Final answer:
Tumor registry information is reported to the NCDB, a nationwide cancer outcomes database for CoC-accredited programs, jointly created by the CoC of the ACoS and the ACS.
Step-by-step explanation:
Tumor registry information is primarily reported to the NCDB, which stands for the National Cancer Data Base. The NCDB is a nationwide oncology outcomes database for more than 1,500 Commission on Cancer (CoC)-accredited cancer programs in the United States and Puerto Rico. It is a joint project of the Commission on Cancer (CoC) of the American College of Surgeons (ACoS) and the American Cancer Society (ACS). The tumor registry data collected by the NCDB includes patient demographics, cancer staging, tumor characteristics, treatment, and outcomes information, which is used for tracking and analyzing cancer incidence and treatment patterns.
Other agencies mentioned, such as the NCHS (National Center for Health Statistics), the HCUP (Healthcare Cost and Utilization Project), and the CMS (Centers for Medicare & Medicaid Services), also have their respective data collection and reporting systems, but for tumor registry information, the NCDB is the specific recipient.