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. Author manuscript; available in PMC: 2021 Feb 1.
Published in final edited form as: Am J Ind Med. 2019 Nov 19;63(2):105–114. doi: 10.1002/ajim.23062

TABLE 1.

Statutory basis for US cancer surveillance

Statutory basis for US cancer surveillance
Cancer is a reportable disease in all the US states and territories
• Healthcare providers and facilities are required to report cancer cases to state cancer registries
• Health Insurance Portability and Accountability Act (HIPAA) permits cancer registries to access and maintain identifiable cancer data
National Cancer Act of 1971 authorized NCI to conduct population-based cancer surveillance, led to the SEER program in 1973
Cancer Registries Amendment Act of 1992 authorized CDC to provide funds to states and territories to enhance existing cancer registries and establish new ones
Caroline Pryce Walker Conquer Childhood Cancer Act of 2008 required CDC to award a grant to enhance and expand tracking of pediatric cancer and include actual occurrences within weeks
Survivorship, Treatment, Access, and Research Act of 2018 (STAR) extended and expanded the Caroline Pryce Walker Act

Note: In the United States, cancer is a reportable illness and cancer surveillance is supported by the NCI and CDC. There is precedent for legislation requiring a specialized program for rapid reporting of a particular type of cancer soon after diagnosis. The Carolyn Pryce Walker Act and subsequent STAR act required rapid reporting of pediatric cancer.

Abbreviations: CDC, Centers for Disease Control and Prevention; National Cancer Institute (NCI); SEER, Surveillance, Epidemiology, and End Results.