A new way to address missing data in late-stage clinical trials

被引:0
|
作者
Ganju, Jitendra [1 ]
Yu, Ron Xiaolong [2 ]
机构
[1] Ganju Clin Trials LLC, San Francisco, CA 94109 USA
[2] Gilead Sci, Biostat, Foster City, CA USA
关键词
Benefit-risk; Mann-Whitney method; Missing data; Win ratio; COMPOSITE END-POINTS; WIN RATIO APPROACH; OUTCOMES;
D O I
10.1016/j.cct.2024.107750
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
According to ICH E9(R1), defining the estimand comes before defining the analysis approach, and the strategies for addressing intercurrent events are key components of the estimand. With the composite strategy, the problem of missing data disappears, because it becomes part of the endpoint definition. It is this perspective that we adopt in addressing the problem of missing data. We propose comparing patients in a pairwise manner to determine which patient fared better, one patient from each group, taking into account the reason for and timing of missingness. For purposes of illustration, reasons for missingness are placed into three categories: (1) death or adverse events, (2) administration of rescue medication (treated as missing even if patient continues in the study, or a poor score is assigned), and (3) other reasons such as loss to follow-up or withdrawal of consent. Each pair of patients is compared on the endpoint of interest. The comparison outcomes are determined based on the presence of missing data, its category, and timing. For instance, if both patients in a pair have received rescue medication, the patient with the later time of rescue medication is considered to have fared better. The overall treatment effect is estimated from combining results across all pairwise comparisons. This method allows the reason and timing of missing data to contribute to the assessment of treatment effects, providing a solution to some limitations of existing methods. Thus, the pairwise comparison approach addresses the missing data problem transparently via the composite strategy.
引用
收藏
页数:5
相关论文
共 50 条
  • [1] A review of therapeutic failures in late-stage clinical trials
    Jain, Ritu
    Subramanian, Janakiraman
    Rathore, Anurag S.
    EXPERT OPINION ON PHARMACOTHERAPY, 2023, 24 (03) : 389 - 399
  • [2] DRUGMAKERS HURT BY LATE-STAGE TRIALS
    不详
    CHEMICAL & ENGINEERING NEWS, 2009, 87 (09) : 23 - 23
  • [3] Carbon footprint of industry-sponsored late-stage clinical trials
    Mackillop, Neil
    Shah, Jayesh
    Collins, Michael
    Costelloe, Thomas
    Ohman, Daniel
    BMJ OPEN, 2023, 13 (08):
  • [4] Quantifying burden to improve patient experience in late-stage clinical trials
    Nowojewski, Andrzej
    Riesbeck, Ingrid
    Scetinina, Tatiana
    Teufel, Michele
    Esparza-Franco, Alejandro
    Schneider, Ian
    Dearden, Richard
    QUALITY OF LIFE RESEARCH, 2022, 31 : S45 - S45
  • [5] Migraine mAbs crowd into late-stage trials
    Gunjan Sinha
    Nature Biotechnology, 2015, 33 : 676 - 677
  • [6] Migraine mAbs crowd into late-stage trials
    Sinha, Gunjan
    NATURE BIOTECHNOLOGY, 2015, 33 (07) : 676 - 677
  • [7] General guidance on exploratory and confirmatory subgroup analysis in late-stage clinical trials
    Dmitrienko, Alex
    Muysers, Christoph
    Fritsch, Arno
    Lipkovich, Ilya
    JOURNAL OF BIOPHARMACEUTICAL STATISTICS, 2016, 26 (01) : 71 - 98
  • [8] NCI begins overhaul of late-stage cancer trials
    Alicia Ault
    Nature Medicine, 1998, 4 : 1219 - 1219
  • [9] NCI begins overhaul of late-stage cancer trials
    Ault, A
    NATURE MEDICINE, 1998, 4 (11) : 1219 - 1219
  • [10] The inclusion of pregnant women in vaccine clinical trials: An overview of late-stage clinical trials' records between 2018 and 2023
    Salloum, Maha
    Paviotti, Antea
    Bastiaens, Hilde
    Van Geertruyden, Jean-Pierre
    VACCINE, 2023, 41 (48) : 7076 - 7083