Investigating a new way of treating poor-prognosis rhabdomyosarcoma
Evaluating a novel protein methyltransferase inhibitor for poor-prognosis rhabdomyosarcoma therapy
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.
Evaluating a novel protein methyltransferase inhibitor for poor-prognosis rhabdomyosarcoma therapy
Assessing rhabdomyosarcoma risk prediction markers based on the biological conditions in the tumour, like low oxygen levels, few blood vessels, and genetics.
How the 3D shape of fusion gene genetic code affects cancer cell behaviour and whether shape-modifying medicines could mitigate these effects.
Finding the biological differences between teenage and young adult cancers cells compared to older adults.
Looking for differences in newly diagnosed RMS patient samples to see if there are any that could be used to show whether treatments are working.
Developing a living systematic review of studies into new treatments for relapsed and refractory rhabdomyosarcoma.
Developing better models of rhabdomyosarcoma to test available treatments.
MG-fnRMS and CINSARC gene expression signatures to predict relapse in fusion gene negative rhabdomyosarcomas: assessing an approach to improve patient outcomes
Understanding treatment decision-making processes in families where a child or young person has relapsed/refractory rhabdomyosarcoma