor prognosis. Next, we'll cover results from TRANSCEND CLL 004, a phase 1 study of the CAR T cell therapy, liso-cel, in patients with relapsed or refractory CLL. We will close with research that provides new insights into how analysis of circulating tumor DNA could inform management of patients with aggressive B-cell lymphomas.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week's podcast, we’ll cover a research article that describes two novel subgroups of adult B-cell ALL with high expression of CDX2 and IDH mutations that are linked to poor prognosis. Next, we'll cover results from TRANSCEND CLL 004, a phase 1 study of the CAR T cell therapy, liso-cel, in patients with relapsed or refractory CLL. We will close with research that provides new insights into how analysis of circulating tumor DNA could inform management of patients with aggressive B-cell lymphomas.]]>
      </content:encoded>
      <pubDate>Thu, 24 Mar 2022 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/84fe2ae8/a7447c46.mp3" length="17238630" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1074</itunes:duration>
      <itunes:summary>In this week's podcast, we’ll cover a research article that describes two novel subgroups of adult B-cell ALL with high expression of CDX2 and IDH mutations that are linked to poor prognosis. Next, we'll cover results from TRANSCEND CLL 004, a phase 1 study of the CAR T cell therapy, liso-cel, in patients with relapsed or refractory CLL. We will close with research that provides new insights into how analysis of circulating tumor DNA could inform management of patients with aggressive B-cell lymphomas.</itunes:summary>
      <itunes:subtitle>In this week's podcast, we’ll cover a research article that describes two novel subgroups of adult B-cell ALL with high expression of CDX2 and IDH mutations that are linked to poor prognosis. Next, we'll cover results from TRANSCEND CLL 004, a phase 1 stu</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Effective treatments for kaposiform hemangioendothelioma, causes of vascular dysfunction in sickle cell patients, and better strategies to select therapy in older adults with AML</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:title>Effective treatments for kaposiform hemangioendothelioma, causes of vascular dysfunction in sickle cell patients, and better strategies to select therapy in older adults with AML</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">44b9c560-3861-4c15-b0ce-42e72f53f87b</guid>
      <link>https://share.transistor.fm/s/c26a8f5d</link>
      <description>
        <![CDATA[In this week's podcast, discuss the efficacy of siroliumus plus prednisolone in kaposiform hemangioendothelioma with the Kasabach-Merritt phenomenon, learn more about the association between SOD2 V16A and vascular dysfunction in patients with sickle cell disease, and discuss the value of geriatric assessment in predicting outcomes in older adults with AML.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week's podcast, discuss the efficacy of siroliumus plus prednisolone in kaposiform hemangioendothelioma with the Kasabach-Merritt phenomenon, learn more about the association between SOD2 V16A and vascular dysfunction in patients with sickle cell disease, and discuss the value of geriatric assessment in predicting outcomes in older adults with AML.]]>
      </content:encoded>
      <pubDate>Thu, 17 Mar 2022 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/c26a8f5d/2057628c.mp3" length="18685011" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1165</itunes:duration>
      <itunes:summary>In this week's podcast, discuss the efficacy of siroliumus plus prednisolone in kaposiform hemangioendothelioma with the Kasabach-Merritt phenomenon, learn more about the association between SOD2 V16A and vascular dysfunction in patients with sickle cell disease, and discuss the value of geriatric assessment in predicting outcomes in older adults with AML.</itunes:summary>
      <itunes:subtitle>In this week's podcast, discuss the efficacy of siroliumus plus prednisolone in kaposiform hemangioendothelioma with the Kasabach-Merritt phenomenon, learn more about the association between SOD2 V16A and vascular dysfunction in patients with sickle cell </itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>COVID-19 vaccination in patients with blood cancers and recalibrating the HLA barrier in haploidentical stem cell transplantation  </title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:title>COVID-19 vaccination in patients with blood cancers and recalibrating the HLA barrier in haploidentical stem cell transplantation  </itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">1fe67069-e484-4a7f-a8a4-a5e94fa7e082</guid>
      <link>https://share.transistor.fm/s/d532e061</link>
      <description>
        <![CDATA[In this week's podcast, we’ll focus on 2 reports on clinical outcomes following COVID-19 vaccination in patients with hematologic malignancies. Despite full or partial vaccination, these patients have an increased risk of poor outcomes compared to matched controls or the general population. In a third report, we discuss new data on HLA-mismatching and outcomes of haploidentical transplants. ]]>
      </description>
      <content:encoded>
        <![CDATA[In this week's podcast, we’ll focus on 2 reports on clinical outcomes following COVID-19 vaccination in patients with hematologic malignancies. Despite full or partial vaccination, these patients have an increased risk of poor outcomes compared to matched controls or the general population. In a third report, we discuss new data on HLA-mismatching and outcomes of haploidentical transplants. ]]>
      </content:encoded>
      <pubDate>Thu, 10 Mar 2022 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/d532e061/117b9a0a.mp3" length="18611428" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1160</itunes:duration>
      <itunes:summary>In this week's podcast, we’ll focus on 2 reports on clinical outcomes following COVID-19 vaccination in patients with hematologic malignancies. Despite full or partial vaccination, these patients have an increased risk of poor outcomes compared to matched controls or the general population. In a third report, we discuss new data on HLA-mismatching and outcomes of haploidentical transplants. </itunes:summary>
      <itunes:subtitle>In this week's podcast, we’ll focus on 2 reports on clinical outcomes following COVID-19 vaccination in patients with hematologic malignancies. Despite full or partial vaccination, these patients have an increased risk of poor outcomes compared to matched</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Cell therapy options for chemo-sensitive DLBCL, PIGA mutations in a novel subtype of hemochromatosis, and triplet combination therapy in high-risk CLL  </title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:title>Cell therapy options for chemo-sensitive DLBCL, PIGA mutations in a novel subtype of hemochromatosis, and triplet combination therapy in high-risk CLL  </itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">94029743-0e15-4efa-a035-b3fc9a49b50e</guid>
      <link>https://share.transistor.fm/s/2e256559</link>
      <description>
        <![CDATA[In this week's podcast, we’ll compare the efficacy of autologous stem cell transplant to CAR T-cell therapy for relapsed diffuse large B-cell lymphoma, learn more about a novel subtype of hemochromatosis caused by constitutional PIGA mutations, and discuss the findings from a phase 2 trial of obinutuzumab, ibrutinib and venetoclax in patients with untreated high-risk CLL.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week's podcast, we’ll compare the efficacy of autologous stem cell transplant to CAR T-cell therapy for relapsed diffuse large B-cell lymphoma, learn more about a novel subtype of hemochromatosis caused by constitutional PIGA mutations, and discuss the findings from a phase 2 trial of obinutuzumab, ibrutinib and venetoclax in patients with untreated high-risk CLL.]]>
      </content:encoded>
      <pubDate>Thu, 03 Mar 2022 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/2e256559/1d24c75d.mp3" length="20646889" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1287</itunes:duration>
      <itunes:summary>In this week's podcast, we’ll compare the efficacy of autologous stem cell transplant to CAR T-cell therapy for relapsed diffuse large B-cell lymphoma, learn more about a novel subtype of hemochromatosis caused by constitutional PIGA mutations, and discuss the findings from a phase 2 trial of obinutuzumab, ibrutinib and venetoclax in patients with untreated high-risk CLL.</itunes:summary>
      <itunes:subtitle>In this week's podcast, we’ll compare the efficacy of autologous stem cell transplant to CAR T-cell therapy for relapsed diffuse large B-cell lymphoma, learn more about a novel subtype of hemochromatosis caused by constitutional PIGA mutations, and discus</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Germline predisposition mutations in AML, a new way to resolve NETs, and venetoclax and BAX mutations in normal myeloid cells of CLL patients</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:title>Germline predisposition mutations in AML, a new way to resolve NETs, and venetoclax and BAX mutations in normal myeloid cells of CLL patients</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">5125191f-e9fe-46ca-a96c-d9bdc8d27547</guid>
      <link>https://share.transistor.fm/s/da41ce78</link>
      <description>
        <![CDATA[In this week's podcast, we’ll look at work from researchers who found pathogenic or likely pathogenic variants of cancer predisposition genes in nearly 14% of adults with AML. Next, we’ll review research demonstrating that a recently identified series of resolvins reduces neutrophil extracellular trap formation and enhances clearance of these NETs by macrophages, suggesting a new mechanism for the resolution of inflammation and coagulopathies associated with various infections. We’ll conclude with research demonstrating that patients with CLL undergoing long-term venetoclax treatment exhibit a high incidence of cytopenias, clonal hematopoiesis, and myeloid neoplasms, and may acquire BAX mutations in normal myeloid cells.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week's podcast, we’ll look at work from researchers who found pathogenic or likely pathogenic variants of cancer predisposition genes in nearly 14% of adults with AML. Next, we’ll review research demonstrating that a recently identified series of resolvins reduces neutrophil extracellular trap formation and enhances clearance of these NETs by macrophages, suggesting a new mechanism for the resolution of inflammation and coagulopathies associated with various infections. We’ll conclude with research demonstrating that patients with CLL undergoing long-term venetoclax treatment exhibit a high incidence of cytopenias, clonal hematopoiesis, and myeloid neoplasms, and may acquire BAX mutations in normal myeloid cells.]]>
      </content:encoded>
      <pubDate>Thu, 24 Feb 2022 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/da41ce78/9ec56f3f.mp3" length="18065428" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1126</itunes:duration>
      <itunes:summary>In this week's podcast, we’ll look at work from researchers who found pathogenic or likely pathogenic variants of cancer predisposition genes in nearly 14% of adults with AML. Next, we’ll review research demonstrating that a recently identified series of resolvins reduces neutrophil extracellular trap formation and enhances clearance of these NETs by macrophages, suggesting a new mechanism for the resolution of inflammation and coagulopathies associated with various infections. We’ll conclude with research demonstrating that patients with CLL undergoing long-term venetoclax treatment exhibit a high incidence of cytopenias, clonal hematopoiesis, and myeloid neoplasms, and may acquire BAX mutations in normal myeloid cells.</itunes:summary>
      <itunes:subtitle>In this week's podcast, we’ll look at work from researchers who found pathogenic or likely pathogenic variants of cancer predisposition genes in nearly 14% of adults with AML. Next, we’ll review research demonstrating that a recently identified series of </itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Ovarian reserve in sickle cell anemia, genomic landscape of adult T-cell leukemia/lymphoma, and a new prognostic index for HLH-associated heme malignancies </title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:title>Ovarian reserve in sickle cell anemia, genomic landscape of adult T-cell leukemia/lymphoma, and a new prognostic index for HLH-associated heme malignancies </itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">f4df67da-4179-425b-a383-3e74f8f67435</guid>
      <link>https://share.transistor.fm/s/b8eb2c8a</link>
      <description>
        <![CDATA[In this week’s podcast, we’ll discuss diminished ovarian reserve in young women with sickle cell anemia, learn more about genomic alterations in adult T-cell leukemia/lymphoma, and review a novel diagnostic and prognostic index for malignancies associated with hemophagocytic lymphohistiocytosis.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s podcast, we’ll discuss diminished ovarian reserve in young women with sickle cell anemia, learn more about genomic alterations in adult T-cell leukemia/lymphoma, and review a novel diagnostic and prognostic index for malignancies associated with hemophagocytic lymphohistiocytosis.]]>
      </content:encoded>
      <pubDate>Thu, 17 Feb 2022 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/b8eb2c8a/91e3a426.mp3" length="19339783" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1206</itunes:duration>
      <itunes:summary>In this week’s podcast, we’ll discuss diminished ovarian reserve in young women with sickle cell anemia, learn more about genomic alterations in adult T-cell leukemia/lymphoma, and review a novel diagnostic and prognostic index for malignancies associated with hemophagocytic lymphohistiocytosis.</itunes:summary>
      <itunes:subtitle>In this week’s podcast, we’ll discuss diminished ovarian reserve in young women with sickle cell anemia, learn more about genomic alterations in adult T-cell leukemia/lymphoma, and review a novel diagnostic and prognostic index for malignancies associated</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Role of HBO1 in HSC function, robust MRD analysis in multiple myeloma, and cardiac ferroptosis in sickle cell disease</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:title>Role of HBO1 in HSC function, robust MRD analysis in multiple myeloma, and cardiac ferroptosis in sickle cell disease</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">faa4c286-68f8-47f1-91db-b60a33c4c14a</guid>
      <link>https://share.transistor.fm/s/c89817aa</link>
      <description>
        <![CDATA[In this week’s podcast, we’ll look at research demonstrating that the histone acetyltransferase HBO1 is an essential regulator of hematopoietic stem cell function during adult hematopoiesis. Next, we’ll review a large, combined analysis confirming the prognostic value of MRD assessed with next-generation sequencing in 4 randomized trials evaluating daratumumab-based therapies. We’ll conclude with research demonstrating that ferroptosis, a specific type of regulated cell death, is a key mechanism of cardiomyopathy in sickle cell disease.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s podcast, we’ll look at research demonstrating that the histone acetyltransferase HBO1 is an essential regulator of hematopoietic stem cell function during adult hematopoiesis. Next, we’ll review a large, combined analysis confirming the prognostic value of MRD assessed with next-generation sequencing in 4 randomized trials evaluating daratumumab-based therapies. We’ll conclude with research demonstrating that ferroptosis, a specific type of regulated cell death, is a key mechanism of cardiomyopathy in sickle cell disease.]]>
      </content:encoded>
      <pubDate>Thu, 10 Feb 2022 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/c89817aa/b2d3ba1d.mp3" length="15728194" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>980</itunes:duration>
      <itunes:summary>In this week’s podcast, we’ll look at research demonstrating that the histone acetyltransferase HBO1 is an essential regulator of hematopoietic stem cell function during adult hematopoiesis. Next, we’ll review a large, combined analysis confirming the prognostic value of MRD assessed with next-generation sequencing in 4 randomized trials evaluating daratumumab-based therapies. We’ll conclude with research demonstrating that ferroptosis, a specific type of regulated cell death, is a key mechanism of cardiomyopathy in sickle cell disease.</itunes:summary>
      <itunes:subtitle>In this week’s podcast, we’ll look at research demonstrating that the histone acetyltransferase HBO1 is an essential regulator of hematopoietic stem cell function during adult hematopoiesis. Next, we’ll review a large, combined analysis confirming the pro</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>The ARID3A transcription factor suppresses leukemia, a COVID-19 booster shot benefits CLL patients, and advances in the genetics of congenital neutropenia</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:title>The ARID3A transcription factor suppresses leukemia, a COVID-19 booster shot benefits CLL patients, and advances in the genetics of congenital neutropenia</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">7173be7a-9958-42ff-ada6-0df016f85ae4</guid>
      <link>https://share.transistor.fm/s/da6b0384</link>
      <description>
        <![CDATA[In this week’s podcast, we’ll discuss the role of megakaryocytic transcription factor ARID3A in leukemia suppression, learn more about the efficacy of a third Pfizer BNT162b2 mRNA COVID-19 vaccine dose in patients with chronic lymphocytic leukemia, and discuss the association of heterozygous caseinolytic peptidase B variants with congenital neutropenia.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s podcast, we’ll discuss the role of megakaryocytic transcription factor ARID3A in leukemia suppression, learn more about the efficacy of a third Pfizer BNT162b2 mRNA COVID-19 vaccine dose in patients with chronic lymphocytic leukemia, and discuss the association of heterozygous caseinolytic peptidase B variants with congenital neutropenia.]]>
      </content:encoded>
      <pubDate>Thu, 03 Feb 2022 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/da6b0384/fa5dfc7b.mp3" length="19097899" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1191</itunes:duration>
      <itunes:summary>In this week’s podcast, we’ll discuss the role of megakaryocytic transcription factor ARID3A in leukemia suppression, learn more about the efficacy of a third Pfizer BNT162b2 mRNA COVID-19 vaccine dose in patients with chronic lymphocytic leukemia, and discuss the association of heterozygous caseinolytic peptidase B variants with congenital neutropenia.</itunes:summary>
      <itunes:subtitle>In this week’s podcast, we’ll discuss the role of megakaryocytic transcription factor ARID3A in leukemia suppression, learn more about the efficacy of a third Pfizer BNT162b2 mRNA COVID-19 vaccine dose in patients with chronic lymphocytic leukemia, and di</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Sustained MRD negativity &amp; outcomes in myeloma, therapeutic targeting of VWF in TTP, and improving CAR T-cells in CLL with PI3 kinase inhibition</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:title>Sustained MRD negativity &amp; outcomes in myeloma, therapeutic targeting of VWF in TTP, and improving CAR T-cells in CLL with PI3 kinase inhibition</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">3441a333-a135-4769-8697-1ab0ef973aae</guid>
      <link>https://share.transistor.fm/s/4f3d25bd</link>
      <description>
        <![CDATA[On this week’s podcast, we’ll review a recent analysis of phase 3 daratumumab studies looking at the prognostic impact of sustained minimal residual disease, or MRD negativity in patients with multiple myeloma. Next, we’ll hear more about a novel thrombolytic agent targeting von Willebrand factor that may represent a promising approach for the treatment of thrombotic thrombocytopenic purpura. We’ll conclude with a study demonstrating that PI3 kinase inhibitor duvelisib can be used to enhance the in vivo efficacy of CAR T cells in CLL.]]>
      </description>
      <content:encoded>
        <![CDATA[On this week’s podcast, we’ll review a recent analysis of phase 3 daratumumab studies looking at the prognostic impact of sustained minimal residual disease, or MRD negativity in patients with multiple myeloma. Next, we’ll hear more about a novel thrombolytic agent targeting von Willebrand factor that may represent a promising approach for the treatment of thrombotic thrombocytopenic purpura. We’ll conclude with a study demonstrating that PI3 kinase inhibitor duvelisib can be used to enhance the in vivo efficacy of CAR T cells in CLL.]]>
      </content:encoded>
      <pubDate>Fri, 28 Jan 2022 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/4f3d25bd/cf157ecd.mp3" length="18796900" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1172</itunes:duration>
      <itunes:summary>On this week’s podcast, we’ll review a recent analysis of phase 3 daratumumab studies looking at the prognostic impact of sustained minimal residual disease, or MRD negativity in patients with multiple myeloma. Next, we’ll hear more about a novel thrombolytic agent targeting von Willebrand factor that may represent a promising approach for the treatment of thrombotic thrombocytopenic purpura. We’ll conclude with a study demonstrating that PI3 kinase inhibitor duvelisib can be used to enhance the in vivo efficacy of CAR T cells in CLL.</itunes:summary>
      <itunes:subtitle>On this week’s podcast, we’ll review a recent analysis of phase 3 daratumumab studies looking at the prognostic impact of sustained minimal residual disease, or MRD negativity in patients with multiple myeloma. Next, we’ll hear more about a novel thrombol</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Does route of CNS prophylaxis for DLBCL matter?, the connection between CHIP and COPD, and ATRA plus low-dose rituximab in ITP</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:title>Does route of CNS prophylaxis for DLBCL matter?, the connection between CHIP and COPD, and ATRA plus low-dose rituximab in ITP</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">a779b536-cbdb-4957-92d1-325448dbb78e</guid>
      <link>https://share.transistor.fm/s/dc50a517</link>
      <description>
        <![CDATA[In this week’s podcast, we’ll discuss real-world outcomes comparing route of CNS prophylaxis for aggressive non-Hodgkin lymphomas, learn more about the association of clonal hematopoiesis with chronic obstructive pulmonary disease, and discuss the efficacy of all-trans retinoic acid plus low-dose rituximab in corticosteroid-resistant or relapsed immune thrombocytopenia.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s podcast, we’ll discuss real-world outcomes comparing route of CNS prophylaxis for aggressive non-Hodgkin lymphomas, learn more about the association of clonal hematopoiesis with chronic obstructive pulmonary disease, and discuss the efficacy of all-trans retinoic acid plus low-dose rituximab in corticosteroid-resistant or relapsed immune thrombocytopenia.]]>
      </content:encoded>
      <pubDate>Thu, 20 Jan 2022 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/dc50a517/c657e874.mp3" length="20917671" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1304</itunes:duration>
      <itunes:summary>In this week’s podcast, we’ll discuss real-world outcomes comparing route of CNS prophylaxis for aggressive non-Hodgkin lymphomas, learn more about the association of clonal hematopoiesis with chronic obstructive pulmonary disease, and discuss the efficacy of all-trans retinoic acid plus low-dose rituximab in corticosteroid-resistant or relapsed immune thrombocytopenia.</itunes:summary>
      <itunes:subtitle>In this week’s podcast, we’ll discuss real-world outcomes comparing route of CNS prophylaxis for aggressive non-Hodgkin lymphomas, learn more about the association of clonal hematopoiesis with chronic obstructive pulmonary disease, and discuss the efficac</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>A spectrum of ALK-positive histiocytosis, and metabolites as biomarkers for GvHD diagnosis and risk assignment</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:title>A spectrum of ALK-positive histiocytosis, and metabolites as biomarkers for GvHD diagnosis and risk assignment</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">74bf8340-8cdc-4084-9d9c-449c869cd0d8</guid>
      <link>https://share.transistor.fm/s/b3e2d506</link>
      <description>
        <![CDATA[On today’s podcast, we’ll explore the largest case series to date describing ALK-positive histiocytosis. The authors provide new insights on the disease and its treatment with ALK inhibitors, which can provide durable responses. We’ll also review with a study that pinpoints alpha-ketoglutaric acid as consistently elevated in pediatric chronic GvHD, and finds unique metabolomic patterns that appear to distinguish different GvHD subtypes.]]>
      </description>
      <content:encoded>
        <![CDATA[On today’s podcast, we’ll explore the largest case series to date describing ALK-positive histiocytosis. The authors provide new insights on the disease and its treatment with ALK inhibitors, which can provide durable responses. We’ll also review with a study that pinpoints alpha-ketoglutaric acid as consistently elevated in pediatric chronic GvHD, and finds unique metabolomic patterns that appear to distinguish different GvHD subtypes.]]>
      </content:encoded>
      <pubDate>Thu, 13 Jan 2022 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/b3e2d506/6a6a1745.mp3" length="14110884" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>879</itunes:duration>
      <itunes:summary>On today’s podcast, we’ll explore the largest case series to date describing ALK-positive histiocytosis. The authors provide new insights on the disease and its treatment with ALK inhibitors, which can provide durable responses. We’ll also review with a study that pinpoints alpha-ketoglutaric acid as consistently elevated in pediatric chronic GvHD, and finds unique metabolomic patterns that appear to distinguish different GvHD subtypes.</itunes:summary>
      <itunes:subtitle>On today’s podcast, we’ll explore the largest case series to date describing ALK-positive histiocytosis. The authors provide new insights on the disease and its treatment with ALK inhibitors, which can provide durable responses. We’ll also review with a s</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Long-term outcomes in severe aplastic anemia, cytoprotective effects of factor VIIa, and the role of IL-1 in hematopoietic stem cell ageing</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:title>Long-term outcomes in severe aplastic anemia, cytoprotective effects of factor VIIa, and the role of IL-1 in hematopoietic stem cell ageing</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">871a4e65-3a9c-46b1-b1e6-a2eab667df5e</guid>
      <link>https://share.transistor.fm/s/eae1d656</link>
      <description>
        <![CDATA[In this week’s podcast, we’ll talk about the long-term outcomes in patients with severe aplastic anemia treated with immunosuppression and eltrombopag, learn more about anti-inflammatory and cytoprotective effects of factor VIIa, and discuss the role of IL-1 in microbiome-induced ageing of hematopoietic stem cells in mice.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s podcast, we’ll talk about the long-term outcomes in patients with severe aplastic anemia treated with immunosuppression and eltrombopag, learn more about anti-inflammatory and cytoprotective effects of factor VIIa, and discuss the role of IL-1 in microbiome-induced ageing of hematopoietic stem cells in mice.]]>
      </content:encoded>
      <pubDate>Thu, 06 Jan 2022 13:53:48 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/eae1d656/d19e2316.mp3" length="19814189" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1235</itunes:duration>
      <itunes:summary>In this week’s podcast, we’ll talk about the long-term outcomes in patients with severe aplastic anemia treated with immunosuppression and eltrombopag, learn more about anti-inflammatory and cytoprotective effects of factor VIIa, and discuss the role of IL-1 in microbiome-induced ageing of hematopoietic stem cells in mice.</itunes:summary>
      <itunes:subtitle>In this week’s podcast, we’ll talk about the long-term outcomes in patients with severe aplastic anemia treated with immunosuppression and eltrombopag, learn more about anti-inflammatory and cytoprotective effects of factor VIIa, and discuss the role of I</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>CRISPR cure for XMEN disease?, JAK inhibition in T-cell lymphomas, and intracranial hemorrhage in hemophilia</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>CRISPR cure for XMEN disease?, JAK inhibition in T-cell lymphomas, and intracranial hemorrhage in hemophilia</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">a98976df-d5ba-4687-b4e5-c3ce9ed08911</guid>
      <link>https://share.transistor.fm/s/b846db9d</link>
      <description>
        <![CDATA[In this week’s episode, we’ll review a research article that provides the first description of a targeted gene insertion approach to correct the genetic mutation underlying XMEN disease. Next, we’ll cover results of a phase 2 study that provides proof-of-principle that the JAK/STAT pathway is a promising target for the treatment of peripheral T-cell lymphomas. We’ll close with a study providing precise and up-to-date estimates on the incidence of  intracranial hemorrhage in patients with hemophilia that could have important implications for preventive strategies.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we’ll review a research article that provides the first description of a targeted gene insertion approach to correct the genetic mutation underlying XMEN disease. Next, we’ll cover results of a phase 2 study that provides proof-of-principle that the JAK/STAT pathway is a promising target for the treatment of peripheral T-cell lymphomas. We’ll close with a study providing precise and up-to-date estimates on the incidence of  intracranial hemorrhage in patients with hemophilia that could have important implications for preventive strategies.]]>
      </content:encoded>
      <pubDate>Thu, 30 Dec 2021 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/b846db9d/430ee42f.mp3" length="18912245" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1179</itunes:duration>
      <itunes:summary>In this week’s episode, we’ll review a research article that provides the first description of a targeted gene insertion approach to correct the genetic mutation underlying XMEN disease. Next, we’ll cover results of a phase 2 study that provides proof-of-principle that the JAK/STAT pathway is a promising target for the treatment of peripheral T-cell lymphomas. We’ll close with a study providing precise and up-to-date estimates on the incidence of  intracranial hemorrhage in patients with hemophilia that could have important implications for preventive strategies.</itunes:summary>
      <itunes:subtitle>In this week’s episode, we’ll review a research article that provides the first description of a targeted gene insertion approach to correct the genetic mutation underlying XMEN disease. Next, we’ll cover results of a phase 2 study that provides proof-of-</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Antigen presentation by platelet extracellular vesicles, fibril-reactive monoclonal antibody therapy for AL amyloidosis, and targeting gasdermin D in sepsis</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Antigen presentation by platelet extracellular vesicles, fibril-reactive monoclonal antibody therapy for AL amyloidosis, and targeting gasdermin D in sepsis</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">ca9a32f5-1498-4c77-8d4f-617840901caa</guid>
      <link>https://share.transistor.fm/s/132d018d</link>
      <description>
        <![CDATA[In this week’s episode, we’ll review a research article demonstrating that some platelet-derived extracellular vesicles harbor proteasomes that can process and present antigens via MHC class I molecules. Next, we’ll review results of a phase 1 study of a fibril-reactive monoclonal antibody that was well tolerated and led to rapid, sustained organ responses in patients with AL amyloidosis. We’ll close with a research article suggesting that the pore-forming protein gasdermin D, which plays a crucial role in the release of neutrophil extracellular traps, is a promising drug target in sepsis.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we’ll review a research article demonstrating that some platelet-derived extracellular vesicles harbor proteasomes that can process and present antigens via MHC class I molecules. Next, we’ll review results of a phase 1 study of a fibril-reactive monoclonal antibody that was well tolerated and led to rapid, sustained organ responses in patients with AL amyloidosis. We’ll close with a research article suggesting that the pore-forming protein gasdermin D, which plays a crucial role in the release of neutrophil extracellular traps, is a promising drug target in sepsis.]]>
      </content:encoded>
      <pubDate>Thu, 23 Dec 2021 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/132d018d/6fc1f18b.mp3" length="18441355" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1149</itunes:duration>
      <itunes:summary>In this week’s episode, we’ll review a research article demonstrating that some platelet-derived extracellular vesicles harbor proteasomes that can process and present antigens via MHC class I molecules. Next, we’ll review results of a phase 1 study of a fibril-reactive monoclonal antibody that was well tolerated and led to rapid, sustained organ responses in patients with AL amyloidosis. We’ll close with a research article suggesting that the pore-forming protein gasdermin D, which plays a crucial role in the release of neutrophil extracellular traps, is a promising drug target in sepsis.</itunes:summary>
      <itunes:subtitle>In this week’s episode, we’ll review a research article demonstrating that some platelet-derived extracellular vesicles harbor proteasomes that can process and present antigens via MHC class I molecules. Next, we’ll review results of a phase 1 study of a </itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Mesenchymal stromal cells in SCD, CAR T-cell-mediated hematotoxicity in B-cell lymphoma, and dual cytokine blockade in GVHD</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Mesenchymal stromal cells in SCD, CAR T-cell-mediated hematotoxicity in B-cell lymphoma, and dual cytokine blockade in GVHD</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">858cea94-15fc-4196-87c3-2035a39fc057</guid>
      <link>https://share.transistor.fm/s/1bdaeb00</link>
      <description>
        <![CDATA[In this week’s episode, we’ll talk about the functional properties of mesenchymal stromal cells in sickle cell disease, learn more about CAR T-cell-mediated hematotoxicity in relapsed/refractory B-cell lymphoma, and discuss dual cytokine blockade in graft-versus-host disease.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we’ll talk about the functional properties of mesenchymal stromal cells in sickle cell disease, learn more about CAR T-cell-mediated hematotoxicity in relapsed/refractory B-cell lymphoma, and discuss dual cytokine blockade in graft-versus-host disease.]]>
      </content:encoded>
      <pubDate>Thu, 16 Dec 2021 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/1bdaeb00/6e8e3bea.mp3" length="17454683" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1088</itunes:duration>
      <itunes:summary>In this week’s episode, we’ll talk about the functional properties of mesenchymal stromal cells in sickle cell disease, learn more about CAR T-cell-mediated hematotoxicity in relapsed/refractory B-cell lymphoma, and discuss dual cytokine blockade in graft-versus-host disease.</itunes:summary>
      <itunes:subtitle>In this week’s episode, we’ll talk about the functional properties of mesenchymal stromal cells in sickle cell disease, learn more about CAR T-cell-mediated hematotoxicity in relapsed/refractory B-cell lymphoma, and discuss dual cytokine blockade in graft</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>PROTACs for JAKs in CRLF2-rearranged ALL, risk stratification in Down syndrome-associated leukemia, and how losing sialic acid activates immune cells in ITP</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>PROTACs for JAKs in CRLF2-rearranged ALL, risk stratification in Down syndrome-associated leukemia, and how losing sialic acid activates immune cells in ITP</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">f30028ae-7fe0-4176-ae37-8ef582765d11</guid>
      <link>https://share.transistor.fm/s/3af19840</link>
      <description>
        <![CDATA[In this week’s episode, we’ll learn about a new approach for targeting Janus kinases in CRLF2-rearranged ALL, discuss risk stratification for myeloid leukemia in children with Down syndrome and learn more about how sialic acid alterations on megakaryocyte antigens regulate immune cells and platelet production.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we’ll learn about a new approach for targeting Janus kinases in CRLF2-rearranged ALL, discuss risk stratification for myeloid leukemia in children with Down syndrome and learn more about how sialic acid alterations on megakaryocyte antigens regulate immune cells and platelet production.]]>
