This article deals with comparing a test with a control therapy using meta-analyses of data from randomized controlled trials with a time-to-event endpoint. Such analyses can often benefit from prior information about the distribution of control group outcomes. One possible source of this information is the published aggregate data about control groups of historical trials from the medical literature. We review methods for making posterior inference about exponentially distributed event times more robust to prior-data conflicts by discounting the prior information based on the extent of observed prior-data conflict. We use simulations to compare analyses without prior information with the meta-analytic combined, meta-analytic predictive and robust meta-analytic predictive approaches, as well as Bayesian model averaging using shrinkage priors. Bayesian model averaging via shrinkage priors with well-chosen hyperpriors performed best in terms of credible interval coverage and mean-squared error across scenarios. For the robust meta-analytic predictive approach, there was little benefit in increasing the weight of the informative mixture components beyond 0.2-0.5. This was the case even when little prior-data conflict was expected, except with very sparse data or substantial between-trial heterogeneity in control group hazard rates. for this article are available online.
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Univ Hosp Besancon, Methodol & Qual Life Oncol Unit, Besancon, France
Univ Hosp Besancon, Dept Med Oncol, Besancon, France
European Org Res Treatment Canc, Dept Med, Brussels, BelgiumUniv Hosp Besancon, Methodol & Qual Life Oncol Unit, Besancon, France
Fiteni, Frederic
Paillard, Marie-Justine
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Univ Hosp Besancon, Methodol & Qual Life Oncol Unit, Besancon, France
Univ Hosp Besancon, Dept Med Oncol, Besancon, FranceUniv Hosp Besancon, Methodol & Qual Life Oncol Unit, Besancon, France
Paillard, Marie-Justine
Westeel, Virginie
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Univ Hosp Besancon, Chest Dis Dept, Besancon, FranceUniv Hosp Besancon, Methodol & Qual Life Oncol Unit, Besancon, France
Westeel, Virginie
Bonnetain, Franck
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Univ Hosp Besancon, Methodol & Qual Life Oncol Unit, Besancon, France
Univ Hosp Besancon, Dept Med Oncol, Besancon, France
Univ Franche Comte, EA 3181, Besancon, FranceUniv Hosp Besancon, Methodol & Qual Life Oncol Unit, Besancon, France
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East China Normal Univ, Sch Stat, Shanghai 200241, Peoples R China
Univ Texas MD Anderson Canc Ctr, Dept Biostat, Houston, TX 77030 USAEast China Normal Univ, Sch Stat, Shanghai 200241, Peoples R China
Mu, Rongji
Xu, Jin
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East China Normal Univ, Sch Stat, Shanghai 200241, Peoples R ChinaEast China Normal Univ, Sch Stat, Shanghai 200241, Peoples R China
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Univ Paris Saclay, Inst Gustave Roussy, Serv Biostat & Epidemiol, Villejuif, France
Univ Paris Sud, Univ Paris Saclay, INSERM, CESP,UVSQ, Villejuif, FranceUniv Paris Saclay, Inst Gustave Roussy, Serv Biostat & Epidemiol, Villejuif, France
Rotolo, Federico
Paoletti, Xavier
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Univ Paris Saclay, Inst Gustave Roussy, Serv Biostat & Epidemiol, Villejuif, France
Univ Paris Sud, Univ Paris Saclay, INSERM, CESP,UVSQ, Villejuif, FranceUniv Paris Saclay, Inst Gustave Roussy, Serv Biostat & Epidemiol, Villejuif, France
Paoletti, Xavier
Burzykowski, Tomasz
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Univ Hasselt, I BioStat, Diepenbeek, Belgium
Int Inst Drug Dev, Louvain La Neuve, BelgiumUniv Paris Saclay, Inst Gustave Roussy, Serv Biostat & Epidemiol, Villejuif, France
Burzykowski, Tomasz
Buyse, Marc
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Univ Hasselt, I BioStat, Diepenbeek, Belgium
Int Inst Drug Dev, Louvain La Neuve, BelgiumUniv Paris Saclay, Inst Gustave Roussy, Serv Biostat & Epidemiol, Villejuif, France
Buyse, Marc
Michiels, Stefan
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Univ Paris Saclay, Inst Gustave Roussy, Serv Biostat & Epidemiol, Villejuif, France
Univ Paris Sud, Univ Paris Saclay, INSERM, CESP,UVSQ, Villejuif, FranceUniv Paris Saclay, Inst Gustave Roussy, Serv Biostat & Epidemiol, Villejuif, France