Mechanisms of resistance to anti-EGFR therapy in colorectal cancer

被引:230
作者
Zhao, Ben [1 ]
Wang, Lu [1 ]
Qiu, Hong [1 ]
Zhang, Mingsheng [1 ]
Sun, Li [1 ]
Peng, Ping [1 ]
Yu, Qianqian [1 ]
Yuan, Xianglin [1 ]
机构
[1] Huazhong Univ Sci & Technol, Tongji Hosp, Dept Oncol, Wuhan, Hubei Province, Peoples R China
基金
中国国家自然科学基金;
关键词
colorectal cancer; epidermal growth factor receptor; targeted drug; primary resistance; acquired resistance; GROWTH-FACTOR RECEPTOR; FACTOR-I-RECEPTOR; GENE COPY NUMBER; CETUXIMAB PLUS IRINOTECAN; CELL LUNG-CANCER; PHASE-III TRIAL; KRAS WILD-TYPE; EPITHELIAL-MESENCHYMAL TRANSITION; ACQUIRED-RESISTANCE; 1ST-LINE TREATMENT;
D O I
10.18632/oncotarget.14012
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Targeting the epidermal growth factor receptor (EGFR) either alone or in combination with chemotherapy is effective for patients with RAS wild type metastatic colorectal cancer (mCRC). However, only a small percentage of mCRC patients are sensitive to anti-EGFR therapy and even the best cases finally become refractory to this therapy. It has become apparent that the RAS mutations correlate with resistance to anti-EGFR therapy. However, these resistance mechanisms only account for nearly 35% to 50% of nonresponsive patients, suggesting that there might be additional mechanisms. In fact, several novel pathways leading to escape from anti-EGFR therapy have been reported in recent years. In this review, we provide an overview of known and novel mechanisms that contribute to both primary and acquired anti-EGFR therapy resistance, and enlist possible treatment strategies to overcome or reverse this resistance.
引用
收藏
页码:3980 / 4000
页数:21
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