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Exploring the impact of Proton Beam Therapy on paediatric cancers

At the start of January, Dr Amy Chadwick and Dr Emma Biglin began the second year of a research project funded by the Children’s Cancer Research Fund (aka Friends of Rosie) to explore the potential of proton beam therapy in treating paediatric cancers. Over the first year of this study, they made significant strides in their research, focusing on how cells respond to this advanced form of radiotherapy under low oxygen conditions and in combination with different drugs. We recently caught with up Amy to hear more about their objectives for the second year of the project and how it may help children with Ewing sarcoma, osteosarcoma and rhabdomyosarcoma in the future.

Amy Chadwick The Christie
Dr Amy Chadwick
Emma Biglin
Dr Emma Biglin

Explains Amy, “There’s a growing body of evidence to show how cells respond to proton therapy, but it’s largely in adult cancers or using adult cancer models. However, a large proportion of the patients that are treated with protons are paediatric patients or teenagers and young adults. Today, there is very little published research looking specifically at proton beam therapy in children. That’s why we’ve picked childhood cancer models that represent diseases that are currently treated with proton therapy or that could benefit from being treated with proton therapy. Our research looks at the difference in how cells respond to conventional radiotherapy using X-rays or proton beam therapy using protons.

“We also know that some of these tumours are quite resistant to radiotherapy. So, our project is focused on how we can combine other drugs or medicines with radiotherapy to see whether we can make it more effective. The long-term goal will be to increase the effectiveness of proton beam therapy or conventional radiotherapy in children with these cancers, while at the same time minimising the side effects.

Continues Amy, “On the run up to 2025, we’d already managed to conduct several experiments and gather valuable data which meant we were able to hit the ground running once the project formally commenced in January.

“Doing experiments using the proton beam differs significantly from conventional radiotherapy with X-rays. It is very precise and involves physics expertise. It’s critical to get the position of your samples right and we’re fortunate at the Proton Beam Therapy Centre to have a multidisciplinary team of biologists and physicists working in collaboration with us.”

Unique Research Facility

One of the unique aspects of Amy and Emma’s work is the dedicated research facility they have access to – The Proton Beam Therapy Centre at The Christie Hospital in Manchester. This facility, located within a clinical proton therapy treatment centre, allows them to conduct experiments in their dedicated proton therapy research facility, alongside clinicians who treat patients. This collaboration has been instrumental in identifying key research questions and maximizing their experimental output.

Research room at The Proton Beam Therapy Centre Continues Amy,Conducting experiments with proton beam therapy is no easy feat. We can only access the proton beam during late evenings or at night when it is not being used for patient treatments. To make the most of this limited and expensive resource, we have developed infrastructure to maximize our throughput.

“This includes studying the impact of proton beam therapy under low oxygen conditions, termed hypoxia, which are common in solid tumours and can make them resistant to radiation. Most solid tumours will have some regions of hypoxia, and these regions are important for radiation because they are radio resistant. The presence of hypoxia in a tumour is a key predictor of poor outcome following radiotherapy in multiple tumour types. So, we were keen to study the impact of proton beam therapy under low oxygen conditions.”

In their first year, the team carried out high-throughput drug screening on 355 compounds in combination with proton beam therapy under hypoxic conditions. This leading-edge work has yielded promising results in year one, and we believe they are the only team in the world with this capability, making this research particularly significant.

Looking Ahead

proton beam therapy
Robotic arm holding a sample in the proton beam.

As they move into their second year of research, Amy and Emma aim to validate the drug combinations they found to be effective. They will expand their research to different models and further understand how these combinations work.

Concludes Amy, “Our goal is to increase the effectiveness of proton beam therapy, with potential to decrease the dose of radiation to reduce the side effects for children with cancer. We’re already having discussions with other collaborators to look at the potential to translate our findings into real-world treatments that could benefit children with cancer. By the end of our second year, we aim to publish our work and secure larger grants to continue this pioneering research.”

This research has been made possible thanks to the donations of our supporters. A two-year study like this one costs around £150k and it’s only possible because of the various fun-runs, bake sales, raffles, donations, and corporate support from people up and down the country.

You can make a difference to children with cancer by supporting more research.

Be the difference and get involved today.
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.