Overview
The Cancer Registries (RT) are structures responsible for the collection and registration of all tumors occurring in a given territory. The primary role of a Cancer Registry is to establish and manage over time an archive of all new cancer cases diagnosed and to ensure that the data is recorded rigorously and continuously and systematically.
Most of the Italian registers are population registers, that is, they collect data relating to cancer diseases of all the residents of a given territory (it can be a single city or an entire region, a province or the territory of an ASL).
Alongside the general population registers, there are specialized registers, which collect information on a single type of tumor or on specific age groups or on occupational cancers.
Decree of the President of the Council of Ministers (DPCM) on Registers and Surveillances of diseases.
Public and private funding
Demographics
Dataset
Access to the AIRTUM database is only granted to specifically authorized persons.
The data collected in it are owned by the accredited registers that feed it and are made available for the statutory purposes of the Association for the promotion of data quality and their use for scientific purposes.
Before being granted, to carry out studies and research, it is necessary that each Director explicitly gives consent to the use of their data.
The release of data is limited to the records and variables actually necessary for the study and can only be used within the study for which they were requested and only for the duration of the project.
Contact
U.O. Prevenzione Oncologica Forlì-Cesena, Azienda Unità Sanitaria Locale della Romagna, via Carlo Forlanini 34, 47121 Forlì, Italy