Rapid communication absence of epidermal growth factor receptor gene mutations in patients with hormone refractory prostate cancer not responding to gefitinib

被引:14
作者
Curigliano, Giuseppe
Pelosi, Giuseppe
De Pas, Tommaso
Renne, Giuseppe
De Cobelli, Ottavio
Manzotti, Michela
Spitaleri, Gianluca
de Braud, Filippo
机构
[1] European Inst Oncol, Clin Pharmacol & New Drugs Dev Unit, Div Med Oncol, I-20141 Milan, Italy
[2] Univ Milan, Sch Med, I-20122 Milan, Italy
[3] European Inst Oncol, Div Pathol, Milan, Italy
[4] European Inst Oncol, Div Urol, Milan, Italy
关键词
EGFR mutations; prostate cancer; gefitinib;
D O I
10.1002/pros.20530
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND. Mutations in the tyrosine kinase (TK) domain of the epidermal growth factor receptor (EGFR) gene in human cancers are associated with increased sensitivity to anilinoquinazoline EGFR inhibitors. To our knowledge no data have been reported on EGFR gene mutations in hormone refractory prostate cancer (HRPC). METHODS. Between March 2003 and December 2004,23 patients with HRPC received 250 mg oral gefitinib daily in addition to antiandrogen plus luteinizing hormone-releasing hormone (LH-RH) analog for at least 2 months or until disease progression. Patients with unresected prostate cancer prospectively underwent trans-rectal biopsy of primary tumor (before starting gefitinib treatment). RESULTS. None of the patients demonstrated PSA or objective response to gefitinib. We sequenced exons 18-21 of the EGFR TK domain from genomic DNA isolated from 8 HRPC patients. No patient showed EGFR TK domain mutations. CONCLUSIONS. Our results show EGFR mutations did not occur in these patients suggesting that gefitinib is unlikely to be effective in patients with tumors not harboring specific EGFR TK domain.
引用
收藏
页码:603 / 604
页数:2
相关论文
共 5 条
[1]   Assessing the construct validity of the adjustment scales for children and adolescents [J].
Canivez, GL ;
Sprouls, K .
JOURNAL OF PSYCHOEDUCATIONAL ASSESSMENT, 2005, 23 (01) :3-14
[2]   Cancer statistics, 2006 [J].
Jemal, A ;
Siegel, R ;
Ward, E ;
Murray, T ;
Xu, JQ ;
Smigal, C ;
Thun, MJ .
CA-A CANCER JOURNAL FOR CLINICIANS, 2006, 56 (02) :106-130
[3]   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
[4]   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
[5]   Gefitinib-sensitizing EGFR mutations in lung cancer activate anti-apoptotic pathways [J].
Sordella, R ;
Bell, DW ;
Haber, DA ;
Settleman, J .
SCIENCE, 2004, 305 (5687) :1163-1167