Optimizing the order of hypotheses in serial testing of multiple endpoints in clinical trials

被引:3
|
作者
Zhang, Zhiwei [1 ]
Wang, Chenguang [2 ]
Troendle, James F. [3 ]
机构
[1] US FDA, Div Biostat, Off Surveillance & Biometr, Ctr Devices & Radiol Hlth, Silver Spring, MD USA
[2] Johns Hopkins Univ, Sch Med, Sidney Kimmel Comprehens Canc Ctr, Div Biostat & Bioinformat, Baltimore, MD USA
[3] NHLBI, Off Biostat Res, Div Cardiovasc Sci, NIH, Bethesda, MD 20892 USA
关键词
chain procedure; fixed sequence; hierarchical testing; multiple comparisons; multiplicity; secondary endpoint; BONFERRONI PROCEDURE; FIXED-SEQUENCE; GATEKEEPING STRATEGIES; ADJUSTMENT METHODS; SELECTION; EFFICACY; WEIGHTS;
D O I
10.1002/sim.6425
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Clinical trials usually collect information on a large number of variables or endpoints, including one or more primary endpoints as well as a number of secondary endpoints representing different aspects of treatment effectiveness and safety. In this article, we focus on serial testing procedures that test multiple endpoints in a pre-specified order, and consider how to optimize the order of endpoints subject to any clinical constraints, with respect to the expected number of successes (i.e., endpoints that reach statistical significance) or the expected gain (if endpoints are associated with numerical utilities). We consider some common approaches to this problem and propose two new approaches: a greedy algorithm based on conditional power and a simulated annealing algorithm that attempts to improve a given sequence in a random and iterative fashion. Simulation results indicate that the proposed algorithms are useful for finding a high-performing sequence, and that optimized fixed sequence procedures can be competitive against traditional multiple testing procedures such as Holm's. The methods and findings are illustrated with two examples concerning migraine and asthma. Copyright (c) 2015 John Wiley & Sons, Ltd.
引用
收藏
页码:1467 / 1482
页数:16
相关论文
共 50 条
  • [31] Inference on multiple endpoints in clinical trials with adaptive interim analyses
    Kieser, M
    Bauer, P
    Lehmacher, W
    [J]. BIOMETRICAL JOURNAL, 1999, 41 (03) : 261 - 277
  • [32] Recommendations for including multiple symptoms as endpoints in cancer clinical trials
    Cleeland, Charles S.
    Sloan, Jeff A.
    Cella, David
    Chen, Connie
    Dueck, Amylou C.
    Janjan, Nora A.
    Liepa, Astra M.
    Mallick, Rajiv
    O'Mara, Ann
    Pearson, Jay D.
    Torigoe, Yasuhiro
    Wang, Xin Shelley
    Williams, Loretta A.
    Woodruff, Jeanie F.
    [J]. CANCER, 2013, 119 (02) : 411 - 420
  • [33] Recurrent disability progression endpoints in multiple sclerosis clinical trials
    Buehler, Alexandra
    Wolbers, Marcel
    Model, Fabian
    Wang, Qing
    Belachew, Shibeshih
    Manfrini, Marianna
    Lorscheider, Johannes
    Kappos, Ludwig
    Beyersmann, Jan
    [J]. MULTIPLE SCLEROSIS JOURNAL, 2023, 29 (01) : 130 - 139
  • [34] Reducing unnecessary measurements in clinical trials with multiple primary endpoints
    Sozu, Takashi
    Sugimoto, Tomoyuki
    Hamasaki, Toshimitsu
    [J]. JOURNAL OF BIOPHARMACEUTICAL STATISTICS, 2016, 26 (04) : 631 - 643
  • [35] DESIGN OF GROUP SEQUENTIAL CLINICAL-TRIALS WITH MULTIPLE ENDPOINTS
    TANG, DI
    GNECCO, C
    GELLER, NL
    [J]. JOURNAL OF THE AMERICAN STATISTICAL ASSOCIATION, 1989, 84 (407) : 776 - 779
  • [36] Generalized estimating equations in controlled clinical trials: Hypotheses testing
    Dahmen, G
    Ziegler, A
    [J]. BIOMETRICAL JOURNAL, 2004, 46 (02) : 214 - 232
  • [37] Testing Hypotheses of Covariate-Adaptive Randomized Clinical Trials
    Ma, We
    Hu, Feifang
    Zhang, Lixin
    [J]. JOURNAL OF THE AMERICAN STATISTICAL ASSOCIATION, 2015, 110 (510) : 669 - 680
  • [38] THE USE OF RANDOMIZATION TESTS FOR MULTIPLE ENDPOINTS IN CLINICAL-TRIALS
    KARRISON, T
    [J]. CONTROLLED CLINICAL TRIALS, 1985, 6 (03): : 240 - 241
  • [39] Some remaining challenges regarding multiple endpoints in clinical trials
    Snapinn, Steven
    [J]. STATISTICS IN MEDICINE, 2017, 36 (28) : 4441 - 4445
  • [40] One-sided tests in clinical trials with multiple endpoints
    Bloch, DA
    Lai, TL
    Tubert-Bitter, P
    [J]. BIOMETRICS, 2001, 57 (04) : 1039 - 1047