Quarterly Newsletter Autumn 2024 - September Issue
Molecular Radiotherapy Conference 2 day event in London, 8th-9th November
Introducing the Hero Awards 2024! Exciting new awards for the neuroendocrine cancer community Daily Dip 4 Dave - Join in on 12th October! Our incredible supporter, Ruth is taking her 365th dip to raise awareness and funds
www.neuroendocrinecancer.org.uk Registered Charity Number: 1092386
Contents
WELCOME
NEWS
FUNDRAISING
AWARENESS
ADVOCACY
EDUCATION
SUPPORT
STORIES & EXPERIENCES
RESEARCH
www.neuroendocrinecancer.org.uk
Contact details
We’re here to assist you in any way we can. Whether you have questions about neuroendocrine cancer, need support, want to get involved with our activities, or have any other enquiries, we’re ready to help. Please feel free to reach out to us using the contact information provided below. We look forward to hearing from you and offering our assistance.
Helpline 0800 434 6476 Tuesday – Thursday (Excluding Bank Holidays) 10:00am – 4:00pm
Speak confidentially with our support services team for information and advice through our helpline.
Please note – The Helpline is not a general enquiry or emergency line. If you require urgent medical assistance, please contact emergency services and inform your specialist team.
Other Enquiries 01926 883 487 Monday – Thursday (Excluding Bank Holidays) 9:00am – 3:00pm
For general enquiries, or to contact a member of our administration or comms teams.
Alternatively, you can use our contact form to get in touch: CLICK HERE
www.neuroendocrinecancer.org.uk
Welcome
Hi everyone,
September…eeeek! Our world here at Neuroendocrine Cancer UK really ramps up as we prepare for the programme of activities for the end of the year and plan for 2025. I truly hope there is something for everyone in the coming months including: A chance to think about your hero… A chance to support a wonderful lady who has been cold water swimming for the past year and does her 365th swim on the 12th of October – we all have the chance to join her on this momentous occasion. Check out the website and get the date in your diary. Literally any activity related to cold water is brilliant, so PLEASE join us! A chance to attend a healthcare professional education day A chance for patients/families/friends to come together to talk all things treatments with a focus on Molecular Radiotherapy treatments Our grant applications for research go live – a chance to fund your research into neuroendocrine cancers A chance to join the global community and raise awareness on November 10th A chance to get involved in a research study The start of this late summer/early autumn season was such a positive one, as I attended the INCA Summit, and heard about all the inspiring work happening across the globe to improve the lives of those affected by neuroendocrine cancer. Over 30 representatives of INCA member organisations together with the ENETs and NANETs leaders and our own UK expert Professor Ramage came together for 2 days to discuss our challenges, but also our hopes and aspirations for the advancement of education, support and research in neuroendocrine cancers.
Thank you, as always to all who have supported us. It means everything.
If you found this newsletter useful, interesting or inspiring then please do share far and wide!
Catherine Bouvier CEO Cathy
News
Neuroendocrine Cancer UK Hero Awards 2024!
These brand new awards aim to recognise and celebrate members of the neuroendocrine cancer community with 5 award categories to choose from:
Someone living with neuroendocrine cancer Neuroendocrine cancer nurse Neuroendocrine cancer doctor / surgeon Friends / family / supporter Fundraiser
Although neuroendocrine cancer is the 10th most prevalent cancer in England, awareness remains low. Through these awards, we aim to raise the profile of neuroendocrine cancer and increase public awareness. Please help us in this mission by sharing news of the awards directly from our social media pages or by visiting our website below.
I nominate...
KEY DATES:
Nominations open Monday 23rd September Our judging panel will select finalists end of October Public vote in November 2024
For more information please visit our website: www.neuroendocrinecancer.org.uk/hero-awards
or email: comms@nc-uk.org
www.neuroendocrinecancer.org.uk
If you have any news you’d like to share with us – whether it’s about a fundraiser you’re organising or neuroendocrine cancer in the news, please let us know by emailing us : hello@nc-uk.org
News
Thank you so much to the almost 1000 of you who completed our survey to enable us to continue to meet your needs and support you in the way you want to be supported. Your feedback has been so helpful. We have just finished analysing it and including it in our upcoming new strategy. We will come back to you shortly with the information we learned from you and the suggestions we have included in our plans going forward. Shape the future of Neuroendocrine Cancer UK - Update Thank you for your input!
