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曲妥珠单抗-恩美曲妥珠单抗治疗曲妥珠单抗和帕妥珠单抗耐药的人表皮生长因子受体 2 阳性转移性乳腺癌的延长反应:系统评价证据。

Prolonged Responses With Trastuzumab Emtasine Treatment of Human Epidermal Growth Factor Receptor 2-positive Metastatic Breast Cancer Refractory to Trastuzumab and Pertuzumab: Systematic Review of Evidence.

机构信息

Medical Oncology Department, Ramon y Cajal University Hospital, Madrid, Spain.

Medical Oncology Department, Ramon y Cajal University Hospital, Madrid, Spain.

出版信息

Clin Breast Cancer. 2021 Oct;21(5):391-398. doi: 10.1016/j.clbc.2021.01.004. Epub 2021 Jan 7.

Abstract

Amplification of human epidermal growth factor receptor 2 (HER2) occurs in around 25% of breast cancers and has been associated with aggressive disease. Here, we summarize published evidence on efficacy and prolonged responses with trastuzumab emtansine (T-DM1) after first-line trastuzumab plus pertuzumab and provide possible factors related to prolonged responses to T-DM1. We conducted a literature search using PubMed, and articles that were published in English between July 1, 2012 and December 31, 2019 were included. A review of the bibliography included in the articles found was made. Nine articles were eligible; 2 were case reports, and the remaining 7 were nonexperimental studies, all retrospective. Five were multi-center works. The total number of patients was 796 (276 received pertuzumab). The Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) statement was used for this systematic review. The population included was heterogeneous among studies according to hormone receptor status, de novo metastatic disease, number of metastatic sites, visceral involvement, brain metastasis, previous neoadjuvant or adjuvant trastuzumab, and line of therapy in which T-DM1 was administered. Less efficacy in terms of responses (overall response rate, 18%-33%) and progression-free survival (4-6 months) with second-line T-DM1, in patients pretreated with pertuzumab, was shown (if compared with the EMILIA trial). The results are more similar to those of the TH3RESA trial (very pretreated population). Prolonged treatments (6 months or more) were observed in at least 17% of cases. The efficacy of T-DM1 after a previous pertuzumab treatment is lower than if pertuzumab is not given, although prolonged responses are observed in this setting.

摘要

人类表皮生长因子受体 2(HER2)的扩增发生在大约 25%的乳腺癌中,并与侵袭性疾病有关。在这里,我们总结了发表的关于曲妥珠单抗-美坦新偶联物(T-DM1)在曲妥珠单抗联合帕妥珠单抗一线治疗后的疗效和延长反应的证据,并提供了与 T-DM1 延长反应相关的可能因素。我们使用 PubMed 进行了文献检索,纳入了 2012 年 7 月 1 日至 2019 年 12 月 31 日期间发表的英文文章。还对文章中包含的参考文献进行了综述。有 9 篇文章符合条件;2 篇为病例报告,其余 7 篇为非实验研究,均为回顾性研究。其中 5 篇为多中心研究。总共有 796 名患者(276 名接受了帕妥珠单抗治疗)。本系统评价采用系统评价和荟萃分析的首选报告项目(PRISMA)声明。根据激素受体状态、初发转移性疾病、转移部位数量、内脏受累、脑转移、先前新辅助或辅助曲妥珠单抗以及接受 T-DM1 治疗的治疗线,研究人群在不同研究中存在异质性。与 EMILIA 试验相比,先前接受过帕妥珠单抗治疗的患者二线使用 T-DM1 的疗效(总缓解率为 18%-33%,无进展生存期为 4-6 个月)较低。结果与 TH3RESA 试验(预处理人群)更为相似。至少 17%的病例观察到延长治疗(6 个月或更长时间)。与未使用帕妥珠单抗相比,先前使用过帕妥珠单抗治疗后 T-DM1 的疗效较低,但在这种情况下观察到延长反应。

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