Steve chats to Wayne Douglas, formerly of the Alliance, George Hawkins and Sofija Venckute from Pathfinder and Dip Mukherjee, Consultant Upper GI & Laparoscopic Surgeon from BHRUT, about a strategy that lays out how AI can impact cancer care in North East London.

We also hear from George's mum!

Read more about the AI Strategy here: https://www.nelcanceralliance.nhs.uk/artificial-intelligence-strategy 

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Steve is joined by guests including Claremont managing director Ian Fannon; Caroline Cook, Early Diagnosis Programme Lead at the North East London Cancer Alliance and Mansi Tara, the Health Promotion Lead for Breast Screening for North, Central and East London.

Read more about the Health Inequalities Strategy here: https://www.nelcanceralliance.nhs.uk/health-inequalities-strategy 

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With cancer services facing unprecedented demand and ongoing workforce challenges, this strategy sets out a clear, ambitious plan to support, grow, and sustain the cancer workforce across north east London. Listen to find out more!

Read more about the Workforce Strategy here: https://www.nelcanceralliance.nhs.uk/our-workforce-strategy

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On bowel cancer, we also hear about the Bowelbabe Fund hitting the magical £20m mark, almost four years after the death of Bowelbabe herself, Dame Deborah James.

But that's not all. We also talk women's rugby and the BIG PINk WEEKEND and a potentially life-saving blood test that could detect pancreatic cancer.

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In this episode of Taking Control of Cancer, host Steve Bland is joined by Mark Guymer, CEO of the charity Cancer Support UK, and Sarita Yaganti, from the alliance, to explore what going back to work really looks like after a cancer diagnosis, and how both employees and employers can make the process healthier, kinder and more successful.

Together, they unpack the emotional and practical realities cancer patients often face when re-entering the workplace. From managing lingering side effects such as fatigue, brain fog and pain, to navigating awkward conversations with colleagues who may not know what to say, returning to work can feel overwhelming. 

The episode also addresses stigma and fear, including worries about being perceived as less capable, concerns about job security, and the very real fear of cancer recurrence that can resurface under stress.

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Together, they explore the development of the Alliance’s new Workforce Strategy and the extensive collaboration, insight, and commitment that has gone into shaping it. With cancer services facing unprecedented demand and ongoing workforce challenges, this strategy sets out a clear, ambitious plan to support, grow, and sustain the cancer workforce across north east London.

The conversation looks at why workforce planning is such a critical enabler of high-quality cancer care, and how investing in people directly translates into better experiences and outcomes for patients. Sarita and Yvonne discuss how the strategy reflects the realities of working in cancer services today, from recruitment and retention pressures to the need for new roles, new skills, and more personalised approaches to care.

Listeners will hear how the strategy has been informed by staff voices across disciplines and settings, ensuring it is grounded in real-world experience. The episode also explores how workforce development supports personalised cancer care, improves equity of access, and helps ensure that patients receive the right care, from the right professional, at the right time.

For more information about the cancer alliance’s Workforce Strategy, visit: https://www.nelcanceralliance.nhs.uk/our-workforce-strategy

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The discussion begins by addressing the system pressures driving the strategy. Cancer incidence is rising, referrals have increased, and diagnostic services are under sustained strain. 

Against this backdrop, the alliance is exploring how artificial intelligence can help shift the NHS conversation from simply digitising frontline services to improving frontline productivity and clinical capacity. Rather than adopting AI as a novelty or isolated innovation, the alliance is taking a deliberate, proactive approach to embedding it within cancer pathways.

The episode highlights how the strategy links productivity, sustainability, and patient safety. AI solutions such as chest X-ray triage illustrate how technology can prioritise urgent cases more effectively, improving safety while also reducing wasted clinician time and easing pressure on imaging services. Crucially, these productivity gains can help offset the costs of AI tools, supporting financial sustainability at a time when healthcare budgets are under pressure.

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Steve and Femi cover National CNS Day, how the alliance is reducing cancer inequalities for Gypsy, Roma and Traveller communities; research from the European Code Against Cancer which says tackling air pollution should be part of government work to cut cancer rates; 30 years of Maggie's centres and a new study that has found that globally, six cancers are rising faster in younger adults than older ones.

For more information about National Cancer Clinical Nurse Specialist Day and the videos of clinical nurse specialists, visit: https://www.nelcanceralliance.nhs.uk/news/national-cancer-clinical-nurse-specialist-day-16-march-2026 or watch the videos on YouTube:

• Ruth: https://youtu.be/_ZtjNhta1Is
• Jessica: https://youtu.be/0WNlMcLo0iM
• Marisa: https://youtu.be/8IOlI7qgu6U
• Message from Marisa for National Cancer CNS Day: https://youtube.com/shorts/CEXUA73tYFM?feature=share

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Together, they explore what it truly means to be an international nurse in the UK cancer workforce, sharing personal stories, professional challenges, and moments of growth that shape both careers and patient care.

The conversation begins with personal journeys into nursing, uncovering what inspired each guest to choose the profession and what led them to take the bold step of working abroad. The nurses reflect on the realities of relocating to a new country, including the emotional and practical challenges of starting again in an unfamiliar healthcare system.

Moving into work life, the episode explores how nursing in the UK compares with practice in their home countries. Guests discuss transferable skills they bring with them, how they adapt to new clinical pathways and systems, and what it’s like navigating the NHS while maintaining high standards of compassionate cancer care.

This episode is released on National Cancer Clinical Nurse Specialist Day, which recognises the importance of the role, raises awareness of career opportunities, and thanks all CNSs across the country for all the hard work they do.

