Non-responsiveness to gefitinib in a patient with lung adenocarcinoma having rare EGFR mutations S7681 and V769L

被引:55
作者
Asahina, Hajime
Yamazaki, Koichi
Kinoshita, Ichiro
Yokouchi, Hiroshi
Dosaka-Akita, Hirotoshi
Nishimura, Masaharu
机构
[1] Hokkaido Univ, Sch Med, Dept Med 1, Kita Ku, Sapporo, Hokkaido 0608638, Japan
[2] Hokkaido Univ, Sch Med, Dept Med Oncol, Kita Ku, Sapporo, Hokkaido 0608638, Japan
关键词
epidermal growth factor receptor (EGFR); mutation; non-small cell lung cancer (NSCLC); gefitinib; chemotherapy; first-line therapy; FACTOR-RECEPTOR GENE; KINASE DOMAIN; CANCER; PHOSPHORYLATION; RESPONSIVENESS; SENSITIVITY; ACTIVATION; PATTERNS; FEATURES;
D O I
10.1016/j.lungcan.2006.09.005
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) are associated with clinical responsiveness to EGFR-tyrosine kinase inhibitors (EGFR-TKIs) in patients with non-small cell, lung cancers (NSCLCs). However, certain rare EGFR mutations including S7681 are reported to confer less in vitro sensitivity to gefitinib, an EGFR-TKI, than major mutations such as exon 19 deletions and L858R and even the wild-type counterpart. Here, we report the first case of adenocarcinoma of the lung in which the patient had rare mutations S7681 and V769L and was treated with gefitinib. Disease progressed during 6 weeks of treatment. This case suggests that in vitro sensitivity to gefitinib correlates with distinct clinical responsiveness to gefitinib in various types of EGFR mutations. (C) 2006 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:419 / 422
页数:4
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