EGFR mutation status in brain metastases of non-small cell lung carcinoma

被引:94
作者
Burel-Vandenbos, Fanny [1 ]
Ambrosetti, Damien [2 ]
Coutts, Michael [3 ]
Pedeutour, Florence [4 ]
机构
[1] Hop Louis Pasteur, Lab Cent Anat Pathol, F-06000 Nice, France
[2] Univ Nice Sophia Antipolis, Inst Res Canc & Ageing Nice, Nice, France
[3] Maidstone Hlth Author, Dept Pathol, W Kent Oncol Ctr, Maidstone, Kent, England
[4] Univ Nice Sophia Antipolis, Fac Med, Nice, France
关键词
Brain metastases; EGFR; Lung cancer; Mutation status; GROWTH-FACTOR-RECEPTOR; TYROSINE KINASE INHIBITORS; NERVOUS-SYSTEM METASTASES; DOSE WEEKLY ERLOTINIB; LEPTOMENINGEAL METASTASES; ACQUIRED-RESISTANCE; RADIATION-THERAPY; CANCER PATIENTS; INTRACRANIAL METASTASES; CLINICAL-RESPONSE;
D O I
10.1007/s11060-012-0990-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Brain metastases are a frequent and grave complication of non-small cell lung carcinoma (NSCLC). The prognosis is generally poor, despite standard therapy based on surgery and radiotherapy. A degree of understanding of the molecular basis of tumors has led to the development of targeted agents with promising initial findings for the treatment of NSCLC. EGFR mutations have been identified which are associated with significant sensitivity to EGFR tyrosine kinase inhibitors (TKI) and correlate with improved outcome in patients with NSCLC who are treated with these agents. The adoption of treatment tailored to the genetic make-up of individual tumors could lead to substantial therapeutic improvements, and such targeted therapy might be considered as a therapeutic option for brain metastases in the future. We review current knowledge about EGFR mutation status in the specific context of brain metastasis: its association with the response of brain metastases to TKI, its prevalence in brain metastases, and the correlation between mutation status in metastases as compared to the corresponding primary lung carcinoma.
引用
收藏
页码:1 / 10
页数:10
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