To find out more about Cancer Clinical Nurse Specialists, visit: https://www.nelcanceralliance.nhs.uk/cancer-clinical-nurse-specialists

Read more about National Cancer Clinical Nurse Specialist Day: https://www.nelcanceralliance.nhs.uk/news/national-cancer-clinical-nurse-specialist-day-16-march-2026

#NationalCancerCNSDay

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The CDL pilot project is a three-year initiative, delivered in partnership with Macmillan Cancer Support and NHS England, designed to address workforce challenges by embedding a dedicated Development Lead role into each London Integrated Care System area. 

Kate explains why the CDL role was created — highlighting the pressing need to tackle high vacancy rates, retention issues, and limited exposure to cancer nursing during initial training — and how the pilot supports newly qualified and early-career Cancer Clinical Nurse Specialists (CNSs) to build confidence, autonomy and leadership skills.

Through a blend of one-to-one mentoring, group education sessions, and outreach activities, the CDL role also promotes the CNS career pathway and fosters a resilient, skilled workforce capable of meeting future cancer care needs.

This episode is released on National Cancer Clinical Nurse Specialist Day, which recognises the importance of the role, raises awareness of career opportunities, and thanks all CNSs across the country for all the hard work they do.

To find out more about the Macmillan CDL pilot, visit https://www.nelcanceralliance.nhs.uk/macmillan-cancer-cns-development-lead-cdl

Read more about National Cancer Clinical Nurse Specialist Day: https://www.nelcanceralliance.nhs.uk/news/national-cancer-clinical-nurse-specialist-day-16-march-2026

#NationalCancerCNSDay

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In this episode, host Steve Bland is joined by Caroline Cook, Early Diagnosis Programme Lead at the North East London Cancer Alliance, and Tiago Moutela, Associate Director at Claremont. Together, they explore the extensive engagement work that brought together voices from a wide range of diverse communities across north east London.

The conversation highlights why meaningful community input is essential, how different groups shared their experiences of cancer care, and how these insights will be used to shape a strategy designed to improve access, experience and outcomes for everyone affected by cancer.

Listeners will hear how the Cancer Alliance, working in partnership with Claremont, undertook extensive engagement with a diverse range of communities, including groups who are often underrepresented in healthcare decision-making. The discussion explores the methods used to reach these communities, the insights they shared, and how their lived experiences will influence strategic priorities.

The episode demonstrates how co-production and listening to local voices can lead to more inclusive, equitable cancer care and better outcomes across north east London.

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We also highlight why attending these appointments is so essential and how the NHS supports people through this journey, helping to catch problems early when they’re easiest to treat.

Clare McGeady from the bowel screening service helps explain what a colonoscopy is, what it is looking for and why you might need one. She talks through some of the myths and fears to provide reassurance for patients who are invited to attend a colonoscopy, and highlights just how essential it is to attend your appointment.

For more information about what a colonoscopy is, visit https://www.nhs.uk/tests-and-treatments/colonoscopy/

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Plus Steve and Femi look at a new plan from NHS England to change bowel cancer screening to help detect more cancers earlier and potentially save lives across England.

And it's Femi's birthday!

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Designed to help patients prepare for cancer treatment, the virtual tour guides them through how to get to their appointment and what to expect when they arrive, reducing uncertainty and anxiety at a critical moment in their care journey.

Recorded at the launch event at St Bartholomew's Hospital, the episode highlights how technology can improve not only the quality of care but also equity of access. By providing clear, visual, and accessible information, the virtual tour helps patients who may be unfamiliar with hospital settings, travelling from further afield, living with anxiety, or facing language or communication barriers. Importantly, it also aims to improve appointment attendance, ensuring patients are supported to receive timely care.

The discussion places the virtual tour within a broader programme of digital innovation across the North East London Cancer Alliance, including the use of AI to speed up chest X-ray reporting, animated videos to explain tests and procedures in simple terms, and chatbots that offer round-the-clock answers to patient questions. 

Together, these tools demonstrate how technology can support patients before, during, and after diagnosis and treatment. Patients attending St Bartholomew’s Hospital are encouraged to access the virtual tour using the link or QR code in their appointment letter to help them feel more prepared and confident ahead of their visit.

Read more about the tour: https://www.nelcanceralliance.nhs.uk/news/launch-new-virtual-hospital-tour

For more information about innovation in cancer diagnosis and treatment in north east London, watch this short video: https://youtu.be/urpQ6-AnExc

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Together, they explore the significance of World Cancer Day, the launch of the National Cancer Plan for England, and what these national ambitions mean on the ground for patients and communities in north east London.

Following the launch of the National Cancer Plan for England, Femi talks through the key priorities of the plan and what they mean specifically for North East London Cancer Alliance. 

As one of the top-performing cancer alliances in the country, consistently meeting and exceeding the three national cancer standards, the Alliance is well placed to build on strong foundations. Femi reflects on what has driven this performance to date, where there is still more to do, and how the new national plan provides both opportunities and challenges for cancer alliances and the communities they serve.

Drawing on his frontline experience as a GP, Dr John reflects on how cancer policy translates into day-to-day primary care — from prevention and early diagnosis to personalised, compassionate support for people living with and beyond cancer. 

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Steve is joined by Caroline Cook, Programme Lead for Early Diagnosis at the North East London Cancer Alliance, and Leena Khagram from the NHS Bowel Screening Service to explore the efforts being made across North East London to increase uptake, and share how you, your family, and your community can all play a part in helping more people benefit from this simple, but life-saving test. 

