MMWR Morb Mortal Wkly Rep. 1994 Feb 4;43(4):71, 74-5.
Population-based cancer registries have identified cancer incidence rates indicating that the burden of cancer in the United States is substantial and varies widely by geographic location and ethnicity. However, for most existing state cancer registries, resources are inadequate for insuring minimum standards for quality and for completeness of case information. In October 1992, Congress enacted the Cancer Registries Amendment Act* that authorized CDC to establish a national program in support of cancer registries. The goal of this program is to enhance existing state cancer registries and to help establish statewide cancer registries so that all states have population-based cancer registries meeting minimum standards for completeness, timeliness, and quality. To ensure complete and timely reporting of newly diagnosed cases of cancer, the federal statute requires authorization of cancer registries under state-specific laws and promulgation of regulations that ensure case reporting and use of data for research. This report extends efforts by the National Cancer Institute to assess existing state laws and regulations to determine how they compare to state-specific legislation required in the cancer registries act.
基于人群的癌症登记处已确定癌症发病率,这表明美国的癌症负担相当大,且因地理位置和种族而有很大差异。然而,对于大多数现有的州癌症登记处来说,资源不足以确保病例信息质量和完整性的最低标准。1992年10月,国会颁布了《癌症登记修正案法案》*,授权疾病控制与预防中心(CDC)设立一个支持癌症登记处的国家项目。该项目的目标是加强现有的州癌症登记处,并帮助建立全州范围的癌症登记处,以便所有州都有基于人群的癌症登记处,满足完整性、及时性和质量的最低标准。为确保新诊断癌症病例的完整和及时报告,联邦法规要求根据各州特定法律对癌症登记处进行授权,并颁布法规以确保病例报告和数据用于研究。本报告扩展了美国国家癌症研究所的工作,以评估现有的州法律法规,确定它们与癌症登记处法案中要求的各州特定立法相比如何。