      </content:encoded>
      <pubDate>Thu, 09 Dec 2021 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/3af19840/802064af.mp3" length="18411110" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1148</itunes:duration>
      <itunes:summary>In this week’s episode, we’ll learn about a new approach for targeting Janus kinases in CRLF2-rearranged ALL, discuss risk stratification for myeloid leukemia in children with Down syndrome and learn more about how sialic acid alterations on megakaryocyte antigens regulate immune cells and platelet production.</itunes:summary>
      <itunes:subtitle>In this week’s episode, we’ll learn about a new approach for targeting Janus kinases in CRLF2-rearranged ALL, discuss risk stratification for myeloid leukemia in children with Down syndrome and learn more about how sialic acid alterations on megakaryocyte</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Belumosudil for chronic GVHD, mechanistic insights into VITT, and factors driving molecular response in IFNα-treated MPNs </title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Belumosudil for chronic GVHD, mechanistic insights into VITT, and factors driving molecular response in IFNα-treated MPNs </itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">ff290d30-34aa-4ba3-a82c-231deb6f1907</guid>
      <link>https://share.transistor.fm/s/8e05b2ef</link>
      <description>
        <![CDATA[First on today’s podcast, we’ll review results of a randomized phase 2 study demonstrating that inhibition of ROCK2 with belumosudil is well tolerated and effective in patients with steroid-refractory graft-versus-host disease. Next, we’ll review the work of researchers who have uncovered new insights into the immunopathogenesis of vaccine-induced immune thrombotic thrombocytopenia. And we’ll close with a report of a prospective longitudinal analysis that elucidates the dynamics of mutated hematopoietic stem and progenitor cells during therapy with interferon-alpha in patients with BCR-ABL1 negative myeloproliferative neoplasms.]]>
      </description>
      <content:encoded>
        <![CDATA[First on today’s podcast, we’ll review results of a randomized phase 2 study demonstrating that inhibition of ROCK2 with belumosudil is well tolerated and effective in patients with steroid-refractory graft-versus-host disease. Next, we’ll review the work of researchers who have uncovered new insights into the immunopathogenesis of vaccine-induced immune thrombotic thrombocytopenia. And we’ll close with a report of a prospective longitudinal analysis that elucidates the dynamics of mutated hematopoietic stem and progenitor cells during therapy with interferon-alpha in patients with BCR-ABL1 negative myeloproliferative neoplasms.]]>
      </content:encoded>
      <pubDate>Thu, 02 Dec 2021 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/8e05b2ef/aedaa8c3.mp3" length="19609587" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1222</itunes:duration>
      <itunes:summary>First on today’s podcast, we’ll review results of a randomized phase 2 study demonstrating that inhibition of ROCK2 with belumosudil is well tolerated and effective in patients with steroid-refractory graft-versus-host disease. Next, we’ll review the work of researchers who have uncovered new insights into the immunopathogenesis of vaccine-induced immune thrombotic thrombocytopenia. And we’ll close with a report of a prospective longitudinal analysis that elucidates the dynamics of mutated hematopoietic stem and progenitor cells during therapy with interferon-alpha in patients with BCR-ABL1 negative myeloproliferative neoplasms.</itunes:summary>
      <itunes:subtitle>First on today’s podcast, we’ll review results of a randomized phase 2 study demonstrating that inhibition of ROCK2 with belumosudil is well tolerated and effective in patients with steroid-refractory graft-versus-host disease. Next, we’ll review the work</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Post-vaccination COVID-19 in patients with hematologic malignancies</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Post-vaccination COVID-19 in patients with hematologic malignancies</itunes:title>
      <itunes:episodeType>bonus</itunes:episodeType>
      <guid isPermaLink="false">66b22642-93ca-40db-8d3b-5e0a790da139</guid>
      <link>https://share.transistor.fm/s/6e44507b</link>
      <description>
        <![CDATA[All four studies included in this podcast present preliminary data with modest numbers of patients, and therefore, the findings should be interpreted with these limitations. Likewise, the impact of specific strains and waning antibody levels after COVID-19 vaccination will require further follow-up, since the Delta variant was not the dominant strain in circulation at the time of this research. The first two studies assess the immune responses to vaccination in two specific high-risk populations, namely, patients with lymphoma and multiple myeloma. The last two studies, one from a large European consortium and the other based on nationwide data from Israel, report on the incidence, risk factors and short-term outcomes of COVID-19 breakthrough infection in vaccinated patients with hematologic malignancies.]]>
      </description>
      <content:encoded>
        <![CDATA[All four studies included in this podcast present preliminary data with modest numbers of patients, and therefore, the findings should be interpreted with these limitations. Likewise, the impact of specific strains and waning antibody levels after COVID-19 vaccination will require further follow-up, since the Delta variant was not the dominant strain in circulation at the time of this research. The first two studies assess the immune responses to vaccination in two specific high-risk populations, namely, patients with lymphoma and multiple myeloma. The last two studies, one from a large European consortium and the other based on nationwide data from Israel, report on the incidence, risk factors and short-term outcomes of COVID-19 breakthrough infection in vaccinated patients with hematologic malignancies.]]>
      </content:encoded>
      <pubDate>Wed, 01 Dec 2021 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/6e44507b/908a6254.mp3" length="32406875" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1348</itunes:duration>
      <itunes:summary>All four studies included in this podcast present preliminary data with modest numbers of patients, and therefore, the findings should be interpreted with these limitations. Likewise, the impact of specific strains and waning antibody levels after COVID-19 vaccination will require further follow-up, since the Delta variant was not the dominant strain in circulation at the time of this research. The first two studies assess the immune responses to vaccination in two specific high-risk populations, namely, patients with lymphoma and multiple myeloma. The last two studies, one from a large European consortium and the other based on nationwide data from Israel, report on the incidence, risk factors and short-term outcomes of COVID-19 breakthrough infection in vaccinated patients with hematologic malignancies.</itunes:summary>
      <itunes:subtitle>All four studies included in this podcast present preliminary data with modest numbers of patients, and therefore, the findings should be interpreted with these limitations. Likewise, the impact of specific strains and waning antibody levels after COVID-1</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Asciminib versus bosutinib in CML; dopamine signaling and hematopoietic stem cells; complement factor C5 and VTE risk</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Asciminib versus bosutinib in CML; dopamine signaling and hematopoietic stem cells; complement factor C5 and VTE risk</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">f5bf401c-ab97-48af-8984-a02c597707e2</guid>
      <link>https://share.transistor.fm/s/ea833cc6</link>
      <description>
        <![CDATA[In this week’s episode, we’ll learn more about the efficacy of asciminib in patients with chronic myeloid leukemia who are resistant or intolerant to two or more tyrosine kinase inhibitors, discuss the role of dopamine signaling in hematopoietic stem and progenitor cell function, and learn more about elevated plasma concentration of complement factor C5 as a risk factor for venous thromboembolism.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we’ll learn more about the efficacy of asciminib in patients with chronic myeloid leukemia who are resistant or intolerant to two or more tyrosine kinase inhibitors, discuss the role of dopamine signaling in hematopoietic stem and progenitor cell function, and learn more about elevated plasma concentration of complement factor C5 as a risk factor for venous thromboembolism.]]>
      </content:encoded>
      <pubDate>Thu, 25 Nov 2021 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/ea833cc6/c57a03a8.mp3" length="20109378" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1254</itunes:duration>
      <itunes:summary>In this week’s episode, we’ll learn more about the efficacy of asciminib in patients with chronic myeloid leukemia who are resistant or intolerant to two or more tyrosine kinase inhibitors, discuss the role of dopamine signaling in hematopoietic stem and progenitor cell function, and learn more about elevated plasma concentration of complement factor C5 as a risk factor for venous thromboembolism.</itunes:summary>
      <itunes:subtitle>In this week’s episode, we’ll learn more about the efficacy of asciminib in patients with chronic myeloid leukemia who are resistant or intolerant to two or more tyrosine kinase inhibitors, discuss the role of dopamine signaling in hematopoietic stem and </itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Danicopan add-on therapy in PNH, neural networks to identify bone marrow cells, and RNA editome and hematopoiesis</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Danicopan add-on therapy in PNH, neural networks to identify bone marrow cells, and RNA editome and hematopoiesis</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">868044a8-43da-456e-830f-a7491ea44eb6</guid>
      <link>https://share.transistor.fm/s/37635118</link>
      <description>
        <![CDATA[In this week’s episode, we’ll review results of a phase 2 study showing the beneficial effects of a first-in-class factor D inhibitor as add-on therapy in PNH patients who remain anemic and are transfusion-dependent despite C5 inhibition. Next, we’ll review the work of researchers who have developed a neural network that they say is highly accurate in differentiating between bone marrow cell morphologies. We’ll close with a report demonstrating that RNA editing of antizyme inhibitor 1, or Azin1, is a novel regulator of hematopoietic cell fate that can influence self-renewal and differentiation.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we’ll review results of a phase 2 study showing the beneficial effects of a first-in-class factor D inhibitor as add-on therapy in PNH patients who remain anemic and are transfusion-dependent despite C5 inhibition. Next, we’ll review the work of researchers who have developed a neural network that they say is highly accurate in differentiating between bone marrow cell morphologies. We’ll close with a report demonstrating that RNA editing of antizyme inhibitor 1, or Azin1, is a novel regulator of hematopoietic cell fate that can influence self-renewal and differentiation.]]>
      </content:encoded>
      <pubDate>Thu, 18 Nov 2021 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/37635118/11347c94.mp3" length="16954180" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1056</itunes:duration>
      <itunes:summary>In this week’s episode, we’ll review results of a phase 2 study showing the beneficial effects of a first-in-class factor D inhibitor as add-on therapy in PNH patients who remain anemic and are transfusion-dependent despite C5 inhibition. Next, we’ll review the work of researchers who have developed a neural network that they say is highly accurate in differentiating between bone marrow cell morphologies. We’ll close with a report demonstrating that RNA editing of antizyme inhibitor 1, or Azin1, is a novel regulator of hematopoietic cell fate that can influence self-renewal and differentiation.</itunes:summary>
      <itunes:subtitle>In this week’s episode, we’ll review results of a phase 2 study showing the beneficial effects of a first-in-class factor D inhibitor as add-on therapy in PNH patients who remain anemic and are transfusion-dependent despite C5 inhibition. Next, we’ll revi</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Machine learning in classification of AML, aging bone marrow in leukemia, and treating bleeding disorders of unknown cause</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Machine learning in classification of AML, aging bone marrow in leukemia, and treating bleeding disorders of unknown cause</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">1580021b-c3d8-41ee-995d-18f1db6161c1</guid>
      <link>https://share.transistor.fm/s/534f6209</link>
      <description>
        <![CDATA[In this week’s episode, we’ll learn more about the application of machine learning in molecular subclassification and prognostication of acute myeloid leukemia or AML, discuss the role of aging bone marrow in leukemia progression, and learn more about the challenges in treating bleeding disorders of unknown cause.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we’ll learn more about the application of machine learning in molecular subclassification and prognostication of acute myeloid leukemia or AML, discuss the role of aging bone marrow in leukemia progression, and learn more about the challenges in treating bleeding disorders of unknown cause.]]>
      </content:encoded>
      <pubDate>Thu, 11 Nov 2021 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/534f6209/cdf51cd0.mp3" length="18695680" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1165</itunes:duration>
      <itunes:summary>In this week’s episode, we’ll learn more about the application of machine learning in molecular subclassification and prognostication of acute myeloid leukemia or AML, discuss the role of aging bone marrow in leukemia progression, and learn more about the challenges in treating bleeding disorders of unknown cause.</itunes:summary>
      <itunes:subtitle>In this week’s episode, we’ll learn more about the application of machine learning in molecular subclassification and prognostication of acute myeloid leukemia or AML, discuss the role of aging bone marrow in leukemia progression, and learn more about the</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Anti-CD36-antibody therapy of neonatal alloimmune thrombocytopenia, costs of hemophilia B gene therapy, and insights into erythroid maturation</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Anti-CD36-antibody therapy of neonatal alloimmune thrombocytopenia, costs of hemophilia B gene therapy, and insights into erythroid maturation</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">400c06e9-df29-4430-9055-190dcc67e163</guid>
      <link>https://share.transistor.fm/s/933fe46c</link>
      <description>
        <![CDATA[In this week’s episode, we’ll review a research article showing beneficial effects of prenatal immunotherapy in a mouse model of anti-CD36-mediated fetal and neonatal alloimmune thrombocytopenia. Next, we’ll look at results of a simulation analysis suggesting that gene therapy for hemophilia B is more cost-effective than on-demand or prophylactic factor treatment. We’ll conclude with a report which provides important new insights into regulation of terminal erythroid maturation at the transcriptional level that may help improve our understanding of normal and abnormal erythropoiesis. ]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we’ll review a research article showing beneficial effects of prenatal immunotherapy in a mouse model of anti-CD36-mediated fetal and neonatal alloimmune thrombocytopenia. Next, we’ll look at results of a simulation analysis suggesting that gene therapy for hemophilia B is more cost-effective than on-demand or prophylactic factor treatment. We’ll conclude with a report which provides important new insights into regulation of terminal erythroid maturation at the transcriptional level that may help improve our understanding of normal and abnormal erythropoiesis. ]]>
      </content:encoded>
      <pubDate>Thu, 04 Nov 2021 13:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/933fe46c/5790ef5a.mp3" length="17072083" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1064</itunes:duration>
      <itunes:summary>In this week’s episode, we’ll review a research article showing beneficial effects of prenatal immunotherapy in a mouse model of anti-CD36-mediated fetal and neonatal alloimmune thrombocytopenia. Next, we’ll look at results of a simulation analysis suggesting that gene therapy for hemophilia B is more cost-effective than on-demand or prophylactic factor treatment. We’ll conclude with a report which provides important new insights into regulation of terminal erythroid maturation at the transcriptional level that may help improve our understanding of normal and abnormal erythropoiesis. </itunes:summary>
      <itunes:subtitle>In this week’s episode, we’ll review a research article showing beneficial effects of prenatal immunotherapy in a mouse model of anti-CD36-mediated fetal and neonatal alloimmune thrombocytopenia. Next, we’ll look at results of a simulation analysis sugges</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Genetic risks for CMV after BMT, multiplex gene editing to reactivate HbF, and rewiring plasma cells in light chain amyloidosis and myeloma</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Genetic risks for CMV after BMT, multiplex gene editing to reactivate HbF, and rewiring plasma cells in light chain amyloidosis and myeloma</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">76c24413-7616-4591-803d-85fa7ab2a026</guid>
      <link>https://share.transistor.fm/s/76c6d0f3</link>
      <description>
        <![CDATA[In this week’s episode, we’ll discuss an analysis of genetic risks for CMV infection after an allogeneic hematopoietic stem cell transplant, learn more about a new multiplex gene editing approach to reactivate fetal hemoglobin in thalassemia, and discuss transcriptional rewiring of normal plasma cell development in light-chain amyloidosis and myeloma.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we’ll discuss an analysis of genetic risks for CMV infection after an allogeneic hematopoietic stem cell transplant, learn more about a new multiplex gene editing approach to reactivate fetal hemoglobin in thalassemia, and discuss transcriptional rewiring of normal plasma cell development in light-chain amyloidosis and myeloma.]]>
      </content:encoded>
      <pubDate>Thu, 28 Oct 2021 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/76c6d0f3/107b97df.mp3" length="18811147" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1173</itunes:duration>
      <itunes:summary>In this week’s episode, we’ll discuss an analysis of genetic risks for CMV infection after an allogeneic hematopoietic stem cell transplant, learn more about a new multiplex gene editing approach to reactivate fetal hemoglobin in thalassemia, and discuss transcriptional rewiring of normal plasma cell development in light-chain amyloidosis and myeloma.</itunes:summary>
      <itunes:subtitle>In this week’s episode, we’ll discuss an analysis of genetic risks for CMV infection after an allogeneic hematopoietic stem cell transplant, learn more about a new multiplex gene editing approach to reactivate fetal hemoglobin in thalassemia, and discuss </itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Omidubicel vs standard umbilical cord blood transplant, CAR T-cell associated lymphomas, and CD63 and ferritin export</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Omidubicel vs standard umbilical cord blood transplant, CAR T-cell associated lymphomas, and CD63 and ferritin export</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">803b6c93-105e-47a8-ad95-a62b81c79ce0</guid>
      <link>https://share.transistor.fm/s/dc26c2a4</link>
      <description>
        <![CDATA[In this week’s episode, we’ll review results of a phase 3 randomized study demonstrating shorter time to neutrophil and platelet recovery with an ex vivo expanded hematopoietic progenitor cell product called omidubicel as compared to standard umbilical cord transplantation. Next, we’ll look at preliminary data on the development of lymphomas originating from piggyBac-modified CD19 CAR T-cells, sounding a note of caution for researchers exploring new gene modification methodologies for CAR T-cell production. We’ll conclude with a report suggesting that the vesicular protein CD63 may orchestrate the transfer of iron-rich ferritin among cells.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we’ll review results of a phase 3 randomized study demonstrating shorter time to neutrophil and platelet recovery with an ex vivo expanded hematopoietic progenitor cell product called omidubicel as compared to standard umbilical cord transplantation. Next, we’ll look at preliminary data on the development of lymphomas originating from piggyBac-modified CD19 CAR T-cells, sounding a note of caution for researchers exploring new gene modification methodologies for CAR T-cell production. We’ll conclude with a report suggesting that the vesicular protein CD63 may orchestrate the transfer of iron-rich ferritin among cells.]]>
      </content:encoded>
      <pubDate>Thu, 21 Oct 2021 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/dc26c2a4/a3378e13.mp3" length="19234249" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1199</itunes:duration>
      <itunes:summary>In this week’s episode, we’ll review results of a phase 3 randomized study demonstrating shorter time to neutrophil and platelet recovery with an ex vivo expanded hematopoietic progenitor cell product called omidubicel as compared to standard umbilical cord transplantation. Next, we’ll look at preliminary data on the development of lymphomas originating from piggyBac-modified CD19 CAR T-cells, sounding a note of caution for researchers exploring new gene modification methodologies for CAR T-cell production. We’ll conclude with a report suggesting that the vesicular protein CD63 may orchestrate the transfer of iron-rich ferritin among cells.</itunes:summary>
      <itunes:subtitle>In this week’s episode, we’ll review results of a phase 3 randomized study demonstrating shorter time to neutrophil and platelet recovery with an ex vivo expanded hematopoietic progenitor cell product called omidubicel as compared to standard umbilical co</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Iron homeostasis and anemia of inflammation in TB, and long-term outcomes of gene therapy in adenosine deaminase-deficient SCID patients</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Iron homeostasis and anemia of inflammation in TB, and long-term outcomes of gene therapy in adenosine deaminase-deficient SCID patients</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">6ffcc4a9-5033-49ca-abf5-a8a8cd133df3</guid>
      <link>https://share.transistor.fm/s/135373fd</link>
      <description>
        <![CDATA[In this week’s episode, we will review a study that prospectively followed tuberculosis patients after treatment initiation to evaluate iron handling during the resolution of inflammatory anemia. We will also examine clinical benefit and long-term safety of gamma-retroviral gene therapy in patients with adenosine deaminase deficient severe combined immunodeficiency.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we will review a study that prospectively followed tuberculosis patients after treatment initiation to evaluate iron handling during the resolution of inflammatory anemia. We will also examine clinical benefit and long-term safety of gamma-retroviral gene therapy in patients with adenosine deaminase deficient severe combined immunodeficiency.]]>
      </content:encoded>
      <pubDate>Thu, 14 Oct 2021 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/135373fd/1389b07c.mp3" length="14012163" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>873</itunes:duration>
      <itunes:summary>In this week’s episode, we will review a study that prospectively followed tuberculosis patients after treatment initiation to evaluate iron handling during the resolution of inflammatory anemia. We will also examine clinical benefit and long-term safety of gamma-retroviral gene therapy in patients with adenosine deaminase deficient severe combined immunodeficiency.</itunes:summary>
      <itunes:subtitle>In this week’s episode, we will review a study that prospectively followed tuberculosis patients after treatment initiation to evaluate iron handling during the resolution of inflammatory anemia. We will also examine clinical benefit and long-term safety </itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Immune megakaryocytes, PD1 deletions in CTCL, and COVID-19 vaccine and VITT</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Immune megakaryocytes, PD1 deletions in CTCL, and COVID-19 vaccine and VITT</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">4b48725e-881f-43dd-b70a-11efcb6c1722</guid>
      <link>https://share.transistor.fm/s/f89a391e</link>
      <description>
        <![CDATA[In this week’s episode, we’ll review a study providing new insights on megakaryocyte diversity and function, including a unique subpopulation that may act as immune cells. Next, we’ll review research that intriguingly reveals a putative role for the PD1 gene in cutaneous T-cell lymphoma. Lastly, we’ll conclude with a report demonstrating a lack of cross-reaction between the antibodies that cause vaccine-induced thrombocytopenia and thrombosis, and the COVID-19 spike protein.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we’ll review a study providing new insights on megakaryocyte diversity and function, including a unique subpopulation that may act as immune cells. Next, we’ll review research that intriguingly reveals a putative role for the PD1 gene in cutaneous T-cell lymphoma. Lastly, we’ll conclude with a report demonstrating a lack of cross-reaction between the antibodies that cause vaccine-induced thrombocytopenia and thrombosis, and the COVID-19 spike protein.]]>
      </content:encoded>
      <pubDate>Thu, 07 Oct 2021 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/f89a391e/c7219799.mp3" length="18323512" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1142</itunes:duration>
      <itunes:summary>In this week’s episode, we’ll review a study providing new insights on megakaryocyte diversity and function, including a unique subpopulation that may act as immune cells. Next, we’ll review research that intriguingly reveals a putative role for the PD1 gene in cutaneous T-cell lymphoma. Lastly, we’ll conclude with a report demonstrating a lack of cross-reaction between the antibodies that cause vaccine-induced thrombocytopenia and thrombosis, and the COVID-19 spike protein.</itunes:summary>
      <itunes:subtitle>In this week’s episode, we’ll review a study providing new insights on megakaryocyte diversity and function, including a unique subpopulation that may act as immune cells. Next, we’ll review research that intriguingly reveals a putative role for the PD1 g</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Inhibition of P-selectin as an anticoagulant, prognostic implications of CEBPA mutations in AML, and treating sickle cell disease with voxelitor</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Inhibition of P-selectin as an anticoagulant, prognostic implications of CEBPA mutations in AML, and treating sickle cell disease with voxelitor</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">04a35eb9-b017-4032-aeb2-6b1895507b09</guid>
      <link>https://share.transistor.fm/s/f3f83d82</link>
      <description>
        <![CDATA[In this week’s episode, we’ll review a study that demonstrates the efficacy of a synthetic inhibitor termed P-G6 that blocks P-selectin signaling and reduces thrombus formation in a pre-clinical model of non-occlusive venous thrombosis, learn more about how biallelic and single bZip CEBPA mutations have an equally favorable prognostic impact in acute myeloid leukemia, and examine the effects of modifying the pathophysiology of sickle cell anemia with therapeutic agents that increase oxygen affinity.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we’ll review a study that demonstrates the efficacy of a synthetic inhibitor termed P-G6 that blocks P-selectin signaling and reduces thrombus formation in a pre-clinical model of non-occlusive venous thrombosis, learn more about how biallelic and single bZip CEBPA mutations have an equally favorable prognostic impact in acute myeloid leukemia, and examine the effects of modifying the pathophysiology of sickle cell anemia with therapeutic agents that increase oxygen affinity.]]>
      </content:encoded>
      <pubDate>Thu, 30 Sep 2021 13:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/f3f83d82/22709636.mp3" length="14873029" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>926</itunes:duration>
      <itunes:summary>In this week’s episode, we’ll review a study that demonstrates the efficacy of a synthetic inhibitor termed P-G6 that blocks P-selectin signaling and reduces thrombus formation in a pre-clinical model of non-occlusive venous thrombosis, learn more about how biallelic and single bZip CEBPA mutations have an equally favorable prognostic impact in acute myeloid leukemia, and examine the effects of modifying the pathophysiology of sickle cell anemia with therapeutic agents that increase oxygen affinity.</itunes:summary>
      <itunes:subtitle>In this week’s episode, we’ll review a study that demonstrates the efficacy of a synthetic inhibitor termed P-G6 that blocks P-selectin signaling and reduces thrombus formation in a pre-clinical model of non-occlusive venous thrombosis, learn more about h</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Caution on JAK inhibitors in HLH, CD44 loss sensitizes AML to venetoclax, and new insights on cell cycle control in Richter transformation</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Caution on JAK inhibitors in HLH, CD44 loss sensitizes AML to venetoclax, and new insights on cell cycle control in Richter transformation</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">c8ab8c00-683c-4d1a-b402-cb8a47ecf0b9</guid>
      <link>https://share.transistor.fm/s/71eeff89</link>
      <description>
        <![CDATA[In this week’s episode, we review results of preclinical investigations that sound a note of caution regarding the potential use of JAK inhibitors as treatment for hemophagocytic lymphohistiocytosis (or HLH), research that provides new insights on how CD44 loss of function sensitizes AML cells to the BCL-2 inhibitor venetoclax, and conclude with a report that demonstrates cooperation between B cell receptor signaling and genetic lesions in CDKN2A, CDKN2B and TP53 in Richter transformation.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we review results of preclinical investigations that sound a note of caution regarding the potential use of JAK inhibitors as treatment for hemophagocytic lymphohistiocytosis (or HLH), research that provides new insights on how CD44 loss of function sensitizes AML cells to the BCL-2 inhibitor venetoclax, and conclude with a report that demonstrates cooperation between B cell receptor signaling and genetic lesions in CDKN2A, CDKN2B and TP53 in Richter transformation.]]>
      </content:encoded>
      <pubDate>Thu, 23 Sep 2021 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/71eeff89/d1a1d3ab.mp3" length="14875923" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>927</itunes:duration>
      <itunes:summary>In this week’s episode, we review results of preclinical investigations that sound a note of caution regarding the potential use of JAK inhibitors as treatment for hemophagocytic lymphohistiocytosis (or HLH), research that provides new insights on how CD44 loss of function sensitizes AML cells to the BCL-2 inhibitor venetoclax, and conclude with a report that demonstrates cooperation between B cell receptor signaling and genetic lesions in CDKN2A, CDKN2B and TP53 in Richter transformation.</itunes:summary>
      <itunes:subtitle>In this week’s episode, we review results of preclinical investigations that sound a note of caution regarding the potential use of JAK inhibitors as treatment for hemophagocytic lymphohistiocytosis (or HLH), research that provides new insights on how CD4</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Improved risk assessment in adult BCR-ABL1-negative B-ALL, value of clone metrics in clonal cytopenias, a placental protease generates a peptide to inhibit NET formation</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Improved risk assessment in adult BCR-ABL1-negative B-ALL, value of clone metrics in clonal cytopenias, a placental protease generates a peptide to inhibit NET formation</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">27a497fa-aaf5-4809-9a39-194f01ea2c0b</guid>
      <link>https://share.transistor.fm/s/326d290e</link>
      <description>
        <![CDATA[In this week’s episode, we will review an integrated analysis of one of the largest adult BCR-ABL1-negative B-ALL patient cohorts treated in a single trial, learn more about the genotypic and phenotypic features of patients with clonal cytopenias, and look at a study showing that a serine protease expressed in the placenta cleaves α1-antitrypsin to generate a fragment that inhibits formation of neutrophil extracellular traps in neonates.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we will review an integrated analysis of one of the largest adult BCR-ABL1-negative B-ALL patient cohorts treated in a single trial, learn more about the genotypic and phenotypic features of patients with clonal cytopenias, and look at a study showing that a serine protease expressed in the placenta cleaves α1-antitrypsin to generate a fragment that inhibits formation of neutrophil extracellular traps in neonates.]]>
      </content:encoded>
      <pubDate>Thu, 16 Sep 2021 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/326d290e/f089f619.mp3" length="17093570" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1065</itunes:duration>
      <itunes:summary>In this week’s episode, we will review an integrated analysis of one of the largest adult BCR-ABL1-negative B-ALL patient cohorts treated in a single trial, learn more about the genotypic and phenotypic features of patients with clonal cytopenias, and look at a study showing that a serine protease expressed in the placenta cleaves α1-antitrypsin to generate a fragment that inhibits formation of neutrophil extracellular traps in neonates.</itunes:summary>
      <itunes:subtitle>In this week’s episode, we will review an integrated analysis of one of the largest adult BCR-ABL1-negative B-ALL patient cohorts treated in a single trial, learn more about the genotypic and phenotypic features of patients with clonal cytopenias, and loo</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Fixed-duration venetoclax in relapsed CLL, differing effects of invariant NK T cells, and under recognition of rare TERT variants in MDS</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Fixed-duration venetoclax in relapsed CLL, differing effects of invariant NK T cells, and under recognition of rare TERT variants in MDS</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">bdf174b7-f5c4-4f8d-b2a2-a081c33feaae</guid>
      <link>https://share.transistor.fm/s/f257eac5</link>
      <description>
        <![CDATA[In this week’s episode, we’ll review updated results of a phase 1b study that provide strong support for the use of fixed-duration venetoclax in patients with relapsed or refractory CLL. Next, we’ll review a research paper that provides new insights on the different subtypes of invariant natural killer T cells, which appear to have diverse immunoregulatory properties and anti-tumor effects. We will finish up with a report indicating that rare variants in the telomerase gene, TERT, are underrecognized in patients with myelodysplastic syndromes, providing a new insight into the germline genetic component of disease pathophysiology.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we’ll review updated results of a phase 1b study that provide strong support for the use of fixed-duration venetoclax in patients with relapsed or refractory CLL. Next, we’ll review a research paper that provides new insights on the different subtypes of invariant natural killer T cells, which appear to have diverse immunoregulatory properties and anti-tumor effects. We will finish up with a report indicating that rare variants in the telomerase gene, TERT, are underrecognized in patients with myelodysplastic syndromes, providing a new insight into the germline genetic component of disease pathophysiology.]]>
      </content:encoded>
      <pubDate>Thu, 09 Sep 2021 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/f257eac5/7e087e3d.mp3" length="21834389" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1361</itunes:duration>
