Re-Print: Developing and then Confirming a Hypothesis Based on a Chronology of Several Clinical Trials: A Bayesian Application to Pirfenidone Mortality Results

Zhengning Lin, Donald A Berry
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Abstract

Designing a study for independent confirmation of a treatment effect is sometimes not practical due to required large sample size. Post hoc pooling of studies including those for learning purposes is subject to selection bias and therefore generally not suitable for confirmation of a treatment effect. We propose a Bayesian approach which calibrates the role of prior information from historical studies for learning and confirming purposes. The amount of prior information to be combined with current study data for the purpose of hypothesis confirmation depends on the overall strength of prior information for hypothesis generation. The method is illustrated in the analysis of mortality data for the pirfenidone NDA. The Bayesian analysis provides a formal method to calibrate the role of information from historical evidence in the overall interpretation of results from both historical and concurrent clinical studies. The increased efficiency of using all available data is especially important in drug development for rare diseases with serious consequences, where limited patient source prohibits large trials, and unmet medical needs demand rapid access to treatment options.
基于几项临床试验年表的假设的发展和确认:吡非尼酮死亡率结果的贝叶斯应用
设计一项研究来独立确认治疗效果有时是不现实的,因为需要大样本量。包括以学习为目的的研究在内的事后汇总研究受到选择偏差的影响,因此通常不适合确认治疗效果。我们提出了一种贝叶斯方法,该方法校准了历史研究中先验信息的作用,用于学习和确认目的。为了验证假设,需要与当前研究数据相结合的先验信息的数量取决于生成假设的先验信息的总体强度。该方法在吡非尼酮NDA的死亡率数据分析中得到说明。贝叶斯分析提供了一种正式的方法来校准来自历史证据的信息在历史和同期临床研究结果的整体解释中的作用。提高利用所有现有数据的效率,对于治疗后果严重的罕见疾病的药物开发尤其重要,因为患者来源有限,无法进行大规模试验,而未得到满足的医疗需求要求迅速获得治疗方案。
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