Documentation for U.S. Data (2001–2017)

U.S. Cancer Statistics Public Use Database

Two United States Cancer Statistics public use databases are available for researchers: the U.S. (2001–2017) database, described in this section, and the U.S. and Puerto Rico (2005–2017) database.

The U.S. (2001–2017) database—

  • Includes race and ethnicity variables.
  • Does not include Puerto Rico data.
  • The population denominators are race-specific, ethnicity-specific, and sex-specific county population estimates from the U.S. Census (July 1, 2010–2018 bridged–race vintage 2018 population estimates), modified by SEER and aggregated to the state and national levels.

Population Coverage by Diagnosis Year

For cases diagnosed from 2003 through 2017, 100% of the population is covered for all 50 states and the District of Columbia. In 2001 and 2002, cases that were diagnosed in Mississippi are not available, so 99% of the U.S. population is covered for those two years.

Suggested Citations

Please use these standard citations for tables and figures when presented in presentations or publications.

For population coverage: Data are from population-based registries that participate in CDC’s National Program of Cancer Registries and/or NCI’s Surveillance, Epidemiology, and End Results Program and meet high-quality data criteria. These registries cover approximately [XX]% of the U.S. population.

For age-adjusted rates: Rates are per 100,000 persons and are age-adjusted to the 2000 U.S. standard population (19 age groups – Census P25–1130).

For the database: National Program of Cancer Registries and Surveillance, Epidemiology, and End Results SEER*Stat Database: NPCR and SEER Incidence – U.S. Cancer Statistics 2001–2017 Public Use Research Database, 2019 submission (2001–2017), United States Department of Health and Human Services, Centers for Disease Control and Prevention and National Cancer Institute. Released June 2020. Available at www.cdc.gov/cancer/uscs/public-use.

Archived Documentation