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Association of differential censoring with survival and suboptimal control arms among oncology clinical trials.

Eric J HsuTimothy A LinDor R DabushZachary McCawAlex KoongChristine LinJoseph Abi JaoudeRoshal PatelRamez KouzyMolly B El AlamSonal NoticewalaYumeng YangAlexander D SherryClifton D FullerCharles R ThomasChad TangPavlos MsaouelPrajnan DasBo HuangLu TianRyan SunJ Jack LeeTomer MeirsonEthan Bernard Ludmir
Published in: Journal of the National Cancer Institute (2024)
Differential censoring, which refers to censoring imbalance between treatment arms, may bias the interpretation of survival outcomes in clinical trials. In 146 phase III oncology trials with statistically significant time-to-event surrogate primary endpoints, we evaluated the association between differential censoring in the surrogate primary endpoints, control arm adequacy, and the subsequent statistical significance of overall survival results. Twenty-four (16%) trials exhibited differential censoring that favored the control arm, whereas 15 (10%) exhibited differential censoring that favored the experimental arm. Positive overall survival was more common in control arm differential censoring trials (63%) than in trials without differential censoring (37%) or with experimental arm differential censoring (47%; odds ratio = 2.64, 95% confidence interval = 1.10 to 7.20; P = .04). Control arm differential censoring trials more frequently used suboptimal control arms at 46% compared with 20% without differential censoring and 13% with experimental arm differential censoring (odds ratio = 3.60, 95% confidence interval = 1.29 to 10.0; P = .007). The presence of control arm differential censoring in trials with surrogate primary endpoints, especially in those with overall survival conversion, may indicate an inadequate control arm and should be examined and explained.
Keyphrases
  • clinical trial
  • randomized controlled trial
  • open label