A cancer registry is a data system designed for the compilation, handling
and analysis of data of people with a diagnosis of cancer or neoplasic
disease. The basic source of information is the clinical file of the patient,
from where the pertinent data is obtained for the registry.
The hospital cancer registry is a system where the information of all
patients with cancer diagnosed or treated in the hospital institution
is compiled. This type of registry can exist in community hospitals and
medical centers.
Cancer registry objectives
Educative: To produce statistical information of registry data to
facilitate result evaluation of cancer processing. This information
is useful for the education of doctors on results of different modalities
of treatment on the different types of cancer.
Systematic tracking for life: To establish and maintain contact with
each registered patient, at least once a year. To stimulate the patient
so that he/she fulfills his/her treatment and stays under medical supervision.
Research: The compiled, analyzed, classified and codified data in
the registry serve as a valuable source for scientists interested in
the causes, diagnoses and treatments for cancer. Fundamental research
in cancer epidemiology usually starts using data compiled in the cancer
registries.