We really appreciate the time you all spent providing us with this invaluable insight, thank you for your support.
NHS Long Term Planning & Integrated Care Board Meeting On Tuesday 10th September, our Campaigns Lead, Lisa attended the NHS Long Term Planning and Integrated Care Board meeting at the Royal College of Medicine. Overall, the event was both productive and insightful, and we remain dedicated to advocating for the neuroendocrine cancer community, now and in the future.
www.neuroendocrinecancer.org.uk
Fundraising
Daily Dip for Dave
Another member of our remarkable fundraising community is Ruth and her ‘Daily Dip 4 Dave’ challenge.
Since October 2023, Ruth has been taking a daily dip in the cold sea, every single day, in honour of her husband, Dave, who was diagnosed with neuroendocrine cancer. Ruth’s journey has been nothing short of incredible— dipping through stormy weather, freezing temperatures, and relentless waves—all to raise awareness and funds for Neuroendocrine Cancer UK. It’s been tough, both physically and emotionally, but Ruth’s determination and love for Dave have inspired so many along the way.
Feeling inspired to take the plunge!? Well, here’s your chance!
On 12th October, Ruth will mark her 365th dip, a full year of showing up, no matter what. To celebrate this milestone, we are inviting 365 people to join us in any way they can—whether it’s dipping in the sea, a lake, a cold shower, or even dipping your feet in a bucket of cold water at home.
Please CLICK HERE to visit our website to read more details of how you can take part!
www.neuroendocrinecancer.org.uk
Fundraising
The dulcet tones of a very special fundraiser! Jane & Rumer
We would like to take this opportunity to highlight one of our amazing fundraisers this month. Jane Kenny was diagnosed with neuroendocrine cancer 7 years ago and after some recent treatments she decided she wanted to create her own fundraising event. Jane has been a fan of a British singer-songwriter Rumer for years. She attended a gig to see her, unfortunately she was no longer performing that night. A friendship was created between Rumer and Jane, she reached out and Rumer agreed to perform at her charity night.
We reached out to Rumer for a comment:
“When I started to get to know Jane, I admired her strength and her spirit. Despite all that was on her plate, she was determined to organise an event to raise awareness for neuroendocrine cancer. I knew I had to help Jane in any way I could. It was such a great night at Wood Lane Social Club and I was delighted to help raise awareness for this important cause”.
Jane has worked tirelessly during this event, with a radio interview on Liverpool Live Radio and her story in the Liverpool Echo all in the pursuit of awareness of neuroendocrine cancer. To date, Jane’s page has raised an amazing £2046.55!
Thank you, Jane & Rumer!
Here is a lovely video from the day:
www.neuroendocrinecancer.org.uk
Cakes for a Cause
Thank you so much to those of you who took part in our Cakes for a Cause event in June. It was lovely to see the community come together to have a cup of tea and a cake and talk about neuroendocrine cancer.
We raised an incredible £4451.50 and will be repeating this event in June 2025 where hopefully we can raise even more awareness of the condition.
The money raised will go towards our support services, which this month alone has seen a 70% increase in Helpline calls compared with June 2023
You raised an amazing £4451.50, THANK YOU!
www.neuroendocrinecancer.org.uk
Fundraising
We’ve had some truly incredible fundraising recently as well as some more exciting events coming up, so keep reading to find out more!
Loz runs 145 miles in memory of his parents.
We are so honoured that Loz undertook this incredible feat to raise funds for Neuroendocrine Cancer UK as well as Birmingham Children’s Hospital and the British Heart Foundation. Loz decided to run a coast to coast route from Seascale in Cumbria to Whitby in Yorkshire. As a passionate runner, Loz said: “Through panic attacks and dark days, I’ve found solace in putting one foot in front of the other, knowing each step is a step forward in healing. This run is my tribute to my parents and a way to support the causes that meant so much to them”. Thank you, Loz. What an incredible achievement! At the time of writing this, Loz has raised an incredible £5215 for charity! HE DID IT! 145 MILES !
@neuroendocrinecanceruk @ncukcharity www.neuroendocrinecancer.org.uk
www.neuroendocrinecancer.org.uk
Awareness Centres of Excellence Outreach Can you help? As part of our outreach work and continued support for healthcare professionals, we will be visiting the neuroendocrine cancer centres of excellence over the coming months to highlight the full range of services we offer and encouraging them to let their patients know about us. Please see the poster below to learn how you can help or email comms@nc-uk.org if you feel you can volunteer to visit one of the CoE near you.