      <itunes:summary>In this week’s episode, we’ll review updated results of a phase 1b study that provide strong support for the use of fixed-duration venetoclax in patients with relapsed or refractory CLL. Next, we’ll review a research paper that provides new insights on the different subtypes of invariant natural killer T cells, which appear to have diverse immunoregulatory properties and anti-tumor effects. We will finish up with a report indicating that rare variants in the telomerase gene, TERT, are underrecognized in patients with myelodysplastic syndromes, providing a new insight into the germline genetic component of disease pathophysiology.</itunes:summary>
      <itunes:subtitle>In this week’s episode, we’ll review updated results of a phase 1b study that provide strong support for the use of fixed-duration venetoclax in patients with relapsed or refractory CLL. Next, we’ll review a research paper that provides new insights on th</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Activated BCL11B in acute leukemias, SARS-CoV-2 antibody responses in lymphoma patients receiving B-cell therapies, and PD-L1 in neutrophil apoptosis and tissue inflammation</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Activated BCL11B in acute leukemias, SARS-CoV-2 antibody responses in lymphoma patients receiving B-cell therapies, and PD-L1 in neutrophil apoptosis and tissue inflammation</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">dd832b56-7100-4368-a39b-6b681f142ca1</guid>
      <link>https://share.transistor.fm/s/e7815bba</link>
      <description>
        <![CDATA[In this week’s episode, we will review a study that shows that BCL11B is an important oncogene in acute leukemias with myeloid and T-lymphoid features, learn more about antibody responses to SARS-CoV-2 vaccination in lymphoma patients receiving B-cell directed therapies, and examine the role of programmed death ligand 1 (or PD-L1) and the PI 3 kinase-AKT survival pathway in delayed neutrophil apoptosis at sites of tissue inflammation.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we will review a study that shows that BCL11B is an important oncogene in acute leukemias with myeloid and T-lymphoid features, learn more about antibody responses to SARS-CoV-2 vaccination in lymphoma patients receiving B-cell directed therapies, and examine the role of programmed death ligand 1 (or PD-L1) and the PI 3 kinase-AKT survival pathway in delayed neutrophil apoptosis at sites of tissue inflammation.]]>
      </content:encoded>
      <pubDate>Thu, 02 Sep 2021 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/e7815bba/3eca79f5.mp3" length="17284998" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1077</itunes:duration>
      <itunes:summary>In this week’s episode, we will review a study that shows that BCL11B is an important oncogene in acute leukemias with myeloid and T-lymphoid features, learn more about antibody responses to SARS-CoV-2 vaccination in lymphoma patients receiving B-cell directed therapies, and examine the role of programmed death ligand 1 (or PD-L1) and the PI 3 kinase-AKT survival pathway in delayed neutrophil apoptosis at sites of tissue inflammation.</itunes:summary>
      <itunes:subtitle>In this week’s episode, we will review a study that shows that BCL11B is an important oncogene in acute leukemias with myeloid and T-lymphoid features, learn more about antibody responses to SARS-CoV-2 vaccination in lymphoma patients receiving B-cell dir</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Review Series on Mechanisms of Hematologic Malignancies</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Review Series on Mechanisms of Hematologic Malignancies</itunes:title>
      <itunes:episodeType>bonus</itunes:episodeType>
      <guid isPermaLink="false">a13cf06a-3109-49f0-a94d-a7e9265c3763</guid>
      <link>https://share.transistor.fm/s/06cbbe0e</link>
      <description>
        <![CDATA[<p>To reach the goal of curing currently incurable hematologic malignancies, we need to go beyond focusing on single gene mutations and gain deeper understanding of the consequences of genetic alterations on gene-regulatory pathways. Edited by John Crispino, these 5 cutting-edge reviews from leaders in the their fields not only summarize our current understanding of key pathways that contribute to myeloid malignancies, but also discuss new therapeutic avenues related to them. They provide a springboard for further groundbreaking basic and clinical advances in hematologic malignancies.</p><p><a href="https://ashpublications.org/blood/article/138/8/587/476233/Introduction-to-a-review-series-on-molecular?searchresult=1">Review Series on Mechanisms of Hematologic Malignancies<br></a><br></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>To reach the goal of curing currently incurable hematologic malignancies, we need to go beyond focusing on single gene mutations and gain deeper understanding of the consequences of genetic alterations on gene-regulatory pathways. Edited by John Crispino, these 5 cutting-edge reviews from leaders in the their fields not only summarize our current understanding of key pathways that contribute to myeloid malignancies, but also discuss new therapeutic avenues related to them. They provide a springboard for further groundbreaking basic and clinical advances in hematologic malignancies.</p><p><a href="https://ashpublications.org/blood/article/138/8/587/476233/Introduction-to-a-review-series-on-molecular?searchresult=1">Review Series on Mechanisms of Hematologic Malignancies<br></a><br></p>]]>
      </content:encoded>
      <pubDate>Thu, 26 Aug 2021 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/06cbbe0e/6800992c.mp3" length="27109158" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/m84_N2uEetj-MtMsMHlI79eqiCq6Ft3vNG7SXTD8mPU/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS83M2Yz/MTEyNjFlMmRkMzRh/YmVjOGE2MGMyMThj/OGI2Yy5qcGc.jpg"/>
      <itunes:duration>1691</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>To reach the goal of curing currently incurable hematologic malignancies, we need to go beyond focusing on single gene mutations and gain deeper understanding of the consequences of genetic alterations on gene-regulatory pathways. Edited by John Crispino, these 5 cutting-edge reviews from leaders in the their fields not only summarize our current understanding of key pathways that contribute to myeloid malignancies, but also discuss new therapeutic avenues related to them. They provide a springboard for further groundbreaking basic and clinical advances in hematologic malignancies.</p><p><a href="https://ashpublications.org/blood/article/138/8/587/476233/Introduction-to-a-review-series-on-molecular?searchresult=1">Review Series on Mechanisms of Hematologic Malignancies<br></a><br></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>IFN-λ therapy for GvHD, mechanism of decitabine in ITP, and TET2 mutations in chronic NK-LGL leukemia</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>IFN-λ therapy for GvHD, mechanism of decitabine in ITP, and TET2 mutations in chronic NK-LGL leukemia</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">432d2770-76b9-4c03-a0e0-4d2ed61b53c9</guid>
      <link>https://share.transistor.fm/s/562c7141</link>
      <description>
        <![CDATA[In this week's episode, we will review a study that proposes IFN-λ therapy as a novel strategy to boost gut protection in GvHD, examine the immunomodulatory effects of decitabine in ITP, and learn about the discovery of TET2 mutations in chronic natural killer large granular lymphocyte leukemia]]>
      </description>
      <content:encoded>
        <![CDATA[In this week's episode, we will review a study that proposes IFN-λ therapy as a novel strategy to boost gut protection in GvHD, examine the immunomodulatory effects of decitabine in ITP, and learn about the discovery of TET2 mutations in chronic natural killer large granular lymphocyte leukemia]]>
      </content:encoded>
      <pubDate>Thu, 26 Aug 2021 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/562c7141/400f1f69.mp3" length="17647356" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1100</itunes:duration>
      <itunes:summary>In this week's episode, we will review a study that proposes IFN-λ therapy as a novel strategy to boost gut protection in GvHD, examine the immunomodulatory effects of decitabine in ITP, and learn about the discovery of TET2 mutations in chronic natural killer large granular lymphocyte leukemia</itunes:summary>
      <itunes:subtitle>In this week's episode, we will review a study that proposes IFN-λ therapy as a novel strategy to boost gut protection in GvHD, examine the immunomodulatory effects of decitabine in ITP, and learn about the discovery of TET2 mutations in chronic natural k</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Choosing chemotherapy for older patients with AML,  the role of the microenvironment in pediatric ALL, and efficacy of thrombopoietin receptor agonists in elderly patients with ITP</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Choosing chemotherapy for older patients with AML,  the role of the microenvironment in pediatric ALL, and efficacy of thrombopoietin receptor agonists in elderly patients with ITP</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">2b55ed37-4ed3-4402-bc55-d207ec6f74f0</guid>
      <link>https://share.transistor.fm/s/ea632a67</link>
      <description>
        <![CDATA[In this week's episode, we will review a report on a clinical prognostic tool that identifies which group of older, fit acute myeloid leukemia patients may derive survival benefit from intensive induction and consolidation chemotherapy, learn more about how pediatric acute myeloid leukemia cells connect with mesenchymal stromal cells and the potential to exploit these cell-cell contacts in AML treatments, and examine the effects of eltrombopag and romiplostim in elderly patients with immune thrombocytopenia.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week's episode, we will review a report on a clinical prognostic tool that identifies which group of older, fit acute myeloid leukemia patients may derive survival benefit from intensive induction and consolidation chemotherapy, learn more about how pediatric acute myeloid leukemia cells connect with mesenchymal stromal cells and the potential to exploit these cell-cell contacts in AML treatments, and examine the effects of eltrombopag and romiplostim in elderly patients with immune thrombocytopenia.]]>
      </content:encoded>
      <pubDate>Thu, 19 Aug 2021 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/ea632a67/af209d06.mp3" length="17354961" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1082</itunes:duration>
      <itunes:summary>In this week's episode, we will review a report on a clinical prognostic tool that identifies which group of older, fit acute myeloid leukemia patients may derive survival benefit from intensive induction and consolidation chemotherapy, learn more about how pediatric acute myeloid leukemia cells connect with mesenchymal stromal cells and the potential to exploit these cell-cell contacts in AML treatments, and examine the effects of eltrombopag and romiplostim in elderly patients with immune thrombocytopenia.</itunes:summary>
      <itunes:subtitle>In this week's episode, we will review a report on a clinical prognostic tool that identifies which group of older, fit acute myeloid leukemia patients may derive survival benefit from intensive induction and consolidation chemotherapy, learn more about h</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Brentuximab plus nivolumab in refractory/relapsed Hodgkin lymphoma, the signature of aging hematopoietic stem cells, and hepatocyte neogenin in iron homeostasis</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Brentuximab plus nivolumab in refractory/relapsed Hodgkin lymphoma, the signature of aging hematopoietic stem cells, and hepatocyte neogenin in iron homeostasis</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">b517448a-bd4c-4446-8378-d3ffa655b907</guid>
      <link>https://share.transistor.fm/s/98f61fef</link>
      <description>
        <![CDATA[In this week's episode, we’ll discuss the safety and efficacy of brentuximab vedotin in combination with nivolumab in patients with relapsed and refractory classical Hodgkin lymphoma, learn more about the aging signature of murine hematopoietic stem cells, and discuss the role of hepatocyte neogenin in iron homeostasis.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week's episode, we’ll discuss the safety and efficacy of brentuximab vedotin in combination with nivolumab in patients with relapsed and refractory classical Hodgkin lymphoma, learn more about the aging signature of murine hematopoietic stem cells, and discuss the role of hepatocyte neogenin in iron homeostasis.]]>
      </content:encoded>
      <pubDate>Thu, 12 Aug 2021 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/98f61fef/af17de9f.mp3" length="15763784" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>982</itunes:duration>
      <itunes:summary>In this week's episode, we’ll discuss the safety and efficacy of brentuximab vedotin in combination with nivolumab in patients with relapsed and refractory classical Hodgkin lymphoma, learn more about the aging signature of murine hematopoietic stem cells, and discuss the role of hepatocyte neogenin in iron homeostasis.</itunes:summary>
      <itunes:subtitle>In this week's episode, we’ll discuss the safety and efficacy of brentuximab vedotin in combination with nivolumab in patients with relapsed and refractory classical Hodgkin lymphoma, learn more about the aging signature of murine hematopoietic stem cells</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Latest Research on the Intensity of AML Therapy in Older Patients, Platelets and T cell Activity in Sepsis, and Genotyping for CNS Lymphoma</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Latest Research on the Intensity of AML Therapy in Older Patients, Platelets and T cell Activity in Sepsis, and Genotyping for CNS Lymphoma</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">f13eb86c-bd41-45f4-99d8-1efb6b15bc7e</guid>
      <link>https://share.transistor.fm/s/952b2928</link>
      <description>
        <![CDATA[In this week's episode, we’ll start by reviewing an intriguing study that, while not randomized, calls into question whether less-intensive induction therapies provide a survival or quality of life benefit in older patients with AML. Next, we will review the somewhat surprising findings from human and mouse model studies demonstrating that platelets downregulate T cell activity during sepsis, a finding that is associated with reduced survival. We will close with a report on a targeted genotyping approach that could reduce diagnostic and treatment delays in patients with primary CNS lymphoma.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week's episode, we’ll start by reviewing an intriguing study that, while not randomized, calls into question whether less-intensive induction therapies provide a survival or quality of life benefit in older patients with AML. Next, we will review the somewhat surprising findings from human and mouse model studies demonstrating that platelets downregulate T cell activity during sepsis, a finding that is associated with reduced survival. We will close with a report on a targeted genotyping approach that could reduce diagnostic and treatment delays in patients with primary CNS lymphoma.]]>
      </content:encoded>
      <pubDate>Thu, 05 Aug 2021 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/952b2928/3c355859.mp3" length="18631078" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1161</itunes:duration>
      <itunes:summary>In this week's episode, we’ll start by reviewing an intriguing study that, while not randomized, calls into question whether less-intensive induction therapies provide a survival or quality of life benefit in older patients with AML. Next, we will review the somewhat surprising findings from human and mouse model studies demonstrating that platelets downregulate T cell activity during sepsis, a finding that is associated with reduced survival. We will close with a report on a targeted genotyping approach that could reduce diagnostic and treatment delays in patients with primary CNS lymphoma.</itunes:summary>
      <itunes:subtitle>In this week's episode, we’ll start by reviewing an intriguing study that, while not randomized, calls into question whether less-intensive induction therapies provide a survival or quality of life benefit in older patients with AML. Next, we will review </itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Vaccine-induced Immune Thrombotic Thrombocytopenia</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Vaccine-induced Immune Thrombotic Thrombocytopenia</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">2abf7f2d-893e-49fb-838c-8dad8438e470</guid>
      <link>https://share.transistor.fm/s/fa613592</link>
      <description>
        <![CDATA[Today’s episode is a special edition that focuses exclusively on vaccine-induced immune thrombotic thrombocytopenia, or VITT, a rare but potentially fatal syndrome associated with adenovirus-based COVID-19 vaccines. The VITT syndrome is characterized by thrombocytopenia and thrombosis in association with platelet-activating anti-platelet factor 4 antibodies. First, we’ll review an insightful Spotlight article on what is known about VITT to date. Then we’ll discuss two new brief reports in Blood that provide additional insights on VITT clinical manifestations, laboratory findings, and disease management.]]>
      </description>
      <content:encoded>
        <![CDATA[Today’s episode is a special edition that focuses exclusively on vaccine-induced immune thrombotic thrombocytopenia, or VITT, a rare but potentially fatal syndrome associated with adenovirus-based COVID-19 vaccines. The VITT syndrome is characterized by thrombocytopenia and thrombosis in association with platelet-activating anti-platelet factor 4 antibodies. First, we’ll review an insightful Spotlight article on what is known about VITT to date. Then we’ll discuss two new brief reports in Blood that provide additional insights on VITT clinical manifestations, laboratory findings, and disease management.]]>
      </content:encoded>
      <pubDate>Thu, 29 Jul 2021 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/fa613592/357509e3.mp3" length="16975388" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1058</itunes:duration>
      <itunes:summary>Today’s episode is a special edition that focuses exclusively on vaccine-induced immune thrombotic thrombocytopenia, or VITT, a rare but potentially fatal syndrome associated with adenovirus-based COVID-19 vaccines. The VITT syndrome is characterized by thrombocytopenia and thrombosis in association with platelet-activating anti-platelet factor 4 antibodies. First, we’ll review an insightful Spotlight article on what is known about VITT to date. Then we’ll discuss two new brief reports in Blood that provide additional insights on VITT clinical manifestations, laboratory findings, and disease management.</itunes:summary>
      <itunes:subtitle>Today’s episode is a special edition that focuses exclusively on vaccine-induced immune thrombotic thrombocytopenia, or VITT, a rare but potentially fatal syndrome associated with adenovirus-based COVID-19 vaccines. The VITT syndrome is characterized by t</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Latest research in post-transplant cyclophosphamide in matched unrelated versus haploidentical donors, outcomes in patients with AITL, and high molecular weight kininogen in acetaminophen-induced liver injury</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Latest research in post-transplant cyclophosphamide in matched unrelated versus haploidentical donors, outcomes in patients with AITL, and high molecular weight kininogen in acetaminophen-induced liver injury</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">7f4f6e94-1792-44e7-a9a2-39f8983902c1</guid>
      <link>https://share.transistor.fm/s/2223098a</link>
      <description>
        <![CDATA[In this week’s episode, we will learn more about the use of high-dose post-transplant cyclophosphamide in matched unrelated donors versus HLA haploidentical grafts, review prognostic factors and outcomes from the largest cohort of patients with angioimmunoblastic T-cell lymphoma reported to date, and look at a study that suggests that high molecular weight kininogen contributes to acetaminophen-induced liver injury.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we will learn more about the use of high-dose post-transplant cyclophosphamide in matched unrelated donors versus HLA haploidentical grafts, review prognostic factors and outcomes from the largest cohort of patients with angioimmunoblastic T-cell lymphoma reported to date, and look at a study that suggests that high molecular weight kininogen contributes to acetaminophen-induced liver injury.]]>
      </content:encoded>
      <pubDate>Thu, 22 Jul 2021 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/2223098a/95be4c3d.mp3" length="16807720" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1047</itunes:duration>
      <itunes:summary>In this week’s episode, we will learn more about the use of high-dose post-transplant cyclophosphamide in matched unrelated donors versus HLA haploidentical grafts, review prognostic factors and outcomes from the largest cohort of patients with angioimmunoblastic T-cell lymphoma reported to date, and look at a study that suggests that high molecular weight kininogen contributes to acetaminophen-induced liver injury.</itunes:summary>
      <itunes:subtitle>In this week’s episode, we will learn more about the use of high-dose post-transplant cyclophosphamide in matched unrelated donors versus HLA haploidentical grafts, review prognostic factors and outcomes from the largest cohort of patients with angioimmun</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Latest research in thrombosis in pediatric COVID-19, prognostic tool for very early stage CLL, and frontline treatment for newly diagnosed myeloma</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Latest research in thrombosis in pediatric COVID-19, prognostic tool for very early stage CLL, and frontline treatment for newly diagnosed myeloma</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">252e1d00-6da9-4b8f-bab4-68defab8001c</guid>
      <link>https://share.transistor.fm/s/1fddb955</link>
      <description>
        <![CDATA[In this week's episode, our studies include an analysis of thrombosis in pediatric patients with COVID-19, the predictive value of the CLL-international prognostic index in monoclonal B-cell lymphocytosis and Rai 0 stage CLL, and results from a phase 2 trial in newly diagnosed multiple myeloma patients treated with frontline carfilzomib, lenalidomide, and dexamethasone with autologous stem cell transplant.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week's episode, our studies include an analysis of thrombosis in pediatric patients with COVID-19, the predictive value of the CLL-international prognostic index in monoclonal B-cell lymphocytosis and Rai 0 stage CLL, and results from a phase 2 trial in newly diagnosed multiple myeloma patients treated with frontline carfilzomib, lenalidomide, and dexamethasone with autologous stem cell transplant.]]>
      </content:encoded>
      <pubDate>Thu, 15 Jul 2021 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/1fddb955/b5f8c358.mp3" length="17223864" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1073</itunes:duration>
      <itunes:summary>In this week's episode, our studies include an analysis of thrombosis in pediatric patients with COVID-19, the predictive value of the CLL-international prognostic index in monoclonal B-cell lymphocytosis and Rai 0 stage CLL, and results from a phase 2 trial in newly diagnosed multiple myeloma patients treated with frontline carfilzomib, lenalidomide, and dexamethasone with autologous stem cell transplant.</itunes:summary>
      <itunes:subtitle>In this week's episode, our studies include an analysis of thrombosis in pediatric patients with COVID-19, the predictive value of the CLL-international prognostic index in monoclonal B-cell lymphocytosis and Rai 0 stage CLL, and results from a phase 2 tr</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Latest Research: Immunity to CMV, lymphoma microenvironment, and tPA induced bleeding</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Latest Research: Immunity to CMV, lymphoma microenvironment, and tPA induced bleeding</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">2fdac2c9-392d-453e-aa0d-f443e902ed9f</guid>
      <link>https://share.transistor.fm/s/553573cf</link>
      <description>
        <![CDATA[In this week's episode, we will review a study that addresses the issue of reconstitution of immunity to cytomegalovirus in transplant patients receiving the antiviral drug letermovir, learn more about the role extracellular vesicles play in forming a tumor supportive stromal cell niche in follicular lymphoma, and finally, look at a report identifying a mechanism that couples the treatment of acute ischemic stroke with tissue plasminogen activator to the development of intracerebral hemorrhage.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week's episode, we will review a study that addresses the issue of reconstitution of immunity to cytomegalovirus in transplant patients receiving the antiviral drug letermovir, learn more about the role extracellular vesicles play in forming a tumor supportive stromal cell niche in follicular lymphoma, and finally, look at a report identifying a mechanism that couples the treatment of acute ischemic stroke with tissue plasminogen activator to the development of intracerebral hemorrhage.]]>
      </content:encoded>
      <pubDate>Thu, 08 Jul 2021 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/553573cf/f871d949.mp3" length="14239145" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>887</itunes:duration>
      <itunes:summary>In this week's episode, we will review a study that addresses the issue of reconstitution of immunity to cytomegalovirus in transplant patients receiving the antiviral drug letermovir, learn more about the role extracellular vesicles play in forming a tumor supportive stromal cell niche in follicular lymphoma, and finally, look at a report identifying a mechanism that couples the treatment of acute ischemic stroke with tissue plasminogen activator to the development of intracerebral hemorrhage.</itunes:summary>
      <itunes:subtitle>In this week's episode, we will review a study that addresses the issue of reconstitution of immunity to cytomegalovirus in transplant patients receiving the antiviral drug letermovir, learn more about the role extracellular vesicles play in forming a tum</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>VEXAS:  A Newly Identified Adult-onset Hemato-inflammatory Syndrome</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>VEXAS:  A Newly Identified Adult-onset Hemato-inflammatory Syndrome</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">5d7b2bf2-bba3-40d1-8e32-ae82607e860e</guid>
      <link>https://share.transistor.fm/s/64f592ae</link>
      <description>
        <![CDATA[Today’s podcast is a special edition that focuses exclusively on VEXAS syndrome, a newly identified adult-onset inflammatory syndrome with associated hematologic manifestations. VEXAS syndrome is a poor-prognosis disease caused by somatic mutations in the X-linked gene, UBA1. It was first reported by Beck and colleagues in the New England Journal of Medicine in December 2020.]]>
      </description>
      <content:encoded>
        <![CDATA[Today’s podcast is a special edition that focuses exclusively on VEXAS syndrome, a newly identified adult-onset inflammatory syndrome with associated hematologic manifestations. VEXAS syndrome is a poor-prognosis disease caused by somatic mutations in the X-linked gene, UBA1. It was first reported by Beck and colleagues in the New England Journal of Medicine in December 2020.]]>
      </content:encoded>
      <pubDate>Thu, 01 Jul 2021 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/64f592ae/236e950f.mp3" length="16577061" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1033</itunes:duration>
      <itunes:summary>Today’s podcast is a special edition that focuses exclusively on VEXAS syndrome, a newly identified adult-onset inflammatory syndrome with associated hematologic manifestations. VEXAS syndrome is a poor-prognosis disease caused by somatic mutations in the X-linked gene, UBA1. It was first reported by Beck and colleagues in the New England Journal of Medicine in December 2020.</itunes:summary>
      <itunes:subtitle>Today’s podcast is a special edition that focuses exclusively on VEXAS syndrome, a newly identified adult-onset inflammatory syndrome with associated hematologic manifestations. VEXAS syndrome is a poor-prognosis disease caused by somatic mutations in the</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 2, Episode 25</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Season 2, Episode 25</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">32fbd3df-3386-445c-b525-2b2647f5e46b</guid>
      <link>https://share.transistor.fm/s/2961cd1b</link>
      <description>
        <![CDATA[In this week’s episode, we will review a study that uses a combination of mouse models to identify IL-19 as a potent cytokine capable of promoting expansion and proliferation of neutrophils, examine the effects of targeted therapies on autoimmune cytopenia in patients with chronic lymphocytic leukemia, and learn about the mechanism of excessive complement activation caused by mutations in factor H-related protein 1 in patients with atypical hemolytic uremic syndrome.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we will review a study that uses a combination of mouse models to identify IL-19 as a potent cytokine capable of promoting expansion and proliferation of neutrophils, examine the effects of targeted therapies on autoimmune cytopenia in patients with chronic lymphocytic leukemia, and learn about the mechanism of excessive complement activation caused by mutations in factor H-related protein 1 in patients with atypical hemolytic uremic syndrome.]]>
      </content:encoded>
      <pubDate>Thu, 24 Jun 2021 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/2961cd1b/062ef04f.mp3" length="18008245" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1122</itunes:duration>
      <itunes:summary>In this week’s episode, we will review a study that uses a combination of mouse models to identify IL-19 as a potent cytokine capable of promoting expansion and proliferation of neutrophils, examine the effects of targeted therapies on autoimmune cytopenia in patients with chronic lymphocytic leukemia, and learn about the mechanism of excessive complement activation caused by mutations in factor H-related protein 1 in patients with atypical hemolytic uremic syndrome.</itunes:summary>
      <itunes:subtitle>In this week’s episode, we will review a study that uses a combination of mouse models to identify IL-19 as a potent cytokine capable of promoting expansion and proliferation of neutrophils, examine the effects of targeted therapies on autoimmune cytopeni</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 2, Episode 24</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Season 2, Episode 24</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">87dcea1b-dd79-41a0-a1ec-5bbc31ace45b</guid>
      <link>https://share.transistor.fm/s/cb71c386</link>
      <description>
        <![CDATA[In this week’s episode, we will review the role of the hypoxia pathway in regulating neutrophil migration, explore the relationship between endothelial extracellular vesicles and the hemostatic effects of clotting Factor VIIa, and finally look at long-term outcomes with the BTK-inhibitor acalabrutinib in treatment-naive chronic lymphocytic leukemia patients.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we will review the role of the hypoxia pathway in regulating neutrophil migration, explore the relationship between endothelial extracellular vesicles and the hemostatic effects of clotting Factor VIIa, and finally look at long-term outcomes with the BTK-inhibitor acalabrutinib in treatment-naive chronic lymphocytic leukemia patients.]]>
      </content:encoded>
      <pubDate>Thu, 17 Jun 2021 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/cb71c386/02648467.mp3" length="21244384" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1325</itunes:duration>
      <itunes:summary>In this week’s episode, we will review the role of the hypoxia pathway in regulating neutrophil migration, explore the relationship between endothelial extracellular vesicles and the hemostatic effects of clotting Factor VIIa, and finally look at long-term outcomes with the BTK-inhibitor acalabrutinib in treatment-naive chronic lymphocytic leukemia patients.</itunes:summary>
      <itunes:subtitle>In this week’s episode, we will review the role of the hypoxia pathway in regulating neutrophil migration, explore the relationship between endothelial extracellular vesicles and the hemostatic effects of clotting Factor VIIa, and finally look at long-ter</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Review Series on Platelets and Cancer</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Review Series on Platelets and Cancer</itunes:title>
      <itunes:episodeType>bonus</itunes:episodeType>
      <guid isPermaLink="false">842c52b4-21ee-41a9-9eb9-d8fa486507b6</guid>
      <link>https://share.transistor.fm/s/7b7e2282</link>
      <description>
        <![CDATA[<p>Platelets are critical for hemostasis and thrombosis, but recent research highlights their role in many other processes, including inflammation, wound healing, and lymphangiogenesis. In this episode, Drs. José López, Elisabeth Battinelli, Craig Williams, and Owen McCarty discuss the review series on platelets and cancer. The series focuses on the emerging role of platelets in cancer, influencing tumor growth and metastasis, immune evasion, and tumor angiogenesis. The reviews present the current understanding of mutual cross talk between platelets and tumors, communication mediated by RNA transfer and extracellular vesicles, and the potential of antiplatelet agents for cancer treatment.</p><p><a href="https://ashpublications.org/blood/article/137/23/3151/475893/Introduction-to-a-review-series-on-platelets-and?searchresult=1">Review Series on Platelets and Cancer</a></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>Platelets are critical for hemostasis and thrombosis, but recent research highlights their role in many other processes, including inflammation, wound healing, and lymphangiogenesis. In this episode, Drs. José López, Elisabeth Battinelli, Craig Williams, and Owen McCarty discuss the review series on platelets and cancer. The series focuses on the emerging role of platelets in cancer, influencing tumor growth and metastasis, immune evasion, and tumor angiogenesis. The reviews present the current understanding of mutual cross talk between platelets and tumors, communication mediated by RNA transfer and extracellular vesicles, and the potential of antiplatelet agents for cancer treatment.</p><p><a href="https://ashpublications.org/blood/article/137/23/3151/475893/Introduction-to-a-review-series-on-platelets-and?searchresult=1">Review Series on Platelets and Cancer</a></p>]]>
      </content:encoded>
      <pubDate>Thu, 10 Jun 2021 13:45:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/7b7e2282/4bb62227.mp3" length="34077613" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/xyt2nJg0bKMWtRXQvQwBFiY7d0chwPwdC8_SlNdyplA/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS9kOGU4/MGQzNzIwMmE0MDI2/ZWE4MTMxMTU4YzA2/ZDZmOS5qcGc.jpg"/>
      <itunes:duration>2127</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>Platelets are critical for hemostasis and thrombosis, but recent research highlights their role in many other processes, including inflammation, wound healing, and lymphangiogenesis. In this episode, Drs. José López, Elisabeth Battinelli, Craig Williams, and Owen McCarty discuss the review series on platelets and cancer. The series focuses on the emerging role of platelets in cancer, influencing tumor growth and metastasis, immune evasion, and tumor angiogenesis. The reviews present the current understanding of mutual cross talk between platelets and tumors, communication mediated by RNA transfer and extracellular vesicles, and the potential of antiplatelet agents for cancer treatment.</p><p><a href="https://ashpublications.org/blood/article/137/23/3151/475893/Introduction-to-a-review-series-on-platelets-and?searchresult=1">Review Series on Platelets and Cancer</a></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 2, Episode 23</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Season 2, Episode 23</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">3940a83d-9f1c-4329-9099-d2b76c68abd0</guid>
      <link>https://share.transistor.fm/s/c584032f</link>
      <description>
        <![CDATA[In this week’s episode, we will review a study demonstrating low rates of response to the Pfizer-BioNTech COVID-19 vaccine among patients with chronic lymphocytic leukemia, review a study looking at associations between post-transplantation cyclophosphamide and cytomegalovirus infection according to donor source, and look at new research indicating that abnormal venous calf muscle pump function in the legs is a risk factor for venous thromboembolism (VTE) and predictor of all-cause mortality.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we will review a study demonstrating low rates of response to the Pfizer-BioNTech COVID-19 vaccine among patients with chronic lymphocytic leukemia, review a study looking at associations between post-transplantation cyclophosphamide and cytomegalovirus infection according to donor source, and look at new research indicating that abnormal venous calf muscle pump function in the legs is a risk factor for venous thromboembolism (VTE) and predictor of all-cause mortality.]]>
