Teikyo University Graduate School of Public Health, 2-11-1 Kaga, Itabashi-ku, Tokyo, Japan.
Clinical Development Department, Daiichi Sankyo RD Novare Co., Ltd., Tokyo, Japan.
Breast Cancer Res Treat. 2020 May;181(1):189-198. doi: 10.1007/s10549-020-05615-4. Epub 2020 Apr 3.
Earlier studies suggest progression-free survival (PFS) may be used as a surrogate endpoint for overall survival (OS) in metastatic breast cancer, which could shorten follow-up duration and speed up assessment of treatment effects. However, to our knowledge, the association between them is still unclear in advanced or metastatic triple-negative breast cancer (TNBC).
A literature-based meta-analysis followed by correlation analysis was conducted in advanced or metastatic TNBC. Weighted multiple regression analysis was then used to test the strength of the association between medians of PFS and OS, and the association between HR and HR.
Fourteen randomized clinical trials published between January 2007 and August 2019, 31 median pairs for PFS and OS, and 17 pairs for HR and HR from 3,880 patients were selected. The Pearson correlation coefficient between medians of PFS and OS was 0.84 (95% confidence interval (CI) 0.68-0.92, p < 0.001), and the correlation coefficient between HR and HR was 0.86 (95% CI 0.63-0.95, p < 0.001). Weighted multiple regression analysis showed HR was the most significant predictor of HR among covariates analyzed (p < 0.001). Both the medians of PFS and OS correlation, and the HR and HR correlation were 0.79 (p < 0.001), 0.80 (p = 0.001), respectively, in the 11 trials excluding immunotherapy and bevacizumab-based therapy trials.
Our analysis suggests PFS can be strongly correlated with OS and considered a valid surrogate endpoint for OS in advanced or metastatic TNBC.
早期研究表明,无进展生存期(PFS)可能可作为转移性乳腺癌的总生存期(OS)替代终点,从而缩短随访时间并加快评估治疗效果。然而,据我们所知,在晚期或转移性三阴性乳腺癌(TNBC)中,两者之间的关联仍不清楚。
对晚期或转移性 TNBC 进行基于文献的荟萃分析和相关性分析。然后,使用加权多重回归分析来检验 PFS 和 OS 中位数之间以及 HR 和 HR 之间关联的强度。
共纳入 2007 年 1 月至 2019 年 8 月期间发表的 14 项随机临床试验,涉及 31 对 PFS 和 OS 中位数,以及来自 3880 名患者的 17 对 HR 和 HR。PFS 和 OS 中位数之间的 Pearson 相关系数为 0.84(95%置信区间(CI)0.68-0.92,p<0.001),HR 和 HR 之间的相关系数为 0.86(95% CI 0.63-0.95,p<0.001)。加权多重回归分析表明,在分析的协变量中,HR 是 HR 最显著的预测因子(p<0.001)。在排除免疫治疗和贝伐珠单抗治疗试验的 11 项试验中,PFS 和 OS 中位数的相关性以及 HR 和 HR 的相关性分别为 0.79(p<0.001)和 0.80(p=0.001)。
我们的分析表明,PFS 与 OS 具有很强的相关性,可以作为晚期或转移性 TNBC 中 OS 的有效替代终点。