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癌症筛查试验的设计与分析。

Design and analysis of cancer screening trials.

作者信息

Etzioni R D, Connor R J, Porok P C, Self S G

机构信息

Fred Hutchinson Cancer Research Center, Division of Public Health Sciences, Seattle, WA 98104, USA.

出版信息

Stat Methods Med Res. 1995 Mar;4(1):3-17. doi: 10.1177/096228029500400102.

Abstract

This article reviews approaches to the design and analysis of cancer screening trials. After summarizing some basic screening concepts and potential pitfalls, we introduce several possible screening trial designs with examples from the literature. We review in detail methods for analyzing screening trial data, including testing for a significant difference in disease-specific mortality between the control and intervention groups, estimating the mortality differential if one exists, and evaluating the programme lead time, the screen sensitivity and the role of stage shifting. We consider Overall mortality analyses, which are based on the experience of the trial population, and Limited mortality analyses, which are based on the experience of comparable groups of cases in the control and intervention groups. We discuss methods for selecting candidate comparable case groups and confirming that they are in fact comparable. We conclude by showing how the principles discussed have been used in the planning and design of a current screening trial for multiple cancers.

摘要

本文回顾了癌症筛查试验的设计与分析方法。在总结了一些基本的筛查概念和潜在陷阱之后,我们通过文献中的实例介绍了几种可能的筛查试验设计。我们详细回顾了分析筛查试验数据的方法,包括检测对照组和干预组之间疾病特异性死亡率的显著差异、估计存在差异时的死亡率差异,以及评估项目提前期、筛查敏感性和分期转移的作用。我们考虑基于试验人群经验的总体死亡率分析,以及基于对照组和干预组中可比病例组经验的有限死亡率分析。我们讨论了选择候选可比病例组并确认它们实际上具有可比性的方法。最后,我们展示了所讨论的原则如何应用于当前多种癌症筛查试验的规划和设计。

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