Targeted Treatment of Triple-Negative Breast Cancer

被引:8
作者
Young, Joanna A. [1 ]
Tan, Antoinette R. [1 ]
机构
[1] Atrium Hlth, Levine Canc Inst, 1021 Morehead Med Dr, Charlotte, NC 28204 USA
关键词
AKT inhibitor; androgen receptor; antibody-drug conjugates; CDK inhibitor; MAP kinase; PI3K; targeted therapy; triple-negative breast cancer; ANTIBODY-DRUG CONJUGATE; FIBROBLAST-GROWTH-FACTOR; RANDOMIZED PHASE-II; GLYCOPROTEIN NONMETASTATIC B; ANDROGEN RECEPTOR; DOSE-ESCALATION; PLUS PACLITAXEL; PATIENTS PTS; GLEMBATUMUMAB VEDOTIN; MEDIATES RESISTANCE;
D O I
10.1097/PPO.0000000000000495
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Triple-negative breast cancer is increasingly recognized as a heterogeneous entity that can be categorized according to histologic, molecular, and clinical subtypes. While chemotherapy remains the backbone of treatment for this disease, there are now several available targeted agents including immunotherapy, poly(adenosine diphosphate-ribose) polymerase inhibitors, and most recently a Food and Drug Administration-approved antibody-drug conjugate sacituzumab govitecan-hziy as a third-line treatment of metastatic triple-negative breast cancer. We review several actionable targets for triple-negative breast cancer and describe promising nonimmunotherapeutic agents including cyclin-dependent kinase inhibitors, androgen receptor inhibitors, mitogen-activated protein kinase inhibitors, phosphoinositide 3-kinase inhibitors, AKT (also known as protein kinase B) inhibitors, and antibody-drug conjugates.
引用
收藏
页码:50 / 58
页数:9
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