      </content:encoded>
      <pubDate>Thu, 10 Jun 2021 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/c584032f/1d7c5d4c.mp3" length="19539282" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1218</itunes:duration>
      <itunes:summary>In this week’s episode, we will review a study demonstrating low rates of response to the Pfizer-BioNTech COVID-19 vaccine among patients with chronic lymphocytic leukemia, review a study looking at associations between post-transplantation cyclophosphamide and cytomegalovirus infection according to donor source, and look at new research indicating that abnormal venous calf muscle pump function in the legs is a risk factor for venous thromboembolism (VTE) and predictor of all-cause mortality.</itunes:summary>
      <itunes:subtitle>In this week’s episode, we will review a study demonstrating low rates of response to the Pfizer-BioNTech COVID-19 vaccine among patients with chronic lymphocytic leukemia, review a study looking at associations between post-transplantation cyclophosphami</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 2, Episode 22</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Season 2, Episode 22</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">2451856f-2187-426d-8b04-bcafa1f8e374</guid>
      <link>https://share.transistor.fm/s/2ee5741e</link>
      <description>
        <![CDATA[In this week’s episode, we will review a study in sickle cell disease patients reporting abnormal retention of mitochondria in circulating red cells and elevated mitochondrial DNA in plasma, learn more about the fate of FLT3-ITD clones in AML patients treated with midostaurin, and look at a study showing, for the first time, that selected elderly patients with newly diagnosed multiple myeloma benefit from modification of standard myeloma treatment based on the level of frailty.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we will review a study in sickle cell disease patients reporting abnormal retention of mitochondria in circulating red cells and elevated mitochondrial DNA in plasma, learn more about the fate of FLT3-ITD clones in AML patients treated with midostaurin, and look at a study showing, for the first time, that selected elderly patients with newly diagnosed multiple myeloma benefit from modification of standard myeloma treatment based on the level of frailty.]]>
      </content:encoded>
      <pubDate>Thu, 03 Jun 2021 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/2ee5741e/5d352672.mp3" length="17570246" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1095</itunes:duration>
      <itunes:summary>In this week’s episode, we will review a study in sickle cell disease patients reporting abnormal retention of mitochondria in circulating red cells and elevated mitochondrial DNA in plasma, learn more about the fate of FLT3-ITD clones in AML patients treated with midostaurin, and look at a study showing, for the first time, that selected elderly patients with newly diagnosed multiple myeloma benefit from modification of standard myeloma treatment based on the level of frailty.</itunes:summary>
      <itunes:subtitle>In this week’s episode, we will review a study in sickle cell disease patients reporting abnormal retention of mitochondria in circulating red cells and elevated mitochondrial DNA in plasma, learn more about the fate of FLT3-ITD clones in AML patients tre</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 2, Episode 21</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Season 2, Episode 21</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">0b2a9279-727b-4533-b019-9d37a16c42f2</guid>
      <link>https://share.transistor.fm/s/9068521f</link>
      <description>
        <![CDATA[In this week’s episode we will review a phase 1 clinical trial looking at novel fully humanized BCMA-targeting CAR in patients with relapsed or refractory multiple myeloma, discuss a plenary paper reporting that different lymph nodes from patients with follicular lymphoma often have distinct clones, and finally, examine a Letter to Blood reporting high levels of markers of complement activation in plasma during quiescent phases in catastrophic antiphospholipid syndrome patients.        ]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode we will review a phase 1 clinical trial looking at novel fully humanized BCMA-targeting CAR in patients with relapsed or refractory multiple myeloma, discuss a plenary paper reporting that different lymph nodes from patients with follicular lymphoma often have distinct clones, and finally, examine a Letter to Blood reporting high levels of markers of complement activation in plasma during quiescent phases in catastrophic antiphospholipid syndrome patients.        ]]>
      </content:encoded>
      <pubDate>Thu, 27 May 2021 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/9068521f/69c3826c.mp3" length="15945239" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>993</itunes:duration>
      <itunes:summary>In this week’s episode we will review a phase 1 clinical trial looking at novel fully humanized BCMA-targeting CAR in patients with relapsed or refractory multiple myeloma, discuss a plenary paper reporting that different lymph nodes from patients with follicular lymphoma often have distinct clones, and finally, examine a Letter to Blood reporting high levels of markers of complement activation in plasma during quiescent phases in catastrophic antiphospholipid syndrome patients.        </itunes:summary>
      <itunes:subtitle>In this week’s episode we will review a phase 1 clinical trial looking at novel fully humanized BCMA-targeting CAR in patients with relapsed or refractory multiple myeloma, discuss a plenary paper reporting that different lymph nodes from patients with fo</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 2, Episode 20</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Season 2, Episode 20</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">63345015-ee1d-40b3-98aa-357c70fe9d4d</guid>
      <link>https://share.transistor.fm/s/74b9c842</link>
      <description>
        <![CDATA[In this week’s episode, we will examine the prognostic significance of co-mutations in IDH-mutated AML, explore an alternative method of warfarin monitoring, and finally, consider the role of tumor suppressor TP53 in determining response to venetoclax and related agents.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we will examine the prognostic significance of co-mutations in IDH-mutated AML, explore an alternative method of warfarin monitoring, and finally, consider the role of tumor suppressor TP53 in determining response to venetoclax and related agents.]]>
      </content:encoded>
      <pubDate>Thu, 20 May 2021 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/74b9c842/9f78662a.mp3" length="19397141" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1209</itunes:duration>
      <itunes:summary>In this week’s episode, we will examine the prognostic significance of co-mutations in IDH-mutated AML, explore an alternative method of warfarin monitoring, and finally, consider the role of tumor suppressor TP53 in determining response to venetoclax and related agents.</itunes:summary>
      <itunes:subtitle>In this week’s episode, we will examine the prognostic significance of co-mutations in IDH-mutated AML, explore an alternative method of warfarin monitoring, and finally, consider the role of tumor suppressor TP53 in determining response to venetoclax and</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 2, Episode 19</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Season 2, Episode 19</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">f6362ab3-c8b8-44b4-8427-39138462af59</guid>
      <link>https://share.transistor.fm/s/ef134235</link>
      <description>
        <![CDATA[In this week’s episode, we will review a randomized phase 3 study of patients with high-risk peripheral T-cell lymphoma that compares results from autologous versus allogeneic stem cell transplant during consolidation, look at a report that examines the significance of ABO-incompatible platelet transfusion on outcomes after intracerebral hemorrhage, and learn about how immune dysregulation mediated by tumor interferon signaling and myeloid-derived suppressor cells is associated with CAR-T-cell resistance in large B-cell lymphoma.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we will review a randomized phase 3 study of patients with high-risk peripheral T-cell lymphoma that compares results from autologous versus allogeneic stem cell transplant during consolidation, look at a report that examines the significance of ABO-incompatible platelet transfusion on outcomes after intracerebral hemorrhage, and learn about how immune dysregulation mediated by tumor interferon signaling and myeloid-derived suppressor cells is associated with CAR-T-cell resistance in large B-cell lymphoma.]]>
      </content:encoded>
      <pubDate>Thu, 13 May 2021 13:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/ef134235/f24ee0c8.mp3" length="18063126" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1126</itunes:duration>
      <itunes:summary>In this week’s episode, we will review a randomized phase 3 study of patients with high-risk peripheral T-cell lymphoma that compares results from autologous versus allogeneic stem cell transplant during consolidation, look at a report that examines the significance of ABO-incompatible platelet transfusion on outcomes after intracerebral hemorrhage, and learn about how immune dysregulation mediated by tumor interferon signaling and myeloid-derived suppressor cells is associated with CAR-T-cell resistance in large B-cell lymphoma.</itunes:summary>
      <itunes:subtitle>In this week’s episode, we will review a randomized phase 3 study of patients with high-risk peripheral T-cell lymphoma that compares results from autologous versus allogeneic stem cell transplant during consolidation, look at a report that examines the s</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 2, Episode 18</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Season 2, Episode 18</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">5e3c97d8-5b93-45f3-b95c-50562b7aa325</guid>
      <link>https://share.transistor.fm/s/0c97cc7f</link>
      <description>
        <![CDATA[In this week’s episode, we will review a prospective study suggesting that eculizumab discontinuation based on complement genetics is a reasonable and safe strategy in patients with atypical hemolytic uremic syndrome, examine a study that provides new insights into resistance mechanisms and immune evasion in T-cell acute lymphoblastic leukemia, and finally look at a research article describing a new disorder associated with variants in the TLR8 gene that is characterized by neutropenia, infections, lymphoproliferation, B-cell defects, and bone marrow failure.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we will review a prospective study suggesting that eculizumab discontinuation based on complement genetics is a reasonable and safe strategy in patients with atypical hemolytic uremic syndrome, examine a study that provides new insights into resistance mechanisms and immune evasion in T-cell acute lymphoblastic leukemia, and finally look at a research article describing a new disorder associated with variants in the TLR8 gene that is characterized by neutropenia, infections, lymphoproliferation, B-cell defects, and bone marrow failure.]]>
      </content:encoded>
      <pubDate>Thu, 06 May 2021 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/0c97cc7f/02cf0295.mp3" length="18772874" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1170</itunes:duration>
      <itunes:summary>In this week’s episode, we will review a prospective study suggesting that eculizumab discontinuation based on complement genetics is a reasonable and safe strategy in patients with atypical hemolytic uremic syndrome, examine a study that provides new insights into resistance mechanisms and immune evasion in T-cell acute lymphoblastic leukemia, and finally look at a research article describing a new disorder associated with variants in the TLR8 gene that is characterized by neutropenia, infections, lymphoproliferation, B-cell defects, and bone marrow failure.</itunes:summary>
      <itunes:subtitle>In this week’s episode, we will review a prospective study suggesting that eculizumab discontinuation based on complement genetics is a reasonable and safe strategy in patients with atypical hemolytic uremic syndrome, examine a study that provides new ins</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 2, Episode 17</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Season 2, Episode 17</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">7012c4b7-6d4e-4773-b33b-e36c3d79f380</guid>
      <link>https://share.transistor.fm/s/87a16671</link>
      <description>
        <![CDATA[In this week’s episode, we will review a study that focuses on the morphologic alterations of stored red blood cells, learn more about how T-cell activation profiles distinguish hemophagocytic lymphohistiocytosis and early sepsis, and, finally, look at a report that describes how the WNT signaling pathway is involved in sclerodermatous chronic graft-versus-host disease and can be blocked by available therapeutics.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we will review a study that focuses on the morphologic alterations of stored red blood cells, learn more about how T-cell activation profiles distinguish hemophagocytic lymphohistiocytosis and early sepsis, and, finally, look at a report that describes how the WNT signaling pathway is involved in sclerodermatous chronic graft-versus-host disease and can be blocked by available therapeutics.]]>
      </content:encoded>
      <pubDate>Thu, 29 Apr 2021 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/87a16671/e240b902.mp3" length="18100924" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1128</itunes:duration>
      <itunes:summary>In this week’s episode, we will review a study that focuses on the morphologic alterations of stored red blood cells, learn more about how T-cell activation profiles distinguish hemophagocytic lymphohistiocytosis and early sepsis, and, finally, look at a report that describes how the WNT signaling pathway is involved in sclerodermatous chronic graft-versus-host disease and can be blocked by available therapeutics.</itunes:summary>
      <itunes:subtitle>In this week’s episode, we will review a study that focuses on the morphologic alterations of stored red blood cells, learn more about how T-cell activation profiles distinguish hemophagocytic lymphohistiocytosis and early sepsis, and, finally, look at a </itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 2, Episode 16</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Season 2, Episode 16</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">725b6a6c-ef40-423b-96b3-bc65efc054d0</guid>
      <link>https://share.transistor.fm/s/159b0a70</link>
      <description>
        <![CDATA[In this week’s episode, we consider the role of MYC and BCL2 copy number variants in double-hit diffuse large B-cell lymphoma, explore megakaryocyte-biased stem cells in JAK2-mutated myeloproliferative neoplasms, and finally, we look at long-term outcomes with emicizumab prophylaxis in patients with hemophilia, which are even better than in the first reports.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we consider the role of MYC and BCL2 copy number variants in double-hit diffuse large B-cell lymphoma, explore megakaryocyte-biased stem cells in JAK2-mutated myeloproliferative neoplasms, and finally, we look at long-term outcomes with emicizumab prophylaxis in patients with hemophilia, which are even better than in the first reports.]]>
      </content:encoded>
      <pubDate>Thu, 22 Apr 2021 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/159b0a70/48d81f4e.mp3" length="19518112" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1217</itunes:duration>
      <itunes:summary>In this week’s episode, we consider the role of MYC and BCL2 copy number variants in double-hit diffuse large B-cell lymphoma, explore megakaryocyte-biased stem cells in JAK2-mutated myeloproliferative neoplasms, and finally, we look at long-term outcomes with emicizumab prophylaxis in patients with hemophilia, which are even better than in the first reports.</itunes:summary>
      <itunes:subtitle>In this week’s episode, we consider the role of MYC and BCL2 copy number variants in double-hit diffuse large B-cell lymphoma, explore megakaryocyte-biased stem cells in JAK2-mutated myeloproliferative neoplasms, and finally, we look at long-term outcomes</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 2, Episode 15</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Season 2, Episode 15</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">86ce52d5-dbcf-4387-8a07-ab5e55dd04a7</guid>
      <link>https://share.transistor.fm/s/66f453db</link>
      <description>
        <![CDATA[In this week’s episode, we will review a manuscript that describes a novel inherited bone marrow failure syndrome associated with defective clearance of formaldehyde by hematopoietic stem cells, learn about the first large scale analysis of the association between cancer-specific mutations in cancer cells and the incidence of cancer-specific thrombosis, and explore results from a large screening study examining the incidence and progression of monoclonal B cell lymphocytosis in families with an inherited predisposition to chronic lymphocytic leukemia. ]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we will review a manuscript that describes a novel inherited bone marrow failure syndrome associated with defective clearance of formaldehyde by hematopoietic stem cells, learn about the first large scale analysis of the association between cancer-specific mutations in cancer cells and the incidence of cancer-specific thrombosis, and explore results from a large screening study examining the incidence and progression of monoclonal B cell lymphocytosis in families with an inherited predisposition to chronic lymphocytic leukemia. ]]>
      </content:encoded>
      <pubDate>Thu, 15 Apr 2021 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/66f453db/9f07f608.mp3" length="17207609" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1072</itunes:duration>
      <itunes:summary>In this week’s episode, we will review a manuscript that describes a novel inherited bone marrow failure syndrome associated with defective clearance of formaldehyde by hematopoietic stem cells, learn about the first large scale analysis of the association between cancer-specific mutations in cancer cells and the incidence of cancer-specific thrombosis, and explore results from a large screening study examining the incidence and progression of monoclonal B cell lymphocytosis in families with an inherited predisposition to chronic lymphocytic leukemia. </itunes:summary>
      <itunes:subtitle>In this week’s episode, we will review a manuscript that describes a novel inherited bone marrow failure syndrome associated with defective clearance of formaldehyde by hematopoietic stem cells, learn about the first large scale analysis of the associatio</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 2, Episode 14</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Season 2, Episode 14</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">1c33db54-fb3c-45b2-843c-4d8b8fa19f80</guid>
      <link>https://share.transistor.fm/s/796131bb</link>
      <description>
        <![CDATA[In this week’s episode, we discuss recent studies providing new insights on the use of minimal residual disease measurements to guide treatment in patients with high-risk ALL; the increasing risk of venous thromboembolism among patients with cancer; and the use of tocilizumab in the prophylaxis of acute graft versus host disease.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we discuss recent studies providing new insights on the use of minimal residual disease measurements to guide treatment in patients with high-risk ALL; the increasing risk of venous thromboembolism among patients with cancer; and the use of tocilizumab in the prophylaxis of acute graft versus host disease.]]>
      </content:encoded>
      <pubDate>Thu, 08 Apr 2021 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/796131bb/d0b25448.mp3" length="18139204" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1131</itunes:duration>
      <itunes:summary>In this week’s episode, we discuss recent studies providing new insights on the use of minimal residual disease measurements to guide treatment in patients with high-risk ALL; the increasing risk of venous thromboembolism among patients with cancer; and the use of tocilizumab in the prophylaxis of acute graft versus host disease.</itunes:summary>
      <itunes:subtitle>In this week’s episode, we discuss recent studies providing new insights on the use of minimal residual disease measurements to guide treatment in patients with high-risk ALL; the increasing risk of venous thromboembolism among patients with cancer; and t</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 2, Episode 13</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Season 2, Episode 13</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">c02987bb-44ce-426d-aa15-7cb499b1e78d</guid>
      <link>https://share.transistor.fm/s/1f5fce54</link>
      <description>
        <![CDATA[In this week’s episode, we will learn more about the feasibility of combining IDH inhibitors with intensive chemotherapy in patients with newly diagnosed IDH-mutant AML, review a phenotypic and functional analysis of the inflammatory infiltrate in the Langerhans Cell Histiocytosis lesion, and discuss the results of a Phase 3 trial in patients with hemophilia A evaluating prophylactic factor replacement therapy targeting two different Factor VIII trough levels for prevention of bleeds.    ]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we will learn more about the feasibility of combining IDH inhibitors with intensive chemotherapy in patients with newly diagnosed IDH-mutant AML, review a phenotypic and functional analysis of the inflammatory infiltrate in the Langerhans Cell Histiocytosis lesion, and discuss the results of a Phase 3 trial in patients with hemophilia A evaluating prophylactic factor replacement therapy targeting two different Factor VIII trough levels for prevention of bleeds.    ]]>
      </content:encoded>
      <pubDate>Thu, 01 Apr 2021 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/1f5fce54/b287aa89.mp3" length="17520515" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1092</itunes:duration>
      <itunes:summary>In this week’s episode, we will learn more about the feasibility of combining IDH inhibitors with intensive chemotherapy in patients with newly diagnosed IDH-mutant AML, review a phenotypic and functional analysis of the inflammatory infiltrate in the Langerhans Cell Histiocytosis lesion, and discuss the results of a Phase 3 trial in patients with hemophilia A evaluating prophylactic factor replacement therapy targeting two different Factor VIII trough levels for prevention of bleeds.    </itunes:summary>
      <itunes:subtitle>In this week’s episode, we will learn more about the feasibility of combining IDH inhibitors with intensive chemotherapy in patients with newly diagnosed IDH-mutant AML, review a phenotypic and functional analysis of the inflammatory infiltrate in the Lan</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 2, Episode 12</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Season 2, Episode 12</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">b210e56d-8ab0-40ef-a9b3-77580b8ae38e</guid>
      <link>https://share.transistor.fm/s/c9efff84</link>
      <description>
        <![CDATA[In this week’s episode, we look at the role of a previously unidentified variant of DNA methyltransferase 1 as a determinant of beta-thalessemia phenotype, report on the association of vascular thromboembolism in cancer patients treated with immune checkpoint inhibitors, and finally we explore preclinical models of acute erythroid leukemia using CRISPR/Cas 9 hematopoietic genome editing.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we look at the role of a previously unidentified variant of DNA methyltransferase 1 as a determinant of beta-thalessemia phenotype, report on the association of vascular thromboembolism in cancer patients treated with immune checkpoint inhibitors, and finally we explore preclinical models of acute erythroid leukemia using CRISPR/Cas 9 hematopoietic genome editing.]]>
      </content:encoded>
      <pubDate>Thu, 25 Mar 2021 12:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/c9efff84/d05ea9bb.mp3" length="18925085" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1180</itunes:duration>
      <itunes:summary>In this week’s episode, we look at the role of a previously unidentified variant of DNA methyltransferase 1 as a determinant of beta-thalessemia phenotype, report on the association of vascular thromboembolism in cancer patients treated with immune checkpoint inhibitors, and finally we explore preclinical models of acute erythroid leukemia using CRISPR/Cas 9 hematopoietic genome editing.</itunes:summary>
      <itunes:subtitle>In this week’s episode, we look at the role of a previously unidentified variant of DNA methyltransferase 1 as a determinant of beta-thalessemia phenotype, report on the association of vascular thromboembolism in cancer patients treated with immune checkp</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 2, Episode 11</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Season 2, Episode 11</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">1846705d-a329-4785-a764-c3d3d754c642</guid>
      <link>https://share.transistor.fm/s/7b77af87</link>
      <description>
        <![CDATA[In this week’s episode, will review a study that looks at primary diffuse large B-cell lymphoma of the central nervous system comparing tumor biologic features associated with Epstein-Barr virus, examine the functions of regulatory T cells in thrombus resolution in a mouse model, and learn more about subsequent malignant neoplasms in treated pediatric patients with Hodgkin lymphoma.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, will review a study that looks at primary diffuse large B-cell lymphoma of the central nervous system comparing tumor biologic features associated with Epstein-Barr virus, examine the functions of regulatory T cells in thrombus resolution in a mouse model, and learn more about subsequent malignant neoplasms in treated pediatric patients with Hodgkin lymphoma.]]>
      </content:encoded>
      <pubDate>Thu, 18 Mar 2021 12:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/7b77af87/52b924de.mp3" length="18605755" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1160</itunes:duration>
      <itunes:summary>In this week’s episode, will review a study that looks at primary diffuse large B-cell lymphoma of the central nervous system comparing tumor biologic features associated with Epstein-Barr virus, examine the functions of regulatory T cells in thrombus resolution in a mouse model, and learn more about subsequent malignant neoplasms in treated pediatric patients with Hodgkin lymphoma.</itunes:summary>
      <itunes:subtitle>In this week’s episode, will review a study that looks at primary diffuse large B-cell lymphoma of the central nervous system comparing tumor biologic features associated with Epstein-Barr virus, examine the functions of regulatory T cells in thrombus res</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 2, Bonus: How I Treat Series: Acquired Hemolytic Anemia</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Season 2, Bonus: How I Treat Series: Acquired Hemolytic Anemia</itunes:title>
      <itunes:episodeType>bonus</itunes:episodeType>
      <guid isPermaLink="false">2af90ef4-31ca-476f-88fc-e561776659e3</guid>
      <link>https://share.transistor.fm/s/31ed1fae</link>
      <description>
        <![CDATA[Diagnosis and treatment of acquired hemolytic anemia can be challenging. In this How I Treat series, edited by Mario Cazzola, clinical experts discuss their approaches to the treatment of patients with 4 different classes of acquired hemolytic anemia.]]>
      </description>
      <content:encoded>
        <![CDATA[Diagnosis and treatment of acquired hemolytic anemia can be challenging. In this How I Treat series, edited by Mario Cazzola, clinical experts discuss their approaches to the treatment of patients with 4 different classes of acquired hemolytic anemia.]]>
      </content:encoded>
      <pubDate>Mon, 15 Mar 2021 12:11:33 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/31ed1fae/7854f0ea.mp3" length="28947826" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1198</itunes:duration>
      <itunes:summary>Diagnosis and treatment of acquired hemolytic anemia can be challenging. In this How I Treat series, edited by Mario Cazzola, clinical experts discuss their approaches to the treatment of patients with 4 different classes of acquired hemolytic anemia.</itunes:summary>
      <itunes:subtitle>Diagnosis and treatment of acquired hemolytic anemia can be challenging. In this How I Treat series, edited by Mario Cazzola, clinical experts discuss their approaches to the treatment of patients with 4 different classes of acquired hemolytic anemia.</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 2, Episode 10</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Season 2, Episode 10</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">37e94a3f-f72a-4236-8629-e400a678aed6</guid>
      <link>https://share.transistor.fm/s/ac3743e6</link>
      <description>
        <![CDATA[In this week’s episode, we will review recent studies providing new insights on frontline use of checkpoint inhibitors in classical Hodgkin lymphoma, immune escape mechanisms in diffuse large B-cell lymphoma, and the role of SRP54 mutations in congenital neutropenia. ]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we will review recent studies providing new insights on frontline use of checkpoint inhibitors in classical Hodgkin lymphoma, immune escape mechanisms in diffuse large B-cell lymphoma, and the role of SRP54 mutations in congenital neutropenia. ]]>
      </content:encoded>
      <pubDate>Thu, 11 Mar 2021 12:00:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/ac3743e6/d06df3d1.mp3" length="16670370" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1039</itunes:duration>
      <itunes:summary>In this week’s episode, we will review recent studies providing new insights on frontline use of checkpoint inhibitors in classical Hodgkin lymphoma, immune escape mechanisms in diffuse large B-cell lymphoma, and the role of SRP54 mutations in congenital neutropenia. </itunes:summary>
      <itunes:subtitle>In this week’s episode, we will review recent studies providing new insights on frontline use of checkpoint inhibitors in classical Hodgkin lymphoma, immune escape mechanisms in diffuse large B-cell lymphoma, and the role of SRP54 mutations in congenital </itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 2, Episode 9</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Season 2, Episode 9</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">a2ac7e05-ecce-47ca-bf36-4262ea7458a3</guid>
      <link>https://share.transistor.fm/s/9dee11c4</link>
      <description>
        <![CDATA[In this week’s episode, we will review a study that provides further evidence of poor prognosis in patients with multiple myeloma who have “double hit” mutations targeting TP53, examine the early use of BCR-ABL1 kinetics to predict the likelihood of treatment free remission in patients with chronic myeloid leukemia receiving tyrosine kinase inhibitors, and learn more about a direct causative link between IL-18 with arrythmias and myocardial fibrosis in sickle cell cardiomyopathy.        ]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we will review a study that provides further evidence of poor prognosis in patients with multiple myeloma who have “double hit” mutations targeting TP53, examine the early use of BCR-ABL1 kinetics to predict the likelihood of treatment free remission in patients with chronic myeloid leukemia receiving tyrosine kinase inhibitors, and learn more about a direct causative link between IL-18 with arrythmias and myocardial fibrosis in sickle cell cardiomyopathy.        ]]>
      </content:encoded>
      <pubDate>Thu, 04 Mar 2021 12:15:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/9dee11c4/12368bd3.mp3" length="15098869" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>941</itunes:duration>
      <itunes:summary>In this week’s episode, we will review a study that provides further evidence of poor prognosis in patients with multiple myeloma who have “double hit” mutations targeting TP53, examine the early use of BCR-ABL1 kinetics to predict the likelihood of treatment free remission in patients with chronic myeloid leukemia receiving tyrosine kinase inhibitors, and learn more about a direct causative link between IL-18 with arrythmias and myocardial fibrosis in sickle cell cardiomyopathy.        </itunes:summary>
      <itunes:subtitle>In this week’s episode, we will review a study that provides further evidence of poor prognosis in patients with multiple myeloma who have “double hit” mutations targeting TP53, examine the early use of BCR-ABL1 kinetics to predict the likelihood of treat</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 2, Episode 8</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Season 2, Episode 8</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">0b5e7700-d741-4823-be22-bd6edf72362c</guid>
      <link>https://share.transistor.fm/s/cef3efbb</link>
      <description>
        <![CDATA[In this week’s episode, we will learn more about pre-clinical work that aims to identify optimal immunotargets for treatment of pediatric AML, report on a novel path for subcutaneous administration of Factor 8, and highlight the performance characteristics of the platelet factor 4-dependent p-selectin expression assay for the diagnosis of heparin-induced thrombocytopenia.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we will learn more about pre-clinical work that aims to identify optimal immunotargets for treatment of pediatric AML, report on a novel path for subcutaneous administration of Factor 8, and highlight the performance characteristics of the platelet factor 4-dependent p-selectin expression assay for the diagnosis of heparin-induced thrombocytopenia.]]>
      </content:encoded>
      <pubDate>Thu, 25 Feb 2021 12:00:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/cef3efbb/849f8cfc.mp3" length="18226640" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1136</itunes:duration>
      <itunes:summary>In this week’s episode, we will learn more about pre-clinical work that aims to identify optimal immunotargets for treatment of pediatric AML, report on a novel path for subcutaneous administration of Factor 8, and highlight the performance characteristics of the platelet factor 4-dependent p-selectin expression assay for the diagnosis of heparin-induced thrombocytopenia.</itunes:summary>
      <itunes:subtitle>In this week’s episode, we will learn more about pre-clinical work that aims to identify optimal immunotargets for treatment of pediatric AML, report on a novel path for subcutaneous administration of Factor 8, and highlight the performance characteristic</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 2, Episode 7</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Season 2, Episode 7</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">a6b2d421-d473-4dc4-bfa8-753cbd3d5cae</guid>
      <link>https://share.transistor.fm/s/49759685</link>
      <description>
        <![CDATA[In this week’s episode, we will learn about the cost effectiveness of caplacizumab in acquired thrombotic thrombocytopenic purpura, review outcomes of a phase 2 trial of pomalidomide in subjects failing prior therapy of chronic graft-versus-host disease, and examine results of a phase 1/2 study looking at the use of ibrutinib and obinutuzimab plus venetoclax in patients with mantle-cell lymphoma. ]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we will learn about the cost effectiveness of caplacizumab in acquired thrombotic thrombocytopenic purpura, review outcomes of a phase 2 trial of pomalidomide in subjects failing prior therapy of chronic graft-versus-host disease, and examine results of a phase 1/2 study looking at the use of ibrutinib and obinutuzimab plus venetoclax in patients with mantle-cell lymphoma. ]]>
      </content:encoded>
      <pubDate>Thu, 18 Feb 2021 12:00:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/49759685/4e7fffca.mp3" length="16732906" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1043</itunes:duration>
      <itunes:summary>In this week’s episode, we will learn about the cost effectiveness of caplacizumab in acquired thrombotic thrombocytopenic purpura, review outcomes of a phase 2 trial of pomalidomide in subjects failing prior therapy of chronic graft-versus-host disease, and examine results of a phase 1/2 study looking at the use of ibrutinib and obinutuzimab plus venetoclax in patients with mantle-cell lymphoma. </itunes:summary>
