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

IF 1.4 Q4 ONCOLOGY Molecular and clinical oncology Pub Date : 2023-02-01 DOI:10.3892/mco.2023.2608
Koshi Matsui, Mitsuharu Earashi, Akemi Yoshikawa, Wataru Fukushima, Zensei Nozaki, Kaeko Oyama, Kiichi Maeda, Akiyoshi Nakakura, Satoshi Morita, Tsutomu Fujii
{"title":"Real-world effect of bevacizumab and eribulin on metastatic breast cancer using a propensity score matching analysis.","authors":"Koshi Matsui,&nbsp;Mitsuharu Earashi,&nbsp;Akemi Yoshikawa,&nbsp;Wataru Fukushima,&nbsp;Zensei Nozaki,&nbsp;Kaeko Oyama,&nbsp;Kiichi Maeda,&nbsp;Akiyoshi Nakakura,&nbsp;Satoshi Morita,&nbsp;Tsutomu Fujii","doi":"10.3892/mco.2023.2608","DOIUrl":null,"url":null,"abstract":"<p><p>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.</p>","PeriodicalId":18737,"journal":{"name":"Molecular and clinical oncology","volume":"18 2","pages":"12"},"PeriodicalIF":1.4000,"publicationDate":"2023-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/4a/9a/mco-18-02-02608.PMC9892966.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular and clinical oncology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3892/mco.2023.2608","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

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.

Abstract Image

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
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。
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。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
2.80
自引率
0.00%
发文量
108
期刊最新文献
Prognostic impact of HLA class I immunohistochemistry staining intensity with regard to the risk of recurrence of adenoid cystic carcinoma. Prognostic value and predictive biomarkers of synergistic interaction between tumor-associated macrophages and cancer stem cells in colorectal cancer. Reduction of seroma by pectoralis fascia dissection using an energy device in total mastectomy for breast cancer: An observational study. Prognostic value of serum uric acid levels following radiotherapy and chemotherapy in nasopharyngeal carcinoma. Integrated multi-omics profiling of plasma extracellular vesicles reveals the hsa-miR-1-3p-LRP1 axis as a potential biomarker in cervical cancer.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1