Influence of first-line chemotherapy and EGFR mutations on second-line gefitinib in advanced non-small cell lung cancer

被引:17
作者
Wu, Jenn-Yu [2 ]
Yu, Chong-Jen [1 ]
Shih, Jin-Yuan [1 ]
Yang, Chih-Hsin [3 ]
Yang, Pan-Chyr [1 ]
机构
[1] Natl Taiwan Univ Hosp, Dept Internal Med, Taipei 100, Taiwan
[2] Natl Taiwan Univ Hosp, Dept Internal Med, Yun Lin Branch, Yunlin, Taiwan
[3] Natl Taiwan Univ Hosp, Dept Oncol, Taipei 10764, Taiwan
关键词
Chemotherapy; EGFR; Gefitinib; Lung cancer; Mutations; Second-line; FACTOR RECEPTOR MUTATIONS; PHASE-III TRIAL; DOCETAXEL; ERLOTINIB; SURVIVAL; ADENOCARCINOMA; THERAPY;
D O I
10.1016/j.lungcan.2009.04.018
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Gefitinib is a valid second-line therapy for previously treated non-small cell lung cancer (NSCLC) patients The influences of various chemotherapy regimens and EGFR mutations on effectiveness of second-line gefitinib are not clear, and laboratory studies revealed that previous chemotherapy changed the effectiveness of treatment with gefitinib In order to clarify the factors changing the effectiveness of second-line gefitinib, we performed a retrospective analysis of the prognosis of NSCLC patients who received gefitinib after first-line chemotherapy Design We analyzed the clinical data and mutational studies of NSCLC patients with EGFR mutations from the National Taiwan University Hospital Results. One hundred and two previously treated patients received second-line gefitinib for stage IIIB or IV NSCLC Fifty of all the 102 patients were sequenced for EGFR status Twenty-eight had EGFR mutation and 22 had wild type EGFR The response rate and progression-free survival of second-line gefitinib was not changed by different previous chemotherapy regimens The potent factor with regards to the effectiveness of second-line gefitinib was EGFR mutation which led to a better response rate and longer progression-free survival of gefitinib than wild type EGFR Conclusions. Gefitinib is effective as a second-line therapy for previously treated NSCLC patients The effectiveness was influenced by EGFR status rather than previous chemotherapy regimens. (C) 2009 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:348 / 354
页数:7
相关论文
共 24 条
[1]  
ALBERTI W, 1995, BRIT MED J, V311, P899
[2]  
[Anonymous], 2004, PATHOLOGY GENETICS T
[3]   Reduced Erlotinib Sensitivity of Epidermal Growth Factor Receptor-Mutant Non-Small Cell Lung Cancer following Cisplatin Exposure: A Cell Culture Model of Second-line Erlotinib Treatment [J].
Chin, Tan Min ;
Quinlan, Margaret P. ;
Singh, Anurag ;
Sequist, Lecia V. ;
Lynch, Thomas J. ;
Haber, Daniel A. ;
Sharma, Sreenath V. ;
Settleman, Jeffrey .
CLINICAL CANCER RESEARCH, 2008, 14 (21) :6867-6876
[4]   Randomized phase III trial of docetaxel versus vinorelbine or ifosfamide in patients with advanced non-small-cell lung cancer previously treated with platinum-containing chemotherapy regimens [J].
Fossella, FV ;
DeVore, R ;
Kerr, RN ;
Crawford, J ;
Natale, RR ;
Dunphy, F ;
Kalman, L ;
Miller, V ;
Lee, JS ;
Moore, M ;
Gandara, D ;
Karp, D ;
Vokes, E ;
Kris, M ;
Kim, Y ;
Gamza, F ;
Hammershaimb, L .
JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (12) :2354-2362
[5]   Radiotherapy in lung adenocarcinoma with brain metastases: Effects of activating epidermal growth factor receptor mutations on clinical response [J].
Gow, Chien-Hung ;
Chien, Chun-Ru ;
Chang, Yih-Leong ;
Chiu, Yueh-Hsia ;
Kuo, Sung-Hsin ;
Shih, Jin-Yuan ;
Chang, Yeun-Chung ;
Yu, Chong-Jen ;
Yang, Chih-Hsin ;
Yang, Pan-Chyr .
CLINICAL CANCER RESEARCH, 2008, 14 (01) :162-168
[6]   Database of somatic mutations in EGFR with analyses revealing indel hotspots but no smoking-associated signature [J].
Gu, Dongqing ;
Scaringe, William A. ;
Li, Kai ;
Saldivar, Juan-Sebastian ;
Hill, Kathleen A. ;
Chen, Zhenbin ;
Gonzalez, Kelly D. ;
Sommer, Steve S. .
HUMAN MUTATION, 2007, 28 (08) :760-770
[7]   Randomized phase III trial of pemetrexed versus docetaxel in patients with non-small-cell lung cancer previously treated with chemotherapy [J].
Hanna, N ;
Shepherd, FA ;
Fossella, FV ;
Pereira, JR ;
De Marinis, F ;
von Pawel, J ;
Gatzemeier, U ;
Tsao, TCY ;
Pless, M ;
Muller, T ;
Lim, HL ;
Desch, C ;
Szondy, K ;
Gervais, R ;
Shaharyar ;
Manegold, C ;
Paul, S ;
Paoletti, P ;
Einhorn, L ;
Bunn, PA .
JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (09) :1589-1597
[8]   Gefitinib versus docetaxel in previously treated non-small-cell lung cancer (INTEREST): a randomised phase III trial [J].
Kim, Edward S. ;
Hirsh, Vera ;
Mok, Tony ;
Socinski, Mark A. ;
Gervais, Radj ;
Wu, Yi-Long ;
Li, Long-Yun ;
Watkins, Claire L. ;
Sellers, Mark V. ;
Lowe, Elizabeth S. ;
Sun, Yan ;
Liao, Mei-Lin ;
Osterlind, Kell ;
Reck, Martin ;
Armour, Alison A. ;
Shepherd, Frances A. ;
Lippman, Scott M. ;
Douillard, Jean-Yves .
LANCET, 2008, 372 (9652) :1809-1818
[9]   Phase III study, V-15-32, of gefitinib versus docetaxel in previously treated Japanese patients with non-small-cell lung cancer [J].
Maruyama, Riichiroh ;
Nishiwaki, Yutaka ;
Tamura, Tomohide ;
Yamamoto, Nobuyuki ;
Tsuboi, Masahiro ;
Nakagawa, Kazuhiko ;
Shinkai, Tetsu ;
Negoro, Shunichi ;
Imamura, Fumio ;
Eguchi, Kenji ;
Takeda, Koji ;
Inoue, Akira ;
Tomii, Keisuke ;
Harada, Masao ;
Masuda, Noriyuki ;
Jiang, Haiyi ;
Itoh, Yohji ;
Ichinose, Yukito ;
Saijo, Nagahiro ;
Fukuoka, Masahiro .
JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (26) :4244-4252
[10]   Mutations of the epidermal growth factor receptor gene predict prolonged survival after gefitinib treatment in patients with non-small-cell lung cancer with postoperative recurrence [J].
Mitsudomi, T ;
Kosaka, T ;
Endoh, H ;
Horio, Y ;
Hida, T ;
Mori, S ;
Hatooka, S ;
Shinoda, M ;
Takahashi, T ;
Yatabe, Y .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (11) :2513-2520