      <itunes:subtitle>In this week’s episode, we will learn about the cost effectiveness of caplacizumab in acquired thrombotic thrombocytopenic purpura, review outcomes of a phase 2 trial of pomalidomide in subjects failing prior therapy of chronic graft-versus-host disease, </itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 2, Episode 6</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Season 2, Episode 6</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">c2ae967b-63f5-45cf-9c53-dba53947456d</guid>
      <link>https://share.transistor.fm/s/a2978e08</link>
      <description>
        <![CDATA[In this week’s episode, we will cover recent research that provides new insights into the treatment of relapsed or refractory acute myeloid leukemia, immune-mediated thrombotic thrombocytopenic purpura, and sickle cell disease.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we will cover recent research that provides new insights into the treatment of relapsed or refractory acute myeloid leukemia, immune-mediated thrombotic thrombocytopenic purpura, and sickle cell disease.]]>
      </content:encoded>
      <pubDate>Thu, 11 Feb 2021 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/a2978e08/35a11aff.mp3" length="24179018" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1004</itunes:duration>
      <itunes:summary>In this week’s episode, we will cover recent research that provides new insights into the treatment of relapsed or refractory acute myeloid leukemia, immune-mediated thrombotic thrombocytopenic purpura, and sickle cell disease.</itunes:summary>
      <itunes:subtitle>In this week’s episode, we will cover recent research that provides new insights into the treatment of relapsed or refractory acute myeloid leukemia, immune-mediated thrombotic thrombocytopenic purpura, and sickle cell disease.</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 2, Episode 5</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Season 2, Episode 5</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">08f1c984-5fd8-40cc-85ea-5d066dfc27eb</guid>
      <link>https://share.transistor.fm/s/72c2b773</link>
      <description>
        <![CDATA[In this week’s episode, we will review a study that describes the pathogenic relevance of retinoic acid-responsive CD8+ T-cells in gastrointestinal graft-versus-host disease, learn more about how storage-induced disturbances of platelets is linked to changes in the number and sphingolipid content of platelet extracellular vesicles which predispose to transfusion related acute lung injury, and lastly, review the findings of a phase II study of venetoclax plus R-CHOP as first-line treatment for patients with diffuse large B-cell lymphoma.       ]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we will review a study that describes the pathogenic relevance of retinoic acid-responsive CD8+ T-cells in gastrointestinal graft-versus-host disease, learn more about how storage-induced disturbances of platelets is linked to changes in the number and sphingolipid content of platelet extracellular vesicles which predispose to transfusion related acute lung injury, and lastly, review the findings of a phase II study of venetoclax plus R-CHOP as first-line treatment for patients with diffuse large B-cell lymphoma.       ]]>
      </content:encoded>
      <pubDate>Thu, 04 Feb 2021 12:00:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/72c2b773/59b5005e.mp3" length="17456273" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1088</itunes:duration>
      <itunes:summary>In this week’s episode, we will review a study that describes the pathogenic relevance of retinoic acid-responsive CD8+ T-cells in gastrointestinal graft-versus-host disease, learn more about how storage-induced disturbances of platelets is linked to changes in the number and sphingolipid content of platelet extracellular vesicles which predispose to transfusion related acute lung injury, and lastly, review the findings of a phase II study of venetoclax plus R-CHOP as first-line treatment for patients with diffuse large B-cell lymphoma.       </itunes:summary>
      <itunes:subtitle>In this week’s episode, we will review a study that describes the pathogenic relevance of retinoic acid-responsive CD8+ T-cells in gastrointestinal graft-versus-host disease, learn more about how storage-induced disturbances of platelets is linked to chan</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 2, Episode 4</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Season 2, Episode 4</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">839fd5e8-9cd6-4d0d-b462-9aae0b75c566</guid>
      <link>https://share.transistor.fm/s/9ebf3cb8</link>
      <description>
        <![CDATA[In this week’s episode, we will explore the characteristics of the tumor and immune environment as predictors of response to blinatumomab in B cell ALL, look at a new predictive tool for guiding decision-making for stem cell transplantation in acute myeloid leukemia, and review the mechanisms of how persistent terminal complement activation can still occur even in the presence of complement inhibitors targeting C3 or C5. ]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we will explore the characteristics of the tumor and immune environment as predictors of response to blinatumomab in B cell ALL, look at a new predictive tool for guiding decision-making for stem cell transplantation in acute myeloid leukemia, and review the mechanisms of how persistent terminal complement activation can still occur even in the presence of complement inhibitors targeting C3 or C5. ]]>
      </content:encoded>
      <pubDate>Thu, 28 Jan 2021 12:00:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/9ebf3cb8/e24800b1.mp3" length="19305076" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1203</itunes:duration>
      <itunes:summary>In this week’s episode, we will explore the characteristics of the tumor and immune environment as predictors of response to blinatumomab in B cell ALL, look at a new predictive tool for guiding decision-making for stem cell transplantation in acute myeloid leukemia, and review the mechanisms of how persistent terminal complement activation can still occur even in the presence of complement inhibitors targeting C3 or C5. </itunes:summary>
      <itunes:subtitle>In this week’s episode, we will explore the characteristics of the tumor and immune environment as predictors of response to blinatumomab in B cell ALL, look at a new predictive tool for guiding decision-making for stem cell transplantation in acute myelo</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 2, Episode 3</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Season 2, Episode 3</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">a9853a39-8f4a-48cc-9304-fbb964453cc3</guid>
      <link>https://share.transistor.fm/s/662c0cb5</link>
      <description>
        <![CDATA[In this week’s episode, we will review a study that shows neutrophils are required for optimum recovery from acute lung injury in a murine model, examine the implication of germline genetic factors in the myeloproliferative neoplasm, polycythemia vera, and learn about the use of emicizumab for bleeding control in a small study of patients with acquired hemophilia A.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we will review a study that shows neutrophils are required for optimum recovery from acute lung injury in a murine model, examine the implication of germline genetic factors in the myeloproliferative neoplasm, polycythemia vera, and learn about the use of emicizumab for bleeding control in a small study of patients with acquired hemophilia A.]]>
      </content:encoded>
      <pubDate>Thu, 21 Jan 2021 12:00:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/662c0cb5/4a24b5bb.mp3" length="20814249" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>864</itunes:duration>
      <itunes:summary>In this week’s episode, we will review a study that shows neutrophils are required for optimum recovery from acute lung injury in a murine model, examine the implication of germline genetic factors in the myeloproliferative neoplasm, polycythemia vera, and learn about the use of emicizumab for bleeding control in a small study of patients with acquired hemophilia A.</itunes:summary>
      <itunes:subtitle>In this week’s episode, we will review a study that shows neutrophils are required for optimum recovery from acute lung injury in a murine model, examine the implication of germline genetic factors in the myeloproliferative neoplasm, polycythemia vera, an</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 2, Episode 2</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Season 2, Episode 2</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">a4e73c38-289e-4647-8359-d70f96fbf12a</guid>
      <link>https://share.transistor.fm/s/5c86ca2e</link>
      <description>
        <![CDATA[This week’s episode covers recent research that provides new insights in erythropoiesis, mastocytosis, and chronic active EBV. First, we’ll review a report describing how interactions between an E3 ubiquitin ligase and a heterochromatin-associated protein may serve as a “toggle” of sorts to regulate the formation of red blood cells. Next, researchers find that presence of hereditary α tryptasemia may predict the risk of severe anaphylaxis in patients with mastocytosis. Finally, we’ll review a report revealing large numbers of myeloid-derived suppressor cells in patients with EBV-associated T/NK cell lymphoproliferative disorders, which may have important implications for understanding disease pathogenesis and targeted approaches to therapy. ]]>
      </description>
      <content:encoded>
        <![CDATA[This week’s episode covers recent research that provides new insights in erythropoiesis, mastocytosis, and chronic active EBV. First, we’ll review a report describing how interactions between an E3 ubiquitin ligase and a heterochromatin-associated protein may serve as a “toggle” of sorts to regulate the formation of red blood cells. Next, researchers find that presence of hereditary α tryptasemia may predict the risk of severe anaphylaxis in patients with mastocytosis. Finally, we’ll review a report revealing large numbers of myeloid-derived suppressor cells in patients with EBV-associated T/NK cell lymphoproliferative disorders, which may have important implications for understanding disease pathogenesis and targeted approaches to therapy. ]]>
      </content:encoded>
      <pubDate>Thu, 14 Jan 2021 12:00:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/5c86ca2e/6b8cb711.mp3" length="26502641" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1101</itunes:duration>
      <itunes:summary>This week’s episode covers recent research that provides new insights in erythropoiesis, mastocytosis, and chronic active EBV. First, we’ll review a report describing how interactions between an E3 ubiquitin ligase and a heterochromatin-associated protein may serve as a “toggle” of sorts to regulate the formation of red blood cells. Next, researchers find that presence of hereditary α tryptasemia may predict the risk of severe anaphylaxis in patients with mastocytosis. Finally, we’ll review a report revealing large numbers of myeloid-derived suppressor cells in patients with EBV-associated T/NK cell lymphoproliferative disorders, which may have important implications for understanding disease pathogenesis and targeted approaches to therapy. </itunes:summary>
      <itunes:subtitle>This week’s episode covers recent research that provides new insights in erythropoiesis, mastocytosis, and chronic active EBV. First, we’ll review a report describing how interactions between an E3 ubiquitin ligase and a heterochromatin-associated protein</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 2, Episode 1</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:title>Season 2, Episode 1</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">1d586752-c1ab-43d0-9a98-6380aa1bef67</guid>
      <link>https://share.transistor.fm/s/5a8fe331</link>
      <description>
        <![CDATA[In this week’s episode, we will review a study that shows that non-invasive imaging of T cell metabolic activity can detect early graft-versus-host disease after allogeneic hematopoietic stem cell transplantation, learn more about how detailed assessment of measurable residual disease in multiple myeloma can better define outcomes and how treatment resistance arises, and finally, examine the mechanism of action and pharmacokinetics of Ciraparantag, a small molecule being developed to rapidly reverse the effects of anticoagulants.  ]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we will review a study that shows that non-invasive imaging of T cell metabolic activity can detect early graft-versus-host disease after allogeneic hematopoietic stem cell transplantation, learn more about how detailed assessment of measurable residual disease in multiple myeloma can better define outcomes and how treatment resistance arises, and finally, examine the mechanism of action and pharmacokinetics of Ciraparantag, a small molecule being developed to rapidly reverse the effects of anticoagulants.  ]]>
      </content:encoded>
      <pubDate>Thu, 07 Jan 2021 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/5a8fe331/33c76759.mp3" length="23984843" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>996</itunes:duration>
      <itunes:summary>In this week’s episode, we will review a study that shows that non-invasive imaging of T cell metabolic activity can detect early graft-versus-host disease after allogeneic hematopoietic stem cell transplantation, learn more about how detailed assessment of measurable residual disease in multiple myeloma can better define outcomes and how treatment resistance arises, and finally, examine the mechanism of action and pharmacokinetics of Ciraparantag, a small molecule being developed to rapidly reverse the effects of anticoagulants.  </itunes:summary>
      <itunes:subtitle>In this week’s episode, we will review a study that shows that non-invasive imaging of T cell metabolic activity can detect early graft-versus-host disease after allogeneic hematopoietic stem cell transplantation, learn more about how detailed assessment </itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 52</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 52</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">d668c602-7c62-4116-adf6-1b97c1682f08</guid>
      <link>https://share.transistor.fm/s/0b277914</link>
      <description>
        <![CDATA[In this week’s episode, we will review a study that evaluates the role of pre-transplant leukocyte telomere length on survival outcomes in patients with myelodysplastic syndrome, learn more about a potential novel treatment for patients with WHIM syndrome, and examine a novel mechanism important for the maintenance of normal hematopoietic stem cell quiescence, and hence, long-term blood formation.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we will review a study that evaluates the role of pre-transplant leukocyte telomere length on survival outcomes in patients with myelodysplastic syndrome, learn more about a potential novel treatment for patients with WHIM syndrome, and examine a novel mechanism important for the maintenance of normal hematopoietic stem cell quiescence, and hence, long-term blood formation.]]>
      </content:encoded>
      <pubDate>Thu, 24 Dec 2020 12:00:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/0b277914/43e4bf33.mp3" length="24617835" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1022</itunes:duration>
      <itunes:summary>In this week’s episode, we will review a study that evaluates the role of pre-transplant leukocyte telomere length on survival outcomes in patients with myelodysplastic syndrome, learn more about a potential novel treatment for patients with WHIM syndrome, and examine a novel mechanism important for the maintenance of normal hematopoietic stem cell quiescence, and hence, long-term blood formation.</itunes:summary>
      <itunes:subtitle>In this week’s episode, we will review a study that evaluates the role of pre-transplant leukocyte telomere length on survival outcomes in patients with myelodysplastic syndrome, learn more about a potential novel treatment for patients with WHIM syndrome</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 51</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 51</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">dbb51398-226f-4b69-9f7d-357283917672</guid>
      <link>https://share.transistor.fm/s/5d5d7269</link>
      <description>
        <![CDATA[In this week’s episode, we will learn more about T-cells from SARS-CoV-2-infected individuals, review a study that describes the rapid clinical and histologic response to anti-PD1 first-line therapy in early-stage, unfavorable Hodgkin lymphoma, and discuss a meta-analysis and systematic review of outcomes of patients with hematologic malignancies and Covid-19.   ]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we will learn more about T-cells from SARS-CoV-2-infected individuals, review a study that describes the rapid clinical and histologic response to anti-PD1 first-line therapy in early-stage, unfavorable Hodgkin lymphoma, and discuss a meta-analysis and systematic review of outcomes of patients with hematologic malignancies and Covid-19.   ]]>
      </content:encoded>
      <pubDate>Thu, 17 Dec 2020 13:00:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/5d5d7269/19d0e396.mp3" length="25199506" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1046</itunes:duration>
      <itunes:summary>In this week’s episode, we will learn more about T-cells from SARS-CoV-2-infected individuals, review a study that describes the rapid clinical and histologic response to anti-PD1 first-line therapy in early-stage, unfavorable Hodgkin lymphoma, and discuss a meta-analysis and systematic review of outcomes of patients with hematologic malignancies and Covid-19.   </itunes:summary>
      <itunes:subtitle>In this week’s episode, we will learn more about T-cells from SARS-CoV-2-infected individuals, review a study that describes the rapid clinical and histologic response to anti-PD1 first-line therapy in early-stage, unfavorable Hodgkin lymphoma, and discus</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 50</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 50</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">79a79fde-736c-4fd1-b047-3b8f2c927142</guid>
      <link>https://share.transistor.fm/s/a8fc3df7</link>
      <description>
        <![CDATA[In this week’s episode, we will review a study describing real-world data where PET scans following chemotherapy for primary mediastinal B-cell lymphoma were used to guide consolidative radiotherapy, learn more about the novel role of the BLOC-2 protein complex in the formation of Weibel-Palade bodies that store von Willebrand Factor in endothelial cells, and finally, examine how mutant TP53 in myelodysplastic syndrome is associated with immune checkpoint overexpression in the bone marrow.  ]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we will review a study describing real-world data where PET scans following chemotherapy for primary mediastinal B-cell lymphoma were used to guide consolidative radiotherapy, learn more about the novel role of the BLOC-2 protein complex in the formation of Weibel-Palade bodies that store von Willebrand Factor in endothelial cells, and finally, examine how mutant TP53 in myelodysplastic syndrome is associated with immune checkpoint overexpression in the bone marrow.  ]]>
      </content:encoded>
      <pubDate>Thu, 10 Dec 2020 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/a8fc3df7/7d0e27cd.mp3" length="24134719" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1002</itunes:duration>
      <itunes:summary>In this week’s episode, we will review a study describing real-world data where PET scans following chemotherapy for primary mediastinal B-cell lymphoma were used to guide consolidative radiotherapy, learn more about the novel role of the BLOC-2 protein complex in the formation of Weibel-Palade bodies that store von Willebrand Factor in endothelial cells, and finally, examine how mutant TP53 in myelodysplastic syndrome is associated with immune checkpoint overexpression in the bone marrow.  </itunes:summary>
      <itunes:subtitle>In this week’s episode, we will review a study describing real-world data where PET scans following chemotherapy for primary mediastinal B-cell lymphoma were used to guide consolidative radiotherapy, learn more about the novel role of the BLOC-2 protein c</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 49</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 49</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">f29bb49f-520f-4749-be16-4289ac1a6ab8</guid>
      <link>https://share.transistor.fm/s/172ae88b</link>
      <description>
        <![CDATA[In this week’s episode, we will review a study that describes how transfer of whole mitochondria from hematopoietic stem cells to bone marrow mesenchymal stem cells helps regenerate the stroma and its capacity to sustain hematopoietic recovery in irradiated mice undergoing stem cell transplant, examine the potential benefit of adding the BCL2-inhibitor, venetoclax, to standard treatment regimens for patients with relapsed or refractory follicular lymphoma, and finally, we will learn more about how NCOA4, the autophagic receptor for ferritin, is necessary for the mobilization of liver iron stores during stress erythropoiesis.      ]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we will review a study that describes how transfer of whole mitochondria from hematopoietic stem cells to bone marrow mesenchymal stem cells helps regenerate the stroma and its capacity to sustain hematopoietic recovery in irradiated mice undergoing stem cell transplant, examine the potential benefit of adding the BCL2-inhibitor, venetoclax, to standard treatment regimens for patients with relapsed or refractory follicular lymphoma, and finally, we will learn more about how NCOA4, the autophagic receptor for ferritin, is necessary for the mobilization of liver iron stores during stress erythropoiesis.      ]]>
      </content:encoded>
      <pubDate>Thu, 03 Dec 2020 12:22:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/172ae88b/090891ca.mp3" length="23770088" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>986</itunes:duration>
      <itunes:summary>In this week’s episode, we will review a study that describes how transfer of whole mitochondria from hematopoietic stem cells to bone marrow mesenchymal stem cells helps regenerate the stroma and its capacity to sustain hematopoietic recovery in irradiated mice undergoing stem cell transplant, examine the potential benefit of adding the BCL2-inhibitor, venetoclax, to standard treatment regimens for patients with relapsed or refractory follicular lymphoma, and finally, we will learn more about how NCOA4, the autophagic receptor for ferritin, is necessary for the mobilization of liver iron stores during stress erythropoiesis.      </itunes:summary>
      <itunes:subtitle>In this week’s episode, we will review a study that describes how transfer of whole mitochondria from hematopoietic stem cells to bone marrow mesenchymal stem cells helps regenerate the stroma and its capacity to sustain hematopoietic recovery in irradiat</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 48</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 48</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">1c07d1e8-970c-440a-ada4-9739dde73a77</guid>
      <link>https://share.transistor.fm/s/b8a9f64a</link>
      <description>
        <![CDATA[In this week’s episode, we will review a study that reveals a previously unknown role for the canonical Wnt signaling pathway in the regulation of granulocyte production in steady state and emergency granulopoiesis, examine the discordance in different assays that measure factor VIII activity after adenoviral-associated gene therapy, and learn about the dynamics of declining antibody levels in repeat Covid-19 convalescent plasma donors.     ]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we will review a study that reveals a previously unknown role for the canonical Wnt signaling pathway in the regulation of granulocyte production in steady state and emergency granulopoiesis, examine the discordance in different assays that measure factor VIII activity after adenoviral-associated gene therapy, and learn about the dynamics of declining antibody levels in repeat Covid-19 convalescent plasma donors.     ]]>
      </content:encoded>
      <pubDate>Thu, 26 Nov 2020 12:00:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/b8a9f64a/95eea1cf.mp3" length="23913552" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>993</itunes:duration>
      <itunes:summary>In this week’s episode, we will review a study that reveals a previously unknown role for the canonical Wnt signaling pathway in the regulation of granulocyte production in steady state and emergency granulopoiesis, examine the discordance in different assays that measure factor VIII activity after adenoviral-associated gene therapy, and learn about the dynamics of declining antibody levels in repeat Covid-19 convalescent plasma donors.     </itunes:summary>
      <itunes:subtitle>In this week’s episode, we will review a study that reveals a previously unknown role for the canonical Wnt signaling pathway in the regulation of granulocyte production in steady state and emergency granulopoiesis, examine the discordance in different as</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 47</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 47</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">b9b348ce-ffb1-41dc-bee3-49fcb0434fbe</guid>
      <link>https://share.transistor.fm/s/17baabdd</link>
      <description>
        <![CDATA[In this week’s episode, we will review an proof-of concept study using the bispecific antibody AFM13 in combination with a check-point inhibitor in patients with relapsed or refractory Hodgkin lymphoma, learn more about how iron restriction might be a promising new therapy for congenital erythropoietic porphyria, and review a manuscript that provides novel molecular insights into the requirement for RUNX1 in a mouse model of inversion 16 acute myeloid leukemia, providing a path forward for new therapies to treat this subgroup of AML.   ]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we will review an proof-of concept study using the bispecific antibody AFM13 in combination with a check-point inhibitor in patients with relapsed or refractory Hodgkin lymphoma, learn more about how iron restriction might be a promising new therapy for congenital erythropoietic porphyria, and review a manuscript that provides novel molecular insights into the requirement for RUNX1 in a mouse model of inversion 16 acute myeloid leukemia, providing a path forward for new therapies to treat this subgroup of AML.   ]]>
      </content:encoded>
      <pubDate>Thu, 19 Nov 2020 13:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/17baabdd/a64226e2.mp3" length="25400424" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1054</itunes:duration>
      <itunes:summary>In this week’s episode, we will review an proof-of concept study using the bispecific antibody AFM13 in combination with a check-point inhibitor in patients with relapsed or refractory Hodgkin lymphoma, learn more about how iron restriction might be a promising new therapy for congenital erythropoietic porphyria, and review a manuscript that provides novel molecular insights into the requirement for RUNX1 in a mouse model of inversion 16 acute myeloid leukemia, providing a path forward for new therapies to treat this subgroup of AML.   </itunes:summary>
      <itunes:subtitle>In this week’s episode, we will review an proof-of concept study using the bispecific antibody AFM13 in combination with a check-point inhibitor in patients with relapsed or refractory Hodgkin lymphoma, learn more about how iron restriction might be a pro</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 46</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 46</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">fae9694c-9793-4174-9595-5358bdf586dd</guid>
      <link>https://share.transistor.fm/s/b3a5fe20</link>
      <description>
        <![CDATA[In this week’s episode, we will review a study on the involvement of lysine-specific, we’ll cover some of the latest findings in COVID-19, multiple myeloma, and myelodysplastic syndromes. First, we’ll review an observational, multicenter study suggesting that convalescent plasma with anti-SARS-CoVid-2 antibodies may be a promising therapy in B-cell depleted patients who have prolonged COVID-19 symptoms. Next, we’ll discuss a research article showing that inhibition of JAK-STAT3 signaling with ruxolitinib could upregulate CD38 expression, thereby enhancing daratumumab-mediated cytotoxicity in multiple myeloma. Finally, we’ll review a report showing for the first time that in MDS, machine learning algorithms can be used to reveal novel associations between morphologic features and genetic lesions that may have important prognostic implications.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we will review a study on the involvement of lysine-specific, we’ll cover some of the latest findings in COVID-19, multiple myeloma, and myelodysplastic syndromes. First, we’ll review an observational, multicenter study suggesting that convalescent plasma with anti-SARS-CoVid-2 antibodies may be a promising therapy in B-cell depleted patients who have prolonged COVID-19 symptoms. Next, we’ll discuss a research article showing that inhibition of JAK-STAT3 signaling with ruxolitinib could upregulate CD38 expression, thereby enhancing daratumumab-mediated cytotoxicity in multiple myeloma. Finally, we’ll review a report showing for the first time that in MDS, machine learning algorithms can be used to reveal novel associations between morphologic features and genetic lesions that may have important prognostic implications.]]>
      </content:encoded>
      <pubDate>Thu, 12 Nov 2020 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/b3a5fe20/d4478910.mp3" length="26564940" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1104</itunes:duration>
      <itunes:summary>In this week’s episode, we will review a study on the involvement of lysine-specific, we’ll cover some of the latest findings in COVID-19, multiple myeloma, and myelodysplastic syndromes. First, we’ll review an observational, multicenter study suggesting that convalescent plasma with anti-SARS-CoVid-2 antibodies may be a promising therapy in B-cell depleted patients who have prolonged COVID-19 symptoms. Next, we’ll discuss a research article showing that inhibition of JAK-STAT3 signaling with ruxolitinib could upregulate CD38 expression, thereby enhancing daratumumab-mediated cytotoxicity in multiple myeloma. Finally, we’ll review a report showing for the first time that in MDS, machine learning algorithms can be used to reveal novel associations between morphologic features and genetic lesions that may have important prognostic implications.</itunes:summary>
      <itunes:subtitle>In this week’s episode, we will review a study on the involvement of lysine-specific, we’ll cover some of the latest findings in COVID-19, multiple myeloma, and myelodysplastic syndromes. First, we’ll review an observational, multicenter study suggesting </itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 45</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 45</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">b6d949ee-2832-4f88-9037-ae802cc3a22f</guid>
      <link>https://share.transistor.fm/s/bc3b390b</link>
      <description>
        <![CDATA[In this week’s episode, we will review a study on the involvement of lysine-specific demethylase 1A in hematopoietic stem cell expansion, examine the role of platelet receptor PAR4 in venous thromboembolism; and finally, investigate the relative contributions of maternal versus fetal hepcidin in embryonic iron endowment in both healthy and inflammatory states.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we will review a study on the involvement of lysine-specific demethylase 1A in hematopoietic stem cell expansion, examine the role of platelet receptor PAR4 in venous thromboembolism; and finally, investigate the relative contributions of maternal versus fetal hepcidin in embryonic iron endowment in both healthy and inflammatory states.]]>
      </content:encoded>
      <pubDate>Thu, 05 Nov 2020 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/bc3b390b/6ffbfa7a.mp3" length="27684192" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1149</itunes:duration>
      <itunes:summary>In this week’s episode, we will review a study on the involvement of lysine-specific demethylase 1A in hematopoietic stem cell expansion, examine the role of platelet receptor PAR4 in venous thromboembolism; and finally, investigate the relative contributions of maternal versus fetal hepcidin in embryonic iron endowment in both healthy and inflammatory states.</itunes:summary>
      <itunes:subtitle>In this week’s episode, we will review a study on the involvement of lysine-specific demethylase 1A in hematopoietic stem cell expansion, examine the role of platelet receptor PAR4 in venous thromboembolism; and finally, investigate the relative contribut</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 44</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 44</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">3d50949d-d073-4557-9a59-5e27c53b1cd8</guid>
      <link>https://share.transistor.fm/s/77dd9ba4</link>
      <description>
        <![CDATA[In this week’s episode, we will review a study that uncovers a role for CLCX4 in inducing the two hallmark features of primary myelofibrosis, bone marrow fibrosis and inflammation. We will next examine how genetic predisposition and altered gut microbiome can trigger the development of Precursor B-ALL in mice, and finally, learn how SARS-CoV2 spike proteins activate complement by engaging the alternative pathway, a novel finding which raises the prospect for targeted therapy of COVID-19-associated micro-angiopathy.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we will review a study that uncovers a role for CLCX4 in inducing the two hallmark features of primary myelofibrosis, bone marrow fibrosis and inflammation. We will next examine how genetic predisposition and altered gut microbiome can trigger the development of Precursor B-ALL in mice, and finally, learn how SARS-CoV2 spike proteins activate complement by engaging the alternative pathway, a novel finding which raises the prospect for targeted therapy of COVID-19-associated micro-angiopathy.]]>
      </content:encoded>
      <pubDate>Thu, 29 Oct 2020 12:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/77dd9ba4/a95b21c0.mp3" length="29328588" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1219</itunes:duration>
      <itunes:summary>In this week’s episode, we will review a study that uncovers a role for CLCX4 in inducing the two hallmark features of primary myelofibrosis, bone marrow fibrosis and inflammation. We will next examine how genetic predisposition and altered gut microbiome can trigger the development of Precursor B-ALL in mice, and finally, learn how SARS-CoV2 spike proteins activate complement by engaging the alternative pathway, a novel finding which raises the prospect for targeted therapy of COVID-19-associated micro-angiopathy.</itunes:summary>
      <itunes:subtitle>In this week’s episode, we will review a study that uncovers a role for CLCX4 in inducing the two hallmark features of primary myelofibrosis, bone marrow fibrosis and inflammation. We will next examine how genetic predisposition and altered gut microbiome</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 43</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 43</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">0a18c9e3-f2db-4793-b172-089973b50b1d</guid>
      <link>https://share.transistor.fm/s/83d17c6c</link>
      <description>
        <![CDATA[In this week’s episode, we will learn more about the immune defects and granule dysfunction in the leukocytes of patients with the rare recessive platelet disorder, gray platelet syndrome, review a study that examines the cost effectiveness of first-line versus third-line ibrutinib in patients with chronic lymphocytic leukemia, and review a manuscript that proposes a diagnostic classifier to facilitate the diagnosis of childhood autoimmune lymphoproliferative syndrome.  ]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we will learn more about the immune defects and granule dysfunction in the leukocytes of patients with the rare recessive platelet disorder, gray platelet syndrome, review a study that examines the cost effectiveness of first-line versus third-line ibrutinib in patients with chronic lymphocytic leukemia, and review a manuscript that proposes a diagnostic classifier to facilitate the diagnosis of childhood autoimmune lymphoproliferative syndrome.  ]]>
      </content:encoded>
      <pubDate>Thu, 22 Oct 2020 12:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/83d17c6c/84a26225.mp3" length="28193046" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1171</itunes:duration>