Plus they cover how a sample of poo really can save your life and most importantly, the techniques you need to collect your samples!

Work still needs to be done to encourage more people to complete and return the bowel screening test kit. This episode explores some of the specific barriers and challenges in north east London, where the population is amongst the most diverse in England, and is also in some of the most deprived areas of the country.

For more information about bowel screening, visit https://www.nelcanceralliance.nhs.uk/bowel-screening

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Plus, it's Cervical Cancer Prevention Week (Jan 19-25) and Steve and Femi are myth-busting! For example, did you know that cervical screening doesn't actually look for cancer?! Cervical screening usually looks for high-risk HPV, not cancer itself. If HPV is found, the sample is then checked for cell changes that could develop into cancer if untreated. Find out more here.

For more info, visit the Eve Appeal or for info on the alliance Health Hubs, head to the North East London Cancer Alliance website.

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Caroline explains what the term ‘psychosocial support’ means, how patients and families can access these services in north east London, and why this kind of care is a vital part of improving outcomes and quality of life. 

For more information about the support services in north east London, visit https://www.nelcanceralliance.nhs.uk/mental-health-and-psychosocial-support.

We also have a directory of training resources for healthcare professionals involved in the delivery of psychosocial services, which can be accessed via this webpage: https://www.nelcanceralliance.nhs.uk/personalised-care-and-psychosocial-care

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In this episode:

1. The UK's National Screening Committee has recommended that only a very small group of men at high risk of prostate cancer should be screened for the disease. Read more here, check out our podcast episode with prostate cancer patients Mike and Yinka and read about the alliance's 'It's Not a Game' campaign here.
2. Adrian Chiles has revealed he’s undergone an operation to remove a cancerous patch of skin from his shoulder. The TV presenter’s diagnosis arrived after he spotted a suspicious skin patch, which a biopsy later confirmed to be cancerous. Read more here.
3. The National Cancer Patient Experience Survey (NCPES) is now live. NCPES gives people who have received cancer treatment the opportunity to share their experiences directly with the NHS. Every response plays a vital role in shaping how cancer services are designed, delivered, and improved. For more information on NCPES, click here.
4. Stand Up To Cancer returned on Friday with new campaign by Channel 4 and Cancer Research UK to drive awareness of NHS cancer screening programmes and raise funds for groundbreaking cancer research. Read more here.

And finally....we'd love to hear what you think of this podcast. We've got big plans for 2026 but this is your chance to shape what we cover! Click here to fill out our (very short) survey.

Host Steve Bland welcomes two remarkable guests, Yinka and Mike, both prostate cancer survivors whose journeys have transformed them into advocates and community voices. 

Through honesty and humour, they share how their diagnoses changed their lives, how they navigated treatment, and why they now dedicate their time to helping other men, especially those in diverse and underserved communities across north east London, recognise the importance of knowing their risk and getting checked early.

For more prostate cancer advice, check out the resources available at Prostate Cancer UK.

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The survey, commissioned by NHS England and conducted annually, is sent to patients who have received cancer treatment as an inpatient or outpatient during a specific period (April, May & June). It asks about every stage of the cancer journey, from diagnosis, tests, and treatment, through to support after care, giving patients the chance to share what went well and what could be improved.

The feedback from tens of thousands of patients across England helps the NHS understand what matters most to those affected by cancer. It plays a vital role in shaping how services are designed and delivered, from improving communication between healthcare teams, to ensuring timely diagnosis, better emotional support, and equitable access to care.

However, in North East London, as in other parts of the country, some communities are underrepresented in the survey responses, particularly patients from Black African and Caribbean backgrounds. This means that their voices and experiences may not be fully reflected in how services are improved, which is why encouraging greater participation from all communities is so important.

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Steve and Femi also celebrate the news that Taking Control of Cancer has been downloaded in 50 countries around the world AND introduce the Alliance's new WhatsApp channel, launched to share all the latest news from the Alliance. You can access the channel using this link https://bit.ly/4oSF8Ku.

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Steve is joined by Alfie Bailey-Bearfield, Head of Influencing and Health Improvement at Pancreatic Cancer UK, and Rishi Athwal, Early Diagnosis Project Manager, North East London Cancer Alliance, to shine a light on one of the toughest cancers to detect.

Together, they discuss the key signs and symptoms everyone should know, along with the latest facts and statistics about pancreatic cancer in the UK. Alfie also shares exciting developments in research, including a new breath test that could transform early detection, and explains why spotting pancreatic cancer early is so critical.

The conversation also covers the work of EUROPAC, which looks at the role of genetics and family history in pancreatic cancer, and introduces Pancreatic Cancer UK’s Family History Checker, a tool designed to help people understand their own risk.

This is an essential listen for anyone who wants to understand more about pancreatic cancer, the importance of early diagnosis, and how we can all play a part in raising awareness.

For more information, visit the Pancreatic Cancer UK website: https://www.pancreaticcancer.org.uk/

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Steve and Femi talk Strictly, hip-shaking, Movember moustaches, breast screening and why there are calls for menopause support to be included in cancer treatment plans.

Plus Femi explains why he's excited about an article in the British Journal of Urology International on prostate cancer which was co-authored by a leading North East London surgeon. Read that right here.

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In this deeply moving episode, host Steve Bland speaks to Chris Soltysiak, a patient and carer representative from the North East London Cancer Alliance, as he shares the story of his late wife, Lynda. 

Lynda dedicated over 30 years of her life to the NHS, supporting others with compassion and commitment, yet when her own symptoms of breast cancer emerged, her journey through the healthcare system was marked by delays, missed opportunities, and heartbreaking loss.

