European Standards of Care
for Children & Adolescents with Cancer
Every child and young person diagnosed with cancer deserves access to the best possible care, no matter where they live in Europe. The European Standards of Care for Children and Adolescents with Cancer are designed to make that a reality. Originally published in 2008, the Standards set clear, evidence-based requirements for paediatric oncology care. Over a decade later, with new scientific evidence and evolving needs of families, these Standards have been revised and updated to reflect today’s realities.
What are the European Standards of Care for Children and Adolescents with Cancer?
The European Standards of Care for Children and Adolescents with Cancer are a set of guidelines that define what high-quality care for young cancer patients should look like across Europe. They bring together the latest medical evidence, expert knowledge, and the lived experiences of patients, families, and survivors. The goal is to ensure that no matter where a child or teenager lives, they have access to the same level of specialised treatment, supportive care, and long-term follow-up.
Why it matters
Childhood cancer is rare, but its impact is profound. By setting clear standards, we can reduce inequalities, improve survival, and enhance the quality of life for children, adolescents, and their families. These Standards are not just a document, they are a call to action for clinicians, policymakers, advocates, and organisations across Europe to work together for lasting change.
How to use them
The Standards are a tool for:
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Patient organisations and advocates: to strengthen advocacy efforts with evidence-based recommendations
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Families and survivors: to understand what care they should expect and demand
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Clinicians: to guide daily practice and ensure consistent, high-quality care
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Policymakers: to inform healthcare planning and resource allocation