      <itunes:summary>In this week’s episode, we will learn more about the immune defects and granule dysfunction in the leukocytes of patients with the rare recessive platelet disorder, gray platelet syndrome, review a study that examines the cost effectiveness of first-line versus third-line ibrutinib in patients with chronic lymphocytic leukemia, and review a manuscript that proposes a diagnostic classifier to facilitate the diagnosis of childhood autoimmune lymphoproliferative syndrome.  </itunes:summary>
      <itunes:subtitle>In this week’s episode, we will learn more about the immune defects and granule dysfunction in the leukocytes of patients with the rare recessive platelet disorder, gray platelet syndrome, review a study that examines the cost effectiveness of first-line </itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 42</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 42</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">19c0d729-dd41-44f2-aa5a-239a29e70e69</guid>
      <link>https://share.transistor.fm/s/fe627970</link>
      <description>
        <![CDATA[In this week’s episode, we will review a study that utilized whole-genome sequencing to define the mutational spectrum and clonal architecture of myelodysplastic/ myeloproliferative neoplasms, learn more about the association between plasma levels of growth differentiation factor 15 and the risk of venous thromboembolism, and examine the role of microenvironment myeloid cells in supporting the growth of T-cell acute lymphoblastic leukemia.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we will review a study that utilized whole-genome sequencing to define the mutational spectrum and clonal architecture of myelodysplastic/ myeloproliferative neoplasms, learn more about the association between plasma levels of growth differentiation factor 15 and the risk of venous thromboembolism, and examine the role of microenvironment myeloid cells in supporting the growth of T-cell acute lymphoblastic leukemia.]]>
      </content:encoded>
      <pubDate>Thu, 15 Oct 2020 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/fe627970/395242f7.mp3" length="23648517" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>982</itunes:duration>
      <itunes:summary>In this week’s episode, we will review a study that utilized whole-genome sequencing to define the mutational spectrum and clonal architecture of myelodysplastic/ myeloproliferative neoplasms, learn more about the association between plasma levels of growth differentiation factor 15 and the risk of venous thromboembolism, and examine the role of microenvironment myeloid cells in supporting the growth of T-cell acute lymphoblastic leukemia.</itunes:summary>
      <itunes:subtitle>In this week’s episode, we will review a study that utilized whole-genome sequencing to define the mutational spectrum and clonal architecture of myelodysplastic/ myeloproliferative neoplasms, learn more about the association between plasma levels of grow</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 41</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 41</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">406a9fd0-36e9-471f-9d92-0bb67ed34fce</guid>
      <link>https://share.transistor.fm/s/683f4f97</link>
      <description>
        <![CDATA[In this week’s episode, we will learn about two molecular brakes that regulate platelet activation and production, review a study showing that giving BCR-ABL1 tyrosine kinase inhibitors after allogeneic stem cell transplantation for Philadelphia-positive ALL prevents relapse, and lastly, see how investigators deciphered the role of a micro-RNA that increases platelet formation by reducing the expression of the actin-bundling protein, L-plastin, in megakaryocytes.       ]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we will learn about two molecular brakes that regulate platelet activation and production, review a study showing that giving BCR-ABL1 tyrosine kinase inhibitors after allogeneic stem cell transplantation for Philadelphia-positive ALL prevents relapse, and lastly, see how investigators deciphered the role of a micro-RNA that increases platelet formation by reducing the expression of the actin-bundling protein, L-plastin, in megakaryocytes.       ]]>
      </content:encoded>
      <pubDate>Thu, 08 Oct 2020 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/683f4f97/59909cf8.mp3" length="24614074" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1021</itunes:duration>
      <itunes:summary>In this week’s episode, we will learn about two molecular brakes that regulate platelet activation and production, review a study showing that giving BCR-ABL1 tyrosine kinase inhibitors after allogeneic stem cell transplantation for Philadelphia-positive ALL prevents relapse, and lastly, see how investigators deciphered the role of a micro-RNA that increases platelet formation by reducing the expression of the actin-bundling protein, L-plastin, in megakaryocytes.       </itunes:summary>
      <itunes:subtitle>In this week’s episode, we will learn about two molecular brakes that regulate platelet activation and production, review a study showing that giving BCR-ABL1 tyrosine kinase inhibitors after allogeneic stem cell transplantation for Philadelphia-positive </itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Review Series on Mechanisms and Clinical Implications of Clonal Hematopoiesis</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Review Series on Mechanisms and Clinical Implications of Clonal Hematopoiesis</itunes:title>
      <itunes:episodeType>bonus</itunes:episodeType>
      <guid isPermaLink="false">aa85d09e-1ff4-4c89-8d8c-ba369d4f9694</guid>
      <link>https://share.transistor.fm/s/4d256479</link>
      <description>
        <![CDATA[<p>In this bonus episode, we welcome Blood Associate Editor, Dr. Margaret Goodell, along with colleagues Dr. Grant Challen and Dr. David Steensma as they discuss the Blood review series on  mechanisms and clinical implications of clonal hematopoiesis. The articles in this series review the mechanisms driving the development of clonal hematopoiesis, the associated risks posed by clonal hematopoiesis for patients with hematologic and nonhematologic disorders and patients with inherited bone marrow syndromes, and the clinical ramifications of discovering clonal hematopoiesis and sharing the results with patients.</p><p><a href="https://ashpublications.org/blood/article/136/14/1567/461669/Introduction-to-a-review-series-on-mechanisms-and?searchresult=1">Review Series on Mechanisms and Clinical Implications of Clonal Hematopoiesis</a></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this bonus episode, we welcome Blood Associate Editor, Dr. Margaret Goodell, along with colleagues Dr. Grant Challen and Dr. David Steensma as they discuss the Blood review series on  mechanisms and clinical implications of clonal hematopoiesis. The articles in this series review the mechanisms driving the development of clonal hematopoiesis, the associated risks posed by clonal hematopoiesis for patients with hematologic and nonhematologic disorders and patients with inherited bone marrow syndromes, and the clinical ramifications of discovering clonal hematopoiesis and sharing the results with patients.</p><p><a href="https://ashpublications.org/blood/article/136/14/1567/461669/Introduction-to-a-review-series-on-mechanisms-and?searchresult=1">Review Series on Mechanisms and Clinical Implications of Clonal Hematopoiesis</a></p>]]>
      </content:encoded>
      <pubDate>Thu, 01 Oct 2020 17:45:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/4d256479/5525a792.mp3" length="27339548" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/S18YuCWWNNDHNJYnWMWUO0tpgLIMasvDbx9v47HHLOs/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS85MWZk/N2I0OWFmYWQ2Yjcy/OTA1NzZmYjQwNmFi/Nzk0Ny5qcGc.jpg"/>
      <itunes:duration>1132</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this bonus episode, we welcome Blood Associate Editor, Dr. Margaret Goodell, along with colleagues Dr. Grant Challen and Dr. David Steensma as they discuss the Blood review series on  mechanisms and clinical implications of clonal hematopoiesis. The articles in this series review the mechanisms driving the development of clonal hematopoiesis, the associated risks posed by clonal hematopoiesis for patients with hematologic and nonhematologic disorders and patients with inherited bone marrow syndromes, and the clinical ramifications of discovering clonal hematopoiesis and sharing the results with patients.</p><p><a href="https://ashpublications.org/blood/article/136/14/1567/461669/Introduction-to-a-review-series-on-mechanisms-and?searchresult=1">Review Series on Mechanisms and Clinical Implications of Clonal Hematopoiesis</a></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 40</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 40</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">8bd1b2a8-14c1-4c1f-a031-d22c7991f78b</guid>
      <link>https://share.transistor.fm/s/0aeaa6a7</link>
      <description>
        <![CDATA[In this week’s episode, we will learn more about the pre-clinical and clinical development of optimized, bivalent, tandem CD20 and CD19 chimeric antigen receptor T cells for treatment of relapsed/refractory non-Hodgkin lymphoma, examine a study that reveals the first stage in the clearance of senescent red blood cells by the spleen, and review a manuscript that describes the first transgenic mouse model fully reproducing specific renal lesions and kidney dysfunction observed in human light chain deposition disease.   ]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we will learn more about the pre-clinical and clinical development of optimized, bivalent, tandem CD20 and CD19 chimeric antigen receptor T cells for treatment of relapsed/refractory non-Hodgkin lymphoma, examine a study that reveals the first stage in the clearance of senescent red blood cells by the spleen, and review a manuscript that describes the first transgenic mouse model fully reproducing specific renal lesions and kidney dysfunction observed in human light chain deposition disease.   ]]>
      </content:encoded>
      <pubDate>Thu, 01 Oct 2020 13:15:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/0aeaa6a7/692d3a8a.mp3" length="23215963" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>964</itunes:duration>
      <itunes:summary>In this week’s episode, we will learn more about the pre-clinical and clinical development of optimized, bivalent, tandem CD20 and CD19 chimeric antigen receptor T cells for treatment of relapsed/refractory non-Hodgkin lymphoma, examine a study that reveals the first stage in the clearance of senescent red blood cells by the spleen, and review a manuscript that describes the first transgenic mouse model fully reproducing specific renal lesions and kidney dysfunction observed in human light chain deposition disease.   </itunes:summary>
      <itunes:subtitle>In this week’s episode, we will learn more about the pre-clinical and clinical development of optimized, bivalent, tandem CD20 and CD19 chimeric antigen receptor T cells for treatment of relapsed/refractory non-Hodgkin lymphoma, examine a study that revea</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 39</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 39</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">51a442cf-14ae-4de9-b2b8-f6b17dc467f7</guid>
      <link>https://share.transistor.fm/s/f78002c0</link>
      <description>
        <![CDATA[In this week’s episode, we will learn more about the role of hepcidin in fetal iron homeostasis, review a new study with improved outcomes in HLA-antigen mismatched transplantation, and examine how two splicing factor mutations can coexist in the same cell in patients with myeloid malignancies. ]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we will learn more about the role of hepcidin in fetal iron homeostasis, review a new study with improved outcomes in HLA-antigen mismatched transplantation, and examine how two splicing factor mutations can coexist in the same cell in patients with myeloid malignancies. ]]>
      </content:encoded>
      <pubDate>Thu, 24 Sep 2020 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/f78002c0/6fb611e3.mp3" length="25696550" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1066</itunes:duration>
      <itunes:summary>In this week’s episode, we will learn more about the role of hepcidin in fetal iron homeostasis, review a new study with improved outcomes in HLA-antigen mismatched transplantation, and examine how two splicing factor mutations can coexist in the same cell in patients with myeloid malignancies. </itunes:summary>
      <itunes:subtitle>In this week’s episode, we will learn more about the role of hepcidin in fetal iron homeostasis, review a new study with improved outcomes in HLA-antigen mismatched transplantation, and examine how two splicing factor mutations can coexist in the same cel</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 38</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 38</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">c530acf5-8c24-4fa7-a54e-d6099f556f32</guid>
      <link>https://share.transistor.fm/s/9e32afb4</link>
      <description>
        <![CDATA[In this week’s episode, we will examine the effects of protecting and regenerating Paneth cells and intestinal stem cells in acute-graft-versus-host-disease, learn more about how Plasmodium falciparum gametocytes develop in the bone marrow by invading erythroblasts, and look at a meta-analysis of direct oral anticoagulants for treating cancer patients with acute venous thromboembolism.  ]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we will examine the effects of protecting and regenerating Paneth cells and intestinal stem cells in acute-graft-versus-host-disease, learn more about how Plasmodium falciparum gametocytes develop in the bone marrow by invading erythroblasts, and look at a meta-analysis of direct oral anticoagulants for treating cancer patients with acute venous thromboembolism.  ]]>
      </content:encoded>
      <pubDate>Thu, 17 Sep 2020 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/9e32afb4/9f777653.mp3" length="24903919" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1034</itunes:duration>
      <itunes:summary>In this week’s episode, we will examine the effects of protecting and regenerating Paneth cells and intestinal stem cells in acute-graft-versus-host-disease, learn more about how Plasmodium falciparum gametocytes develop in the bone marrow by invading erythroblasts, and look at a meta-analysis of direct oral anticoagulants for treating cancer patients with acute venous thromboembolism.  </itunes:summary>
      <itunes:subtitle>In this week’s episode, we will examine the effects of protecting and regenerating Paneth cells and intestinal stem cells in acute-graft-versus-host-disease, learn more about how Plasmodium falciparum gametocytes develop in the bone marrow by invading ery</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Review Series on Inherited Anemias</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Review Series on Inherited Anemias</itunes:title>
      <itunes:episodeType>bonus</itunes:episodeType>
      <guid isPermaLink="false">f65bbbaf-af05-4e24-9e29-32a9576f1438</guid>
      <link>https://share.transistor.fm/s/4a767138</link>
      <description>
        <![CDATA[<p>In this bonus episode, we welcome Drs. Mario Cazzola, Rachel Grace, and Achille Iolascon as they discuss the Blood Review Series on Inherited Anemias. In this series, experts review the biology and pathophysiology of prominent inherited anemias and provide updated information on their management.</p><p><a href="https://ashpublications.org/blood/article/136/11/1215/461554/Introduction-to-a-review-series-on-inherited?searchresult=1">Review Series on Inherited Anemias</a></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this bonus episode, we welcome Drs. Mario Cazzola, Rachel Grace, and Achille Iolascon as they discuss the Blood Review Series on Inherited Anemias. In this series, experts review the biology and pathophysiology of prominent inherited anemias and provide updated information on their management.</p><p><a href="https://ashpublications.org/blood/article/136/11/1215/461554/Introduction-to-a-review-series-on-inherited?searchresult=1">Review Series on Inherited Anemias</a></p>]]>
      </content:encoded>
      <pubDate>Thu, 10 Sep 2020 14:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/4a767138/85396750.mp3" length="31108628" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/is_ZawbF5I9lINVOlo_H4FOXUmSGuVK-kvnT89O8NpQ/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS9mN2I0/NDYzYzJhNDM1NWQ0/MDUxNWY2NjA3MDVi/M2E3OC5qcGc.jpg"/>
      <itunes:duration>1293</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this bonus episode, we welcome Drs. Mario Cazzola, Rachel Grace, and Achille Iolascon as they discuss the Blood Review Series on Inherited Anemias. In this series, experts review the biology and pathophysiology of prominent inherited anemias and provide updated information on their management.</p><p><a href="https://ashpublications.org/blood/article/136/11/1215/461554/Introduction-to-a-review-series-on-inherited?searchresult=1">Review Series on Inherited Anemias</a></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 37</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 37</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">ea9ea35f-dae6-441a-b36b-c0b682534546</guid>
      <link>https://share.transistor.fm/s/2327baac</link>
      <description>
        <![CDATA[In this week’s episode, we start by reviewing two studies on the risks of transmitting HIV from transfusion. The first study asks whether changing the US blood donation policy for men who have sex with men from an indefinite deferral, to a deferral of 12 months from last sex, increases the risk of transfusion-transmitted HIV. The second study examines the frequency of detecting anti-HIV retroviral drugs in the serum of people attempting to donate blood. We will also review a manuscript examining the impact of Myc in HIV-associated non-Hodgkin lymphomas treated with EPOCH chemotherapy with or without vorinostat. And lastly, we learn more about platelet hyperactivity in two recent studies of patients with COVID-19.  ]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we start by reviewing two studies on the risks of transmitting HIV from transfusion. The first study asks whether changing the US blood donation policy for men who have sex with men from an indefinite deferral, to a deferral of 12 months from last sex, increases the risk of transfusion-transmitted HIV. The second study examines the frequency of detecting anti-HIV retroviral drugs in the serum of people attempting to donate blood. We will also review a manuscript examining the impact of Myc in HIV-associated non-Hodgkin lymphomas treated with EPOCH chemotherapy with or without vorinostat. And lastly, we learn more about platelet hyperactivity in two recent studies of patients with COVID-19.  ]]>
      </content:encoded>
      <pubDate>Thu, 10 Sep 2020 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/2327baac/9e60a4f2.mp3" length="26502608" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1100</itunes:duration>
      <itunes:summary>In this week’s episode, we start by reviewing two studies on the risks of transmitting HIV from transfusion. The first study asks whether changing the US blood donation policy for men who have sex with men from an indefinite deferral, to a deferral of 12 months from last sex, increases the risk of transfusion-transmitted HIV. The second study examines the frequency of detecting anti-HIV retroviral drugs in the serum of people attempting to donate blood. We will also review a manuscript examining the impact of Myc in HIV-associated non-Hodgkin lymphomas treated with EPOCH chemotherapy with or without vorinostat. And lastly, we learn more about platelet hyperactivity in two recent studies of patients with COVID-19.  </itunes:summary>
      <itunes:subtitle>In this week’s episode, we start by reviewing two studies on the risks of transmitting HIV from transfusion. The first study asks whether changing the US blood donation policy for men who have sex with men from an indefinite deferral, to a deferral of 12 </itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 36</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 36</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">15903071-104e-4ee7-b239-14d35fc7f036</guid>
      <link>https://share.transistor.fm/s/a7c9c544</link>
      <description>
        <![CDATA[In this week’s episode, we will learn about vasomotor hyper-responsiveness in sickle cell disease, examine the role of neutrophil extracellular traps in the pathophysiology of immunothrombosis in COVID-19-associated acute respiratory distress syndrome, and discuss a large series evaluating allogeneic hemopoietic cell transplantation in chronic granulomatous disease.   ]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we will learn about vasomotor hyper-responsiveness in sickle cell disease, examine the role of neutrophil extracellular traps in the pathophysiology of immunothrombosis in COVID-19-associated acute respiratory distress syndrome, and discuss a large series evaluating allogeneic hemopoietic cell transplantation in chronic granulomatous disease.   ]]>
      </content:encoded>
      <pubDate>Thu, 03 Sep 2020 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/a7c9c544/60dd24aa.mp3" length="21794731" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>905</itunes:duration>
      <itunes:summary>In this week’s episode, we will learn about vasomotor hyper-responsiveness in sickle cell disease, examine the role of neutrophil extracellular traps in the pathophysiology of immunothrombosis in COVID-19-associated acute respiratory distress syndrome, and discuss a large series evaluating allogeneic hemopoietic cell transplantation in chronic granulomatous disease.   </itunes:summary>
      <itunes:subtitle>In this week’s episode, we will learn about vasomotor hyper-responsiveness in sickle cell disease, examine the role of neutrophil extracellular traps in the pathophysiology of immunothrombosis in COVID-19-associated acute respiratory distress syndrome, an</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 35</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 35</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">f901455e-c338-4f32-ac9c-5b783f237cce</guid>
      <link>https://share.transistor.fm/s/7a7c3430</link>
      <description>
        <![CDATA[In this week’s episode, we will review a study that identifies a new modular organization of erythropoiesis and offers a novel strategy to overcome chronic anemias, summarize a study that used data from two large phase three trials to examine the risk of thrombosis in patients with newly diagnosed multiple myeloma, and review the first report of autosomal recessive germline TET2 deficiency, which results in immunodeficiency, autoimmune lymphoproliferation, and lymphoma.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode, we will review a study that identifies a new modular organization of erythropoiesis and offers a novel strategy to overcome chronic anemias, summarize a study that used data from two large phase three trials to examine the risk of thrombosis in patients with newly diagnosed multiple myeloma, and review the first report of autosomal recessive germline TET2 deficiency, which results in immunodeficiency, autoimmune lymphoproliferation, and lymphoma.]]>
      </content:encoded>
      <pubDate>Thu, 27 Aug 2020 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/7a7c3430/d54ba819.mp3" length="25792381" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1071</itunes:duration>
      <itunes:summary>In this week’s episode, we will review a study that identifies a new modular organization of erythropoiesis and offers a novel strategy to overcome chronic anemias, summarize a study that used data from two large phase three trials to examine the risk of thrombosis in patients with newly diagnosed multiple myeloma, and review the first report of autosomal recessive germline TET2 deficiency, which results in immunodeficiency, autoimmune lymphoproliferation, and lymphoma.</itunes:summary>
      <itunes:subtitle>In this week’s episode, we will review a study that identifies a new modular organization of erythropoiesis and offers a novel strategy to overcome chronic anemias, summarize a study that used data from two large phase three trials to examine the risk of </itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 34</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 34</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">4dff7846-9f7a-40b9-9d38-394598627226</guid>
      <link>https://share.transistor.fm/s/5ec69426</link>
      <description>
        <![CDATA[In this week’s episode we will review a study exploring recurrent somatic deletions at chromosome 13q12.2 in acute lymphoblastic leukemia leading to upregulation of FLT3, examine how matriptase-2 plays a key role in suppressing hepatic hepcidin expression, and learn about the addition of daratumumab to lenalidomide, bortezomib, and dexamethasone as a quadruple therapy for transplant eligible patients with newly diagnosed multiple myeloma. ]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode we will review a study exploring recurrent somatic deletions at chromosome 13q12.2 in acute lymphoblastic leukemia leading to upregulation of FLT3, examine how matriptase-2 plays a key role in suppressing hepatic hepcidin expression, and learn about the addition of daratumumab to lenalidomide, bortezomib, and dexamethasone as a quadruple therapy for transplant eligible patients with newly diagnosed multiple myeloma. ]]>
      </content:encoded>
      <pubDate>Thu, 20 Aug 2020 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/5ec69426/93fc7071.mp3" length="24576538" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1021</itunes:duration>
      <itunes:summary>In this week’s episode we will review a study exploring recurrent somatic deletions at chromosome 13q12.2 in acute lymphoblastic leukemia leading to upregulation of FLT3, examine how matriptase-2 plays a key role in suppressing hepatic hepcidin expression, and learn about the addition of daratumumab to lenalidomide, bortezomib, and dexamethasone as a quadruple therapy for transplant eligible patients with newly diagnosed multiple myeloma. </itunes:summary>
      <itunes:subtitle>In this week’s episode we will review a study exploring recurrent somatic deletions at chromosome 13q12.2 in acute lymphoblastic leukemia leading to upregulation of FLT3, examine how matriptase-2 plays a key role in suppressing hepatic hepcidin expression</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 33</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 33</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">1489dece-55ce-4629-a8d6-5b589a700b2f</guid>
      <link>https://share.transistor.fm/s/9e2b6cb6</link>
      <description>
        <![CDATA[In this week’s episode we will review a study exploring the use of demethylating agents in patients with adult T-cell leukemia-lymphoma, learn more about hematopoietic stem cell formation, and examine treatment timing and prognosis in newly diagnosed patients with acute myeloid leukemia.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode we will review a study exploring the use of demethylating agents in patients with adult T-cell leukemia-lymphoma, learn more about hematopoietic stem cell formation, and examine treatment timing and prognosis in newly diagnosed patients with acute myeloid leukemia.]]>
      </content:encoded>
      <pubDate>Thu, 13 Aug 2020 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/9e2b6cb6/dd387d5d.mp3" length="24943757" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1035</itunes:duration>
      <itunes:summary>In this week’s episode we will review a study exploring the use of demethylating agents in patients with adult T-cell leukemia-lymphoma, learn more about hematopoietic stem cell formation, and examine treatment timing and prognosis in newly diagnosed patients with acute myeloid leukemia.</itunes:summary>
      <itunes:subtitle>In this week’s episode we will review a study exploring the use of demethylating agents in patients with adult T-cell leukemia-lymphoma, learn more about hematopoietic stem cell formation, and examine treatment timing and prognosis in newly diagnosed pati</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 32</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 32</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">6a3c54ef-6808-4717-8043-7f6495fab54f</guid>
      <link>https://share.transistor.fm/s/a5e9578c</link>
      <description>
        <![CDATA[In this week’s episode we will review a study exploring the use of a novel hemophilia A mouse model to examine emicizumab function in vivo, a new approach to fighting the cytokine storm of HLH with a combination of glucocorticoids and ruxolitinib, and a timely Letter to Blood about red cell-bound antibodies and transfusion requirements in hospitalized patients with COVID-19.   ]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode we will review a study exploring the use of a novel hemophilia A mouse model to examine emicizumab function in vivo, a new approach to fighting the cytokine storm of HLH with a combination of glucocorticoids and ruxolitinib, and a timely Letter to Blood about red cell-bound antibodies and transfusion requirements in hospitalized patients with COVID-19.   ]]>
      </content:encoded>
      <pubDate>Thu, 06 Aug 2020 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/a5e9578c/50f4ca86.mp3" length="22192778" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>921</itunes:duration>
      <itunes:summary>In this week’s episode we will review a study exploring the use of a novel hemophilia A mouse model to examine emicizumab function in vivo, a new approach to fighting the cytokine storm of HLH with a combination of glucocorticoids and ruxolitinib, and a timely Letter to Blood about red cell-bound antibodies and transfusion requirements in hospitalized patients with COVID-19.   </itunes:summary>
      <itunes:subtitle>In this week’s episode we will review a study exploring the use of a novel hemophilia A mouse model to examine emicizumab function in vivo, a new approach to fighting the cytokine storm of HLH with a combination of glucocorticoids and ruxolitinib, and a t</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 31</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 31</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">d96e4a28-5361-4077-bf0d-a0bb815e30d9</guid>
      <link>https://share.transistor.fm/s/805057bf</link>
      <description>
        <![CDATA[In this week's episode we will review a study that demonstrates how the impaired hematopoietic stem cells (HSCs) observed in β-thalassemia can be rescued by administration of parathyroid hormone, learn more about genetic variants that can increase the risk of venous thromboembolism, and explore the identification of two DNA methylation subtypes of Waldenström’s macroglobulinemia.    ]]>
      </description>
      <content:encoded>
        <![CDATA[In this week's episode we will review a study that demonstrates how the impaired hematopoietic stem cells (HSCs) observed in β-thalassemia can be rescued by administration of parathyroid hormone, learn more about genetic variants that can increase the risk of venous thromboembolism, and explore the identification of two DNA methylation subtypes of Waldenström’s macroglobulinemia.    ]]>
      </content:encoded>
      <pubDate>Thu, 30 Jul 2020 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/805057bf/69189786.mp3" length="24208170" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1004</itunes:duration>
      <itunes:summary>In this week's episode we will review a study that demonstrates how the impaired hematopoietic stem cells (HSCs) observed in β-thalassemia can be rescued by administration of parathyroid hormone, learn more about genetic variants that can increase the risk of venous thromboembolism, and explore the identification of two DNA methylation subtypes of Waldenström’s macroglobulinemia.    </itunes:summary>
      <itunes:subtitle>In this week's episode we will review a study that demonstrates how the impaired hematopoietic stem cells (HSCs) observed in β-thalassemia can be rescued by administration of parathyroid hormone, learn more about genetic variants that can increase the ris</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 30</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 30</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">bbe1e7ef-3a9d-4296-b0c4-3871f321d143</guid>
      <link>https://share.transistor.fm/s/10dacc72</link>
      <description>
        <![CDATA[In this episode we will review a study identifying cyclin-dependent kinase 6 (or CDK6) as a therapeutic target of NUP98-driven acute myeloid leukemia (or AML), learn more about the largest clinical dataset on cold agglutinin disease, and examine the effects of COVID-19 on coagulation parameters as well as bleeding and thrombosis in hospitalized patients. ]]>
      </description>
      <content:encoded>
        <![CDATA[In this episode we will review a study identifying cyclin-dependent kinase 6 (or CDK6) as a therapeutic target of NUP98-driven acute myeloid leukemia (or AML), learn more about the largest clinical dataset on cold agglutinin disease, and examine the effects of COVID-19 on coagulation parameters as well as bleeding and thrombosis in hospitalized patients. ]]>
      </content:encoded>
      <pubDate>Thu, 23 Jul 2020 12:00:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/10dacc72/53df3f06.mp3" length="28467846" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1183</itunes:duration>
      <itunes:summary>In this episode we will review a study identifying cyclin-dependent kinase 6 (or CDK6) as a therapeutic target of NUP98-driven acute myeloid leukemia (or AML), learn more about the largest clinical dataset on cold agglutinin disease, and examine the effects of COVID-19 on coagulation parameters as well as bleeding and thrombosis in hospitalized patients. </itunes:summary>
      <itunes:subtitle>In this episode we will review a study identifying cyclin-dependent kinase 6 (or CDK6) as a therapeutic target of NUP98-driven acute myeloid leukemia (or AML), learn more about the largest clinical dataset on cold agglutinin disease, and examine the effec</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 29</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 29</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">3f19bf64-0eae-40dc-86c6-3b3d25875345</guid>
      <link>https://share.transistor.fm/s/f06cadc4</link>
      <description>
        <![CDATA[In this episode we’ll review the risk of bleeding after initiating treatment for acquired hemophilia A, examine the functional effect of antibodies leading to immune TTP and how this can be used as a biomarker, and finally, a blast from the past – we will discuss a study that explores the intriguing possibility that a core component driving globin gene expression became active long ago.]]>
      </description>
      <content:encoded>
        <![CDATA[In this episode we’ll review the risk of bleeding after initiating treatment for acquired hemophilia A, examine the functional effect of antibodies leading to immune TTP and how this can be used as a biomarker, and finally, a blast from the past – we will discuss a study that explores the intriguing possibility that a core component driving globin gene expression became active long ago.]]>
      </content:encoded>
      <pubDate>Thu, 16 Jul 2020 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/f06cadc4/847f9b4e.mp3" length="25276983" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1049</itunes:duration>
      <itunes:summary>In this episode we’ll review the risk of bleeding after initiating treatment for acquired hemophilia A, examine the functional effect of antibodies leading to immune TTP and how this can be used as a biomarker, and finally, a blast from the past – we will discuss a study that explores the intriguing possibility that a core component driving globin gene expression became active long ago.</itunes:summary>
      <itunes:subtitle>In this episode we’ll review the risk of bleeding after initiating treatment for acquired hemophilia A, examine the functional effect of antibodies leading to immune TTP and how this can be used as a biomarker, and finally, a blast from the past – we will</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 28</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 28</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">63f180c4-cb3c-4e6f-a4f3-127dbff6fe08</guid>
      <link>https://share.transistor.fm/s/515bc486</link>
      <description>
        <![CDATA[This week we’ll review data that suggests the pro-inflammatory environment associated with aging alters hematopoietic stem cell function by inducing IL27 receptor alpha expression, examine a study attempting to optimize antiplatelet therapy in essential thrombocythemia, and learn more about a study by investigators who have proposed that myelodysplastic syndrome patients with mutations in SF3B1 identify a new subtype of that disease. ]]>
      </description>
      <content:encoded>
        <![CDATA[This week we’ll review data that suggests the pro-inflammatory environment associated with aging alters hematopoietic stem cell function by inducing IL27 receptor alpha expression, examine a study attempting to optimize antiplatelet therapy in essential thrombocythemia, and learn more about a study by investigators who have proposed that myelodysplastic syndrome patients with mutations in SF3B1 identify a new subtype of that disease. ]]>