Chris opens up about Lynda’s courage, her love for her family, and her enduring dedication to others, even in the final weeks of her life. He also reflects on the challenges faced by carers, the impact of missed diagnoses, and the changes that are needed in cancer awareness and support. 

Through this story, Chris offers powerful lessons for patients, carers, and healthcare professionals alike — reminding us of the importance of persistence, advocacy, and compassion in the face of cancer.

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Steve is joined by Cathy Bouvier-Ellis, CEO and Co-Founder of Neuroendocrine Cancer UK, along with Jane Aylott, a patient sharing her lived experience, and Sarita Yaganti, Programme Lead for Personalised Cancer Care at the North East London Cancer Alliance, to discuss the challenges of diagnosing neuroendocrine cancer, the signs and symptoms to look out for, treatment options available, and the importance of connecting patients with specialist support networks.

Whether you are a patient, carer, or healthcare professional, this conversation sheds light on why early recognition matters and how support can make a huge difference for patients with neuroendocrine cancer.

Key facts and stats

·      Around 6,000 people are diagnosed with neuroendocrine tumours (NETs) each year in the UK.

·      NETs account for about 1–2% of all cancers, but incidence has been increasing over the past two decades.

·      Many patients experience delays of 5–7 years on average before receiving an accurate diagnosis.

·      Common sites include the gastrointestinal tract, pancreas, and lungs.

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From two of sport's biggest names inspiring through talking about their own cancer stories, to a chart topper rerturning to the stage after breast cancer surgery, this episode has it all. Plus we cover what's going on in Demmark to set them apart when it comes to early diagnosis.

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We explore how his personal experience with a stage 2, grade 2 pancreatic neuroendocrine tumour shaped his leadership, deepened his commitment to equity and integration, and influenced his vision for the hospital and broader healthcare services in north east London.

Amanjit, Harvard-trained epidemiologist, McKinsey alumnus, entrepreneur, and pancreatic cancer survivor, shares candid reflections on how becoming a patient opened his eyes to the strengths, gaps, and emotional complexities within NHS care. 

From witnessing integration across Whipps Cross, The Royal London, and St Bartholomew’s, to championing equality, diversity, and inclusion, his dual perspective offers a rare lens on service improvement. 

This heartfelt and inspiring episode will resonate with anyone interested in leadership, resilience, and the human face of cancer care.

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So in these episodes Steve Bland is joined by Mansi Tara, Health Promotion Lead, and Claire Mabena, Lead Nurse, both from the North London and Central and East London Breast Screening Service to take you through everything you need to know, from what actually happens at a breast screening appointment to why it’s so important, and what the latest facts and figures tell us.

We also address some of the most common concerns and misconceptions, as we know that fear, confusion, and lack of information can be real barriers. Whether you’ve never been for a screening before or you’re encouraging a friend or family member to go, we want to offer clarity, reassurance, and honest answers. Breast screening isn’t just another appointment, it’s a powerful step in protecting your health.

The first part of this episode will be a ‘back-to-basics’ guide, covering every aspect of the patient’s journey, from receiving the invite letter to making the appointment, attending and receiving the results. It will look at why it is so important, what it checks for and what the age ranges are.

The second part will look at some of the myths and barriers to attending and how we can overcome these to help increase the uptake.

Read some essential information about breast screening: https://www.nelcanceralliance.nhs.uk/breast-screening

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So in this episode Steve Bland is joined by Mansi Tara, Health Promotion Lead, and Claire Mabena, Lead Nurse, both from the North London and Central and East London Breast Screening Service to take you through everything you need to know, from what actually happens at a breast screening appointment to why it’s so important, and what the latest facts and figures tell us.

We also address some of the most common concerns and misconceptions, as we know that fear, confusion, and lack of information can be real barriers. Whether you’ve never been for a screening before or you’re encouraging a friend or family member to go, we want to offer clarity, reassurance, and honest answers. Breast screening isn’t just another appointment, it’s a powerful step in protecting your health.

The first part of this episode will be a ‘back-to-basics’ guide, covering every aspect of the patient’s journey, from receiving the invite letter to making the appointment, attending and receiving the results. It will look at why it is so important, what it checks for and what the age ranges are.

The second part will look at some of the myths and barriers to attending and how we can overcome these to help increase the uptake.

Read some essential information about breast screening: https://www.nelcanceralliance.nhs.uk/breast-screening

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In this episode host Steve Bland is joined by Steph and Sarita Yaganti, the Programme Lead for Personalised Cancer Care at the North East London Cancer Alliance, to explore some of these challenges in more detail and offer some top tips for cancer patients in how they can improve their quality of life after going through their cancer treatment.

From practical, every day steps people can introduce to their daily routine, to more in-depth levels of support, this podcast is a must for cancer patients, and their families, friends and colleagues.

Steph Davies is an ICF trained coach, NLP Practitioner and Mental Health First Aider. She facilitates our support groups and coaching programmes.

After completing chemotherapy for Hodgkins Lymphoma, Steph realised that the world was a very different colour post cancer. Cancer shaped her life, so she created this space to support others in shaping theirs. Visit https://www.life-aftercancer.co.uk/.

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Together, they unpack the latest cancer headlines from across England, exploring what they mean for patients, cancer services, and the work of the Alliance. From new research developments and celebrities speaking out about their experiences, to updates in cancer care and Formula 1 drivers, this is your monthly round-up of the news that matters.

