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Friends of

£66,500 grant for immunotherapy study

We’re delighted to report encouraging results from our research project investigating the use of immunotherapy to treat childhood brain tumours that are resistant to conventional treatment methods. Results obtained so far and the great potential of this project have now led to a further £66,500 being granted by Friends of Rosie to continue this research for a second year.

During 2017/18 we funded a £65,000 project, conducted at the Manchester Cancer Research Centre facilities on the Christie campus in south Manchester, to research the use of immunotherapy to treat childhood brain tumours that have a poor prognosis.

The project is investigating the feasibility of using cells called Tumour Infiltrating Lymphocytes (TILs), created by a child’s own immune system, to shrink or destroy brain tumours in children, also known as immunotherapy. Solid tumours are made up of a variety of cells, not just cancer cells. TILs are white blood cells that have left the bloodstream and travelled into the tumour to destroy cancer cells. However, there may not be enough of them within the tumour to shrink or eradicate it.

Exciting findings

Dr Gray Kueberuwa, lead Friends of Rosie funded researcher, reveals the exciting findings from year one of this immunotherapy research, “Within tumours there is a constant battle. The immune system attempts to destroy tumours, while tumours attempt to adapt and evolve to survive this attack. In children that develop tumours, the immune system is losing the battle. Immune cells are often suppressed or “switched off” by the tumour cells.

“The past twelve months of this project have focused on four key areas. Firstly, we needed to adapt our methods to the use of small numbers of cells. When removing a tumour from a child’s brain it is clearly of the upmost importance not to inflict damage. This is often the barrier to surgeons being able to remove the whole tumour. Then, once removed, the majority of the tumour will be used by the diagnosing doctor to characterise the type of tumour and therefore, the types of treatments that stand the best chance of working. This leaves just a small sample for our research.

“So we needed to come up with an effective way to grow more TILs in the lab. We did this by using other tumour types, such as breast cancers, to identity the best conditions for growth. We then obtained two childhood brain tumour samples and applied these techniques to grow more TILs.

Next steps

The next stage of the project was to better understand the component parts of the TILs using a process called cytometry. Says Dr Kueberuwa, “During this project we were able to use the most advanced technology to analyse the cells. This allowed us to identify the immune cells present in the brain tumour samples in a way that has not been possible before now.”

The final step was to see how the lab-grown immune cells affect the tumour. A new and advanced measurement method was used to measure multiple parameters of the immune response. This showed that TILs activated their cell-killing mechanisms when they were in contact with tumour cells, providing evidence that they could potentially be developed as a therapy for paediatric brain tumours.

These promising first year findings led to the Friends of Rosie Scientific Advisory Board (SAB) recommending a further year of funding for this project. Says SAB Chair, Professor John Hickman, “The results we’ve seen so far are very exciting as they provide evidence that TILs and immunotherapy could have the potential to be used as a therapy for rare childhood brain tumours. This second year of funding is needed to obtain more samples to investigate whether the results seen so far are reproducible in other types of childhood brain tumours, particularly those with very few treatment options.”

In May 2017, 20-month old Gracie Greenwood lost her battle with cancer after a nine-month fight against an extremely rare brain tumour. Says Gracie’s mum, Lauren, “I wish something like this had of been available when Gracie was diagnosed. It would be amazing if there was a treatment for children in the future so other parents would not have to suffer the horrific pain of losing a child.”

In addition to the Royal Manchester Children’s Hospital, Alder Hey Children’s Hospital in Liverpool and potentially Birmingham Children’s Hospital will be joining the study to help enable access to more tumour samples.

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.