Which registry is responsible for collecting cancer data from multiple states?

The SEER (Surveillance, Epidemiology, and End Results) Program is responsible for collecting cancer data from multiple states. This national program, established by the National Cancer Institute, operates through a network of population-based cancer registries across the United States. Its comprehensive data collection efforts aim to provide information about cancer incidence, survival, mortality, and prevalence. The SEER program is known for its robust dataset, which helps inform cancer research, policy making, and public health initiatives.

SEER's role is vital in understanding cancer trends and outcomes over time, which is essential for health care planning and improving cancer control efforts. By utilizing multiple state registries, SEER can compile a diverse and extensive range of data that reflects the cancer burden across different populations and geographies, making it a crucial resource in the fight against cancer.

In contrast, other options, such as the National Cancer Database, focus on data from accredited programs rather than being a multi-state registry; the American Cancer Society is primarily an advocacy and education organization that focuses on cancer awareness and fundraising; and the FDA Oncology Registry does not compile population-wide cancer data but rather focuses on safety and effectiveness regarding oncology drugs and treatments.