A group sequential design and sample size estimation for an immunotherapy trial with a delayed treatment effect

被引:5
|
作者
Li, Bosheng [1 ]
Su, Liwen [1 ]
Gao, Jun [1 ]
Jiang, Liyun [1 ]
Yan, Fangrong [1 ]
机构
[1] China Pharmaceut Univ, Res Ctr Biostat & Computat Pharm, Nanjing 211198, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
Cancer immunotherapy; delayed treatment effect; piecewise weighted log-rank test; group sequential design; maximum sample size;
D O I
10.1177/0962280220980780
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
A delayed treatment effect is often observed in the confirmatory trials for immunotherapies and is reflected by a delayed separation of the survival curves of the immunotherapy groups versus the control groups. This phenomenon makes the design based on the log-rank test not applicable because this design would violate the proportional hazard assumption and cause loss of power. Thus, we propose a group sequential design allowing early termination on the basis of efficacy based on a more powerful piecewise weighted log-rank test for an immunotherapy trial with a delayed treatment effect. We present an approach on the group sequential monitoring, in which the information time is defined based on the number of events occurring after the delay time. Furthermore, we developed a one-dimensional search algorithm to determine the required maximum sample size for the proposed design, which uses an analytical estimation obtained by the inflation factor as an initial value and an empirical power function calculated by a simulation-based procedure as an objective function. In the simulation, we tested the unstable accuracy of the analytical estimation, the consistent accuracy of the maximum sample size determined by the search algorithm and the advantages of the proposed design on saving sample size.
引用
收藏
页码:904 / 915
页数:12
相关论文
共 50 条
  • [31] Sample size calculation for planning group sequential longitudinal trials
    Liu, AY
    Boyett, JM
    Xiong, XP
    STATISTICS IN MEDICINE, 2000, 19 (02) : 221 - 237
  • [32] A group sequential t-test with updating of sample size
    Denne, JS
    Jennison, C
    BIOMETRIKA, 2000, 87 (01) : 125 - 134
  • [33] Development of Adaptive Group Sequential Procedure for Changing Sample Size
    Nakamura, Tomohiro
    Douke, Hideyuki
    COMMUNICATIONS IN STATISTICS-SIMULATION AND COMPUTATION, 2010, 39 (05) : 950 - 970
  • [34] Adaptive promising zone design for cancer immunotherapy with heterogeneous delayed treatment effect
    Li, Bosheng
    Yan, Fangrong
    Jiang, Depeng
    JOURNAL OF BIOPHARMACEUTICAL STATISTICS, 2024,
  • [35] Sample size calculations for mixture alternatives in a control group vs. treatment group design
    Jeske, Daniel R.
    Yao, Weixin
    STATISTICS, 2020, 54 (01) : 97 - 113
  • [36] On Group Sequential Enrichment Design for Basket Trial
    Yuan, Shuai S.
    Chen, Aiying
    He, Li
    Chen, Cong
    Gause, Christine K.
    Beckman, Robert A.
    STATISTICS IN BIOPHARMACEUTICAL RESEARCH, 2016, 8 (03): : 293 - 306
  • [37] Conditional estimation following a group sequential clinical trial
    Troendle, JF
    Yu, KF
    COMMUNICATIONS IN STATISTICS-THEORY AND METHODS, 1999, 28 (07) : 1617 - 1634
  • [38] On asymptotic normality in estimation after a group sequential trial
    Berckmoes, Ben
    Ivanova, Anna
    Molenberghs, Geert
    SEQUENTIAL ANALYSIS-DESIGN METHODS AND APPLICATIONS, 2020, 39 (04): : 443 - 466
  • [39] Estimation of a secondary parameter in a group sequential clinical trial
    Gorfine, M
    BIOMETRICS, 2001, 57 (02) : 589 - 597
  • [40] A randomized group sequential enrichment design for immunotherapy and targeted therapy
    Park, Yeonhee
    Liu, Suyu
    CONTEMPORARY CLINICAL TRIALS, 2022, 116