To find out more about the projects mentioned in this podcast, visit https://www.nelcanceralliance.nhs.uk/

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Host Steve Bland headed to Highgate School to speak to James Green, Consultant Urological Surgeon at Barts Health, and Vicky Stubbs, National Education Expert, about all things testicular cancer: the warning signs, how to self-check, and when - and how - to take action.

Aimed at boys, young men, parents, teachers, and anyone supporting boys’ health, this episode covers the key facts, busts common myths, and offers practical, potentially life-saving advice.

In part two the guests are also joined by Head of Year 7, Phil Bartlett, who shares how schools are playing a key role in raising awareness, and why talking openly about this topic could save a life.

The key, as with other forms of cancer, is early diagnosis. This is achieved through knowing the signs of symptoms, regular self-checking and then taking action if you do find anything. It is unlikely to be cancer or anything serious, but if there is something that needs looking into, the earlier the better as treatment is likely to be easier.

James and Vicky talk about the fantastic range of education resources available, co-developed with Highgate School in north London. For more information visit www.testicularhealth.info

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Host Steve Bland headed to Highgate School to speak to James Green, Consultant Urological Surgeon at Barts Health, and Vicky Stubbs, National Education Expert, about all things testicular cancer: the warning signs, how to self-check, and when - and how - to take action.

Aimed at boys, young men, parents, teachers, and anyone supporting boys’ health, this episode covers the key facts, busts common myths, and offers practical, potentially life-saving advice.

The guests are also joined by Head of Year 7, Phil Bartlett, who shares how schools are playing a key role in raising awareness, and why talking openly about this topic could save a life.

The key, as with other forms of cancer, is early diagnosis. This is achieved through knowing the signs of symptoms, regular self-checking and then taking action if you do find anything. It is unlikely to be cancer or anything serious, but if there is something that needs looking into, the earlier the better as treatment is likely to be easier.

James and Vicky talk about the fantastic range of education resources available, co-developed with Highgate School in north London. For more information visit www.testicularhealth.info

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As the summer holidays approach, many of us look forward to enjoying the sun, but without proper precautions, that sunshine can carry serious risks. In this episode, we explore how skin cancer, one of the most common forms of cancer in the UK, can often be prevented or cured if caught early.

Tom and Rosie talk about the essential steps individuals and families can take to protect their skin both at home and abroad, from choosing the right sunscreen, how to apply it to kids, and recognising early warning signs, to knowing when to seek medical advice.

We also go behind the scenes to explore the groundbreaking work underway to revolutionise skin cancer diagnosis. From Artificial Intelligence tools helping clinicians prioritise and assess images faster, to streamlined referral systems and digital dermatology services, innovation is helping provide quicker reassurance for the majority and faster treatment for those who need it most.

For information about the latest campaign from the cancer alliance on sun safety visit: https://www.nelcanceralliance.nhs.uk/LDN-get-sun-set

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In particular, we're looking at a project in North East London which aims to reduce the wait time for chest X-ray results from three weeks to just three days for scans with significant findings (https://www.nelcanceralliance.nhs.uk/news/using-artificial-intelligence-faster-chest-x-ray-results) 

In collaboration with Sectra and Qure.ai, North East London Cancer Alliance is using the Sectra Amplifier services integrating Qure.ai qXR AI tool to help radiologists and reporting radiographers prioritise urgent cases, enhance decision-making, and streamline the patient journey.

By prioritising urgent cases and quickly sorting through unremarkable ones, the AI system reduces delays in diagnosing critical conditions like lung cancer. This means patients can receive faster treatment when needed, improving their outcomes by ensuring timely care. For those without cancer, the system provides quicker reassurance, giving them peace of mind sooner.

This podcast discusses the benefits of using AI, as well as the challenges and barriers. It also focuses on patient safety as a key priority and helps explain how the nee technology is being introduced safely into cancer care.

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Steve and Wayne are joined by Dr Francesca Jackson-Spence, Clinical Research fellow in Genitourinary oncology at Bart’s Cancer Institute, Queen Mary University of London, PhD candidate; and Dr Angel A. Rodriguez, MD Oncology and Senior Medical Director at Natera.

The project will evaluate the real-world impact in an NHS setting of circulating tumour DNA (ctDNA) testing using Signatera™ to inform follow-on treatment decisions of early stage urothelial and gastro-intestinal cancer patients. Signatera™ is a personalised and highly sensitive tumour-informed cDNA test for molecular residual disease detection (MRD), to inform treatment decisions for cancer patients with solid tumours.

This pilot will help better select the patients who need treatments, and de-escalate therapy for those who don’t need it.

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In part one, Steve Bland is joined by Wayne Douglas, Programme Lead for Diagnosis and Treatment; and Project Manager Rosie O'Dea, both from the North East London Cancer Alliance; and Molly Pipping, Senior Programme Lead for Workforce & Education at the Greater Manchester Cancer Alliance, to talk about innovation and collaboration between the cancer alliances.

This episode explores how cutting-edge innovation is transforming cancer diagnosis and treatment. We spotlight the game-changing role of AI, emerging technologies, and the power of cancer alliances in delivering faster, more accurate diagnostics - and ultimately, saving lives. 

We also reflect on the vital role of collaboration, both across cancer alliances and with wider system partners, as a driving force behind progress.

Look out for part two!

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At the age of 43, Jean-Pierre was initially given three weeks to live as his cancer had spread so much. However, after changing his chemotherapy treatment, he responded well and survived beyond the three weeks. A year later, Annamaria Minicozzi from Barts Health performed a rare and intense procedure on Jean-Pierre to try to remove all the cancer that was too small to be visible to the human eye.