Full list of Centres of Excellence can be found HERE
www.neuroendocrinecancer.org.uk
Advocacy
PODCAST NOT JUST NE CANCER For those affected by neuroendocrine cancer.
The Realities of Living with Neuroendocrine Cancer
Join us for a truly insightful conversation with two of Neuroendocrine Cancer UK's Ambassadors, Lisa and Alan. Lisa and Alan share their personal journey, offering an honest account of navigating medical appointments, seeking the best treatment options, and dealing with the emotional ups and downs that come with being your own advocate. In our latest Not Just NE Cancer podcast, we discuss the realities of self-advocacy while living with neuroendocrine cancer. Join us as we explore the challenges and triumphs of advocating for oneself in the healthcare system. Submit Questions or Topics: Have a question or topic you’d like us to cover? Click here to submit your suggestions and we might feature them in a future episode!
www.neuroendocrinecancer.org.uk
Education - HCPs
PERT Webinars for HCPs Healthcare Professional Webinars: PERT and what to do during current shortages As part of our ongoing commitment to work together with healthcare and allied healthcare professionals, alongside charity colleagues, to improve patient care, access to best treatments, and ultimately to improve the patient experience, and outcomes, we are delighted to share 2 key information and educational opportunities.
These free to access webinars were hosted by Pancreatic Cancer UK:
On Tuesday 17th September from 9am-10:15am the 1st webinar is for HCPs & CNSs – for further details and to check for recordings of the event visit: https://www.pancreaticcancer.org.uk/health-professionals/events-for-health- professionals/pert-shortage-guidance-cns-dietitian On Wednesday 18th September from 6pm-7pm the 2nd webinar is for GPs and Pharmacists – for further details and to check for recordings of the event visit: https://www.pancreaticcancer.org.uk/health-professionals/events-for-health- professionals/pert-shortage-guidance-gps-pharmacists
**The charities collaborative working group are meeting monthly to advocate and work on solutions**
To keep up to date with the latest news from Neuroendocrine Cancer UK, please visit the News section of our website: https://www.neuroendocrinecancer.org.uk/news/
www.neuroendocrinecancer.org.uk
Education - HCPs Spotlight on Neuroendocrine Cancer Update The ‘spotlight on neuroendocrine cancer’ campaign aims to raise awareness of neuroendocrine cancer among non-NC specialist healthcare professionals. The campaign is in collaboration with the UK and Ireland Neuroendocrine Tumour Society (UKINETS). An overview of neuroendocrine cancer for healthcare professionals’ series To enable us to raise awareness of neuroendocrine cancer for healthcare professionals we are creating a series of overviews for different HCP disciplines. The aim of these is to act as a bite-size, practical educational aid to support HCPs to suspect and know how to support potential neuroendocrine cancer patients. We have just completed an overview for endocrinologists and oncologists to add to the collection. To date we have created an overview for GPs, gastroenterologists, general surgeons and a general one for all HCPs. Dissemination of our educational and awareness materials It is so important not just to create the materials we do but to ensure that they go out to the relevant healthcare professionals. Please help us spread the word by directing your medical team to the HCP page on the website: www.neuroendocrinecancer.org.uk/hcp Neuroendocrine cancer awareness for medical students Neuroendocrine cancer, like many less common cancers, is not included in the syllabus at many medical schools. We would like to increase awareness of the disease among medical students and to this end are working on a series of videos to raise awareness of neuroendocrine cancer among medical students and healthcare professionals. The format will be a Q&A between a patient and a student. In the videos those with the disease discuss their symptoms and journey to diagnosis. We are currently in the process of editing them.
www.neuroendocrinecancer.org.uk
Education
Molecular Radiotherapy Conference In partnership with UKINETS - 8th & 9th November 2024 This conference is intended to provide a platform to discuss issues that we have here in the UK regarding access and availability of Molecular Radiotherapy (MRT). The conference will take place over 2 days; the first day is designed for medical professionals and the second will be a face to face patient meeting on treatments in neuroendocrine cancer with a specific focus on molecular radiotherapy.
Interested medical professionals can CLICK HERE to learn more and can sign up using the button below.