      </content:encoded>
      <pubDate>Thu, 09 Jul 2020 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/515bc486/19d8f658.mp3" length="28898121" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1201</itunes:duration>
      <itunes:summary>This week we’ll review data that suggests the pro-inflammatory environment associated with aging alters hematopoietic stem cell function by inducing IL27 receptor alpha expression, examine a study attempting to optimize antiplatelet therapy in essential thrombocythemia, and learn more about a study by investigators who have proposed that myelodysplastic syndrome patients with mutations in SF3B1 identify a new subtype of that disease. </itunes:summary>
      <itunes:subtitle>This week we’ll review data that suggests the pro-inflammatory environment associated with aging alters hematopoietic stem cell function by inducing IL27 receptor alpha expression, examine a study attempting to optimize antiplatelet therapy in essential t</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Review Series on Secondary Leukemia</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Review Series on Secondary Leukemia</itunes:title>
      <itunes:episodeType>bonus</itunes:episodeType>
      <guid isPermaLink="false">8ea3e543-6a13-4188-b76a-9b55d036acef</guid>
      <link>https://share.transistor.fm/s/058746a3</link>
      <description>
        <![CDATA[<p>In this bonus podcast episode Dr. Jean Soulier shares highlights of the Blood Review Series on Secondary Leukemia. In this review series, experts provide new insights into the pathobiology of secondary acute myeloid leukemias arising in diverse genetic or acquired, benign or malignant hematologic disorders.</p><p><a href="https://ashpublications.org/blood/article/136/1/1/456030/Introduction-to-a-review-series-on-secondary?searchresult=1">Review Series on Secondary Leukemia</a></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this bonus podcast episode Dr. Jean Soulier shares highlights of the Blood Review Series on Secondary Leukemia. In this review series, experts provide new insights into the pathobiology of secondary acute myeloid leukemias arising in diverse genetic or acquired, benign or malignant hematologic disorders.</p><p><a href="https://ashpublications.org/blood/article/136/1/1/456030/Introduction-to-a-review-series-on-secondary?searchresult=1">Review Series on Secondary Leukemia</a></p>]]>
      </content:encoded>
      <pubDate>Thu, 02 Jul 2020 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/058746a3/05f1f40e.mp3" length="31108702" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/hbamxDVaGp5ITUzUi34NG5uqD2RuPCsQX-hkj2UtDcM/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS9jMDBk/YzBkYTA3ZTQ3NTkx/YTY5NDYzOTMwNWYz/NjgzZC5qcGc.jpg"/>
      <itunes:duration>1293</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this bonus podcast episode Dr. Jean Soulier shares highlights of the Blood Review Series on Secondary Leukemia. In this review series, experts provide new insights into the pathobiology of secondary acute myeloid leukemias arising in diverse genetic or acquired, benign or malignant hematologic disorders.</p><p><a href="https://ashpublications.org/blood/article/136/1/1/456030/Introduction-to-a-review-series-on-secondary?searchresult=1">Review Series on Secondary Leukemia</a></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 27</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 27</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">24e7cfd2-6aa4-47a6-aa77-51187e9f19a8</guid>
      <link>https://share.transistor.fm/s/7d89fef1</link>
      <description>
        <![CDATA[This week we will explore the impact of calreticulin (or CALR) haploinsufficiency on hematopoietic stem cell activity in the context of myeloproliferative neoplasms, explore mechanisms of leukemogenesis related to the E2A-PBX1 fusion protein in childhood B-cell acute lymphoblastic leukemia, and learn about the connection between intestinal microbiota, their metabolite short chain fatty acids and chronic graft versus host disease after allogeneic stem cell transplantation.]]>
      </description>
      <content:encoded>
        <![CDATA[This week we will explore the impact of calreticulin (or CALR) haploinsufficiency on hematopoietic stem cell activity in the context of myeloproliferative neoplasms, explore mechanisms of leukemogenesis related to the E2A-PBX1 fusion protein in childhood B-cell acute lymphoblastic leukemia, and learn about the connection between intestinal microbiota, their metabolite short chain fatty acids and chronic graft versus host disease after allogeneic stem cell transplantation.]]>
      </content:encoded>
      <pubDate>Thu, 02 Jul 2020 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/7d89fef1/1cb3c769.mp3" length="25944645" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1077</itunes:duration>
      <itunes:summary>This week we will explore the impact of calreticulin (or CALR) haploinsufficiency on hematopoietic stem cell activity in the context of myeloproliferative neoplasms, explore mechanisms of leukemogenesis related to the E2A-PBX1 fusion protein in childhood B-cell acute lymphoblastic leukemia, and learn about the connection between intestinal microbiota, their metabolite short chain fatty acids and chronic graft versus host disease after allogeneic stem cell transplantation.</itunes:summary>
      <itunes:subtitle>This week we will explore the impact of calreticulin (or CALR) haploinsufficiency on hematopoietic stem cell activity in the context of myeloproliferative neoplasms, explore mechanisms of leukemogenesis related to the E2A-PBX1 fusion protein in childhood </itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 26</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 26</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">0967f549-5c78-47d4-9f6d-c9d5f12616e7</guid>
      <link>https://share.transistor.fm/s/524a781d</link>
      <description>
        <![CDATA[In this week’s episode we’ll examine the cause and clinical significance of dysplastic hematopoiesis at time of diagnosis in patients with multiple myeloma, review a multi‐omics analysis of patients that have undergone blastic transformation of chronic myeloid leukemia, and learn about HLA alleles that are either risk factors or protective for immune-mediated TTP in Japan.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode we’ll examine the cause and clinical significance of dysplastic hematopoiesis at time of diagnosis in patients with multiple myeloma, review a multi‐omics analysis of patients that have undergone blastic transformation of chronic myeloid leukemia, and learn about HLA alleles that are either risk factors or protective for immune-mediated TTP in Japan.]]>
      </content:encoded>
      <pubDate>Thu, 25 Jun 2020 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/524a781d/d00aecdd.mp3" length="25030093" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1040</itunes:duration>
      <itunes:summary>In this week’s episode we’ll examine the cause and clinical significance of dysplastic hematopoiesis at time of diagnosis in patients with multiple myeloma, review a multi‐omics analysis of patients that have undergone blastic transformation of chronic myeloid leukemia, and learn about HLA alleles that are either risk factors or protective for immune-mediated TTP in Japan.</itunes:summary>
      <itunes:subtitle>In this week’s episode we’ll examine the cause and clinical significance of dysplastic hematopoiesis at time of diagnosis in patients with multiple myeloma, review a multi‐omics analysis of patients that have undergone blastic transformation of chronic my</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 25</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 25</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">f274c007-636c-4282-bbc2-8333427402dc</guid>
      <link>https://share.transistor.fm/s/c0126617</link>
      <description>
        <![CDATA[In this week’s episode we’ll review a study focusing on the causes and impact of the inflammation of aging on hematopoietic stem cell function, learn about the potential influence of the endothelial cell protein C receptor in the pathogenesis of hemophilic arthropathy, and assess a novel function of GPS2 on erythropoiesis.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode we’ll review a study focusing on the causes and impact of the inflammation of aging on hematopoietic stem cell function, learn about the potential influence of the endothelial cell protein C receptor in the pathogenesis of hemophilic arthropathy, and assess a novel function of GPS2 on erythropoiesis.]]>
      </content:encoded>
      <pubDate>Thu, 18 Jun 2020 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/c0126617/efdf8869.mp3" length="23980274" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>995</itunes:duration>
      <itunes:summary>In this week’s episode we’ll review a study focusing on the causes and impact of the inflammation of aging on hematopoietic stem cell function, learn about the potential influence of the endothelial cell protein C receptor in the pathogenesis of hemophilic arthropathy, and assess a novel function of GPS2 on erythropoiesis.</itunes:summary>
      <itunes:subtitle>In this week’s episode we’ll review a study focusing on the causes and impact of the inflammation of aging on hematopoietic stem cell function, learn about the potential influence of the endothelial cell protein C receptor in the pathogenesis of hemophili</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 24</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 24</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">4fc93617-53be-4bdd-8d77-be3f63aa7e0a</guid>
      <link>https://share.transistor.fm/s/c7be24f9</link>
      <description>
        <![CDATA[In this week’s episode we’ll review results of a trial of venetoclax plus low-dose cytarabine in untreated patients with acute myeloid leukemia who are ineligible for intensive chemotherapy, learn how HRI-regulated transcription factor ATF4 activates BCL11A transcription to silence fetal hemoglobin expression, and assess new data demonstrating that aromatase is a novel neosubstrate of cereblon responsible for thrombocytopenia caused by immunomodulatory drugs.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode we’ll review results of a trial of venetoclax plus low-dose cytarabine in untreated patients with acute myeloid leukemia who are ineligible for intensive chemotherapy, learn how HRI-regulated transcription factor ATF4 activates BCL11A transcription to silence fetal hemoglobin expression, and assess new data demonstrating that aromatase is a novel neosubstrate of cereblon responsible for thrombocytopenia caused by immunomodulatory drugs.]]>
      </content:encoded>
      <pubDate>Thu, 11 Jun 2020 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/c7be24f9/945aade7.mp3" length="26467103" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1099</itunes:duration>
      <itunes:summary>In this week’s episode we’ll review results of a trial of venetoclax plus low-dose cytarabine in untreated patients with acute myeloid leukemia who are ineligible for intensive chemotherapy, learn how HRI-regulated transcription factor ATF4 activates BCL11A transcription to silence fetal hemoglobin expression, and assess new data demonstrating that aromatase is a novel neosubstrate of cereblon responsible for thrombocytopenia caused by immunomodulatory drugs.</itunes:summary>
      <itunes:subtitle>In this week’s episode we’ll review results of a trial of venetoclax plus low-dose cytarabine in untreated patients with acute myeloid leukemia who are ineligible for intensive chemotherapy, learn how HRI-regulated transcription factor ATF4 activates BCL1</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 23</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 23</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">c08d309f-4a9f-489d-98c2-f6835982de7e</guid>
      <link>https://share.transistor.fm/s/374b1064</link>
      <description>
        <![CDATA[This week’s episode will discuss the impact of sickle cell disease on the bone marrow vascular niche, highlight more about the evolution of retrovirus-infected premalignant T-cell clones in adult T-cell leukemia/lymphoma, and assess the outcomes following hematopoietic cell transplantation for Wiskott-Aldrich syndrome.]]>
      </description>
      <content:encoded>
        <![CDATA[This week’s episode will discuss the impact of sickle cell disease on the bone marrow vascular niche, highlight more about the evolution of retrovirus-infected premalignant T-cell clones in adult T-cell leukemia/lymphoma, and assess the outcomes following hematopoietic cell transplantation for Wiskott-Aldrich syndrome.]]>
      </content:encoded>
      <pubDate>Thu, 04 Jun 2020 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/374b1064/31084050.mp3" length="25248183" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1048</itunes:duration>
      <itunes:summary>This week’s episode will discuss the impact of sickle cell disease on the bone marrow vascular niche, highlight more about the evolution of retrovirus-infected premalignant T-cell clones in adult T-cell leukemia/lymphoma, and assess the outcomes following hematopoietic cell transplantation for Wiskott-Aldrich syndrome.</itunes:summary>
      <itunes:subtitle>This week’s episode will discuss the impact of sickle cell disease on the bone marrow vascular niche, highlight more about the evolution of retrovirus-infected premalignant T-cell clones in adult T-cell leukemia/lymphoma, and assess the outcomes following</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 22</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 22</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">c34f5f64-52a6-4909-9676-449f67368254</guid>
      <link>https://share.transistor.fm/s/fde58c65</link>
      <description>
        <![CDATA[In this week’s episode we will review a report on the use of hydroxyurea as an alternative to transfusion therapy for the prevention of recurrent strokes in patients with sickle cell anemia, learn more about why some erythroblasts continue to produce hemoglobin F in adults, and review a study that explores cancer outcomes in patients with short telomere syndromes.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode we will review a report on the use of hydroxyurea as an alternative to transfusion therapy for the prevention of recurrent strokes in patients with sickle cell anemia, learn more about why some erythroblasts continue to produce hemoglobin F in adults, and review a study that explores cancer outcomes in patients with short telomere syndromes.]]>
      </content:encoded>
      <pubDate>Thu, 28 May 2020 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/fde58c65/005bf195.mp3" length="27189628" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1130</itunes:duration>
      <itunes:summary>In this week’s episode we will review a report on the use of hydroxyurea as an alternative to transfusion therapy for the prevention of recurrent strokes in patients with sickle cell anemia, learn more about why some erythroblasts continue to produce hemoglobin F in adults, and review a study that explores cancer outcomes in patients with short telomere syndromes.</itunes:summary>
      <itunes:subtitle>In this week’s episode we will review a report on the use of hydroxyurea as an alternative to transfusion therapy for the prevention of recurrent strokes in patients with sickle cell anemia, learn more about why some erythroblasts continue to produce hemo</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 21</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 21</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">ff6116fe-d4b4-4aec-9547-beb4c5edfb5f</guid>
      <link>https://share.transistor.fm/s/8b716b8b</link>
      <description>
        <![CDATA[Today we’ll review data on the high frequency of germline RUNX1 mutations in patients with acute myeloid leukemia, learn more about the development of an international prognostic score that predicts time to first treatment in CLL patients with early, asymptomatic disease, and explore the possibility of improving the activity of virus-directed immunotherapies against certain types of EBV tumors.]]>
      </description>
      <content:encoded>
        <![CDATA[Today we’ll review data on the high frequency of germline RUNX1 mutations in patients with acute myeloid leukemia, learn more about the development of an international prognostic score that predicts time to first treatment in CLL patients with early, asymptomatic disease, and explore the possibility of improving the activity of virus-directed immunotherapies against certain types of EBV tumors.]]>
      </content:encoded>
      <pubDate>Thu, 21 May 2020 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/8b716b8b/1ed44fa3.mp3" length="28736773" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1193</itunes:duration>
      <itunes:summary>Today we’ll review data on the high frequency of germline RUNX1 mutations in patients with acute myeloid leukemia, learn more about the development of an international prognostic score that predicts time to first treatment in CLL patients with early, asymptomatic disease, and explore the possibility of improving the activity of virus-directed immunotherapies against certain types of EBV tumors.</itunes:summary>
      <itunes:subtitle>Today we’ll review data on the high frequency of germline RUNX1 mutations in patients with acute myeloid leukemia, learn more about the development of an international prognostic score that predicts time to first treatment in CLL patients with early, asym</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 20</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 20</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">866516ce-6cd2-47df-a312-f8b3be5cabae</guid>
      <link>https://share.transistor.fm/s/2c259fe1</link>
      <description>
        <![CDATA[In this week’s episode we’ll learn why anticoagulation may play a role in the prevention of vaso-occlusive events in sickle cell disease, review data that could help predict the risk of VTE and bleeding in hospitalized patients, and find out if Ruxolitinib is a viable treatment of steroid-refractory acute graft-versus-host disease.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode we’ll learn why anticoagulation may play a role in the prevention of vaso-occlusive events in sickle cell disease, review data that could help predict the risk of VTE and bleeding in hospitalized patients, and find out if Ruxolitinib is a viable treatment of steroid-refractory acute graft-versus-host disease.]]>
      </content:encoded>
      <pubDate>Thu, 14 May 2020 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/2c259fe1/06b8ad5e.mp3" length="22756017" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>945</itunes:duration>
      <itunes:summary>In this week’s episode we’ll learn why anticoagulation may play a role in the prevention of vaso-occlusive events in sickle cell disease, review data that could help predict the risk of VTE and bleeding in hospitalized patients, and find out if Ruxolitinib is a viable treatment of steroid-refractory acute graft-versus-host disease.</itunes:summary>
      <itunes:subtitle>In this week’s episode we’ll learn why anticoagulation may play a role in the prevention of vaso-occlusive events in sickle cell disease, review data that could help predict the risk of VTE and bleeding in hospitalized patients, and find out if Ruxolitini</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 19</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 19</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">5854c671-b41e-46d8-acb6-8588937b6cb3</guid>
      <link>https://share.transistor.fm/s/7a5cafdb</link>
      <description>
        <![CDATA[This week’s episode will review a report on a new mouse model with an enhanced ability to support human hematopoietic and tumor engraftment, explore more about increased mTOR activation in idiopathic multicentric Castleman disease, and assess the feasibility and efficacy of CD19-targeted CAR-T cells with concurrent ibrutinib for CLL.]]>
      </description>
      <content:encoded>
        <![CDATA[This week’s episode will review a report on a new mouse model with an enhanced ability to support human hematopoietic and tumor engraftment, explore more about increased mTOR activation in idiopathic multicentric Castleman disease, and assess the feasibility and efficacy of CD19-targeted CAR-T cells with concurrent ibrutinib for CLL.]]>
      </content:encoded>
      <pubDate>Thu, 07 May 2020 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/7a5cafdb/e610af92.mp3" length="23652005" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>982</itunes:duration>
      <itunes:summary>This week’s episode will review a report on a new mouse model with an enhanced ability to support human hematopoietic and tumor engraftment, explore more about increased mTOR activation in idiopathic multicentric Castleman disease, and assess the feasibility and efficacy of CD19-targeted CAR-T cells with concurrent ibrutinib for CLL.</itunes:summary>
      <itunes:subtitle>This week’s episode will review a report on a new mouse model with an enhanced ability to support human hematopoietic and tumor engraftment, explore more about increased mTOR activation in idiopathic multicentric Castleman disease, and assess the feasibil</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 18</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 18</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">bc24e71d-18b3-41d3-92d0-c5ff054202d9</guid>
      <link>https://share.transistor.fm/s/856f7084</link>
      <description>
        <![CDATA[This week’s episode will review the incidence and fate of clonal hematopoiesis among donors and recipients of related allogeneic hematopoietic stem cell transplantation, examine the manifestations and clinical course of patients with a particular subtype of Fanconi anemia, and assess three clinical studies that demonstrate high rates of efficacy and low rates of toxicity of daratumumab in patients with previously treated AL amyloidosis.]]>
      </description>
      <content:encoded>
        <![CDATA[This week’s episode will review the incidence and fate of clonal hematopoiesis among donors and recipients of related allogeneic hematopoietic stem cell transplantation, examine the manifestations and clinical course of patients with a particular subtype of Fanconi anemia, and assess three clinical studies that demonstrate high rates of efficacy and low rates of toxicity of daratumumab in patients with previously treated AL amyloidosis.]]>
      </content:encoded>
      <pubDate>Thu, 30 Apr 2020 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/856f7084/0207223d.mp3" length="34002987" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1413</itunes:duration>
      <itunes:summary>This week’s episode will review the incidence and fate of clonal hematopoiesis among donors and recipients of related allogeneic hematopoietic stem cell transplantation, examine the manifestations and clinical course of patients with a particular subtype of Fanconi anemia, and assess three clinical studies that demonstrate high rates of efficacy and low rates of toxicity of daratumumab in patients with previously treated AL amyloidosis.</itunes:summary>
      <itunes:subtitle>This week’s episode will review the incidence and fate of clonal hematopoiesis among donors and recipients of related allogeneic hematopoietic stem cell transplantation, examine the manifestations and clinical course of patients with a particular subtype </itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 17</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 17</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">69c9ed16-c030-482f-b68b-357797fdbfea</guid>
      <link>https://share.transistor.fm/s/26073bf3</link>
      <description>
        <![CDATA[This week’s episode will highlight the development of a factor VIII replacement therapy for patients with severe Hemophilia A, examine a novel pathway of resistance of FLT3-ITD+ AML cells to FLIT3 inhibitors, and review long-term results of a pilot study in children with low risk B-cell ALL conducted in a limited-resource setting.]]>
      </description>
      <content:encoded>
        <![CDATA[This week’s episode will highlight the development of a factor VIII replacement therapy for patients with severe Hemophilia A, examine a novel pathway of resistance of FLT3-ITD+ AML cells to FLIT3 inhibitors, and review long-term results of a pilot study in children with low risk B-cell ALL conducted in a limited-resource setting.]]>
      </content:encoded>
      <pubDate>Thu, 23 Apr 2020 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/26073bf3/e067b0c3.mp3" length="17012697" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1058</itunes:duration>
      <itunes:summary>This week’s episode will highlight the development of a factor VIII replacement therapy for patients with severe Hemophilia A, examine a novel pathway of resistance of FLT3-ITD+ AML cells to FLIT3 inhibitors, and review long-term results of a pilot study in children with low risk B-cell ALL conducted in a limited-resource setting.</itunes:summary>
      <itunes:subtitle>This week’s episode will highlight the development of a factor VIII replacement therapy for patients with severe Hemophilia A, examine a novel pathway of resistance of FLT3-ITD+ AML cells to FLIT3 inhibitors, and review long-term results of a pilot study </itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Review Series on Rare Systemic Hematologic Disorders</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Review Series on Rare Systemic Hematologic Disorders</itunes:title>
      <itunes:episodeType>bonus</itunes:episodeType>
      <guid isPermaLink="false">aa9aef35-2014-4909-a320-3fd779892ab1</guid>
      <link>https://share.transistor.fm/s/2167d055</link>
      <description>
        <![CDATA[<p>In this bonus podcast episode, Drs. Nancy Berliner and Laurie Sehn lead a discussion on this series of authoritative reviews on a collection of rare systemic hematologic disorders that are frequently difficult to recognize, diagnose, and treat. The series highlights new genomic and proteomic insights that inform our understanding of their pathophysiology and treatment.</p><p><a href="https://ashpublications.org/blood/article/135/16/1305/452570/Introduction-to-a-review-series-on-rare-systemic?searchresult=1">Review Series on Rare Systemic Hematologic Disorders</a></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this bonus podcast episode, Drs. Nancy Berliner and Laurie Sehn lead a discussion on this series of authoritative reviews on a collection of rare systemic hematologic disorders that are frequently difficult to recognize, diagnose, and treat. The series highlights new genomic and proteomic insights that inform our understanding of their pathophysiology and treatment.</p><p><a href="https://ashpublications.org/blood/article/135/16/1305/452570/Introduction-to-a-review-series-on-rare-systemic?searchresult=1">Review Series on Rare Systemic Hematologic Disorders</a></p>]]>
      </content:encoded>
      <pubDate>Thu, 16 Apr 2020 14:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/2167d055/9e958473.mp3" length="17765141" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/kDWojwiSnn68F7JnNVQyJaBQfUsuyj9clvl-2wYUEHI/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS9jMTY1/Mzk0NjMyY2Y5MDUw/Y2QwZGZlMDEwNzZj/NmE3MC5qcGc.jpg"/>
      <itunes:duration>1107</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this bonus podcast episode, Drs. Nancy Berliner and Laurie Sehn lead a discussion on this series of authoritative reviews on a collection of rare systemic hematologic disorders that are frequently difficult to recognize, diagnose, and treat. The series highlights new genomic and proteomic insights that inform our understanding of their pathophysiology and treatment.</p><p><a href="https://ashpublications.org/blood/article/135/16/1305/452570/Introduction-to-a-review-series-on-rare-systemic?searchresult=1">Review Series on Rare Systemic Hematologic Disorders</a></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 16</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 16</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">f131b301-b796-46e4-9872-a177b073b57a</guid>
      <link>https://share.transistor.fm/s/d3e92a4b</link>
      <description>
        <![CDATA[This week’s episode will review evidence that selecting donors with specific types of natural killer cells leads to improved outcome in stem cell transplantation, review an analysis of platelet transfusion in cerebral hemorrhage, and explore the challenges of diagnosing recurrent ipsilateral deep vein thrombosis.]]>
      </description>
      <content:encoded>
        <![CDATA[This week’s episode will review evidence that selecting donors with specific types of natural killer cells leads to improved outcome in stem cell transplantation, review an analysis of platelet transfusion in cerebral hemorrhage, and explore the challenges of diagnosing recurrent ipsilateral deep vein thrombosis.]]>
      </content:encoded>
      <pubDate>Thu, 16 Apr 2020 13:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/d3e92a4b/9acc148c.mp3" length="22513746" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>935</itunes:duration>
      <itunes:summary>This week’s episode will review evidence that selecting donors with specific types of natural killer cells leads to improved outcome in stem cell transplantation, review an analysis of platelet transfusion in cerebral hemorrhage, and explore the challenges of diagnosing recurrent ipsilateral deep vein thrombosis.</itunes:summary>
      <itunes:subtitle>This week’s episode will review evidence that selecting donors with specific types of natural killer cells leads to improved outcome in stem cell transplantation, review an analysis of platelet transfusion in cerebral hemorrhage, and explore the challenge</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 15</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 15</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">637e77a0-a2aa-496d-a514-0b33ddfef681</guid>
      <link>https://share.transistor.fm/s/9015112c</link>
      <description>
        <![CDATA[This week’s episode will examine data on the impact of the FDG uptake level on predicting subsequent high-grade histological transformation in follicular lymphoma, explore clonal tracking in gene therapy patients as a method for understanding human hematopoiesis, and review a study on the recognition of platelet factor 4-von Willebrand factor complexes by heparin-induced thrombocytopenia antibodies as a basis for the pathogenesis of HIT.]]>
      </description>
      <content:encoded>
        <![CDATA[This week’s episode will examine data on the impact of the FDG uptake level on predicting subsequent high-grade histological transformation in follicular lymphoma, explore clonal tracking in gene therapy patients as a method for understanding human hematopoiesis, and review a study on the recognition of platelet factor 4-von Willebrand factor complexes by heparin-induced thrombocytopenia antibodies as a basis for the pathogenesis of HIT.]]>
      </content:encoded>
      <pubDate>Thu, 09 Apr 2020 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/9015112c/5696fce7.mp3" length="17400466" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1084</itunes:duration>
      <itunes:summary>This week’s episode will examine data on the impact of the FDG uptake level on predicting subsequent high-grade histological transformation in follicular lymphoma, explore clonal tracking in gene therapy patients as a method for understanding human hematopoiesis, and review a study on the recognition of platelet factor 4-von Willebrand factor complexes by heparin-induced thrombocytopenia antibodies as a basis for the pathogenesis of HIT.</itunes:summary>
      <itunes:subtitle>This week’s episode will examine data on the impact of the FDG uptake level on predicting subsequent high-grade histological transformation in follicular lymphoma, explore clonal tracking in gene therapy patients as a method for understanding human hemato</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 14</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 14</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">f4d0bfd8-a5ad-465b-aa7e-74a2520b7716</guid>
      <link>https://share.transistor.fm/s/1bd4c969</link>
      <description>
        <![CDATA[In this week’s episode we’ll learn about novel insights into the link between innate immune responses and activation of coagulation during gram-negative sepsis, examine the impact of GPRASP proteins on hematopoietic stem cell transplantation, and explore the dynamics of clonal hematopoiesis in anemia of older individuals.]]>
      </description>
      <content:encoded>
        <![CDATA[In this week’s episode we’ll learn about novel insights into the link between innate immune responses and activation of coagulation during gram-negative sepsis, examine the impact of GPRASP proteins on hematopoietic stem cell transplantation, and explore the dynamics of clonal hematopoiesis in anemia of older individuals.]]>
      </content:encoded>
      <pubDate>Thu, 02 Apr 2020 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/1bd4c969/0db80290.mp3" length="19699436" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1228</itunes:duration>
      <itunes:summary>In this week’s episode we’ll learn about novel insights into the link between innate immune responses and activation of coagulation during gram-negative sepsis, examine the impact of GPRASP proteins on hematopoietic stem cell transplantation, and explore the dynamics of clonal hematopoiesis in anemia of older individuals.</itunes:summary>
      <itunes:subtitle>In this week’s episode we’ll learn about novel insights into the link between innate immune responses and activation of coagulation during gram-negative sepsis, examine the impact of GPRASP proteins on hematopoietic stem cell transplantation, and explore </itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 13</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 13</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">db970d65-5370-4b39-8314-516a7342904c</guid>
      <link>https://share.transistor.fm/s/85eaed08</link>
      <description>
        <![CDATA[This week’s episode will review data on spliceosomal gene mutations, evaluate the impact of Ruxolitinib on weight gain, and assess the effect of compliment blockade with eculizumab on high risk patients with stem cell transplant associated thrombotic microangiopathy. ]]>
      </description>
      <content:encoded>
        <![CDATA[This week’s episode will review data on spliceosomal gene mutations, evaluate the impact of Ruxolitinib on weight gain, and assess the effect of compliment blockade with eculizumab on high risk patients with stem cell transplant associated thrombotic microangiopathy. ]]>
      </content:encoded>
      <pubDate>Thu, 26 Mar 2020 12:45:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/85eaed08/8c3090a8.mp3" length="15771202" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>983</itunes:duration>
      <itunes:summary>This week’s episode will review data on spliceosomal gene mutations, evaluate the impact of Ruxolitinib on weight gain, and assess the effect of compliment blockade with eculizumab on high risk patients with stem cell transplant associated thrombotic microangiopathy. </itunes:summary>
      <itunes:subtitle>This week’s episode will review data on spliceosomal gene mutations, evaluate the impact of Ruxolitinib on weight gain, and assess the effect of compliment blockade with eculizumab on high risk patients with stem cell transplant associated thrombotic micr</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 12</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 12</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">deca1d0f-6a15-47e6-a8a4-ca2af6b4ee3e</guid>
      <link>https://share.transistor.fm/s/d09c4807</link>
      <description>
        <![CDATA[This week’s episode will review the clinical correlates of NT5C2 mutations in relapsed ALL, the impact of Crovalimab, a recycling monoclonal antibody against complement component C5 in paroxysmal nocturnal hemoglobinuria, and the relationship between leukocyte NADPH oxidase and leukotriene B4 and neutrophilic inflammation in the context of chronic granulomatous disease]]>
      </description>
      <content:encoded>
        <![CDATA[This week’s episode will review the clinical correlates of NT5C2 mutations in relapsed ALL, the impact of Crovalimab, a recycling monoclonal antibody against complement component C5 in paroxysmal nocturnal hemoglobinuria, and the relationship between leukocyte NADPH oxidase and leukotriene B4 and neutrophilic inflammation in the context of chronic granulomatous disease]]>
      </content:encoded>
      <pubDate>Thu, 19 Mar 2020 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/d09c4807/2d5a7ecb.mp3" length="16516343" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1029</itunes:duration>
      <itunes:summary>This week’s episode will review the clinical correlates of NT5C2 mutations in relapsed ALL, the impact of Crovalimab, a recycling monoclonal antibody against complement component C5 in paroxysmal nocturnal hemoglobinuria, and the relationship between leukocyte NADPH oxidase and leukotriene B4 and neutrophilic inflammation in the context of chronic granulomatous disease</itunes:summary>
