Molecularly targeted therapies for metastatic triple-negative breast cancer

被引:141
作者
Bayraktar, Soley [1 ]
Glueck, Stefan [2 ,3 ,4 ]
机构
[1] Mercy Canc Ctr, Dept Med Oncol, Ardmore, OK USA
[2] Univ Miami, Dept Med, Div Hematol Med Oncol, Miami, FL USA
[3] Sylvester Comprehens Canc Ctr, Miami, FL USA
[4] Univ Miami, Leonard L Miller Sch Med, Sylvester Comprehens Canc Ctr, Miami, FL 33136 USA
关键词
Metastatic; Targeted agents; Triple-negative breast cancer; PARP; VEGFR; EGFR; GROWTH-FACTOR RECEPTOR; BEVACIZUMAB-CONTAINING THERAPY; RANDOMIZED PHASE-II; ESTROGEN-RECEPTOR; 1ST-LINE TREATMENT; DRUG-RESISTANCE; CLINICAL-TRIALS; CELL-LINES; COMBINATION; EXPRESSION;
D O I
10.1007/s10549-013-2421-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Triple-negative breast cancer (TNBC) refers to a heterogeneous group of tumors that do not express the estrogen/progesterone-receptor (ER/PR), and human epidermal growth factor receptor-2 (HER2). TNBC is an aggressive histological subtype with limited treatment options and very poor prognosis following progression after standard chemotherapy regimens. There have been significant improvements in the outcome of other subtypes of breast cancer, including ER-positive/HER2 overexpressed tumors, attributed to the addition of targeted therapy, including hormonal agents and trastuzumab. However, no specific targeted agents are currently available for the treatment of TNBC. This review aims to collate and describe the most recent data on targeted therapies that have demonstrated efficacy in the management of metastatic TNBC. Targeted agents that have been investigated in the treatment of metastatic TNBC include inhibitors of poly(ADP-ribose) polymerase, angiogenesis, mammalian target of rapamycin, epidermal growth factor receptor, HDAC, Jak2, and Src. Several of these agents have shown considerable promise.
引用
收藏
页码:21 / 35
页数:15
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