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Journal of the NATIONAL CANCER INSTITUTE November 1974 Vol. 53, No.5 (DREW Publication No. NIH 7413) NATIONAL INSTITUTES OF HEALTH PUBLIC HEALTH SERVICE THE JOURNAL of the National Cancer Institute
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National Cancer refers to the official cancer registry of a specific country or region, which is used to collect and track data related to cancer incidence, prevalence, mortality, and survival rates.
Healthcare providers, hospitals, and cancer treatment centers are typically required to file national cancer data to ensure accurate reporting and analysis of cancer-related statistics.
National cancer data is usually filled out electronically through online portals or software provided by the relevant health authorities. Detailed instructions and guidelines are typically available to assist with the process.
The main purpose of national cancer registries is to monitor trends in cancer incidence, improve cancer prevention and control efforts, facilitate research on cancer causes and treatments, and ultimately reduce the burden of cancer on the population.
Information typically reported on national cancer registries includes patient demographics, tumor characteristics, treatment modalities, and outcomes. Additional data on risk factors, screenings, and genetic predispositions may also be included.
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