The registry collects data and provides advice. Therapy should be carried out in accordance with the standard of care.
Collection of epidemiological data
Collection of information on treatment and treatment outcome and retrospective evaluation of the relationship between intervention and outcome
Recording of late effects
Assessment of the quality of treatment through data collection, data review and consultation by the registry centre and the reference institutions
Creation of a tumour bank as a basis for future biological research projects to identify new risk factors and targets for targeted therapeutics.
