Strategies to overcome resistance to epidermal growth factor receptor monoclonal antibody therapy in metastatic colorectal cancer

被引:21
|
作者
Jeong, Woo-Jeong [1 ]
Cha, Pu-Hyeon [1 ]
Choi, Kang-Yell [1 ]
机构
[1] Yonsei Univ, Coll Life Sci & Biotechnol, Dept Biotechnol, Translat Res Ctr Prot Funct Control, Seoul 120749, South Korea
关键词
Colorectal cancer; Epidermal growth factor receptor; Resistance; K-ras mutation; Combinational therapy; PHOSPHATIDYLINOSITOL 3-KINASE/MAMMALIAN TARGET; TRANSFERASE INHIBITOR R115777; CETUXIMAB PLUS IRINOTECAN; SIGNAL-REGULATED KINASE; KRAS CODON 12; PHASE-II; COLON-CANCER; ANTITUMOR ACTIVITIES; RAPAMYCIN INHIBITOR; AZD6244; ARRY-142886;
D O I
10.3748/wjg.v20.i29.9862
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Administration of monoclonal antibodies (mAbs) against epidermal growth factor receptor (EGFR) such as cetuximab and panitumumab in combination with conventional chemotherapy substantially prolongs survival of patients with metastatic colorectal cancer (mCRC). However, the efficacy of these mAbs is limited due to genetic variation among patients, in particular K-ras mutations. The discovery of K-ras mutation as a predictor of non-responsiveness to EGFR mAb therapy has caused a major change in the treatment of mCRC. Drugs that inhibit transformation caused by oncogenic alterations of Ras and its downstream components such as BRAF, MEK and AKT seem to be promising cancer therapeutics as single agents or when given with EGFR inhibitors. Although multiple therapeutic strategies to overcome EGFR mAb-resistance are under investigation, our understanding of their mode of action is limited. Rational drug development based on stringent preclinical data, biomarker validation, and proper selection of patients is of paramount importance in the treatment of mCRC. In this review, we will discuss diverse approaches to overcome the problem of resistance to existing anti-EGFR therapies and potential future directions for cancer therapies related to the mutational status of genes associated with EGFR-Ras-ERK and PI3K signalings. (C) 2014 Baishideng Publishing Group Inc. All rights reserved.
引用
收藏
页码:9862 / 9871
页数:10
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