Identification of EGFR kinase domain mutations among lung cancer patients in China: implication for targeted cancer therapy

被引:61
作者
Qin, BM
Chen, X
Zhu, JD
Pei, DQ [1 ]
机构
[1] Chinese Acad Sci, Guangzhou Inst Biomed & Hlth, Guangzhou 510663, Peoples R China
[2] Shanghai Jiao Tong Univ, Shanghai Canc Inst, State Key Lab Oncogenes & Related Genes, Shanghai 200032, Peoples R China
关键词
lung cancer; epidermal growth factor receptor (EGFR); somatic mutation;
D O I
10.1038/sj.cr.7290289
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Lung cancer is one of the leading causes of death with one of the lowest survival rates. However, a subset of lung cancer patients who are of Asian origin and carry somatic mutations in epidermal growth factor receptor or EGFR have responded remarkable well to two tyrosine kinase inhibitors, gefitinib and erlotinib. While EGFR mutation profiles have been reported from Japan, South Korea, and Taiwan, there is no such report from mainland of China where the largest pool of patients reside. In this report, we identified ten somatic mutations from a total of 41 lung cancer patients in China. Among them, seven mutations were found in 17 adenocarcinomas. In contrast to previous reports, eight of these mutations are deletions in exon 19 and two of these deletions are homozygous. These results suggest that a large portion of Chinese adenocarcinoma patients could benefit from gefitinib or erlotinib. This unique mutation profile provides a rationale to develop the next generation of EGFR inhibitors more suitable for the Chinese population.
引用
收藏
页码:212 / 217
页数:6
相关论文
共 11 条
[1]   Chasing mutations in the epidermal growth factor in lung cancer [J].
Dowell, JE ;
Minna, JD .
NEW ENGLAND JOURNAL OF MEDICINE, 2005, 352 (08) :830-832
[2]  
HAN SW, 2005, J CLIN ONCOL 0214
[3]   High frequency of epidermal growth factor receptor mutations with complex patterns in non-small cell lung cancers related to gefitinib responsiveness in Taiwan [J].
Huang, SF ;
Liu, HP ;
Li, LH ;
Ku, YC ;
Fu, YN ;
Tsai, HY ;
Chen, YT ;
Lin, YF ;
Chang, WC ;
Kuo, HP ;
Wu, YC ;
Chen, YR ;
Tsai, SF .
CLINICAL CANCER RESEARCH, 2004, 10 (24) :8195-8203
[4]   Mutations of the epidermal growth factor receptor gene in lung cancer:: Biological and clinical implications [J].
Kosaka, T ;
Yatabe, Y ;
Endoh, H ;
Kuwano, H ;
Takahashi, T ;
Mitsudomi, T .
CANCER RESEARCH, 2004, 64 (24) :8919-8923
[5]   Activating mutations in the epidermal growth factor receptor underlying responsiveness of non-small-cell lung cancer to gefitinib [J].
Lynch, TJ ;
Bell, DW ;
Sordella, R ;
Gurubhagavatula, S ;
Okimoto, RA ;
Brannigan, BW ;
Harris, PL ;
Haserlat, SM ;
Supko, JG ;
Haluska, FG ;
Louis, DN ;
Christiani, DC ;
Settleman, J ;
Haber, DA .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 350 (21) :2129-2139
[6]   Cancer - A bull's eye for targeted lung cancer therapy [J].
Minna, JD ;
Gazdar, AF ;
Sprang, SR ;
Herz, J .
SCIENCE, 2004, 304 (5676) :1458-+
[7]   EGFR mutations in lung cancer:: Correlation with clinical response to gefitinib therapy [J].
Paez, JG ;
Jänne, PA ;
Lee, JC ;
Tracy, S ;
Greulich, H ;
Gabriel, S ;
Herman, P ;
Kaye, FJ ;
Lindeman, N ;
Boggon, TJ ;
Naoki, K ;
Sasaki, H ;
Fujii, Y ;
Eck, MJ ;
Sellers, WR ;
Johnson, BE ;
Meyerson, M .
SCIENCE, 2004, 304 (5676) :1497-1500
[8]   Targeted therapies for cancer 2004 [J].
Ross, JS ;
Schenkein, DP ;
Pietrusko, R ;
Rolfe, M ;
Linette, GP ;
Stec, J ;
Stagliano, NE ;
Ginsburg, GS ;
Symmans, WF ;
Pusztai, L ;
Hortobagyi, GN .
AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 2004, 122 (04) :598-609
[9]   EGFR gene mutations: A call for global x global views of cancer [J].
Sellers, WR ;
Meyerson, M .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2005, 97 (05) :326-328
[10]   Clinical and biological features associated with epidermal growth factor receptor gene mutations in lung cancers [J].
Shigematsu, H ;
Lin, L ;
Takahashi, T ;
Nomura, M ;
Suzuki, M ;
Wistuba, II ;
Fong, KM ;
Lee, H ;
Toyooka, S ;
Shimizu, N ;
Fujisawa, T ;
Feng, ZD ;
Roth, JA ;
Herz, J ;
Minna, JD ;
Gazdar, AF .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2005, 97 (05) :339-346