Design and Estimation for Evaluating Principal Surrogate Markers in Vaccine Trials
From MaRDI portal
Publication:2846433
DOI10.1111/biom.12014zbMath1274.62794WikidataQ39467318 ScholiaQ39467318MaRDI QIDQ2846433
Julian Wolfson, Ying Huang, Peter B. Gilbert
Publication date: 5 September 2013
Published in: Biometrics (Search for Journal in Brave)
Full work available at URL: http://europepmc.org/articles/pmc3713795
two-phase sampling design; pseudo-score; estimated likelihood; principal surrogate; closeout placebo vaccination; immune correlate
62P10: Applications of statistics to biology and medical sciences; meta analysis
Related Items
A unified evaluation of differential vaccine efficacy, Predicting overall vaccine efficacy in a new setting by re-calibrating baseline covariate and intermediate response endpoint effect modifiers of type-specific vaccine efficacy, Sensitivity analysis for evaluating principal surrogate endpoints relaxing the equal early clinical risk assumption, Evaluating principal surrogate markers in vaccine trials in the presence of multiphase sampling
Cites Work
- The evaluation of surrogate endpoints.
- Assessing surrogate endpoints in vaccine trials with case-cohort sampling and the Cox model
- Comparing Biomarkers as Principal Surrogate Endpoints
- Statistical Identifiability and the Surrogate Endpoint Problem, with Application to Vaccine Trials
- Principal Stratification in Causal Inference
- Evaluating Candidate Principal Surrogate Endpoints
- A Bayesian Approach to Surrogacy Assessment Using Principal Stratification in Clinical Trials
- Related Causal Frameworks for Surrogate Outcomes
- A Pseudoscore Estimator for Regression Problems With Two-Phase Sampling
- The validation of surrogate endpoints in meta-analyses of randomized experiments
- Augmented Designs to Assess Immune Response in Vaccine Trials
- A Generalization of Sampling Without Replacement From a Finite Universe
- Assessing Vaccine Effects in Repeated Low‐Dose Challenge Experiments