使用倾向评分匹配分析贝伐单抗和伊瑞布林对转移性乳腺癌的实际影响。

IF 1.4 Q4 ONCOLOGY
Koshi Matsui, Mitsuharu Earashi, Akemi Yoshikawa, Wataru Fukushima, Zensei Nozaki, Kaeko Oyama, Kiichi Maeda, Akiyoshi Nakakura, Satoshi Morita, Tsutomu Fujii
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引用次数: 0

摘要

贝伐单抗和伊瑞布林是治疗her2阴性转移性乳腺癌(MBC)的新药物;然而,在贝伐单抗和埃瑞布林之间选择治疗MBC是很困难的。本研究旨在比较两种治疗策略,即埃利布林联合贝伐单抗和紫杉醇(BEV + PTX)与BEV + PTX联合埃利布林,以确定给药顺序是否会影响现实世界中MBC的预后。从2011年8月至2018年6月,共有180例her2阴性MBC患者开始了BEV + PTX和埃瑞布林治疗。其中,84例患者先后接受BEV + PTX和伊瑞布林治疗。为了评估治疗顺序的影响,我们比较了BEV + PTX加依瑞布林(B-E组)与相反顺序治疗(E-B组)的疗效。采用倾向得分匹配法(PSMA)来提高本研究结果的稳健性。共有60例患者接受了BEV + PTX或伊瑞布林作为一线或二线治疗。在整个队列中,B-E组和E-B组的中位策略失败时间(TFS)分别为16.8和9.9个月[风险比(HR)=0.515, 95% CI 0.298-0.889, P=0.017]。类似的HR来源于TFS的PSMA。使用PSMA, B-E组和E-B组的TFS分别为16.9和9.9个月(HR=0.491, 95% CI 0.253-0.952, P=0.031)。这些结果提示,当同时使用贝伐单抗和伊瑞布林时,应先使用贝伐单抗,后使用伊瑞布林,以确保每种药物的最有效使用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Real-world effect of bevacizumab and eribulin on metastatic breast cancer using a propensity score matching analysis.

Real-world effect of bevacizumab and eribulin on metastatic breast cancer using a propensity score matching analysis.

Real-world effect of bevacizumab and eribulin on metastatic breast cancer using a propensity score matching analysis.

Bevacizumab and eribulin are novel agents for the treatment of HER2-negative metastatic breast cancer (MBC); however, the choice between bevacizumab and eribulin for MBC can be difficult. The present study aimed to compare two treatment strategies, eribulin followed by bevacizumab and paclitaxel (BEV + PTX) versus BEV + PTX followed by eribulin, to determine whether the order of administration affects the outcome of MBC in the real world. A total of 180 patients who started BEV + PTX and eribulin treatment for HER2-negative MBC from August 2011 to June 2018 were selected. Of these, 84 patients were treated with both BEV + PTX and eribulin sequentially. To evaluate the influence of the sequential order, the efficacy of BEV + PTX followed by eribulin (B-E arm) was compared to treatment with the reverse sequence (E-B arm). The propensity score matching method (PSMA) was used to improve the robustness of the findings from the present study. A total of 60 cases analyzed received BEV + PTX or eribulin as either first- or second-line treatment. In the entire cohort, the median time to failure of strategy (TFS) was 16.8 and 9.9 months in the B-E and E-B arms, respectively [hazard ratio (HR)=0.515, 95% CI 0.298-0.889, P=0.017). A similar HR was derived from PSMA for TFS. Using PSMA, TFS was 16.9 and 9.9 months in the B-E and E-B arms, respectively (HR=0.491, 95% CI 0.253-0.952, P=0.031). These results suggested that when both bevacizumab and eribulin are administered, bevacizumab should be administered first and eribulin should be administered later to ensure the most effective use of each drug.

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