Some statistical methods for multiple endpoints in clinical trials

被引:133
作者
Zhang, J
Quan, H
Ng, J
Stepanavage, ME
机构
[1] Merck Research Laboratories, Clin. Biostatist. Res. Data Syst., Rahway, NJ
[2] Merck Research Laboratories, Clin. Biostatist. Res. Data Syst., RY 33-404, Rahway
来源
CONTROLLED CLINICAL TRIALS | 1997年 / 18卷 / 03期
关键词
composite endpoint; control of type I error; experimentwise error rate; p-value adjustment; alpha-level;
D O I
10.1016/S0197-2456(96)00129-8
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
This paper summarizes, defines, and discusses multiple endpoints comparison procedures, concepts, and methodologies for applications to clinical trials. We address the more widely used methods of alpha-level, p-value, and critical value adjustments. We examine global assessment measures such as O'Brien's test and Simes' procedure and contrast them with the alpha-adjustment procedures of Bonferroni and Helm. We propose a global assessment procedure based on categorization of the individual endpoints to form an overall composite endpoint. Additionally, we discuss a new weighting scheme for Helm's sequentially rejective alpha-adjustment procedure. investigation of the correlation between endpoints is examined in relation to adjustment of the alpha-level. In the context of a clinical trial, the above multiplicity procedures are applied and compared. Finally, some comments concerning ease of use and relevance are summarized for the above methods. (C) Elsevier Science Inc. 1997.
引用
收藏
页码:204 / 221
页数:18
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