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Postprogression therapy and confounding for the estimated treatment effect on overall survival in phase III oncology trials

Authors :
Pavlos Msaouel
Ramez Kouzy
Joseph Abi Jaoude
Ethan B Ludmir
Alexander D Sherry
Timothy A Lin
Esther J Beck
Avital M Miller
Adina H Passy
Gabrielle S Kupferman
Eugene J Koay
Clifton David Fuller
Charles R Thomas
Zachary R McCaw
Source :
BMJ Oncology, Vol 3, Iss 1 (2024)
Publication Year :
2024
Publisher :
BMJ Publishing Group, 2024.

Abstract

Objective Estimations of the treatment effect on overall survival (OS) may be influenced by post-progression therapies (PPTs). It is unclear how often OS analyses account for PPT effects. The purpose of this cross-sectional analysis was to determine the prevalence of OS analyses accounting for PPT effects in phase III oncology trials.Methods and analysis We screened two-arm, superiority design, phase III, randomised, oncology trials reporting OS from ClinicalTrials.gov. The primary outcome was the frequency of OS analyses adjusting for PPT confounding. Logistic regressions computed ORs for the association between trial-level covariates and the outcome.Results A total of 334 phase III trials enrolling 265 310 patients were included, with publications between 2004 and 2020. PPTs were reported in 47% of trials (157 of 334), and an analysis accounting for PPTs was performed in only 12% of trials (N=41). PPT adjustments were often prespecified (N=23, 56%), and appeared to be more likely in cross-over studies (OR 5.04, 95% CI 2.42 to 10.38) and studies with discordant surrogate-OS findings (OR 2.26, 95% CI 1.16 to 4.38). In key subgroup analyses, PPT analyses were infrequent, including 8% of trials among those studying locoregional/first-line therapy and 11% of trials among those powered for OS.Conclusions Although time on PPTs is an important component of OS, PPTs are rarely considered in OS analyses, which may introduce confounding on estimates of the treatment effect on OS. PPTs and methods to account for their effects on OS estimates should be considered at the time of trial design and reporting.

Details

Language :
English
ISSN :
27527948
Volume :
3
Issue :
1
Database :
Directory of Open Access Journals
Journal :
BMJ Oncology
Publication Type :
Academic Journal
Accession number :
edsdoj.284718e1663b466c99a570c4fdc80d03
Document Type :
article
Full Text :
https://doi.org/10.1136/bmjonc-2024-000322