Department of Clinical Medicine and Surgery, University of Naples Federico II, Via Sergio Pansini 5, Naples, Italy.
IRCCS Ospedale San Raffaele, Department of Medical Oncology, Milan, Italy; Università Vita-Salute San Raffaele, Milan, Italy.
Eur J Cancer. 2024 Dec;213:115077. doi: 10.1016/j.ejca.2024.115077. Epub 2024 Oct 20.
Assessment of Progression-free survival (PFS) events by investigators might be inaccurate in randomized controlled trials (RCTs) with open-label design. We explored differences in PFS evaluated by blinded independent central review (BICR) or local investigator assessment (IA) in trials testing immunotherapy (IO) in advanced cancers.
We systematically reviewed articles of RCTs investigating IO in advanced tumors, published in PubMed-indexed journals up to December 2023. For each RCT, we collected PFS results by BICR and by local IA. We calculated the discrepancy index (DI) as the ratio of BICR and IA Hazard Ratios (HR/HR) for PFS. An overall DI and relative confidence interval (CI) were calculated using a fixed-effect model weighted for the inverse of variance.
Only 32/140 (22.9 %) RCTs reported both BICR and local IA PFS data, including 17,054 patients. PFS was the sole primary endpoint in 19/32 (59.4 %) and a co-primary endpoint 9/32 (28.2 %) trials. The study design was open label or double-blind in 17/32 (53.1 %) and 15/32 (46.9 %) RCTs, respectively. The overall DI was 1.07 (95 % CI 1.01-1.13; I =0, p = 0.02), revealing a more optimistic analysis of results in favor of local IA. In the 17 open-label trials, the overall DI was 1.09 (95 % CI 1.02-1.17, I2 =0, p = 0.02), revealing a more favorable interpretation of PFS results by local investigators.
We found a statistically significant difference between BICR and local IA of PFS in trials of IO in cancer. These results suggest that the double assessment is recommended in RCTs testing IO, especially in open-label trials.
This work was supported by the MFAG27826-2022 grant (Dr. Alberto Servetto).
在开放标签设计的随机对照试验(RCT)中,研究者评估的无进展生存期(PFS)事件可能不准确。我们探讨了在晚期癌症免疫治疗(IO)试验中,盲法独立中心评估(BICR)或当地研究者评估(IA)评估的 PFS 之间的差异。
我们系统地回顾了截至 2023 年 12 月在 PubMed 索引期刊上发表的 IO 治疗晚期肿瘤 RCT 的文章。对于每项 RCT,我们收集了 BICR 和当地 IA 的 PFS 结果。我们计算了差异指数(DI),即 BICR 和 IA 的 PFS 风险比(HR/HR)的比值。使用固定效应模型加权方差倒数计算总体 DI 和相对置信区间(CI)。
仅有 32/140(22.9%)项 RCT 报告了 BICR 和当地 IA 的 PFS 数据,包括 17054 名患者。PFS 是 19/32(59.4%)项和 9/32(28.2%)项 RCT 的唯一主要终点和共同主要终点。17/32(53.1%)项和 15/32(46.9%)项 RCT 的研究设计分别为开放标签或双盲。总体 DI 为 1.07(95%CI 1.01-1.13;I=0,p=0.02),表明当地 IA 对结果的分析更为乐观。在 17 项开放标签试验中,总体 DI 为 1.09(95%CI 1.02-1.17,I2=0,p=0.02),表明当地研究者对 PFS 结果的解释更为有利。
我们发现 IO 治疗癌症的 RCT 中,BICR 和当地 IA 的 PFS 存在统计学显著差异。这些结果表明,在 IO 检测 RCT 中,特别是在开放标签试验中,建议进行双重评估。
这项工作得到了 MFAG27826-2022 赠款(Dr. Alberto Servetto)的支持。