Emerging EGFR antagonists for breast cancer

被引:22
|
作者
Lluch, Ana [1 ,2 ]
Eroles, Pilar [2 ]
Perez-Fidalgo, Jose-Alejandro [1 ,2 ]
机构
[1] Hosp Clin Univ, INCLIVA Biomed Res Inst, Dept Hematol & Oncol, Valencia, Spain
[2] INCLIVA Biomed Res Inst, Valencia, Spain
关键词
angiogenesis; breast cancer; cetuximab; EGFR; erlotinib; gefitinib; tyrosine kinase inhibitor; GROWTH-FACTOR-RECEPTOR; TYROSINE KINASE INHIBITOR; PHASE-II TRIAL; ESTROGEN-RECEPTOR; ACQUIRED-RESISTANCE; POSTMENOPAUSAL WOMEN; TAMOXIFEN-RESISTANT; RANDOMIZED-TRIAL; DOUBLE-BLIND; ANTIBODY CETUXIMAB;
D O I
10.1517/14728214.2014.903919
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: The EGFR has been associated with the pathogenesis and progression of breast cancer. Treatment based on an EGFR target is emerging as a promising option, especially in combination with conventional therapies. Unfortunately, there are no validated predictor biomarkers, and combinatorial treatments are meeting new resistance. Areas covered: The purpose of this review is to summarize the existing treatments and the current research based on targeting the EGFR pathway. Expert opinion: The existing EGFR treatments in breast cancer have shown limited benefit. The combination of the monoclonal antibody cetuximab and platinum salts achieves a 15 - 20% response rate. The effectiveness of tyrosine kinase inhibitors is not completely clear, showing modest or no benefits. Gefitinib treatment has offered some promising results in estrogen receptor + breast cancer. However, it has not been identified as a predictive factor for the appropriate selection of patients. Radioimmunotherapy with anti-EGFR radiolabeled antibodies is a promising strategy in BRCA-mutated breast cancer, but it still requires clinical confirmation. Nevertheless, the crosstalk between pathways frequently leads to treatment resistance. Current research is focused on increasing knowledge about the mechanisms of response and the discovery of predictive markers. Targeting several pathways simultaneously and a correct selection of patients seem essential.
引用
收藏
页码:165 / 181
页数:17
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