Goldfeld Keith S, Wu Danni, Tarpey Thaddeus, Liu Mengling, Wu Yinxiang, Troxel Andrea B, Petkova Eva
Division of Biostatistics, Department of Population Health, New York University Grossman School of Medicine, New York, New York, USA.
Department of Environmental Medicine, New York University Grossman School of Medicine, New York, New York, USA.
Stat Med. 2021 Oct 30;40(24):5131-5151. doi: 10.1002/sim.9115. Epub 2021 Jun 23.
As the world faced the devastation of the COVID-19 pandemic in late 2019 and early 2020, numerous clinical trials were initiated in many locations in an effort to establish the efficacy (or lack thereof) of potential treatments. As the pandemic has been shifting locations rapidly, individual studies have been at risk of failing to meet recruitment targets because of declining numbers of eligible patients with COVID-19 encountered at participating sites. It has become clear that it might take several more COVID-19 surges at the same location to achieve full enrollment and to find answers about what treatments are effective for this disease. This paper proposes an innovative approach for pooling patient-level data from multiple ongoing randomized clinical trials (RCTs) that have not been configured as a network of sites. We present the statistical analysis plan of a prospective individual patient data (IPD) meta-analysis (MA) from ongoing RCTs of convalescent plasma (CP). We employ an adaptive Bayesian approach for continuously monitoring the accumulating pooled data via posterior probabilities for safety, efficacy, and harm. Although we focus on RCTs for CP and address specific challenges related to CP treatment for COVID-19, the proposed framework is generally applicable to pooling data from RCTs for other therapies and disease settings in order to find answers in weeks or months, rather than years.
2019年末至2020年初,当世界面临新冠疫情的肆虐时,许多地方启动了大量临床试验,以确定潜在治疗方法的疗效(或缺乏疗效)。由于疫情迅速蔓延至不同地区,个别研究面临无法达到招募目标的风险,因为参与试验的地点遇到的符合条件的新冠患者数量在减少。很明显,同一地点可能还需要经历几次新冠疫情高峰,才能实现充分招募,并找到针对这种疾病的有效治疗方法。本文提出了一种创新方法,用于汇总来自多个正在进行的随机临床试验(RCT)的患者层面数据,这些试验尚未配置为站点网络。我们展示了一项针对正在进行的恢复期血浆(CP)随机对照试验的前瞻性个体患者数据(IPD)荟萃分析(MA)的统计分析计划。我们采用自适应贝叶斯方法,通过安全性、疗效和危害的后验概率持续监测累积的汇总数据。尽管我们专注于CP的随机对照试验,并解决与新冠治疗中CP治疗相关的特定挑战,但所提出的框架通常适用于汇总来自其他疗法和疾病背景的随机对照试验的数据,以便在数周或数月内而非数年内找到答案。