This 12-hour intensive operation - known as HIPEC - has completely changed Jean-Pierre's life - and given him so many more precious moments with his wife and family. Anna is championing for more of this surgery to be available in England, as there are currently only four centres of excellence.

What is HIPEC?

HIPEC stands for Heated Intraoperative Intraperitoneal Chemotherapy. It is a treatment combination used to treat cancers that have spread into the abdominal cavity, affecting the surface which is called ‘peritoneum’.

Traditionally the cancer which affects the peritoneum has been considered a condition not curable surgically and not very responsive to intravenous (IV) chemotherapy. However, there is evidence that if the size and spread of the cancer is limited, then a special surgical procedure called “Cytoreductive Surgery” that removes all the visible disease can be helpful.

This treatment can involve major surgery to remove organs in the abdomen and the peritoneum. Once the tumour has been removed, a heated chemotherapy is delivered directly to the abdominal cavity while the patient is under the anesthetic to kill off any remaining unseen cancerous cells that could otherwise grow.

The cancer cells are exposed to a high dosage of chemotherapy drug and the general undesired effects are minimized. The treatment that can be offered will vary depending on the extent that the cancer has spread.

Anna is aiming for more patients from East London and other areas of London and the South of England to be able to access this curative treatment for peritoneal metastases from colorectal and appendiceal cancer, closer to home.

This will avoid delay in treatment and consequently progression of disease and aims to improve opportunity of care and facilitate continuity of care.

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It’s good to talk. Yet despite incredible advances in cancer diagnosis, treatment and care, “the C word” remains one of the hardest topics to talk about. But could breaking that silence be the key to saving lives?

In this powerful episode, host Steve sits down with Paul to explore how fear, stigma and silence still shape the way we deal with cancer.

From encouraging early GP visits and screening uptake, to creating safe spaces for people to open up, they dive into why conversations really matter, and how we can all play a part in changing the narrative.

Whether you're personally affected or work in healthcare, this episode sheds light on what’s working, what’s not, and what we can all do to help people get the right support at the right time.

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Caroline and Riyad have a look at reasons why women are not coming forward for free, live-saving breast screening, with fear being one of the main reasons. Another reason often given is not having enough time for it. Yet what could be more important than looking after your health?

This episode also looks at an example of the work taking place within the Bengali community as well as some of the wider work the cancer alliance is doing with local people to help encourage the uptake of breast screening.

For more information about breast screening, visit https://www.nelcanceralliance.nhs.uk/breast-screening

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Steve is joined by Ben Lamb, MDT Clinical Lead for the North East London Cancer Alliance and Ellen Quinney, Programme Manager, Diagnosis and Treatment, North East London Cancer Alliance, as they talk about bringing in the experts for a cancer diagnosis.

Ben and Ellen explain how when cancer is diagnosed, you are not just getting a single opinion, but one from a team of experts with a range of different skills and expertise. This is a key area of focus for the cancer alliance, looking at how improvements can be made to this process to speed up the time of results for patients, so that the right treatment can be provided at the right time.

Meetings to discuss a cancer patient’s diagnosis and treatment are called Multi Disciplinary Team Meetings, or MDTs. They are where a group of health and care staff who are members of different organisations and professions (e.g. GPs, clinicians, nurses) come together to make decisions regarding the treatment of individual cancer patients.

Ben and Ellen are leading a vital programme of work to improve the effectiveness of these MDTs. A key part of this is called Streamlining. This helps ensure that more complex cases go through a full MDT and more straightforward, easier-to-treat cases get support via a triage meeting and then progress to treatment quickly.

The benefit of this is that in simpler cases, patients get treatment more quickly and, at the same time, capacity for MDTs is increased for patients with more complex needs, so they can get the specialist levels of support required.

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Jack and Natasha from Cancer Awareness in Teens and Twenties (CATTS) share their experience of working with schools to help empower young minds, raising awareness of cancer at an early age. This benefits both school children - providing them with invaluable health advice - and their families, encouraging more conversations at home.

This is part of an innovative project funded by the cancer alliance and led by project manager Nikki Poland. It is delivering a series of engaging cancer awareness workshops to Year 10 and Year 11 pupils in secondary schools across north east London.

The cancer awareness workshops cover: what is cancer, the signs and symptoms of cancer, how to check your body including breasts and testicles, how to reduce your chances of developing cancers including sun safety and promote healthy living. All this is in line with the PSHE curriculum.

The project has engaged with a number of schools to date, reaching over 5,000 pupils in the last 2 years. It is looking for more schools in north east London to get on board.

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Learn about the role of family history, the importance of attending screening appointments like lung and breast checks, and how early detection can make all the difference. Don’t wait for a symptom to become a problem - take control of your health today.

Plus, find out what's in Toby's box!

Join us for this essential conversation on how staying informed could change, or even save, a life.

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At the age of 22, after Robin died from a late-stage germ cell cancer diagnosis, Toby founded The Robin Cancer Trust with a mission to save lives by raising awareness, delivering education, and offering support to young people affected by testicular or ovarian cancer.

This episode explores the impact of cancer on family members, especially when it comes to losing a sibling and how this can be a different experience from losing a friend or parent. For example, Toby talks about the moment when he became older than his brother, which was a very emotional milestone.

The episode talks about what support is available and what support would be helpful to have in place. It also talks about the work that The Robin Cancer Trust is doing to raise awareness of cancer and offering support to people affected by cancer.

