Trastuzumab Deruxtecan (DS-8201a): The Latest Research and Advances in Breast Cancer

被引:58
作者
Andrikopoulou, Angeliki [1 ]
Zografos, Eleni [1 ]
Liontos, Michalis [1 ]
Koutsoukos, Konstantinos [1 ]
Dimopoulos, Meletios-Athanasios [1 ]
Zagouri, Flora [1 ]
机构
[1] Alexandra Hosp, Med Sch, Dept Clin Therapeut, Athens, Greece
关键词
Antibody-drug conjugate; Breast cancer; DS-8201a; HER2; Trastuzumab deruxtecan; ANTIBODY-DRUG CONJUGATE; TOPOISOMERASE-I INHIBITORS; EMTANSINE T-DM1; ANTITUMOR-ACTIVITY; OPEN-LABEL; INTERSTITIAL PNEUMONITIS; PHYSICIANS CHOICE; TUMOR BIOMARKERS; PHASE-III; MECHANISMS;
D O I
10.1016/j.clbc.2020.08.006
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The development of antibody-drug conjugates composed of a cytotoxic agent and a monoclonal antibody carrier offers an important alternative to classic chemotherapy strategies. Trastuzumab deruxtecan (DS-8201a) is a next-generation antibody-drug conjugate composed of a monoclonal anti-HER2 antibody and a topoisomerase I inhibitor, an exatecan derivative (DX-8951f). DS-8201a resulted in favorable outcomes in HER2-positive heavily pretreated breast cancer patients and also had a promising efficacy in patients with HER2-negative/low-expressing disease, whose options are limited. Interestingly, a recently published phase 2 trial (NCT03248492) reported 60% overall response and 97% disease control in patients with HER2-positive disease previously treated with multiple regimens, including trastuzumab emtansine. On the basis of recent clinical trials, the US Food and Drug Administration granted accelerated approval to DS-8201a in advanced or unresectable HER2-positive breast cancer pretreated with at least two HER2-targeting treatment lines. We review all preclinical and clinical data of DS-8201a regarding breast cancer. (C) 2020 Elsevier Inc. All rights reserved.
引用
收藏
页码:E212 / E219
页数:8
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