Surrogate endpoints in phase III randomized trials of advanced gastroesophageal cancer: A systematic review and meta-analysis
- PMID: 38871262
- DOI: 10.1016/j.critrevonc.2024.104416
Surrogate endpoints in phase III randomized trials of advanced gastroesophageal cancer: A systematic review and meta-analysis
Erratum in
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Corrigendum to "Surrogate endpoints in phase III randomized trials of advanced gastroesophageal cancer: A systematic review and meta-analysis" [Crit. Rev. Oncol./Hematol. 201 (2024) 104416].Crit Rev Oncol Hematol. 2024 Oct;202:104466. doi: 10.1016/j.critrevonc.2024.104466. Epub 2024 Aug 10. Crit Rev Oncol Hematol. 2024. PMID: 39127520 No abstract available.
Abstract
Overall survival (OS) is the most meaningful endpoint in clinical trials. However, owing to their limitations, surrogate endpoints are commonly used and validation studies are required to assess their reliability. Analysis of phase III randomized controlled trials (RCTs) of advanced gastroesophageal cancer (AGC) with > 100 patients, correlation coefficients (r), and determination coefficients (R²) between OS and surrogates were evaluated through meta-analyses. Progression-free survival (PFS), time to progression (TTP), and objective response rate (ORR) were examined to determine their correlations with OS. Analysis of 65 phase III RCTs (29,766 subjects) showed a moderate correlation between PFS/TTP and OS (r = 0.77, R² = 0.59), while ORR correlation was low (r = 0.56, R² = 0.31). Excluding immunotherapy trials improved the PFS/TTP and OS correlations (r = 0.83, R² = 0.70). These findings suggest the potential use of PFS/TTP in AGC phase III investigations, disregarding the use of ORR as a surrogate endpoint.
Keywords: Clinical trials; Correlation analysis; Gastroesophageal cancer; Immunotherapy; Phase III randomized controlled trials; Surrogate endpoints; Surrogate threshold effect.
Copyright © 2024 The Authors. Published by Elsevier B.V. All rights reserved.
Conflict of interest statement
Declaration of Competing Interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: The authors declare the following financial interests/personal relationships which may be considered as potential competing interests. J.VR. has received lecture fees from MSD and travel and education funding from MSD, Astrazeneca, Advanz pharma and AAA; M.B. has received consulting and lecture fees from Astellas and Janssen; R.M. has received consulting and lecture fees from Servier, Roche, MSD and Bristol Myers Squibb and travel and education funding from MSD, Eli Lilly, Bayer, Roche and Astrazeneca. All remaining authors have declared no conflict of interest.
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