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Navigating menopause after a cancer diagnosis can leave you feeling unsupported, isolated and not knowing what your options are. Support is out there, and we explore this with help from Dani, who was diagnosed with breast cancer in her early 30s.

She went on to create Menopause and Cancer, which provides support for all those affected by menopause and cancer and more information about their work is on their website: https://menopauseandcancer.org/

Cancer treatment often triggers the menopause. In fact, 40% of women under 40 and 70%-90% of women over 40 enter permanent menopause as a result of their treatment. Many women say that navigating menopause after cancer feels harder than chemotherapy, radiotherapy, and surgery altogether.

We discuss the facts about cancer and menopause, look at what to expect after a cancer diagnosis and when going through treatment. We talk through experiences of women going through menopause after cancer treatment, and look at the support that is available.

This episode provides some top tips on how to access support, how to connect with other women going through similar experiences, and the importance of getting access to the right information so you can make informed choices.

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In part one, Steve is joined by Kate Williams, the Macmillan Cancer CNS Development Lead, and Yvonne Beadle, from the North East London Cancer Alliance, and in part two, it's the turn of Kim Grove and Chelo Bou, Clinical Nurse Specialists from Barking, Havering and Redbridge University Hospitals NHS Trust, and patient Peter Adams.

The CNS is a vital part of a cancer patient’s treatment, yet it's a role that is not so commonly understood. It is important to recognise the work that Clinical Nurse Specialists undertake and to raise the profile of the role to help encourage more people to work in this specialist field.

A Cancer CNS is a senior nursing role which focuses on the needs of cancer patients and their families. They tend to work in a specific cancer site and build extensive knowledge of the clinical and broader needs of patients with that cancer. They typically first meet patients at the point they are diagnosed with cancer and become an essential contact and support as they progress through treatment and beyond.

As well as exploring the day-to-day activities in more detail, this episode also compares the modern-day role to the past and how things have changed over the years. This includes the role of the cancer alliance in supporting the CNS workforce and the current challenges with recruiting nurses for the role.

It is a unique peak through the eyes of very experienced Clinical Nurse Specialists in north east London!

To find out more about the role of a cancer clinical nurse specialist, visit https://www.nelcanceralliance.nhs.uk/cancer-clinical-nurse-specialists

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#NationalCancerCNSDay

Steve Bland speaks to Susan Piper, a Specialist Nurse at Prostate Cancer UK and Paul Thomas, Communications and Engagement Manager at the North East London Cancer Alliance.

Susan helps sort through the facts from the fiction about prostate cancer, giving key information to boost survival rates that everyone should know - not just men, but their partners, family and friends too.

This includes highlighting the support available from Prostate Cancer UK, encouraging men to have more conversations about prostate cancer and to reach out for advice and get checked.

The episode builds on our previous episodes on prostate cancer: one where a patient talked about his experience of prostate cancer diagnosis, treatment and recovery, and the other where a British Athlete spoke about the risk of getting prostate cancer, particularly in the black community.

Although prostate cancer is the most common cancer in men in England, survival rates for prostate cancer are good – when it is diagnosed early. If found at its earliest stage, all men are expected to survive, compared with around 49% of men when diagnosed at the latest stage.

For more information on prostate cancer, visit the Prostate Cancer UK website: https://prostatecanceruk.org/

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#ProstateCancerAwarenessMonth

This episode takes a unique dive into the day-to-day activities of a cancer alliance MD and a closer look at some of the demands of the role.

It focuses on how a major part of this role is bringing together all partners to work together more closely and effectively to make improvements for patients. This is paying off, as reflected in local cancer performance results for north east London.

Find out more about the work of the North East London Cancer Alliance: https://www.nelcanceralliance.nhs.uk/

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Dr Kaythyn Mannix is leading the way in this subject area, and in this emotional episode she talks to Steve about what she has experienced both as a palliative care doctor, and as a best-selling author, winning an award for her book, ‘With the end in mind .’ Steve also shares how Kathryn helped him know what to look out for in the days and hours leading up to the death of his first wife, Rachael.

Talking about death isn’t easy, but it’s one of the most important conversations we can have. In this powerful episode of Taking Control of Cancer, we explore how opening up about end-of-life matters can help cancer patients and their loved ones navigate this deeply emotional journey.

Kathryn talks about how we can better understand and prepare for death (our own or somebody else’s). From breaking taboos to offering practical guidance, she delves into the ways these honest discussions can bring clarity, connection, and even comfort during life’s most challenging moments.

Find out more about Kathryn's work at https://www.kathrynmannix.com/.

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In her own brutally honest but hilarious way, Karen shares her personal experience of cervical cancer and also talks about her work with The Eve Appeal and the cancer alliance on the ‘You Need To Know’ womb cancer campaign. This campaign raises awareness of the main symptom of womb cancer, which is bleeding after the menopause. Karen brings her humour and vast knowledge to bring about more open conversations about signs and symptoms in private parts of the body, covering all five gynae cancers (womb, cervical, ovarian, vulval and vaginal).

More information about the You Need To Know campaign is here: https://www.nelcanceralliance.nhs.uk/about-you-need-know-campaign

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Farzana is a passionate, charismatic GP from the London Borough of Newham, with a vast experience of supporting local people in north east London. She cares deeply about her patients and has built up close relationships throughout her dedicated support over the years. She is determined to make a difference in cancer, helping people get diagnosed more quickly and getting their treatment at the right time.

This episode provides advice for patients from a GP's perspective, as well as a look at how we can encourage different communities to come forward. It explores specific barriers and ways of overcoming these, for example starting conversations at home about cancer and supporting friends, family and colleagues.

