Question to the Department of Health and Social Care:

To ask the Secretary of State for Health and Social Care, what steps he is taking to ensure that the views and lived experience of teenagers and young adults with cancer are being incorporated into his forthcoming national cancer plan; and how their involvement will be reflected in the plan’s publication and launch.

The Department is committed to improving outcomes for teenagers and young adults with cancer. The Children and Young People Cancer Taskforce was relaunched on 4 February 2025 to identify tangible ways to improve outcomes and experiences for young cancer patients. The taskforce will explore opportunities for improvement in England, including detection and diagnosis, genomic testing and treatment, research and innovation, and patient experience. The taskforce will ensure that the unique needs of children and young people, including teenagers and young adults with cancer, are carefully considered as part of the forthcoming National Cancer Plan.

The Government is committed to including the views and lived experience of teenagers and young adults in the National Cancer Plan. That is why the Department has worked with the Children and Young People Cancer taskforce members to assemble a Patient Experience Panel of people with lived experience of cancer. The panel is made up of a diverse group, including parents of children with cancer, young adults who were diagnosed with cancer as teenagers, and those who were diagnosed as children.

As part of the Department’s engagement to inform the development of the forthcoming National Cancer Plan, officials from the Department’s cancer team have worked closely with patient organisations, clinicians, and cancer partners, and has considered over 11,000 responses to the call for evidence. These included submissions from Teenage Cancer Trust, Ellen MacArthur Cancer Trust, Young Lives vs Cancer, CCLG: The Children and Young People's Cancer Association, and so on.