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Informed Bayesian Survival Analysis

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    0560436 - ÚI 2023 RIV GB eng J - Journal Article
    Bartoš, František - Aust, F. - Haaf, J. M.
    Informed Bayesian Survival Analysis.
    BMC Medical Research Methodology. Roč. 22, č. 1 (2022), č. článku 238. E-ISSN 1471-2288
    Grant - others:Ministerstvo školství, mládeže a tělovýchovy - GA MŠk(CZ) LM2018140
    Institutional support: RVO:67985807
    Keywords : Bayesian * survival analysis * model-averaging * Bayes factor * historical data
    OECD category: Statistics and probability
    Impact factor: 4, year: 2022
    Method of publishing: Open access
    https://dx.doi.org/10.1186/s12874-022-01676-9

    We overview Bayesian estimation, hypothesis testing, and model-averaging and illustrate how they benefit parametric survival analysis. We contrast the Bayesian framework to the currently dominant frequentist approach and highlight advantages, such as seamless incorporation of historical data, continuous monitoring of evidence, and incorporating uncertainty about the true data generating process. We illustrate the application of the Bayesian approaches on an example data set from a colon cancer trial. We compare the Bayesian parametric survival analysis and frequentist models with AIC/BIC model selection in fixed-n and sequential designs with a simulation study. In the example data set, the Bayesian framework provided evidence for the absence of a positive treatment effect on disease-free survival in patients with resected colon cancer. Furthermore, the Bayesian sequential analysis would have terminated the trial 13.3 months earlier than the standard frequentist analysis. In a simulation study with sequential designs, the Bayesian framework on average reached a decision in almost half the time required by the frequentist counterparts, while maintaining the same power, and an appropriate false-positive rate. Under model misspecification, the Bayesian framework resulted in higher false-negative rate compared to the frequentist counterparts, which resulted in a higher proportion of undecided trials. In fixed-n designs, the Bayesian framework showed slightly higher power, slightly elevated error rates, and lower bias and RMSE when estimating treatment effects in small samples. We have made the analytic approach readily available in RoBSA R package. The outlined Bayesian framework provides several benefits when applied to parametric survival analyses. It uses data more efficiently, is capable of greatly shortening the length of clinical trials, and provides a richer set of inferences.
    Permanent Link: https://hdl.handle.net/11104/0333363


    Research data: CRAN
     
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    0560436-aoa.pdf31.9 MBOA CC BY 4:0Publisher’s postprintopen-access
    0560436-pre.pdf0888.1 KBAuthor´s preprintopen-access
     
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