Medical records are the primary source of data on cancer incidence. Staff at health care facilities abstract data from patients’ medical records, enter it into the facility’s cancer registry (if it has one), and then send the data to the central registry. Other data sources include physicians’ offices, radiation facilities, freestanding surgical centers, and pathology laboratories.
Cancer mortality statistics are based on information from all death certificates filed in the 50 states, the District of Columbia, and Puerto Rico, and processed by the National Vital Statistics System.
The population estimates for the denominators of incidence and death rates are race-specific, ethnicity-specific, and sex-specific county population estimates aggregated to the state or metropolitan-area level.
Population estimates used in the calculation of Puerto Rico incidence and death rates are sex-specific, are obtained from the U.S. Census Bureau, and are not available by race or ethnicity. To account for the population shift that occurred due to Hurricane Maria, the population denominators for 2017 were adjusted by dividing the U.S. Census Bureau’s July 1, 2017 (vintage 2021) Puerto Rico population estimate in half.
Cancer screening and risk factor data are based on information obtained from the Behavioral Risk Factor Surveillance System, which collects data in all 50 states, the District of Columbia, and three U.S. territories. Human papillomavirus (HPV) immunization data are collected through the National Immunization Survey-Teen (NIS-Teen).