Anti-EGFR Therapy to Treat Metastatic Colorectal Cancer: Not for All

被引:18
作者
Martins, Marta [1 ]
Mansinho, Andre [2 ]
Cruz-Duarte, Raquel [1 ]
Martins, Soraia Lobo [2 ]
Costa, Luis [1 ,2 ]
机构
[1] Univ Lisbon, Inst Med Mol Joao Lobo Antunes, Fac Med, Lisbon, Portugal
[2] Santa Maria Hosp, Div Oncol, Ctr Hosp Lisboa Norte, Lisbon, Portugal
来源
TARGETED THERAPY OF COLORECTAL CANCER SUBTYPES | 2018年 / 1110卷
关键词
Colorectal cancer; Epidermal growth factor receptor; Primary resistance; Secondary resistance; Targeted therapy; GROWTH-FACTOR RECEPTOR; CETUXIMAB PLUS IRINOTECAN; GENE COPY NUMBER; CONSENSUS MOLECULAR SUBTYPES; CELL LUNG-CANCER; K-RAS MUTATIONS; PHASE-III TRIAL; 1ST-LINE TREATMENT; ACQUIRED-RESISTANCE; COLON-CANCER;
D O I
10.1007/978-3-030-02771-1_8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The development of monoclonal antibodies (mAbs) cetuximab and panitumumab, which target the transmembrane protein epidermal growth factor receptor (EGFR), mark a major step forward in the treatment of metastatic colorectal cancer (mCRC). However, this therapeutic progress proved to be effective only in a very restricted subset of patients. Although several mechanisms of resistance, both primary and acquired, have been identified, the only established predictive tumour biomarker for the treatment of mCRC patients is the RAS mutational status. RAS activating mutations predict a lack of response to these therapies while low levels of primary resistance characterize RAS wild type (WT) patients (only about 15%). However, even WT patients that initially respond to anti-EGFR therapy, eventually undergo tumour progression. In this context, there is still more to be done in the search for effective predictive markers with therapeutic applicability. In this chapter, we provide an overview on the mechanisms that contribute to resistance to EGFR-targeted therapy and highlight what is still missing in our understanding of these molecular mechanisms and approaches to overcome them.
引用
收藏
页码:113 / 131
页数:19
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