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

Author:

Hsu Eric J1ORCID,Lin Timothy A23,Dabush Dor R4,McCaw Zachary5,Koong Alex2,Lin Christine2,Abi Jaoude Joseph2,Patel Roshal2,Kouzy Ramez2,El Alam Molly B2,Noticewala Sonal2,Yang Yumeng6,Sherry Alexander D2,Fuller Clifton D2,Thomas Charles R7,Tang Chad2,Msaouel Pavlos8ORCID,Das Prajnan2,Huang Bo9,Tian Lu10ORCID,Sun Ryan11ORCID,Lee J Jack11,Meirson Tomer412ORCID,Ludmir Ethan B211ORCID

Affiliation:

1. Department of Radiation Oncology, University of Texas Southwestern Medical Center , Dallas, TX, USA

2. Division of Radiation Oncology, University of Texas MD Anderson Cancer Center , Houston, TX, USA

3. Department of Radiation Oncology and Molecular Radiation Sciences, Johns Hopkins University School of Medicine , Baltimore, MD, USA

4. Davidoff Cancer Center, Rabin Medical Center , Petah-Tikva, Israel

5. Department of Biostatistics, The University of North Carolina at Chapel Hill , Chapel Hill, NC, USA

6. School of Bioinformatics, University of Texas Health Science Center at Houston , Houston, TX, USA

7. Radiation Oncology, Dartmouth Cancer Center, Geisel School of Medicine , Lebanon, NH, USA

8. Department of Genitourinary Medical Oncology, University of Texas MD Anderson Cancer Center , Houston, TX, USA

9. Pfizer Inc , Groton, CT, USA

10. Department of Health Research and Policy, Stanford University , Stanford, CA, USA

11. Department of Biostatistics, University of Texas MD Anderson Cancer Center , Houston, TX, USA

12. Faculty of Medicine, Tel Aviv University , Tel Aviv, Israel

Abstract

Abstract 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.

Funder

Sabin Family Foundation Fellowship

Publisher

Oxford University Press (OUP)

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