SIGN UP
Further information on the patient event will be shared on our website, mailing list and social media channels shortly.
VENUE : MARRIOTT HOTEL, REGENTS PARK, LONDON, NW3 3ST NEAREST TUBE : SWISS COTTAGE UNDERGROUND
Thanks to our sponsors:
www.neuroendocrinecancer.org.uk
Education - Community
September’s National Online Webinatter ‘The most important person in the room - YOU!’
Professor Was Mansoor
September's Guest Webinar Speaker was LUNG NETS specialist Prof Was Mansoor from The Christie NHS Foundation Trust which took place on Tues 10th September. During the webinar he discussed why the Patient is the Most Important Person in the room - and he took a Q&A session on Lung NETS. A recording of this webinar will be made available soon after the event, in case you weren’t able to make it. You also check out other past webinars HERE.
CLICK HERE to see all future webinar events on our website.
www.neuroendocrinecancer.org.uk
Support
Manchester In-Person Natter
Manchester’s Natter group met again in-person on 11th September at the beautiful Didsbury Parsonage Trust on Stenner Lane, Didsbury, M20 2RQ with patients attending both from The Christie Manchester and Liverpool NET Centres of Excellence. The Manchester Natter group is going from strength to strength, so please do come along to join us next time, especially if you are newly diagnosed and seeking information and support.
The meeting is free and friendly.
You can bring your partner if you like and we even have an Assistance Dog with us.
The Manchester Natters are held quarterly on a Wednesday: 11:00–13:00 and the next date in 2024 will be 4th December.
www.neuroendocrinecancer.org.uk
Support
New Nottinghamshire Natter We are delighted to announce our new Peer Support Group for Nottinghamshire - and would like to thank Nottingham’s own ‘NET’ nurse specialist Hannah B, and Maggie’s Nottingham, for their support in getting this group up and running. 29 people attended the first meeting, and here is some of the feedback from the 1st meeting:
support
sharing understanding together continuity informal information courage
belonging
contact
networking
community
listening
hope
social
empathy
Hannah has been vital to this group’s start: she has advocated across the hospital, encouraging colleagues to signpost and direct patients, and their loved ones, to the group, and has timetabled her own participation, to facilitate the group, as part of her work schedule.
She asked the group what matters most to them. Topics discussed and suggested included:
Peer Support: Regular meetings, informal setting, shared experiences, being heard, belonging, having someone present their experience...
Diet & Nutrition: Menu sheet, alcohol advice (can they have alcohol?), PERT information, how diet may help symptom management...
Information - and where to find it: NETs / NECs / Carcinoid: ALL types of NC not just the most common, access to info in different forms not just online, alternative and complimentary therapies, treatments, what comes after PRRT?, what happens after surgery - e.g., post-op exercise.
Self-care: Emotional support, financial support, family & friends support, general exercise and activity information
Involvement in research/trials.
www.neuroendocrinecancer.org.uk
Sources of support: Neuroendocrine Cancer UK - a member of the team to come along, Maggie’s - use outside of the group...
Amongst many others... that we’ll be working with Hannah to provide.
The group meets every 3 months on the 1st Tuesday of the month.
The next meeting is scheduled for Tuesday 3rd December - starting at 10am, with dates for 2025 already penciled in.
The meeting is held at Maggie’s Centre, Nottingham - click HERE for information on the Centre and how to get there.
Contact Nikie or Kate for further details of this and other Support Group Meetings held, in person or online, across the UK - or visit the Events Calendar on the website to find one for you.
Click HERE to visit the Natter Support Group Guide
www.neuroendocrinecancer.org.uk
Support
The Virtual Patient Handbook 25,000 views!
We are extremely proud to say that the virtual patient handbook that was released in October 2023 has now received over 25,000 views! We sincerely hope that this resource is a reliable and informative centralised document for those newly diagnosed or living with neuroendocrine cancer. If you haven’t visited the handbook yet, or if you have but found it a bit difficult to navigate, here are a couple of tips that may help you find your way around:
Click on the image above to visit the handbook
At the bottom of the page you will find a toolbar. If you click the icon outlined in red it will show a table of contents. This way, you can quickly move between sections. At the top right hand corner of the page you will find a magnifying glass icon. This is a very powerful search tool. You can type any keyword and it will list every page in the handbook that includes a mention of that search term. You can then click directly to that page.
