French National Registry of Childhood Cancers

The registry includes all children newly diagnosed with cancer, younger than 18 years (since 2011), and whose usual residence is in mainland France or overseas departments at the time of diagnosis. RNCE made up of: The French National Registry of Childhood Haematological Malignancies, which records all diagnoses of haematological malignancies since 1990 and The French National Registry of Childhood Solid Tumours, which records all solid tumours cases since 2000. Until 2011, RNCE covered mainland France's under 15 population. Since 2011, it expanded to the overseas territories and teenagers under 18 years old.