Can Patients with HER2-Low Breast Cancer Benefit from Anti-HER2 Therapies? A Review

被引:1
|
作者
Wang, Jin [1 ,2 ,3 ]
Liao, Dongying [1 ,2 ,3 ]
Zhang, Xuemin [1 ,2 ,3 ]
Miao, Changhong [1 ,2 ,3 ]
Chen, Kuang [1 ,2 ,3 ]
机构
[1] Tianjin Univ Tradit Chinese Med, Teaching Hosp 1, Dept Emergency, Anshanxi Rd, Tianjin 300193, Peoples R China
[2] Natl Clin Res Ctr Chinese Med Acupuncture & Moxibu, Tianjin, Peoples R China
[3] Tianjin Univ Tradit Chinese Med, Tianjin 301617, Peoples R China
来源
关键词
HER2-low breast cancer; monoclonal antibodies; antibody-drug conjugates; trastuzumab deruxtecan; immunotherapy; ANTIBODY-DRUG CONJUGATE; DERUXTECAN T-DXD; TRASTUZUMAB DERUXTECAN; PATIENTS PTS; OPEN-LABEL; ENDOCRINE THERAPY; PHASE-II; ESTROGEN-RECEPTOR; ANTICANCER AGENTS; DOUBLE-BLIND;
D O I
10.2147/BCTT.S407181
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Breast cancer (BC) poses a severe threat to the health of women worldwide. Currently, different therapeutic regimens are used for BC according to the pathological classification of HER2-positive or HER2-negative. Clinical reports of HER2-low expression indicate that the condition is HER2-negative, which was ineligible for HER2-targeted therapy. In contrast to HER2-zero tumors, however, HER2-low BC is a heterogeneous disease with unique genetic characteristics, prognoses, and different therapeutic responses. Clinical efficacy has been demonstrated by numerous potent and innovative anti-HER2 medications, particularly antibody-drug conjugates (ADCs). Certain ADCs, including T-DXd, have demonstrated good efficacy in some trials either used alone or in conjunction with other medications. To enhance outcomes in individuals with HER2-low BC, immunotherapy and other treatments are frequently combined with HER2-targeted therapy. There are also alternative strategies that target both HER2 and HER3 or other antigenic sites. We hope more individuals with HER2-low BC will benefit from more precise treatment regimens in the future. This article provides a review of existing research and clinical trials.
引用
收藏
页码:281 / 294
页数:14
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