Lastly, we would like to thank everyone who completed our recent survey asking for feedback on your experience using the handbook. It is extremely helpful for us to see how certain elements of the handbook work in practice and we have taken your comments onboard. As a result, we will be making changes to the handbook over the next year but you will still be able to access the handbook as usual during this process.
www.neuroendocrinecancer.org.uk
Educational Webinars Empowering our community with knowledge & understanding
We’ve had some fantastic educational webinars throughout 2024 and we are excited to continue hosting these expert-led, hugely informative, free events into 2025 and beyond! If you access these webinars and find them helpful, please consider donating to Neuroendocrine Cancer UK so that we can continue to produce these free resources for the whole community for years to come. More information on how to donate can be found here: https://www.neuroendocrinecancer.org.uk/donate/ Here are a list of webinar speakers and topics that have taken place so far. As an added bonus, you can click on the links to access the recording of the webinar on YouTube. Dr Christine May - Endocrinology & Hormones Dr Zahir Soonawalla - Surgery for Pancreatic Neuroendocrine Tumours Mrs Christina Nuttall & Dr Melissa Frizzerio - MDTs in Cancer Care Dr Elle Reed - Living with a Life-Limiting Illness Mr Mike Tadman - Treatment Decision Making Dr Philip Lodge - Palliative Care Consultant (Video coming soon) Prof Was Mansoor - Medical Oncologist, The Christie (Video coming soon) Mrs Wendy Martin - Advanced Nurse Practitioner (Video coming soon)
www.neuroendocrinecancer.org.uk
Stories & Experiences
Pushing for a Pathway Chris, our newest Ambassador talks about his experience of diagnosis and treatment as well as the importance of a neuroendocrine cancer pathway
Name: Chris Neuroendocrine Cancer Site: Lung Hospital: Royal Free
We’re delighted to welcome Chris from Wiltshire, who has just joined our Neuroendocrine Cancer UK Ambassador team. Chris was diagnosed in February 2021 by a private lung specialist at the Spire Bristol Hospital, with a primary in his lung known as an Atypical Carcinoid. In terms of Lung NET classifications (sometimes called pulmonary NETS or bronchial NETS), there are 2 main classifications: TC (Typical Carcinoid) and AC (Atypical Carcinoid). These are differentiated by their KI67% score and Chris’s was Ki67 <5% … so AC.
Chris’s Story Initial Diagnosis and Chemotherapy
I had a course of chemotherapy quite quickly after diagnosis, doing 4 out of 6 cycles of Carboplatin and Streptozocin but it was unsuccessful. I asked for a second opinion at The Royal Free London but they didn’t think surgery was feasible. Luckily, one of the Consultant Thoracic surgeons – Dr Igor Saftic at Bristol Royal Infirmary – agreed to try to remove my main tumour and I credit him with saving my life. There’s always more than one way to approach cancer, in my experience.
www.neuroendocrinecancer.org.uk
In Sept 2021 I had a right lung pneumonectomy followed by 5 weeks in the hospital and almost a month in ICU (intensive care unit) for a herniation of the heart, pneumonia, and an infection. In August 2022, I started to get some back pain and was referred for an MRI Spine. Then an FDG-PET scan showed multiple sites of bone metastases including my spine, hips, shoulder, left leg, and the base of my skull. This is where I believe self-advocacy comes in. At this point, my local cancer team hadn’t consulted with The Royal Free London NET Centre of Excellence and as a result, told me that only radiotherapy to control pain was an option for me … and that my prognosis was around 12 months. Naturally, I couldn’t accept this. I rang The Royal Free London myself and spoke with Prof Caplin, head of the team. We agreed to try both Lanreotide monthly injections and Everolimus, an oral targeted therapy. I didn’t tolerate Lanreotide very well so came off it – but I’ve tolerated Everolimus well so far and at the time of writing (August 2024) I remain on it. Today, I still take some strong opioids for pain relief but I’m living a fairly normal life. My employer has been fantastic. They understand I have good days and bad days, and hospital appointments – and being able to work keeps me mentally strong. I used to be a keen footballer and cricketer but these days I enjoy watching rather than playing – but that doesn’t stop me from fundraising at these events too. I also enjoy exploring our beautiful coastline and countryside with my partner, Gemma, and our dog, Arnold. Being in nature definitely helps me. So why be an Ambassador? Well, I find it incredible that our NHS still has no formal recognised pathway for neuroendocrine cancer patients. There should be a structured approach to diagnosis, treatment, and follow-up in place, as there are with other, more widely recognised cancers. In my view, it’s only earlier diagnoses that are going to make a difference to us – and we definitely need the ‘age box’ removed from the tick list. I was 34 and although I ticked all the other boxes for a cancer referral, it didn’t happen because I was ‘an under 40 normally fit and healthy person.’ I’m looking forward to helping try to change this.
