Novel therapeutic strategies in the treatment of triple-negative breast cancer

被引:58
|
作者
Oualla, Karima [2 ]
El-Zawahry, Heba M. [1 ,6 ]
Arun, Banu [3 ]
Reuben, James M. [4 ]
Woodward, Wendy A. [5 ]
El-Din, Heba Gamal
Lim, Bora [3 ]
Mellas, Nawfel [2 ]
Ueno, Naoto T. [3 ]
Fouad, Tamer M.
机构
[1] Cairo Univ, Natl Canc Inst, Dept Med Oncol, Kasr El Aini Rd, Cairo 11796, Egypt
[2] Hassan II Univ Hosp, Med Oncol Dept, Fes, Morocco
[3] Univ Texas MD Anderson Canc Ctr, Dept Breast Med Oncol, Houston, TX 77030 USA
[4] Univ Texas MD Anderson Canc Ctr, Dept Hematopathol, Houston, TX 77030 USA
[5] Univ Texas MD Anderson Canc Ctr, Dept Radiat Oncol, Houston, TX 77030 USA
[6] Cairo Univ, Natl Canc Inst, Dept Surg Oncol, Cairo, Egypt
关键词
chemotherapy; clinical trials; immunotherapy; molecular subtypes; targeted therapies; triple-negative breast cancer; TUMOR-INFILTRATING LYMPHOCYTES; GROWTH-FACTOR RECEPTOR; BASAL-LIKE PHENOTYPE; II CLINICAL-TRIAL; PROGNOSTIC VALUE; MOLECULAR CHARACTERIZATION; NEOADJUVANT CHEMOTHERAPY; LOCOREGIONAL RECURRENCE; 1ST-LINE TREATMENT; ANDROGEN RECEPTOR;
D O I
10.1177/1758834017711380
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Triple-negative breast cancer (TNBC) is a heterogeneous subtype of breast cancer that is defined by negative estrogen receptor (ER), progesterone receptor (PR) and human epidermal growth factor receptor 2 (HER2) status. Treating patients with TNBC remains clinically challenging, as patients are not candidates for endocrine or HER2-directed therapy. As a result, chemotherapy with traditional agents such as anthracyclines and taxanes remains the only available option with moderate success. Recent discoveries have revealed that TNBC is a heterogeneous disease at the clinical, histological and molecular levels. The use of biomarkers to identify distinct subsets of TNBC that derive the greatest benefit from presently approved as well as novel therapeutics has become the main focus of current research. The aim of this review is to explore the clinical and biological complexity of TNBC as well as identify novel therapeutic options that target the various molecular subsets of TNBC.
引用
收藏
页码:493 / 511
页数:19
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