Matsui Koshi, Earashi Mitsuharu, Yoshikawa Akemi, Fukushima Wataru, Nozaki Zensei, Oyama Kaeko, Maeda Kiichi, Nakakura Akiyoshi, Morita Satoshi, Fujii Tsutomu
Department of Surgery and Science, Faculty of Medicine, Academic Assembly, University of Toyama, Toyama 930-0194, Japan.
Department of Surgery, Toyama Nishi General Hospital, Toyama 939-2716, Japan.
Mol Clin Oncol. 2023 Jan 13;18(2):12. doi: 10.3892/mco.2023.2608. eCollection 2023 Feb.
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.
贝伐单抗和艾瑞布林是治疗人表皮生长因子受体2阴性转移性乳腺癌(MBC)的新型药物;然而,在MBC治疗中选择贝伐单抗还是艾瑞布林可能会很困难。本研究旨在比较两种治疗策略,即先使用艾瑞布林后使用贝伐单抗和紫杉醇(BEV+PTX)与先使用BEV+PTX后使用艾瑞布林,以确定给药顺序是否会影响现实世界中MBC的治疗结果。选取了2011年8月至2018年6月期间开始接受BEV+PTX和艾瑞布林治疗HER2阴性MBC的180例患者。其中,84例患者先后接受了BEV+PTX和艾瑞布林治疗。为了评估给药顺序的影响,将先使用BEV+PTX后使用艾瑞布林(B-E组)的疗效与相反顺序(E-B组)的治疗进行了比较。采用倾向评分匹配法(PSMA)来提高本研究结果的稳健性。共有60例分析病例接受BEV+PTX或艾瑞布林作为一线或二线治疗。在整个队列中,B-E组和E-B组的策略失败中位时间(TFS)分别为16.8个月和9.9个月[风险比(HR)=0.515,95%置信区间0.298-0.889,P=0.017]。PSMA得出的TFS的HR相似。使用PSMA时,B-E组和E-B组的TFS分别为16.9个月和9.9个月(HR=0.491,95%置信区间0.253-0.952,P=0.031)。这些结果表明,当同时使用贝伐单抗和艾瑞布林时,应先使用贝伐单抗,后使用艾瑞布林,以确保每种药物的最有效使用。