Follow Farzana on X: @fhussain73

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Joe is a British athlete with an impressive array of championship titles across hurdles, long jump and triple jump. Joe’s friend and hurdling rival was diagnosed with prostate cancer himself and encouraged Joe to speak to his GP. Now Joe wants to pass on the favour as he campaigns to raise awareness of the risk of prostate cancer, particular in the black community where the risk is higher. 

This episode also covers key facts and stats about prostate cancer, especially for the black community where the risk is higher. Joe talks about his personal experience of prostate cancer combined with his athletics career, along with the community work he is doing to raise awareness of prostate cancer.

The episode includes a look at the key facts about prostate cancer and what to do if you are at a higher risk, with the key thing being to get a PSA test.

Joe’s story can be seen here: https://prostatecanceruk.org/about-us/news-and-views/2022/03/joe-appiah-says-his-friend-saved-his-life.

Joe produced an awareness raising video with the cancer alliance, which can be viewed here: https://youtu.be/bp-KG7OWdX0

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Our guest is Stephanie Uys, Clinical Director for Targeted Lung Health Check Programme in north east London. Stephanie leads the Targeted Lung Health Check programme in north east London from a clinical perspective. She works for Barts Health and is also working with the cancer alliance on the programme. She is helping to drive uptake from both GP practices to get on board with the programme and also with patients so that more residents come forward for their free lung check. A key part of the programme is also about encouraging smokers to join a free, local smoking cessation programme which can help prevent lung cancer.

Lung cancer is one of the top 10 cancer types in north east London and nationally, around 50,000 cases of lung cancer are diagnosed every year (as stated on the Roy Castle Lung Cancer Foundation website).

Early stages of lung cancer often don’t have any symptoms. However, at an early stage it is easier to treat and so early diagnosis is the key. The Targeted Lung Health Check Programme is designed to find anything early, which is helping to save lives. It is available free to 55-74 year olds who have ever smoked and the programme is going well in north east London, with one of the highest uptake rates in the country.

This episode looks at the impact the programme is having on improving the health of our population through both checking lungs and helping people to quit smoking, while at the same time also helping to reduce health inequalities.

More information on the Targeted Lung Health Check Programme is here: https://www.nelcanceralliance.nhs.uk/tlhc

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Guest speaker: Victoria Curran, Centre Head, Maggie's Barts

Victoria leads the team at the wonderful Maggie’s Barts service, which provides warm, friendly support for cancer patients in a calming and relaxed setting. She is passionate about helping cancer patients through their treatment and has worked with North East London Cancer Alliance on a prehab video to help explain the benefits to patients. The video is available here: https://youtu.be/sQEISRtfAiY

Victoria provides an overview of her role and the support that is available at Maggie’s. The episode covers a wider look at prehab and its three core elements of diet, physical exercise and mental health and wellbeing. It looks at the benefits to patients of prehab and how all cancer patients can access these vital services across north east London.

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When Pamela was diagnosed, her immediate thought was that she was going to die. However, after surgery, chemotherapy, radiotherapy and immunotherapy she is now cancer free. Pamela wants to make a difference in her community by changing the narrative around cancer in minority communities and helping to raise awareness.

Pamela shares her breast cancer story, starting with her diagnosis and then moving on to her treatment and support. She introduces the great work of charity Black Women Rising, for which she is an ambassador, and talks about how we can help minority communities to come forward, like Pamela did, for life-saving treatment.

For more information on the North East London Cancer Alliance click here.

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Kevin has recently joined North East London Cancer Alliance as a patient partner and has lived experience of prostate cancer. Kevin is a Hackney resident and is passionate about the benefits of prehab, which helps cancer patients be as fit and as a healthy as possible for their treatment. He has also set up a community group for men to get together and share their experience of prostate cancer

Kevin explores his cancer story, sharing his experience of his original contact with his GP, his diagnosis, finding out the results, the treatment, and his experience of the prehab service which helped him prepare for his treatment. He provides invaluable insight for prostate cancer patients, as well as important information for men and their families who may not have had any experience yet of prostate cancer. In particular, Kevin talks about the importance of keeping fit and healthy following a cancer diagnosis, and how this gives you the best possible chance of recovery.

Steve and Kevin are also joined by North East London Cancer Alliance Chief Medical Officer Angela Wong.

For more information on the North East London Cancer Alliance click here.

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Professor Knight takes Steve through his own career, and explains how he came to be involved with the Alliance. He also talks about the challenges the Alliance faces in the incredibly diverse North East London, and the work that's going on to tackle those challenges.

About Professor Knight: 

Professor Knight served as honorary secretary of the British Cardiovascular Society from 2008 to 2011 and was associate editor of the journal Heart until 2014. He was a member of the Royal College of Physicians' Cardiology Speciality Advisory Committee.

Professor Knight is a specialist in alcohol septal ablation and a Fellow of the Royal College of Physicians. From 2010 he led the development of the Barts Heart Centre by merging cardiac services from across London to create the largest cardiac centre in the UK. He became the Centre’s first executive director in 2014. In 2015 he was appointed as managing director and then chief executive of St Bartholomew’s Hospital.

In March 2020, Professor Knight was seconded as chief executive officer of NHS Nightingale Hospital London, established to care for patients during the 2020 Covid-19 pandemic. In July he was awarded the Freedom of the City of London in acknowledgment of his role in the NHS’s response to the outbreak. In October 2020 he was awarded an OBE for services to the NHS and people with heart disease.

Find out more about the North East London Cancer Alliance here.

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