Response to gefitinib in bronchioloalveolar carcinoma in the absence of EGFR mutation

被引:8
|
作者
Taja-Chayeb, L
Candelaria, M
Brom, R
Trejo-Becerril, C
Meza, F
Duenas-Gonzalez, A
机构
[1] Univ Nacl Autonoma Mexico, Inst Invest Biomed, Unidad Invest Biomed Canc, Inst Nacl Cancerol, Mexico City 14080, DF, Mexico
[2] Inst Nacl Cancerol, Div Clin Res, Mexico City, DF, Mexico
[3] Fdn Med Sur, Ctr Oncol, Mexico City, DF, Mexico
[4] Inst Nacl Cancerol, Div Radiol, Mexico City, DF, Mexico
关键词
epidermal growth factor receptor; EGFR mutations; bronchioloalveolar carcinoma; gefitinib;
D O I
10.1016/j.lungcan.2005.05.015
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Mutations in the tyrosine kinase (TK) domain of the epidermal growth factor receptor (EGFR) gene in non-small cell lung cancers are associated with increased sensitivity of these cancers to drugs that inhibit EGFR kinase activity such as gefitinib and erlotinib. Responses to TK inhibitors in the absence of EGFR gene mutation for BAC patients have not been reported. A case of a patient with BAC refractory to chemotherapy who responded to gefitinib in the absence of EGFR gene mutations is reported. Tyrosine kinase inhibitors may have a role in BAC in the absence of EGFR gene mutations. Additional studies on other molecular alterations of the EGFR family members are needed to better predict response to these agents. (c) 2005 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:259 / 263
页数:5
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