Pyrotinib combined with trastuzumab and chemotherapy in the treatment of HER2-positive metastatic breast cancer after the progression of trastuzumab therapy.

IF 2.6 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL
Xiangping Mei, Yue Hu, Huijie Liu, Hongge Wu, Linka Xie, Jie Xiong, Yuehua Wang, Jing Yao
{"title":"Pyrotinib combined with trastuzumab and chemotherapy in the treatment of HER2-positive metastatic breast cancer after the progression of trastuzumab therapy.","authors":"Xiangping Mei, Yue Hu, Huijie Liu, Hongge Wu, Linka Xie, Jie Xiong, Yuehua Wang, Jing Yao","doi":"10.1016/j.jfma.2025.03.003","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Retrospective studies have shown that the continuation use of trastuzumab in HER2 positive metastatic breast cancer patients who progressed during treatment with trastuzumab still may have clinical benefits. However, the optimal strategy was still unknown. We conducted this study aiming to explore the efficacy and safety of pyrotinib plus chemotherapy with or without trastuzumab in HER2 positive MBC patients who progressed after previous trastuzumab treatment.</p><p><strong>Methods: </strong>This was a real-world retrospective study that enrolled HER2 positive MBC patients previously treated with trastuzumab. Patients were divided into control group (pyrotinib combined with chemotherapy) and combined group (trastuzumab combined with pyrotinib and chemotherapy). The primary endpoint was progression-free survival (PFS), and the secondary endpoints were objective remission rate (ORR), disease control rate (DCR) and safety.</p><p><strong>Results: </strong>A total of 101 patients were included in the analysis with median follow-up time of 25.5 months (95%CI, 22.5-33.0). The median PFS was 19.1 months (95%CI 10.5-NA, P = 0.039) in combined group and 11.5 months (95%CI 8.1-15.1) in control group. The ORR was 55.6% in the combined group compared with 43.0% in the control group(P = 0.299), and the DCR was 100% compared with 87.7% respectively(P = 0.028). The most common grade 3 or 4 adverse events were diarrhea [7(25.0%)], neutropenia [5(14.3%)] and leukopenia [4(11.4%)] in combined group and diarrhea [3(5.0%)], neutropenia [3(5.0%)] and leukopenia [3(5.0%)] in control group.</p><p><strong>Conclusions: </strong>Trastuzumab combined with pyrotinib and chemotherapy showed clinical benefits and acceptable tolerance in HER2-positive MBC patients previously treated with trastuzumab. Thus, these combination regimens may be potential options for such patients.</p>","PeriodicalId":17305,"journal":{"name":"Journal of the Formosan Medical Association","volume":" ","pages":""},"PeriodicalIF":2.6000,"publicationDate":"2025-03-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the Formosan Medical Association","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.jfma.2025.03.003","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
引用次数: 0

Abstract

Introduction: Retrospective studies have shown that the continuation use of trastuzumab in HER2 positive metastatic breast cancer patients who progressed during treatment with trastuzumab still may have clinical benefits. However, the optimal strategy was still unknown. We conducted this study aiming to explore the efficacy and safety of pyrotinib plus chemotherapy with or without trastuzumab in HER2 positive MBC patients who progressed after previous trastuzumab treatment.

Methods: This was a real-world retrospective study that enrolled HER2 positive MBC patients previously treated with trastuzumab. Patients were divided into control group (pyrotinib combined with chemotherapy) and combined group (trastuzumab combined with pyrotinib and chemotherapy). The primary endpoint was progression-free survival (PFS), and the secondary endpoints were objective remission rate (ORR), disease control rate (DCR) and safety.

Results: A total of 101 patients were included in the analysis with median follow-up time of 25.5 months (95%CI, 22.5-33.0). The median PFS was 19.1 months (95%CI 10.5-NA, P = 0.039) in combined group and 11.5 months (95%CI 8.1-15.1) in control group. The ORR was 55.6% in the combined group compared with 43.0% in the control group(P = 0.299), and the DCR was 100% compared with 87.7% respectively(P = 0.028). The most common grade 3 or 4 adverse events were diarrhea [7(25.0%)], neutropenia [5(14.3%)] and leukopenia [4(11.4%)] in combined group and diarrhea [3(5.0%)], neutropenia [3(5.0%)] and leukopenia [3(5.0%)] in control group.

Conclusions: Trastuzumab combined with pyrotinib and chemotherapy showed clinical benefits and acceptable tolerance in HER2-positive MBC patients previously treated with trastuzumab. Thus, these combination regimens may be potential options for such patients.

求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
6.50
自引率
6.20%
发文量
381
审稿时长
57 days
期刊介绍: Journal of the Formosan Medical Association (JFMA), published continuously since 1902, is an open access international general medical journal of the Formosan Medical Association based in Taipei, Taiwan. It is indexed in Current Contents/ Clinical Medicine, Medline, ciSearch, CAB Abstracts, Embase, SIIC Data Bases, Research Alert, BIOSIS, Biological Abstracts, Scopus and ScienceDirect. As a general medical journal, research related to clinical practice and research in all fields of medicine and related disciplines are considered for publication. Article types considered include perspectives, reviews, original papers, case reports, brief communications, correspondence and letters to the editor.
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信