The Swiss Childhood Cancer Survivor Study - Follow-up (SCCSS-FollowUp)

Critères d'inclusion

This prospective cohort study is based on the Childhood Cancer Registry (ChCR), a national, population-based cancer registry that includes all children and adolescents in Switzerland who were diagnosed with cancer at age 0-20 years. It includes patients diagnosed with leukemia, lymphoma, central nervous system tumors, and malignant solid tumors or Langerhans cell histiocytosis. • Registered in the Childhood Cancer Registry (ChCR) or treated and followed-up in a Swiss pediatric oncology (SPOG) clinic, but not registered in the ChCR because of residency in neighboring countries • Diagnosed at age 0 - 20 years • Childhood cancer treatment completed • All age categories at time of inclusion in the study (children, adolescents, adults) • Written informed consent