What makes ependymoma in infants different?
Looking at molecular makeup and MRIs to characterise infant ependymoma.
We have been funding expert research since 2016, aiming to ensure that every child and young person has a safe and effective treatment for their cancer, and that they can live long and happy lives post-treatment.
Looking at molecular makeup and MRIs to characterise infant ependymoma.
Looking at the genetics of bone marrow samples to see which genes affect resistance to treatment.
Assessing whether blocking a protein's activity could improve survival and reduce side effects.
Developing a living systematic review of studies into new treatments for relapsed and refractory rhabdomyosarcoma.
Looking into whether survivors of childhood cancer are at risk of severe infections.
Developing more effective treatments for patients who have a low chance of survival, while reducing treatment and side effects for other patients.
Finding which regulatory regions of the genome are causing leukaemia by acting on the wrong gene
Developing better models of rhabdomyosarcoma to test available treatments.
Our proposal will deliver novel, less toxic targeted therapies with the potential to advance current treatment regimens for B-ALL. This will improve current outcomes, reduce side-effects in B-ALL patients and ultimately lead to a better quality of life for patients and their families.