Dutch Institute for Clinical Auditing, Leiden, the Netherlands.
Division of Pharmacoepidemiology and Clinical Pharmacology, Utrecht Institute for Pharmaceutical Sciences, Utrecht, The Netherlands.
BMC Med Res Methodol. 2023 Jan 3;23(1):1. doi: 10.1186/s12874-022-01760-0.
Many studies have compared real-world clinical outcomes of immunotherapy in patients with metastatic non-small cell lung cancer (NSCLC) with reported outcomes data from pivotal trials. However, any differences observed could be only limitedly explored further for causation because of the unavailability of individual patient data (IPD) from trial participants. The present study aims to explore the additional benefit of comparison with IPD.
This study compares progression free survival (PFS) and overall survival (OS) of metastatic NSCLC patients treated with second line nivolumab in real-world clinical practice (n = 141) with IPD from participants in the Checkmate-057 clinical trial (n = 292). Univariate and multivariate Cox proportional hazards models were used to construct HRs for real-world practice versus clinical trial.
Real-world patients were older (64 vs. 61 years), had more often ECOG PS ≥ 2 (5 vs. 0%) and were less often treated with subsequent anti-cancer treatment (28.4 vs. 42.5%) compared to trial patients. The median PFS in real-world patients was longer (3.84 (95%CI: 3.19-5.49) vs 2.30 (2.20-3.50) months) and the OS shorter than in trial participants (8.25 (6.93-13.2) vs. 12.2 (9.90-15.1) months). Adjustment with available patient characteristics, led to a shift in the hazard ratio (HR) for OS, but not for PFS (HRs from 1.13 (0.88-1.44) to 1.07 (0.83-1.38), and from 0.82 (0.66-1.03) to 0.79 (0.63-1.00), respectively).
This study is an example how IPD from both real-world and trial patients can be applied to search for factors that could explain an efficacy-effectiveness gap. Making IPD from clinical trials available to the international research community allows this.
许多研究比较了转移性非小细胞肺癌(NSCLC)患者免疫治疗的真实世界临床结局与关键试验报告的结局数据。然而,由于无法从试验参与者获得个体患者数据(IPD),因此只能有限地进一步探讨任何观察到的差异的因果关系。本研究旨在探索与 IPD 进行比较的额外益处。
本研究比较了真实世界中接受二线纳武利尤单抗治疗的转移性 NSCLC 患者(n=141)的无进展生存期(PFS)和总生存期(OS)与 Checkmate-057 临床试验参与者的 IPD(n=292)。使用单变量和多变量 Cox 比例风险模型构建真实世界实践与临床试验的 HR。
与试验患者相比,真实世界患者年龄更大(64 岁 vs. 61 岁),ECOG PS≥2 的比例更高(5% vs. 0%),接受后续抗癌治疗的比例更低(28.4% vs. 42.5%)。真实世界患者的中位 PFS 更长(3.84(95%CI:3.19-5.49)vs. 2.30(2.20-3.50)个月),OS 更短与试验参与者相比(8.25(6.93-13.2)vs. 12.2(9.90-15.1)个月)。在调整了可用的患者特征后,OS 的危险比(HR)发生了变化,但 PFS 没有(HR 分别从 1.13(0.88-1.44)变为 1.07(0.83-1.38)和从 0.82(0.66-1.03)变为 0.79(0.63-1.00))。
本研究是一个例子,说明了如何应用来自真实世界和试验患者的 IPD 来寻找可能解释疗效-有效性差距的因素。使临床试验的 IPD 可供国际研究界使用即可实现这一点。