Updates on targeting human epidermal growth factor receptor 2-positive breast cancer: what's to know in 2021

被引:5
作者
McAndrew, Nicholas P. [1 ]
机构
[1] Univ Calif Los Angeles, David Geffen Sch Med, Beverly Hills, CA USA
关键词
antibody-drug conjugate; breast cancer; human epidermal growth factor receptor 2; targeted therapy; PATHOLOGICAL COMPLETE RESPONSE; NERVOUS-SYSTEM METASTASES; TRASTUZUMAB-BASED THERAPY; CHEMOTHERAPY PLUS; SURVIVAL; POLYMORPHISMS; ANTIBODY; TRIAL;
D O I
10.1097/GCO.0000000000000762
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Purpose of review To highlight recent practice changing clinical trials, focusing on those leading to new drug approvals, in human epidermal growth factor receptor 2-positive (HER2+) breast cancer. Recent findings The improved disease-free survival of adjuvant trastuzumab emtansine (T-DM1) over trastuzumab in patients with residual disease has made neoadjuvant sequencing of therapy standard for most patients with early stage disease. In patients with metastatic HER2+ breast cancer, trastuzumab deruxtecan has recently shown dramatically improved efficacy over T-DM1. Tucatinib is an oral tyrosine kinase inhibitor with best in class blood-brain barrier penetration. Margetuximab, a novel HER2-targeted chimeric monoclonal antibody with an engineered Fc receptor designed to activate local immune response, was recently approved in heavily pretreated patients based on modest but significant improvement in progression-free survival. Patients with HER2+ breast cancer have a variety of therapeutic options in the early stage and metastatic setting. Optimal sequencing of therapy will depend on patient-specific factors such as site of tumor progression and underlying comorbidities. De-escalation of the first-line metastatic regimen may be considered in select patients with hormone positive/HER2+ breast cancer, by using endocrine therapy instead of chemotherapy in combination with HER2-targeted therapy, which may improve side effects without sacrificing efficacy.
引用
收藏
页码:41 / 45
页数:5
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