Key result
The proposed cross-validation method evaluates predictive individual-level general surrogates, though application to rotavirus vaccine trials found no single high-quality surrogate across all regions.
The proposed statistical method allows for the evaluation of predictive individual-level general surrogates to accurately predict individual treatment efficacy in new clinical settings.
Offers a novel statistical tool to validate surrogate endpoints for personalized treatment efficacy; leaves open the identification of universally.
An intermediate response measure that accurately predicts efficacy in a new setting at the individual level could be used both for prediction and personalized medical decisions. In this article, we define a predictive individual-level general surrogate (PIGS), which is an individual-level intermediate response that can be used to accurately predict individual efficacy in a new setting. While methods for evaluating trial-level general surrogates, which are predictors of trial-level efficacy, have been developed previously, few, if any, methods have been developed to evaluate individual-level general surrogates, and no methods have formalized the use of cross-validation to quantify the expected prediction error. Our proposed method uses existing methods of individual-level surrogate evaluation within a given clinical trial setting in combination with cross-validation over a set of clinical trials to evaluate surrogate quality and to estimate the absolute prediction error that is expected in a new trial setting when using a PIGS. Simulations show that our method performs well across a variety of scenarios. We use our method to evaluate and to compare candidate individual-level general surrogates over a set of multi-national trials of a pentavalent rotavirus vaccine.
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Gabriel et al. (2017) studied Rotavirus gastroenteritis. Pentavalent rotavirus vaccine (RV5) vs. Placebo was evaluated on Absolute prediction error of candidate surrogates. The proposed cross-validation method evaluates predictive individual-level general surrogates, though application to rotavirus vaccine trials found no single high-quality surrogate across all regions.
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