Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/43630
Title: Proportion of treatment effect explained: An overview of interpretations
Authors: Stijven, Florian
ALONSO ABAD, Ariel 
MOLENBERGHS, Geert 
Issue Date: 2024
Publisher: SAGE PUBLICATIONS LTD
Source: Statistical methods in medical research, 33 (7) , p. 1278 -1296
Abstract: The selection of the primary endpoint in a clinical trial plays a critical role in determining the trial's success. Ideally, the primary endpoint is the clinically most relevant outcome, also termed the true endpoint. However, practical considerations, like extended follow-up, may complicate this choice, prompting the proposal to replace the true endpoint with so-called surrogate endpoints. Evaluating the validity of these surrogate endpoints is crucial, and a popular evaluation framework is based on the proportion of treatment effect explained (PTE). While methodological advancements in this area have focused primarily on estimation methods, interpretation remains a challenge hindering the practical use of the PTE. We review various ways to interpret the PTE. These interpretations-two causal and one non-causal-reveal connections between the PTE principal surrogacy, causal mediation analysis, and the prediction of trial-level treatment effects. A common limitation across these interpretations is the reliance on unverifiable assumptions. As such, we argue that the PTE is only meaningful when researchers are willing to make very strong assumptions. These challenges are also illustrated in an analysis of three hypothetical vaccine trials.
Notes: Stijven, F (corresponding author), Katholieke Univ Leuven, I BioStat, Leuven, Belgium.
florian.stijven@kuleuven.be
Keywords: Surrogacy;Surrogacy;Prentice's criteria;Prentice's criteria;mediation analysis;mediation analysis;principal stratification;principal stratification;causal inference;causal inference
Document URI: http://hdl.handle.net/1942/43630
ISSN: 0962-2802
e-ISSN: 1477-0334
DOI: 10.1177/09622802241259177
ISI #: 001276826200001
Rights: The Author(s) 2024
Category: A1
Type: Journal Contribution
Appears in Collections:Research publications

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