Key result
A proposed Bayesian non-parametric modeling method successfully evaluated candidate trial level general surrogates, identifying two immune measures that predict pentavalent rotavirus vaccine efficacy.
A novel Bayesian non-parametric modeling and cross-validation method effectively evaluates and compares candidate trial-level general surrogates.
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May enable surrogate-based rotavirus vaccine evaluation; extends Bayesian methods but leaves prospective validation open.
An intermediate response measure that accurately predicts efficacy in a new setting can reduce trial cost and time to product licensure. In this paper, we define a trial level general surrogate as a trial level intermediate response that accurately predicts trial level clinical responses. Methods for evaluating trial level general surrogates have been developed previously. Many methods in the literature use trial level intermediate responses for prediction. However, all existing methods focus on surrogate evaluation and prediction in new settings, rather than comparison of candidate trial level surrogates, and few formalize the use of cross validation to quantify the expected prediction error. Our proposed method uses Bayesian non-parametric modeling and cross-validation to estimate the absolute prediction error for use in evaluating and comparing candidate trial level general surrogates. Simulations show that our method performs well across a variety of scenarios. We use our method to evaluate and to compare candidate trial level general surrogates in several multi-national trials of a pentavalent rotavirus vaccine. We identify two immune measures that have potential value as trial level general surrogates and use the measures to predict efficacy in a trial with no clinical outcomes measured.
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Gabriel et al. (2015) studied Rotavirus infection (vaccine trials). Bayesian non-parametric modeling and cross-validation method vs. Existing methods was evaluated on Absolute prediction error for candidate trial level general surrogates. A proposed Bayesian non-parametric modeling method successfully evaluated candidate trial level general surrogates, identifying two immune measures that predict pentavalent rotavirus vaccine efficacy.
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