Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, Duke University Medical Center, Durham, NC, United States of America.
Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, Massachusetts General Hospital, Boston, MA, United States of America.
Gynecol Oncol. 2019 Mar;152(3):533-539. doi: 10.1016/j.ygyno.2018.11.006.
Clinical research in gynecologic oncology has seen a proliferation of studies that investigate the effectiveness of treatments using existing data sources such as cancer registries, electronic health records, and insurance claims. These observational studies are often feasible when randomized trial may not be, and may be more generalizable than randomized trials, because of greater diversity in the study populations. While statistical methods such as multivariable regression, matching, stratification, and weighting can adjust for the confounding in observational studies, statistical adjustment cannot control for confounders that are unmeasured in the data. Observational studies comparing the effectiveness of treatments for gynecologic malignancies are susceptible to bias from unmeasured confounding because factors like functional status, frailty and disease burden, which influence treatment selection and outcome, are often not reported in existing data sources. Like randomized trials, quasi-experimental designs attempt to account for both measured and unmeasured confounding by exploiting natural experiments arising in the real world. These methods are underutilized in gynecologic oncology research and are particularly relevant to studies that use large datasets to study the effectiveness of treatments. In this review, we consider methodological challenges that arise in the analysis of non-randomized studies, and describe how application of quasi-experimental methodology can estimate unbiased treatment effects even in the presence of unmeasured confounders.
妇科肿瘤学的临床研究已经出现了大量的研究,这些研究利用癌症登记处、电子健康记录和保险索赔等现有数据源来调查治疗效果。当随机试验不可行时,这些观察性研究通常是可行的,并且可能比随机试验更具普遍性,因为研究人群的多样性更大。虽然多变量回归、匹配、分层和加权等统计方法可以调整观察性研究中的混杂因素,但统计调整不能控制数据中未测量的混杂因素。比较妇科恶性肿瘤治疗效果的观察性研究容易受到未测量混杂因素的偏倚影响,因为影响治疗选择和结果的因素,如功能状态、脆弱性和疾病负担,在现有数据源中通常没有报告。与随机试验一样,准实验设计试图通过利用现实世界中出现的自然实验来解释测量和未测量的混杂因素。这些方法在妇科肿瘤学研究中未得到充分利用,特别是对于使用大型数据集研究治疗效果的研究。在这篇综述中,我们考虑了在非随机研究分析中出现的方法学挑战,并描述了如何应用准实验方法即使在存在未测量混杂因素的情况下也可以估计无偏的治疗效果。