Department of Biostatistics and Bioinformatics, Duke University, Durham, North Carolina, USA.
Tufts Medical Center, Division of Clinical Decision Making, Department of Medicine, Tufts University School of Medicine, Boston, Massachusetts, USA.
Stat Med. 2020 Sep 30;39(22):3003-3021. doi: 10.1002/sim.8581. Epub 2020 Jul 9.
With heighted interest in causal inference based on real-world evidence, this empirical study sought to understand differences between the results of observational analyses and long-term randomized clinical trials. We hypothesized that patients deemed "eligible" for clinical trials would follow a different survival trajectory from those deemed "ineligible" and that this factor could partially explain results. In a large observational registry dataset, we estimated separate survival trajectories for hypothetically trial-eligible vs ineligible patients under both coronary artery bypass surgery (CABG) and percutaneous coronary intervention (PCI). We also explored whether results would depend on the causal inference method (inverse probability of treatment weighting vs optimal full propensity matching) or the approach to combine propensity scores from multiple imputations (the "across" vs "within" approaches). We found that, in this registry population of PCI/CABG multivessel patients, 32.5% would have been eligible for contemporaneous RCTs, suggesting that RCTs enroll selected populations. Additionally, we found treatment selection bias with different distributions of propensity scores between PCI and CABG patients. The different methodological approaches did not result in different conclusions. Overall, trial-eligible patients appeared to demonstrate at least marginally better survival than ineligible patients. Treatment comparisons by eligibility depended on disease severity. Among trial-eligible three-vessel diseased and trial-ineligible two-vessel diseased patients, CABG appeared to have at least a slight advantage with no treatment difference otherwise. In conclusion, our analyses suggest that RCTs enroll highly selected populations, and our findings are generally consistent with RCTs but less pronounced than major registry findings.
随着人们对基于真实世界证据的因果推理的兴趣日益浓厚,这项实证研究旨在了解观察性分析和长期随机临床试验结果之间的差异。我们假设,被认为有资格参加临床试验的患者的生存轨迹与被认为无资格参加临床试验的患者不同,而这一因素可能部分解释了结果。在一个大型观察性登记数据集,我们估计了假设的符合试验条件的患者与不符合试验条件的患者的单独生存轨迹,分别在冠状动脉旁路移植术(CABG)和经皮冠状动脉介入治疗(PCI)下。我们还探讨了结果是否取决于因果推理方法(治疗反概率加权与最佳完全倾向匹配)或从多个插补中合并倾向评分的方法(“跨”与“内”方法)。我们发现,在这个 PCI/CABG 多血管患者的登记人群中,32.5%的患者可能有资格参加同期 RCT,这表明 RCT 只招募了部分人群。此外,我们还发现了治疗选择偏倚,PCI 和 CABG 患者之间的倾向评分分布不同。不同的方法学方法并没有导致不同的结论。总的来说,符合试验条件的患者的生存似乎至少略好于不符合试验条件的患者。根据符合试验条件和不符合试验条件的患者的疾病严重程度进行的治疗比较。在符合试验条件的三支血管病变和不符合试验条件的两支血管病变患者中,CABG 似乎至少有轻微优势,否则无治疗差异。总之,我们的分析表明 RCT 招募了高度选择的人群,我们的发现与 RCT 基本一致,但不如主要登记研究结果明显。