Targeting Epidermal Growth Factor Receptor in triple negative breast cancer: New discoveries and practical insights for drug development

被引:135
作者
Costa, Ricardo [1 ]
Shah, Ami N. [3 ]
Santa-Maria, Cesar A. [1 ,2 ]
Cruz, Marcelo R. [1 ]
Mahalingam, Devalingam [4 ,5 ,6 ]
Carneiro, Benedito A. [1 ,2 ]
Chae, Young Kwang [1 ,2 ]
Cristofanilli, Massimo [1 ,2 ]
Gradishar, William J. [1 ,2 ]
Giles, Francis J. [1 ,2 ]
机构
[1] Feinberg Sch Med, Div Hematol Oncol, Dev Therapeut Program, Chicago, IL USA
[2] Northwestern Univ, Robert H Lurie Comprehens Canc Ctr, Chicago, IL 60611 USA
[3] Feinberg Sch Med, Div Hematol Oncol, Chicago, IL USA
[4] Univ Texas Hlth Sci Ctr San Antonio, Dept Med Canc Res, San Antonio, TX 78229 USA
[5] Univ Texas Hlth Sci Ctr San Antonio, Therapy Ctr, San Antonio, TX 78229 USA
[6] Univ Texas Hlth Sci Ctr San Antonio, Sch Med, San Antonio, TX 78229 USA
关键词
Triple negative breast cancer; Epidermal Growth Factor Receptor; Targeted therapy; mTOR; CELL LUNG-CANCER; IXABEPILONE PLUS CAPECITABINE; PATHOLOGICAL COMPLETE RESPONSE; MONOCLONAL-ANTIBODY CETUXIMAB; RANDOMIZED PHASE-II; 1ST-LINE TREATMENT; OPEN-LABEL; PROTEIN EXPRESSION; CLINICAL-PRACTICE; SPORADIC BREAST;
D O I
10.1016/j.ctrv.2016.12.010
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Triple negative breast cancer (TNBC) accounts for 10-20% of cases in breast cancer. Despite recent advances in the treatment of hormonal receptor+ and HER2+ breast cancers, there are no targeted therapies available for TNBC. Evidence supports that most patients with TNBC express the transmembrane Epidermal Growth Factor Receptor (EGFR). However, early phase clinical trials failed to demonstrate significant activity of EGFR-targeted monoclonal antibodies and/or tyrosine kinase inhibitors. Here, we review the recent discoveries related to the underlying biology of the EGFR pathway in TNBC, clinical progress to date and suggest rational future approaches for investigational therapies in TNBC. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:111 / 119
页数:9
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