Treatments / PediaRT
The National Childhood Cancer Registry has been collecting detailed data on treatments since it received ANR funding under the “Investissement d’Avenir” program. These treatment data are supplemented by the response to treatment and the 5-year follow-up of each patient’s diagnosis.
These initial patient follow-up data are the link with the COHOPER cohort, a long-term follow-up cohort for patients included in the French National Childhood Cancer Registry;
The PediaRT database, a component of the HOPE-EPI/ CCOP project, has also been funded by the ANR under the “Investissements d’Avenir” program.
Its aim is to collect dosimetric data on curative radiotherapy treatment of French children and adolescents.
This database has been built up prospectively since 2014 from dosimetric data exported by each treatment center, on a secure online platform. All data is stored anonymously.
These data are transmitted to the CCOP, which performs a correlation analysis with clinical follow-up data. The aim is to study the link between doses to different organs and relapses and/or adverse effects.