      <itunes:subtitle>This week’s episode will review the clinical correlates of NT5C2 mutations in relapsed ALL, the impact of Crovalimab, a recycling monoclonal antibody against complement component C5 in paroxysmal nocturnal hemoglobinuria, and the relationship between leuk</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 11</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 11</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">1d1dec16-9a81-4e4d-bfa3-ad6722fcc757</guid>
      <link>https://share.transistor.fm/s/acd166a4</link>
      <description>
        <![CDATA[This week’s episode will review a novel treatment for Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis, learn more about the behavior of leukemic clones in patients with acute myeloid leukemia receiving venetoclax-based combination therapies, and review the role of the integrin alpha9beta1 in arterial thrombosis.]]>
      </description>
      <content:encoded>
        <![CDATA[This week’s episode will review a novel treatment for Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis, learn more about the behavior of leukemic clones in patients with acute myeloid leukemia receiving venetoclax-based combination therapies, and review the role of the integrin alpha9beta1 in arterial thrombosis.]]>
      </content:encoded>
      <pubDate>Thu, 12 Mar 2020 12:30:00 -0400</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/acd166a4/2db16b5d.mp3" length="14627921" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>911</itunes:duration>
      <itunes:summary>This week’s episode will review a novel treatment for Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis, learn more about the behavior of leukemic clones in patients with acute myeloid leukemia receiving venetoclax-based combination therapies, and review the role of the integrin alpha9beta1 in arterial thrombosis.</itunes:summary>
      <itunes:subtitle>This week’s episode will review a novel treatment for Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis, learn more about the behavior of leukemic clones in patients with acute myeloid leukemia receiving venetoclax-based combination therapi</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 10</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 10</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">1f26b289-3c36-4f49-af28-4bd4f9b0f303</guid>
      <link>https://share.transistor.fm/s/b993895b</link>
      <description>
        <![CDATA[This week's episode will explore interventions that may improve outcomes in sepsis by stabilizing neutrophil extracellular traps, or NETs, discuss the use of a novel strategy to generate CAR T cells that react with surface antigens on AML cells, and review data about how chronic lymphocytic leukemia cells become resistant to Venetoclax.]]>
      </description>
      <content:encoded>
        <![CDATA[This week's episode will explore interventions that may improve outcomes in sepsis by stabilizing neutrophil extracellular traps, or NETs, discuss the use of a novel strategy to generate CAR T cells that react with surface antigens on AML cells, and review data about how chronic lymphocytic leukemia cells become resistant to Venetoclax.]]>
      </content:encoded>
      <pubDate>Thu, 05 Mar 2020 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/b993895b/14e6b9ce.mp3" length="17186259" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1071</itunes:duration>
      <itunes:summary>This week's episode will explore interventions that may improve outcomes in sepsis by stabilizing neutrophil extracellular traps, or NETs, discuss the use of a novel strategy to generate CAR T cells that react with surface antigens on AML cells, and review data about how chronic lymphocytic leukemia cells become resistant to Venetoclax.</itunes:summary>
      <itunes:subtitle>This week's episode will explore interventions that may improve outcomes in sepsis by stabilizing neutrophil extracellular traps, or NETs, discuss the use of a novel strategy to generate CAR T cells that react with surface antigens on AML cells, and revie</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Review Series on Understanding and Treating Primary Immunodeficiency</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Review Series on Understanding and Treating Primary Immunodeficiency</itunes:title>
      <itunes:episodeType>bonus</itunes:episodeType>
      <guid isPermaLink="false">7c0a6783-a324-436b-b5d2-0dfd0d6261b7</guid>
      <link>https://share.transistor.fm/s/905ae3b3</link>
      <description>
        <![CDATA[<p>In this episode Dr. Catherine Bollard, Blood Associate Editor provides highlights of this commissioned review series Understanding and Treating Primary Immunodeficiency, that highlights cutting-edge developments in the biology and management of primary immune deficiencies.</p><p><a href="https://ashpublications.org/blood/article/135/9/591/431022/Introduction-to-a-review-series-on-understanding?searchresult=1">Review Series on Understanding and Treating Primary Immunodeficiency</a></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this episode Dr. Catherine Bollard, Blood Associate Editor provides highlights of this commissioned review series Understanding and Treating Primary Immunodeficiency, that highlights cutting-edge developments in the biology and management of primary immune deficiencies.</p><p><a href="https://ashpublications.org/blood/article/135/9/591/431022/Introduction-to-a-review-series-on-understanding?searchresult=1">Review Series on Understanding and Treating Primary Immunodeficiency</a></p>]]>
      </content:encoded>
      <pubDate>Thu, 27 Feb 2020 16:00:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/905ae3b3/0c8c2aef.mp3" length="7477380" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/ZTqjpSdNNlhNkFGTKi9HpMlCTpmx1Gmosk324U8C1Us/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS82NTQx/YjdiNmRjM2FmMzc1/YmFhOGQ1NGI1YjEy/YzllYy5qcGc.jpg"/>
      <itunes:duration>464</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this episode Dr. Catherine Bollard, Blood Associate Editor provides highlights of this commissioned review series Understanding and Treating Primary Immunodeficiency, that highlights cutting-edge developments in the biology and management of primary immune deficiencies.</p><p><a href="https://ashpublications.org/blood/article/135/9/591/431022/Introduction-to-a-review-series-on-understanding?searchresult=1">Review Series on Understanding and Treating Primary Immunodeficiency</a></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 9</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 9</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">16145b87-94a9-401b-8fc2-bd42edf6f6bb</guid>
      <link>https://share.transistor.fm/s/d8e8f4ce</link>
      <description>
        <![CDATA[This week's episode will review efforts to improve the activity of CAR T cells, explore the impact of Protein C activator AB002 on thrombus development, and look at results from a UK study on minimal residual disease status and outcome after transplantation in NPM1-mutated AML.]]>
      </description>
      <content:encoded>
        <![CDATA[This week's episode will review efforts to improve the activity of CAR T cells, explore the impact of Protein C activator AB002 on thrombus development, and look at results from a UK study on minimal residual disease status and outcome after transplantation in NPM1-mutated AML.]]>
      </content:encoded>
      <pubDate>Thu, 27 Feb 2020 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/d8e8f4ce/a5af5128.mp3" length="19593160" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1221</itunes:duration>
      <itunes:summary>This week's episode will review efforts to improve the activity of CAR T cells, explore the impact of Protein C activator AB002 on thrombus development, and look at results from a UK study on minimal residual disease status and outcome after transplantation in NPM1-mutated AML.</itunes:summary>
      <itunes:subtitle>This week's episode will review efforts to improve the activity of CAR T cells, explore the impact of Protein C activator AB002 on thrombus development, and look at results from a UK study on minimal residual disease status and outcome after transplantati</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 8</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 8</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">d9a3a574-9dab-4bab-8976-fe5806df7bff</guid>
      <link>https://share.transistor.fm/s/3037e558</link>
      <description>
        <![CDATA[This week’s episode will examine how graft versus host disease in the colon is driven by an inflammatory cytokine produced by specialized donor T cells, review a prospective, multicenter study to assess the frequency and clinical relevance of low level mutations in chronic myeloid leukemia, and learn about a potential new therapeutic that blocks the activity of the iron-regulatory hormone Erythroferrone to reduce iron overload in thalassemia. ]]>
      </description>
      <content:encoded>
        <![CDATA[This week’s episode will examine how graft versus host disease in the colon is driven by an inflammatory cytokine produced by specialized donor T cells, review a prospective, multicenter study to assess the frequency and clinical relevance of low level mutations in chronic myeloid leukemia, and learn about a potential new therapeutic that blocks the activity of the iron-regulatory hormone Erythroferrone to reduce iron overload in thalassemia. ]]>
      </content:encoded>
      <pubDate>Thu, 20 Feb 2020 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/3037e558/95723f92.mp3" length="26462371" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1099</itunes:duration>
      <itunes:summary>This week’s episode will examine how graft versus host disease in the colon is driven by an inflammatory cytokine produced by specialized donor T cells, review a prospective, multicenter study to assess the frequency and clinical relevance of low level mutations in chronic myeloid leukemia, and learn about a potential new therapeutic that blocks the activity of the iron-regulatory hormone Erythroferrone to reduce iron overload in thalassemia. </itunes:summary>
      <itunes:subtitle>This week’s episode will examine how graft versus host disease in the colon is driven by an inflammatory cytokine produced by specialized donor T cells, review a prospective, multicenter study to assess the frequency and clinical relevance of low level mu</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 7</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 7</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">a2a635f4-f04f-4012-ab3b-d8feae675f08</guid>
      <link>https://share.transistor.fm/s/3c5da005</link>
      <description>
        <![CDATA[<p>This week’s episode will review treatment for secondary prevention of venous thromboembolism in children, a therapeutic strategy for relapsed or refractory B-cell acute lymphoblastic leukemia, Ivosidenib monotherapy in patients with newly diagnosed AML with mutations in the isocitrate dehydrogenase 1 gene, and survival outcomes of chronic Lymphocytic Leukemia patients treated with Ibrutinib.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>This week’s episode will review treatment for secondary prevention of venous thromboembolism in children, a therapeutic strategy for relapsed or refractory B-cell acute lymphoblastic leukemia, Ivosidenib monotherapy in patients with newly diagnosed AML with mutations in the isocitrate dehydrogenase 1 gene, and survival outcomes of chronic Lymphocytic Leukemia patients treated with Ibrutinib.</p>]]>
      </content:encoded>
      <pubDate>Thu, 13 Feb 2020 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/3c5da005/dd6426cd.mp3" length="26861821" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1116</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>This week’s episode will review treatment for secondary prevention of venous thromboembolism in children, a therapeutic strategy for relapsed or refractory B-cell acute lymphoblastic leukemia, Ivosidenib monotherapy in patients with newly diagnosed AML with mutations in the isocitrate dehydrogenase 1 gene, and survival outcomes of chronic Lymphocytic Leukemia patients treated with Ibrutinib.</p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 6</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 6</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">c21e1ff2-93d7-44fa-8fc9-a1a9c074af45</guid>
      <link>https://share.transistor.fm/s/f676b443</link>
      <description>
        <![CDATA[<p>This week’s episode will examine the critical role of platelet necrosis in ischemic stroke injury, the discovery of the molecular basis for the PEL blood group, and the impact of NPM1/FLT3-ITD genotypes in patients with acute myeloid leukemia.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>This week’s episode will examine the critical role of platelet necrosis in ischemic stroke injury, the discovery of the molecular basis for the PEL blood group, and the impact of NPM1/FLT3-ITD genotypes in patients with acute myeloid leukemia.</p>]]>
      </content:encoded>
      <pubDate>Thu, 06 Feb 2020 13:00:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/f676b443/674e25ae.mp3" length="23578742" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>979</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>This week’s episode will examine the critical role of platelet necrosis in ischemic stroke injury, the discovery of the molecular basis for the PEL blood group, and the impact of NPM1/FLT3-ITD genotypes in patients with acute myeloid leukemia.</p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Review Series on Treatment of Venous Thrombotic Disorders</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Review Series on Treatment of Venous Thrombotic Disorders</itunes:title>
      <itunes:episodeType>bonus</itunes:episodeType>
      <guid isPermaLink="false">81608a63-cc86-45a5-929d-fa2345387a1a</guid>
      <link>https://share.transistor.fm/s/90377bf7</link>
      <description>
        <![CDATA[<p>In this episode we welcome Drs. Thomas Ortel, Jeffrey Weitz, and Kenneth Bauer as they discuss the Blood Review Series on the Treatment of Venous Thrombotic Disorders. In this review series, experts contribute 6 seminal reviews that focus on the treatment of venous thromboembolism (VTE) in adults and children, the management of VTE developing in unusual locations and in the setting of thrombophilia, and new targets and antithrombotic therapies in development.</p><p><a href="https://ashpublications.org/blood/article/135/5/299/430070/Introduction-to-a-review-series-on-treatment-of?searchresult=1">Review Series on Treatment of Venous Thrombotic Disorders</a></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this episode we welcome Drs. Thomas Ortel, Jeffrey Weitz, and Kenneth Bauer as they discuss the Blood Review Series on the Treatment of Venous Thrombotic Disorders. In this review series, experts contribute 6 seminal reviews that focus on the treatment of venous thromboembolism (VTE) in adults and children, the management of VTE developing in unusual locations and in the setting of thrombophilia, and new targets and antithrombotic therapies in development.</p><p><a href="https://ashpublications.org/blood/article/135/5/299/430070/Introduction-to-a-review-series-on-treatment-of?searchresult=1">Review Series on Treatment of Venous Thrombotic Disorders</a></p>]]>
      </content:encoded>
      <pubDate>Fri, 31 Jan 2020 15:00:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/90377bf7/1f36fab8.mp3" length="43742094" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/0bS7sKit-nSrc-QgAcW3KzgYs_RDNtRDz9VvsXYN00g/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS9lNmQ3/YjkxMmI2MDEwYjgx/NmE3ZjRjY2Y4ZTVk/ZmFmNC5qcGc.jpg"/>
      <itunes:duration>1815</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this episode we welcome Drs. Thomas Ortel, Jeffrey Weitz, and Kenneth Bauer as they discuss the Blood Review Series on the Treatment of Venous Thrombotic Disorders. In this review series, experts contribute 6 seminal reviews that focus on the treatment of venous thromboembolism (VTE) in adults and children, the management of VTE developing in unusual locations and in the setting of thrombophilia, and new targets and antithrombotic therapies in development.</p><p><a href="https://ashpublications.org/blood/article/135/5/299/430070/Introduction-to-a-review-series-on-treatment-of?searchresult=1">Review Series on Treatment of Venous Thrombotic Disorders</a></p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 5</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 5</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">15e2737c-3599-4a1f-98be-c84298088a71</guid>
      <link>https://share.transistor.fm/s/0e32d0a9</link>
      <description>
        <![CDATA[<p>In this episode we’ll examine a new strategy to improve the durability of remission after CAR T-cell therapy for pediatric B cell leukemia, explore the genomic landscape of Breast Implant-Associated Anaplastic Large Cell Lymphomas, and discuss a new report showing that the occurrence of arterial thrombotic events following the diagnosis of myeloproliferative neoplasms is associated with a significantly increased risk of a second cancer.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this episode we’ll examine a new strategy to improve the durability of remission after CAR T-cell therapy for pediatric B cell leukemia, explore the genomic landscape of Breast Implant-Associated Anaplastic Large Cell Lymphomas, and discuss a new report showing that the occurrence of arterial thrombotic events following the diagnosis of myeloproliferative neoplasms is associated with a significantly increased risk of a second cancer.</p>]]>
      </content:encoded>
      <pubDate>Thu, 30 Jan 2020 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/0e32d0a9/7ff53eb2.mp3" length="14246958" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>887</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this episode we’ll examine a new strategy to improve the durability of remission after CAR T-cell therapy for pediatric B cell leukemia, explore the genomic landscape of Breast Implant-Associated Anaplastic Large Cell Lymphomas, and discuss a new report showing that the occurrence of arterial thrombotic events following the diagnosis of myeloproliferative neoplasms is associated with a significantly increased risk of a second cancer.</p>]]>
      </itunes:summary>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 4</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 4</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">0a53aa7d-845c-4c2d-8328-5122c83705d4</guid>
      <link>https://share.transistor.fm/s/42d5b616</link>
      <description>
        <![CDATA[    Today we’ll examine the role of heredity vs. environmental factors in the evolution of age-related clonal hematopoiesis, review the first systematic approach to uncover all possible activating point mutations within and around the transmembrane domain of the thrombopoietin receptor in myeloproliferative neoplasms, and discuss the role of complement activation and mutations in complement regulatory genes in patients with thrombotic or catastrophic antiphospholipid syndromes. ]]>
      </description>
      <content:encoded>
        <![CDATA[    Today we’ll examine the role of heredity vs. environmental factors in the evolution of age-related clonal hematopoiesis, review the first systematic approach to uncover all possible activating point mutations within and around the transmembrane domain of the thrombopoietin receptor in myeloproliferative neoplasms, and discuss the role of complement activation and mutations in complement regulatory genes in patients with thrombotic or catastrophic antiphospholipid syndromes. ]]>
      </content:encoded>
      <pubDate>Thu, 23 Jan 2020 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/42d5b616/0b4051a3.mp3" length="28385955" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1179</itunes:duration>
      <itunes:summary>    Today we’ll examine the role of heredity vs. environmental factors in the evolution of age-related clonal hematopoiesis, review the first systematic approach to uncover all possible activating point mutations within and around the transmembrane domain of the thrombopoietin receptor in myeloproliferative neoplasms, and discuss the role of complement activation and mutations in complement regulatory genes in patients with thrombotic or catastrophic antiphospholipid syndromes. </itunes:summary>
      <itunes:subtitle>    Today we’ll examine the role of heredity vs. environmental factors in the evolution of age-related clonal hematopoiesis, review the first systematic approach to uncover all possible activating point mutations within and around the transmembrane domain</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 3</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 3</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">236bf018-59a0-4492-abfd-0f4f711ef641</guid>
      <link>https://share.transistor.fm/s/614c3664</link>
      <description>
        <![CDATA[In this episode we highlight the development of intensified T-cell acute lymphoblastic leukemia-focused protocols, the use of a thrombopoietin agonist for thrombocytopenia following allogeneic hematopoieticstem cell transplantation, and a crucial step forward in the development of miRNA therapies targeting myeloid diseases.]]>
      </description>
      <content:encoded>
        <![CDATA[In this episode we highlight the development of intensified T-cell acute lymphoblastic leukemia-focused protocols, the use of a thrombopoietin agonist for thrombocytopenia following allogeneic hematopoieticstem cell transplantation, and a crucial step forward in the development of miRNA therapies targeting myeloid diseases.]]>
      </content:encoded>
      <pubDate>Thu, 16 Jan 2020 12:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/614c3664/29f80b5d.mp3" length="20695839" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1290</itunes:duration>
      <itunes:summary>In this episode we highlight the development of intensified T-cell acute lymphoblastic leukemia-focused protocols, the use of a thrombopoietin agonist for thrombocytopenia following allogeneic hematopoieticstem cell transplantation, and a crucial step forward in the development of miRNA therapies targeting myeloid diseases.</itunes:summary>
      <itunes:subtitle>In this episode we highlight the development of intensified T-cell acute lymphoblastic leukemia-focused protocols, the use of a thrombopoietin agonist for thrombocytopenia following allogeneic hematopoieticstem cell transplantation, and a crucial step for</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 2</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 2</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">b752168a-22c3-4fdb-b927-3baf203fb094</guid>
      <link>https://share.transistor.fm/s/2b31fd24</link>
      <description>
        <![CDATA[This episode will explore the consequences of a loss of the interaction between mutant calreticulin and another ER resident protein, and how this may promote myeloproliferative neoplasms, the role of a calcium-induced transcription factor in driving diffuse large B-cell lymphoma signaling, and a comparison of two therapies for standard risk acute graft-versus-host disease.]]>
      </description>
      <content:encoded>
        <![CDATA[This episode will explore the consequences of a loss of the interaction between mutant calreticulin and another ER resident protein, and how this may promote myeloproliferative neoplasms, the role of a calcium-induced transcription factor in driving diffuse large B-cell lymphoma signaling, and a comparison of two therapies for standard risk acute graft-versus-host disease.]]>
      </content:encoded>
      <pubDate>Thu, 09 Jan 2020 13:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/2b31fd24/3a77267f.mp3" length="22429567" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>931</itunes:duration>
      <itunes:summary>This episode will explore the consequences of a loss of the interaction between mutant calreticulin and another ER resident protein, and how this may promote myeloproliferative neoplasms, the role of a calcium-induced transcription factor in driving diffuse large B-cell lymphoma signaling, and a comparison of two therapies for standard risk acute graft-versus-host disease.</itunes:summary>
      <itunes:subtitle>This episode will explore the consequences of a loss of the interaction between mutant calreticulin and another ER resident protein, and how this may promote myeloproliferative neoplasms, the role of a calcium-induced transcription factor in driving diffu</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Season 1, Episode 1</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Season 1, Episode 1</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">ccc3fd57-8f0b-4bff-aadf-97d9b9c3fd85</guid>
      <link>https://share.transistor.fm/s/4e6c84da</link>
      <description>
        <![CDATA[This episode will highlight a unique treatment for refractory hematologic malignancies, therapy-induced mutations impacting the genomic landscape of relapsed acute lymphoblastic leukemia, and a unique approach to avoiding chronic graft-versus-host disease.]]>
      </description>
      <content:encoded>
        <![CDATA[This episode will highlight a unique treatment for refractory hematologic malignancies, therapy-induced mutations impacting the genomic landscape of relapsed acute lymphoblastic leukemia, and a unique approach to avoiding chronic graft-versus-host disease.]]>
      </content:encoded>
      <pubDate>Thu, 02 Jan 2020 13:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/4e6c84da/036c6b22.mp3" length="20717491" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>860</itunes:duration>
      <itunes:summary>This episode will highlight a unique treatment for refractory hematologic malignancies, therapy-induced mutations impacting the genomic landscape of relapsed acute lymphoblastic leukemia, and a unique approach to avoiding chronic graft-versus-host disease.</itunes:summary>
      <itunes:subtitle>This episode will highlight a unique treatment for refractory hematologic malignancies, therapy-induced mutations impacting the genomic landscape of relapsed acute lymphoblastic leukemia, and a unique approach to avoiding chronic graft-versus-host disease</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Sneak Peek Episode 2</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Sneak Peek Episode 2</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">b8948654-d983-4af4-96bd-5f999c3b95ff</guid>
      <link>https://share.transistor.fm/s/fb71ee13</link>
      <description>
        <![CDATA[This episode highlights articles and commentaries that help expand our understanding of prognostic biomarkers in CLL, learn more about a streamlined analysis of the granulocyte transcriptome in myeloproliferative neoplasms, explore the role of neutrophil extra cellulartraps in adenosine deaminase deficiency, and examine the function of the plant homeodomain-like finger protein 6, in hematopoietic stem cell self-renewal.]]>
      </description>
      <content:encoded>
        <![CDATA[This episode highlights articles and commentaries that help expand our understanding of prognostic biomarkers in CLL, learn more about a streamlined analysis of the granulocyte transcriptome in myeloproliferative neoplasms, explore the role of neutrophil extra cellulartraps in adenosine deaminase deficiency, and examine the function of the plant homeodomain-like finger protein 6, in hematopoietic stem cell self-renewal.]]>
      </content:encoded>
      <pubDate>Tue, 10 Dec 2019 10:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/fb71ee13/b309bc18.mp3" length="23135618" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1154</itunes:duration>
      <itunes:summary>This episode highlights articles and commentaries that help expand our understanding of prognostic biomarkers in CLL, learn more about a streamlined analysis of the granulocyte transcriptome in myeloproliferative neoplasms, explore the role of neutrophil extra cellulartraps in adenosine deaminase deficiency, and examine the function of the plant homeodomain-like finger protein 6, in hematopoietic stem cell self-renewal.</itunes:summary>
      <itunes:subtitle>This episode highlights articles and commentaries that help expand our understanding of prognostic biomarkers in CLL, learn more about a streamlined analysis of the granulocyte transcriptome in myeloproliferative neoplasms, explore the role of neutrophil </itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Sneak Peek Episode 3</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Sneak Peek Episode 3</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">562b4011-b218-457c-9a6a-adc01c570d28</guid>
      <link>https://share.transistor.fm/s/241872a0</link>
      <description>
        <![CDATA[This episode discusses the immune engine in classical Hodgkin Lymphoma, osteopontin’s keyrole in the chemoattraction of neutrophils in transfusion-related acute lunginjury,B-1 progenitor acute lymphoid leukemia, and exciting new ideas for heparin-induced thrombocytopenia treatment.]]>
      </description>
      <content:encoded>
        <![CDATA[This episode discusses the immune engine in classical Hodgkin Lymphoma, osteopontin’s keyrole in the chemoattraction of neutrophils in transfusion-related acute lunginjury,B-1 progenitor acute lymphoid leukemia, and exciting new ideas for heparin-induced thrombocytopenia treatment.]]>
      </content:encoded>
      <pubDate>Tue, 10 Dec 2019 10:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/241872a0/6d50fb55.mp3" length="23575514" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>980</itunes:duration>
      <itunes:summary>This episode discusses the immune engine in classical Hodgkin Lymphoma, osteopontin’s keyrole in the chemoattraction of neutrophils in transfusion-related acute lunginjury,B-1 progenitor acute lymphoid leukemia, and exciting new ideas for heparin-induced thrombocytopenia treatment.</itunes:summary>
      <itunes:subtitle>This episode discusses the immune engine in classical Hodgkin Lymphoma, osteopontin’s keyrole in the chemoattraction of neutrophils in transfusion-related acute lunginjury,B-1 progenitor acute lymphoid leukemia, and exciting new ideas for heparin-induced </itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Sneak Peek Episode 4</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Sneak Peek Episode 4</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">7c32a46a-2a6c-4dfc-9c38-7c5ad34b8eed</guid>
      <link>https://share.transistor.fm/s/295c41da</link>
      <description>
        <![CDATA[The topics in this episode include studies on the mechanism of progression in myelodysplastic syndromes, the value of gait speed as a predictor of outcomes in older adults with hematologic malignancies, the role of extended eltrombobag therapy on severe aplastic anemia, and the role of the Hedghog pathway mutations in chronic lymphocytic leukemia.]]>
      </description>
      <content:encoded>
        <![CDATA[The topics in this episode include studies on the mechanism of progression in myelodysplastic syndromes, the value of gait speed as a predictor of outcomes in older adults with hematologic malignancies, the role of extended eltrombobag therapy on severe aplastic anemia, and the role of the Hedghog pathway mutations in chronic lymphocytic leukemia.]]>
      </content:encoded>
      <pubDate>Tue, 10 Dec 2019 10:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/295c41da/f28b5b78.mp3" length="25582303" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1063</itunes:duration>
      <itunes:summary>The topics in this episode include studies on the mechanism of progression in myelodysplastic syndromes, the value of gait speed as a predictor of outcomes in older adults with hematologic malignancies, the role of extended eltrombobag therapy on severe aplastic anemia, and the role of the Hedghog pathway mutations in chronic lymphocytic leukemia.</itunes:summary>
      <itunes:subtitle>The topics in this episode include studies on the mechanism of progression in myelodysplastic syndromes, the value of gait speed as a predictor of outcomes in older adults with hematologic malignancies, the role of extended eltrombobag therapy on severe a</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Sneak Peek Episode 1</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Sneak Peek Episode 1</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">ea226097-5516-47cc-989d-829c31804daa</guid>
      <link>https://share.transistor.fm/s/5ba818e1</link>
      <description>
        <![CDATA[This episode explores four compelling topics which include: Hemophagocytic Lymphohistiocytosis, a severe and potentially fatal systemic inflammatory syndrome, CAR T-cell therapy in follicular lymphomas, Sickle Cell Anemia and sickle trait in thrombosis, and mutated calreticulin in myeloproliferative disorders.]]>
      </description>
      <content:encoded>
        <![CDATA[This episode explores four compelling topics which include: Hemophagocytic Lymphohistiocytosis, a severe and potentially fatal systemic inflammatory syndrome, CAR T-cell therapy in follicular lymphomas, Sickle Cell Anemia and sickle trait in thrombosis, and mutated calreticulin in myeloproliferative disorders.]]>
      </content:encoded>
      <pubDate>Tue, 10 Dec 2019 10:30:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/5ba818e1/953108ed.mp3" length="27689566" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>1150</itunes:duration>
      <itunes:summary>This episode explores four compelling topics which include: Hemophagocytic Lymphohistiocytosis, a severe and potentially fatal systemic inflammatory syndrome, CAR T-cell therapy in follicular lymphomas, Sickle Cell Anemia and sickle trait in thrombosis, and mutated calreticulin in myeloproliferative disorders.</itunes:summary>
      <itunes:subtitle>This episode explores four compelling topics which include: Hemophagocytic Lymphohistiocytosis, a severe and potentially fatal systemic inflammatory syndrome, CAR T-cell therapy in follicular lymphomas, Sickle Cell Anemia and sickle trait in thrombosis, a</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Blood Podcast - Trailer</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:title>Blood Podcast - Trailer</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">4ffc3471-d09a-4bfc-b0e0-6efde60f09f9</guid>
      <link>https://share.transistor.fm/s/e5775454</link>
      <description>
        <![CDATA[<p>The article highlighted in this trailer "<a href="https://ashpublications.org/blood/article/133/23/2495/273845/The-chromatin-binding-protein-Phf6-restricts-the"><strong>The chromatin-binding protein Phf6 restricts the self-renewal of hematopoietic stem cells</strong></a>"  was published June 6, 2019; <em>Blood</em>, Volume 133, Issue 23. </p><p>The authors of this article are: Satoru Miyagi , Patrycja Sroczynska , Yuko Kato , Yaeko Nakajima-Takagi , Motohiko Oshima , Ola Rizq , Naoya Takayama , Atsunori Saraya , Seiya Mizuno , Fumihiro Sugiyama , Satoru Takahashi , Yumi Matsuzaki , Jesper Christensen , Kristian Helin , Atsushi Iwama.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>The article highlighted in this trailer "<a href="https://ashpublications.org/blood/article/133/23/2495/273845/The-chromatin-binding-protein-Phf6-restricts-the"><strong>The chromatin-binding protein Phf6 restricts the self-renewal of hematopoietic stem cells</strong></a>"  was published June 6, 2019; <em>Blood</em>, Volume 133, Issue 23. </p><p>The authors of this article are: Satoru Miyagi , Patrycja Sroczynska , Yuko Kato , Yaeko Nakajima-Takagi , Motohiko Oshima , Ola Rizq , Naoya Takayama , Atsunori Saraya , Seiya Mizuno , Fumihiro Sugiyama , Satoru Takahashi , Yumi Matsuzaki , Jesper Christensen , Kristian Helin , Atsushi Iwama.</p>]]>
      </content:encoded>
      <pubDate>Sat, 09 Nov 2019 13:00:00 -0500</pubDate>
      <author>American Society of Hematology</author>
      <enclosure url="https://prfx.byspotify.com/e/media.transistor.fm/e5775454/e9043dab.mp3" length="1137123" type="audio/mpeg"/>
      <itunes:author>American Society of Hematology</itunes:author>
      <itunes:duration>45</itunes:duration>
      <itunes:summary>This is a trailer for the Blood Podcast, a podcast series that will provide timely information about research published in Blood, the most cited peer-reviewed publication in the field of hematology. Each episode will provide a summary of recent Blood articles. We will release a sneak peek of what's to come in December, sometime during the 2019 ASH Annual Meeting. The official series will launch January 2, 2020.  Subscribe now to get each episode as soon as they are released.  

The podcast series is published by the American Society of Hematology.</itunes:summary>
      <itunes:subtitle>This is a trailer for the Blood Podcast, a podcast series that will provide timely information about research published in Blood, the most cited peer-reviewed publication in the field of hematology. Each episode will provide a summary of recent Blood arti</itunes:subtitle>
      <itunes:keywords>hematology, oncology, medical, medical research, lymphoma, leukemia, CAR T, red cells</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
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