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监测、流行病学和最终结果计划数据的代表性:癌症死亡率的近期趋势

Representativeness of the surveillance, epidemiology, and end results program data: recent trends in cancer mortality rates.

作者信息

Frey C M, McMillen M M, Cowan C D, Horm J W, Kessler L G

机构信息

Division of Cancer Prevention and Control, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.

出版信息

J Natl Cancer Inst. 1992 Jun 3;84(11):872-7. doi: 10.1093/jnci/84.11.872.

Abstract

BACKGROUND

Mortality, incidence, and survival rates are the primary measures used by the National Cancer Institute (NCI) to monitor cancer in the United States. The Surveillance, Epidemiology, and End Results (SEER) data system collects data on all cancers diagnosed among residents in geographically defined populations, which comprise about 10% of the U.S. population. This data system is the major component of the NCI system for tracking these rates. Thus, it is important to assess the degree to which SEER data are representative of the entire U.S. population.

PURPOSE

National data on mortality, but not on incidence or survival, are available from the National Center for Health Statistics. These data provide a census against which mortality data from the subset of the SEER regions may be compared.

METHODS

Multivariate regression analyses of age-adjusted mortality rates from 1975 to 1988, computed for the SEER areas and for the entire United States, were performed for race- and sex-specific data from 15 cancer sites. Representativeness was evaluated by testing for differences in trends and levels between the data from the U.S. population and those from the SEER Program.

RESULTS

Data from the SEER regions reflected the correct direction of trend for all sites, although some race-, sex-, and site-specific differences existed for the magnitude of the trends and levels of mortality when compared with data from the U.S. population.

CONCLUSIONS

The demonstration that data from the SEER population do occasionally yield mortality rates that differ from those for the entire U.S. population suggests that data from the SEER coverage population are, in some cases, not representative of the greater U.S. population.

IMPLICATIONS

This issue is of particular relevance to the interpretation of incidence measures, computed from the SEER data, for which there is no national database. Future efforts should be directed at a better understanding of how the SEER population differs from the U.S. population so that SEER rates can be adjusted to be more nationally representative.

摘要

背景

死亡率、发病率和生存率是美国国立癌症研究所(NCI)用于监测美国癌症情况的主要指标。监测、流行病学和最终结果(SEER)数据系统收集地理界定人群中居民所诊断出的所有癌症的数据,这些人群约占美国人口的10%。该数据系统是NCI追踪这些比率的系统的主要组成部分。因此,评估SEER数据在多大程度上代表美国全体人口很重要。

目的

美国国家卫生统计中心可提供全国的死亡率数据,但不提供发病率或生存率数据。这些数据可作为一个普查数据,用于与SEER地区子集的死亡率数据进行比较。

方法

对1975年至1988年SEER地区和整个美国计算得出的年龄调整死亡率进行多变量回归分析,分析针对15个癌症部位的种族和性别特异性数据。通过测试美国人口数据与SEER项目数据之间趋势和水平的差异来评估代表性。

结果

SEER地区的数据反映了所有部位趋势的正确方向,尽管与美国人口数据相比,在趋势幅度和死亡率水平方面存在一些种族、性别和部位特异性差异。

结论

SEER人群数据偶尔会得出与美国全体人口不同的死亡率,这表明在某些情况下,SEER覆盖人群的数据不能代表更广泛的美国人口。

启示

这个问题对于解释从SEER数据计算得出的发病率指标尤为相关,因为没有全国性数据库。未来的努力应致力于更好地了解SEER人群与美国人口的差异,以便调整SEER比率使其更具全国代表性。

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