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

Differential censoring (DC), referring to censoring imbalance between treatment arms, may bias the interpretation of survival outcomes in clinical trials. In 146 phase 3 oncology trials with statistically significant time-to-event surrogate primary endpoints (PEPs), we evaluated the association betw...

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Veröffentlicht in:JNCI : Journal of the National Cancer Institute 2024-02, Vol.116 (6), p.990
Hauptverfasser: Hsu, Eric J, Lin, Timothy A, Dabush, Dor R, McCaw, Zachary, Koong, Alex, Lin, Christine, Abi Jaoude, Joseph, Patel, Roshal, Kouzy, Ramez, El Alam, Molly B, Noticewala, Sonal, Yang, Yumeng, Sherry, Alexander D, Fuller, Clifton D, Thomas, Jr, Charles R, Tang, Chad, Msaouel, Pavlos, Das, Prajnan, Huang, Bo, Tian, Lu, Sun, Ryan, Lee, J Jack, Meirson, Tomer, Ludmir, Ethan B
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Sprache:eng
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Zusammenfassung:Differential censoring (DC), referring to censoring imbalance between treatment arms, may bias the interpretation of survival outcomes in clinical trials. In 146 phase 3 oncology trials with statistically significant time-to-event surrogate primary endpoints (PEPs), we evaluated the association between DC in the surrogate PEP, control arm adequacy, and the subsequent statistical significance of OS results. Twenty-four (16%) trials exhibited DC favoring the control arm (ConDC), while 15 (10%) exhibited experimental arm DC (ExpDC). Positive OS was more common in ConDC trials (63%) than trials without DC (37%) or with ExpDC (47%; odds ratio [OR] 2.64, 95% CI 1.10-7.20; P=.04). ConDC trials more frequently used suboptimal control arms (46%) compared to 20% without DC and 13% with ExpDC (OR 3.60, 95% CI 1.29-10.0; P=.007). The presence of ConDC in trials with surrogate PEPs, especially in those with OS conversion, may indicate an inadequate control arm and should be examined and explained.
ISSN:0027-8874
1460-2105
1460-2105
DOI:10.1093/jnci/djae028