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£70,000 awarded to pioneer new treatment approach for aggressive childhood cancer

To mark International Clinical Trials Day (20 May), we are proud to announce our latest research grant award – pioneering research that could lay the foundations for a completely new way of treating high‑risk neuroblastoma, one of the most aggressive childhood cancers.

This £70,000 research grant, supported by two other charities, Joseph’s Smile and The Bradley Lowery Foundation (BLF), will enable scientists at the University of Bristol to explore a promising new treatment strategy that targets subtle molecular weaknesses in neuroblastoma cells.

Around 100 children in the UK are diagnosed with neuroblastoma each year. Despite intensive treatment, approximately half face a high‑risk form of the disease where long‑term survival rates remain unacceptably low. Progress depends on early‑stage research that can open the door to future clinical trials – making this collaboration especially timely.

Exploring a new therapeutic pathway

Led by Professor Karim Malik, the Bristol team aims to uncover subtle molecular weaknesses that drive the most aggressive neuroblastoma tumours. Unlike many adult cancers, neuroblastoma does not typically carry large numbers of genetic mutations. Instead, it appears to rely on more subtle changes within cancer cells – changes that may expose vulnerabilities researchers can target.

Early findings from Professor Malik’s team suggest that disrupting certain branches of fatty acid metabolism can dramatically reduce neuroblastoma cell survival. Such fatty acids can regulate how proteins function within cells, and neuroblastoma cells appear to be particularly dependent on these processes to survive and grow.

The project will investigate two drugs that interfere with fatty acid metabolism. Crucially, both drugs are already in clinical trials, raising the possibility that – if successful – this research could provide the springboard for the development of new rationalized treatments for neuroblastoma patients in the near future.

The research aims to lay the foundations for an entirely new treatment strategy for children with high‑risk neuroblastoma, and potentially other childhood cancers that share similar biological features.

Thank you for standing with us and helping us continue Rosie’s legacy.

If you wish to make a direct contribution to this promising project, please click below to donate.

“On International Clinical Trials Day, this collaboration shows the power of charities uniting behind a shared mission. By funding early stage research like this, we aim to accelerate discoveries that could genuinely transform the future for children and families affected by neuroblastoma. Rosie, Joseph and Bradley’s legacies drive us to push for better, kinder treatments.”

“This funding allows us to explore an exciting and under‑researched area of neuroblastoma biology. We are extremely grateful to CCRF, Joseph’s Smile and BLF for their support and for their commitment to improving outcomes for children with this devastating disease.”

“At BLF, we are proud to support this vital research. Progress will only come through research, and we hope this contribution helps create a future where more children survive cancer. Having lost Bradley to neuroblastoma, I know how desperately families need hope. Supporting research is one way of fighting for a future where fewer families endure that pain.”

“As a charity created in Joseph’s memory, we are incredibly proud to support this pioneering research. Backing innovative projects like this is at the heart of why we exist. Knowing that this work could one day lead to kinder, more effective treatments for children like my nephew Joseph, Rosie and Bradley gives us real hope, and we are honoured to stand alongside CCRF in driving progress forward.”

Nancy Dykes

Nancy Dykes

Nancy, 11, was diagnosed with rhabdomyosarcoma when she was just 2 years old. She was treated with Proton Beam Therapy (PBT) in Germany but unfortunately relapsed less than a year later. The family were then sent to Germany for a second round of PBT. Although treatment helped to cure Nancy’s cancer, she has been left with lots of lasting effects which will require ongoing treatment throughout her life. Here Nancy and her mum, Antonia, share their story in the hope it will help others, raise awareness, and raise more money for children’s cancer research.

Prof John Hickman

Prof John Hickman

Why I am a Trustee of CCRF
 
I am a relative of the Larkin family and knew Rosie Larkin ( Friends of Rosie, now CCRF) when she had and then died of neuroblastoma, aged six. At that time, I was a scientist and professor at Manchester University, actively working on the problem of why some cancers do not die despite intensive and toxic therapies.  Seeing Rosie during her unsuccessful therapy and then attending her funeral, besides being emotional, drove me to double down on my own research as well as to support the Charity as best I could as a cancer researcher. I spent over a decade as the Chairman of the Scientific Advisory Board of the CCRF, when the Board moulded policies to ensure that funds raised for research into childhood cancers were distributed only to clinicians and researchers who had the brightest ideas that could impact of cancer medicine for children.
 
My role on the Board
 
As a Trustee,  I hope that my many decades of experience in cancer research and medicine can help the CCRF determine where best the funds that are raised can be invested in cutting edge research and medicine. I am also keen that the CCRF brings together UK and international experts in science and cancer medicine to brainstorm on how best to advance the treatment of childhood cancers.
 
My Background
 
I was a Professor of Pharmacology at Manchester University, working on drug resistance in cancer. I then moved to Paris, where I still live, to head cancer drug discovery at a French pharmaceutical company (Servier). I then headed an EU consortium for six years that brought together researchers from the pharmaceutical industry, universities and biotechnology companies, from all over Europe and the UK, to improve cancer drug discovery. I continue to be active in cancer health policy, publishing in the medical literature.
Katrina

Katrina London

Why I am a Trustee of CCRF

I have spent my professional career representing individuals and families affected by the devastating asbestos-related cancer, mesothelioma, which has no cure and for which there are only a limited number of palliative treatments available on the NHS.

I joined CCRF because I wanted to bring my understanding of the need to raise awareness of less well known cancers and passion for the need to secure improved funding for research to children facing a cancer diagnosis.

My role on the Board

I am responsible for oversight of our collaboration agreements with other charities to co-fund research into cures and treatments for childhood cancers. I also manage our challenge events and help with community fundraising. 

My Background

I am a Senior Associate at Irwin Mitchell LLP and specialise in Asbestos Disease Litigation, acting on behalf of victims of asbestos related diseases and their families.  Over the years, I have undertaken a number of fundraising challenges to raise money for cancer research, including a 1000 mile cycle ride from Glasgow to Southampton.   

Carla

Carla Nuttall

Why I’m a Trustee of CCRF
 
I became a trustee of the Children’s Cancer Research Fund because I believe every child deserves the chance to grow up healthy and with everything to look forward to in life. Like many people, I’ve seen the impact cancer can have on families and I wanted to do something that could make a real difference. This started through my work as an ambassador for Cyclists Fighting Cancer, which supported young people and their families in finding strength, confidence, and joy through movement.
 
That experience shaped my understanding of the challenges families face and the importance of community-led support – but crucially, the clear need for that to go hand-in-hand with targeted research and long-term solutions.
 
This is why I’m so passionate about the work CCRF does and proud to contribute to a cause that gives children and their families, the greatest chance of living a life without limits.
 
My Role on the Board
 
I support CCRF’s mission by bringing my experience in brand, marketing, and communications to the board. My focus is on helping CCRF tell its story in a way that resonates with people – whether that’s families, researchers, donors, or the wider public. I work alongside an incredible team to strengthen CCRF’s voice, build trust, and grow awareness so that more children and families can benefit from the breakthroughs we’re helping to fund.
 
My Background
 
I’m the Executive Director of Corporate Affairs and Marketing for The Growth Company, a social enterprise dedicated to helping people, businesses, and places to thrive through its market-leading insight, employment, skills and business support.
My passion is to help the organisations I work with to communicate with clarity, purpose, and integrity. That’s why I’ve spent my career in strategic communications supporting organisations that want to make a positive difference – CCRF could not fit my sense of purpose any better.