Department of Biostatistics and Bioinformatics, Emory University, Atlanta, Georgia, USA.
Division of Biostatistics, Department of Population Health Sciences, Weill Cornell Medicine, New York, New York, USA.
Biometrics. 2021 Dec;77(4):1467-1481. doi: 10.1111/biom.13377. Epub 2020 Oct 11.
Time is of the essence in evaluating potential drugs and biologics for the treatment and prevention of COVID-19. There are currently 876 randomized clinical trials (phase 2 and 3) of treatments for COVID-19 registered on clinicaltrials.gov. Covariate adjustment is a statistical analysis method with potential to improve precision and reduce the required sample size for a substantial number of these trials. Though covariate adjustment is recommended by the U.S. Food and Drug Administration and the European Medicines Agency, it is underutilized, especially for the types of outcomes (binary, ordinal, and time-to-event) that are common in COVID-19 trials. To demonstrate the potential value added by covariate adjustment in this context, we simulated two-arm, randomized trials comparing a hypothetical COVID-19 treatment versus standard of care, where the primary outcome is binary, ordinal, or time-to-event. Our simulated distributions are derived from two sources: longitudinal data on over 500 patients hospitalized at Weill Cornell Medicine New York Presbyterian Hospital and a Centers for Disease Control and Prevention preliminary description of 2449 cases. In simulated trials with sample sizes ranging from 100 to 1000 participants, we found substantial precision gains from using covariate adjustment-equivalent to 4-18% reductions in the required sample size to achieve a desired power. This was the case for a variety of estimands (targets of inference). From these simulations, we conclude that covariate adjustment is a low-risk, high-reward approach to streamlining COVID-19 treatment trials. We provide an R package and practical recommendations for implementation.
评估用于治疗和预防 COVID-19 的潜在药物和生物制剂时,时间至关重要。目前,clinicaltrials.gov 上注册了 876 项 COVID-19 治疗的随机临床试验(第 2 阶段和第 3 阶段)。协变量调整是一种具有提高精度和减少大量试验所需样本量潜力的统计分析方法。尽管美国食品和药物管理局和欧洲药品管理局都推荐使用协变量调整,但它的应用并不广泛,尤其是对于 COVID-19 试验中常见的二分类、有序分类和生存时间等类型的结局。为了证明协变量调整在这种情况下的潜在价值,我们模拟了两项比较假设的 COVID-19 治疗与标准治疗的双臂随机试验,主要结局为二分类、有序分类或生存时间。我们的模拟分布来自两个来源:威尔康奈尔医学院纽约长老会医院 500 多名住院患者的纵向数据和疾病控制与预防中心对 2449 例病例的初步描述。在样本量从 100 到 1000 名参与者的模拟试验中,我们发现使用协变量调整可获得显著的精度增益,相当于所需样本量减少 4-18%,即可达到所需的功效。对于各种估计量(推断目标)都是如此。从这些模拟中,我们得出结论,协变量调整是一种低风险、高回报的方法,可以简化 COVID-19 治疗试验。我们提供了一个 R 包和实施的实用建议。