Huang Yufen, Chang Wan-Jung, Hsiao Chin-Fu
Department of Mathematics, National Chung Cheng University, Min-Hsiung, Chia-Yi, Taiwan.
Pharm Stat. 2013 Mar-Apr;12(2):59-64. doi: 10.1002/pst.1553. Epub 2013 Jan 14.
To accelerate the drug development process and shorten approval time, the design of multiregional clinical trials (MRCTs) incorporates subjects from many countries/regions around the world under the same protocol. After showing the overall efficacy of a drug in all global regions, one can also simultaneously evaluate the possibility of applying the overall trial results to all regions and subsequently support drug registration in each of them. In this paper, we focus on a specific region and establish a statistical criterion to assess the consistency between the specific region and overall results in an MRCT. More specifically, we treat each region in an MRCT as an independent clinical trial, and each perhaps has different treatment effect. We then construct the empirical prior information for the treatment effect for the specific region on the basis of all of the observed data from other regions. We will conclude similarity between the specific region and all regions if the posterior probability of deriving a positive treatment effect in the specific region is large, say 80%. Numerical examples illustrate applications of the proposed approach in different scenarios.
为了加速药物研发进程并缩短审批时间,多区域临床试验(MRCT)的设计纳入了来自世界多个国家/地区的受试者,遵循相同的方案。在证明一种药物在所有全球区域的总体疗效后,还可以同时评估将总体试验结果应用于所有区域的可能性,并随后支持在每个区域进行药物注册。在本文中,我们聚焦于一个特定区域,并建立一个统计标准来评估该特定区域与MRCT中总体结果之间的一致性。更具体地说,我们将MRCT中的每个区域视为一个独立的临床试验,每个区域可能具有不同的治疗效果。然后,我们根据来自其他区域的所有观测数据构建特定区域治疗效果的经验先验信息。如果在特定区域得出阳性治疗效果的后验概率很大,比如80%,我们就得出该特定区域与所有区域相似的结论。数值示例说明了所提出方法在不同场景中的应用。