Clinical registry of childhood cancers

The Clinical Registry of Childhood Cancers (KrOt) was launched in 2018. The KrOt collects all data on patients diagnosed before the age of 20 with any malignant tumor and some in situ and benign tumor. These data are crucial for monitoring and recording the late effects of the treatment of childhood cancers, which are also recorded in the KrOt.

Data analyses are compiled according to the year in which the patients were diagnosed, following the format of the cancer registry, and are published in the KrOt annual reports.