Differential sensitivities to tyrosine kinase inhibitors in NSCLC harboring EGFR mutation and ALK translocation

被引:117
作者
Lee, June Koo [1 ]
Kim, Tae Min [1 ]
Koh, Youngil [1 ]
Lee, Se-Hoon [1 ]
Kim, Dong-Wan [1 ]
Jeon, Yoon-Kyung [2 ]
Chung, Doo Hyun [2 ]
Yang, Seok-Chul [1 ]
Kim, Young Tae [3 ]
Kim, Young-Whan [1 ]
Heo, Dae Seog [1 ]
Bang, Yung-Jue [1 ]
机构
[1] Seoul Natl Univ, Seoul Natl Univ Hosp, Dept Internal Med, Canc Res Inst,Coll Med, Seoul 110744, South Korea
[2] Seoul Natl Univ, Seoul Natl Univ Hosp, Dept Pathol, Canc Res Inst,Coll Med, Seoul 110744, South Korea
[3] Seoul Natl Univ, Seoul Natl Univ Hosp, Dept Thorac Surg, Canc Res Inst,Coll Med, Seoul 110744, South Korea
关键词
Non-small cell lung cancer; EGFR mutation; ALK translocation; EML4-ALK FUSION GENE; CELL LUNG-CANCER; ADENOCARCINOMA; RESISTANCE; GEFITINIB; ADDICTION; LEADS;
D O I
10.1016/j.lungcan.2012.04.012
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Epidermal growth factor receptor (EGFR) mutations and anaplastic lymphoma kinase (ALK) translocations in non-small cell lung cancer (NSCLC) are mutually exclusive. However, several exceptional cases harboring both genetic alterations have been reported. In this study, a total of 444 patients with lung adenocarcinoma were examined for their EGFR and ALK status at Seoul National University Hospital between July 2008 and September 2011. EGFR mutations and ALK translocations were detected in 228 (51.4%) and 34 (7.7%) patients, respectively. Four patients (0.9%) had both genetic alterations and three underwent curative surgery. One patient who received both EGFR tyrosine kinase and ALK inhibitors, separately showed an objective response to the ALK inhibitor alone. Considering our and previous studies, patients harboring both EGFR mutation and ALK translocation showed differential sensitivities to both targeted therapies, suggesting a variable dependence on EGFR and ALK oncogenes. (C) 2012 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:460 / 463
页数:4
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