Thank you, Chris! We’re so happy to have you onboard as a Neuroendocrine Cancer UK Ambassador!
We're always on the lookout for people who are willing to share their experiences with neuroendocrine cancer. If you would like to share yours, please CLICK HERE.
www.neuroendocrinecancer.org.uk
Research
Over the following pages we will be highlighting some current studies that are open for recruitment.
LANTana: RECRUITING
Patients with neuroendocrine tumours (NETs).
Assessing feasibility of ASTX727 to re-express SSR2 in those with negative/low uptake [68Ga]Ga-DOTA-TATE-PET/CT who would be otherwise ineligible for protein radionucleotide receptor therapy.
Key Eligibility:
Histologic diagnosis of NET (Ki67 <55%) No or low uptake on [68Ga]Ga-DOTATATE- PET/CT ≥1 prior therapy
CLICK HERE to read more on the clinicaltrials.gov website.
Referrals for this study will be through your specialist clinical team.
www.neuroendocrinecancer.org.uk
NELMAS Study
Comparison of Adjuvant Treatment With 177Lu-DOTATATE to Best Supportive Care in Patients After Resection of Neuroendocrine Liver Metastases (NELMAS). An international multi-centre, open, randomised, parallel-group phase II study comparing adjuvant treatment with 177Lu-DOTATATE to best supportive care in patients after complete surgical removal of neuroendocrine liver metastases.
CLICK HERE to read the study overview, full eligibility and exclusion criteria.
Referrals for this study will be through your specialist clinical team.
BackSOM Study
A Study to Understand Participant's Experiences in Gastro-enteropancreatic Neuroendocrine Tumors (GEP-NETs) and Acromegaly (BackSOM)
Participants of this study are adults with GEP-NETs and/or acromegaly who were using the Ipsen lanreotide syringe and have transitioned in the last 6 months to the Pharmathen lanreotide syringe, having received at least two injections using the Pharmathen syringe.
CLICK HERE to read the study overview, full eligibility and exclusion criteria.
Referrals for this study will be through your specialist clinical team.
www.neuroendocrinecancer.org.uk
Research
Research is fundamentally important as a means of providing a better understanding of any disease and therefore improving understanding and management options. We are very proud to be using our Advancing Research campaign to have a meaningful impact on how neuroendocrine research is done. Advancing Neuroendocrine Cancer Research Update
The objective of this campaign is to raise funds for NC research to support those with the condition both today and in the future.
We are so grateful to our community for enabling us to fund this research through their generous donations. Thank you so much for your support, we really appreciate it. For those wishing to donate, please visit our website for more information: https://www.neuroendocrinecancer.org.uk/donate/
Neuroendocrine cancer receives very little funding for research. 46% of overall spend on cancer research is on the four most common cancers. 54% of overall spend on cancer research is on rare and less common cancers. However, this 54% is being split among 100+ rare and less common cancers. Source: Cancer52
www.neuroendocrinecancer.org.uk
Practice-changing Grants
The aim of these grants is to find new and practical ways to improve the lives and experience of people with neuroendocrine cancer (outcomes must be shown within 12 months). These grants are practical in nature, open to any healthcare professional and must demonstrate a clear benefit for people with NC. Please see the video below from Dr Charlotte Fribbens, for an update of the practice-changing grant we awarded in December 2023 to the Royal Marsden for their project: Evaluation of the impact on quality of life of a NET specific pathway for patients, utilizing the MyMarsden patient app, together with integration with Advanced Nurse Practitioner led NET clinic.
Pump-priming grant
We are opening the 2024 Pump priming grants now and will award 2 x £25,000 awards in December of this year.
The aim of this grant is to provide pump-priming funds to support research projects designed to improve outcomes for patients with neuroendocrine cancer.
www.neuroendocrinecancer.org.uk
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