Efficacy of epidermal growth factor receptor inhibitors versus chemotherapy as second-line treatment in advanced non-small-cell lung cancer with wild-type EGFR: A meta-analysis of randomized controlled clinical trials

被引:49
作者
Zhao, Ning [1 ,2 ,3 ]
Zhang, Xu-chao [2 ,3 ]
Yan, Hong-hong [2 ,3 ]
Yang, Jin-ji [2 ,3 ]
Wu, Yi-long [2 ,3 ]
机构
[1] Guangdong Gen Hosp, Guangdong Cardiovasc Inst, Guangzhou 510080, Guangdong, Peoples R China
[2] Guangdong Acad Med Sci, Guangzhou 510080, Guangdong, Peoples R China
[3] Guangdong Gen Hosp, Guangdong Lung Canc Inst, Guangzhou 510080, Guangdong, Peoples R China
关键词
EGFR wild-type; EGFR-TKI; Non-small cell lung cancer; Erlotinib; Gefitinib; Chemotherapy; Meta-analysis; OPEN-LABEL; PHASE-III; PRETREATED PATIENTS; 1ST-LINE TREATMENT; GEFITINIB; ERLOTINIB; MUTATIONS; MULTICENTER; DOCETAXEL; MONOTHERAPY;
D O I
10.1016/j.lungcan.2014.03.026
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: EGFR mutation status is closely related to the efficacy of EGFR-TKIs in advanced non-small cell lung cancer (NSCLC). EGFR-TKIs have become the standard first-line treatment for advanced EGFR-mutation NSCLC, while for EGFR wild-type tumors, the preferred first-line treatment is chemotherapy. However, the efficacy of EGFR-TKIs as second-line treatment in EGFR wild-type NSCLC remains controversial. We sought to evaluate the effectiveness of EGFR-TKI as second-line treatment in EGFR wild-type NSCLC. Methods: Randomized controlled trials that compared EGFR-TKIs with chemotherapy in previously treated advanced NSCLC with wild-type EGFR were included. We performed a meta-analysis to evaluate the effectiveness of EGFR-TKIs compared with standard chemotherapy. The endpoints were progression-free survival (PFS), overall survival (OS), and objective response rate (ORR). Results: Six randomized controlled trials with a total of 990 patients with wild-type EGFR were included: 499 in the EGFR-TKIs group and 491 in the chemotherapy group. The results indicated that in the second-line treatment of EGFR wild-type advanced NSCLC, PFS was significantly inferior in the EGFR-TKIs group versus the chemotherapy group (HR = 1.37, 95% CI = 1.20-1.56, P<0.00001). However, this significant difference did not translate into OS (HR = 1.02, 95% CI = 0.87-1.20, P = 0.81). ORR tended to favor chemotherapy but there was no significant difference compared with EGFR-TKI (RR = 1.77, 95% CI = 0.90-3.50, P = 0.10). Conclusions: Chemotherapy improves PFS significantly but not OS, compared with EGFR-TKIs as a second-line treatment in advanced NSCLC with wild-type EGFR. Whether EGFR-TKIs should be used in EGFR wild-type patients should be considered carefully. (C) 2014 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:66 / 73
页数:8
相关论文
共 45 条
[1]  
[Anonymous], J CLIN ONCOL S
[2]   Is the DNA sequence the gold standard in genetic testing? Quality of molecular genetic tests assessed [J].
Bakker, E .
CLINICAL CHEMISTRY, 2006, 52 (04) :557-558
[3]   Mutations of the epidermal growth factor receptor in non-small cell lung cancer - Search and destroy [J].
Chan, SK ;
Gullick, WJ ;
Hill, ME .
EUROPEAN JOURNAL OF CANCER, 2006, 42 (01) :17-23
[4]   Efficacy and safety of erlotinib versus chemotherapy in second-line treatment of patients with advanced, non-small-cell lung cancer with poor prognosis (TITAN): a randomised multicentre, open-label, phase 3 study [J].
Ciuleanu, Tudor ;
Stelmakh, Lilia ;
Cicenas, Saulius ;
Miliauskas, Skaidrius ;
Grigorescu, Alexandru Calin ;
Hillenbach, Carina ;
Johannsdottir, Hrefna Kristin ;
Klughammer, Barbara ;
Esteban Gonzalez, Emilio .
LANCET ONCOLOGY, 2012, 13 (03) :300-308
[5]   Mutation detection and mutation databases [J].
Cotton, RGH .
CLINICAL CHEMISTRY AND LABORATORY MEDICINE, 1998, 36 (08) :519-522
[6]   Molecular Predictors of Outcome With Gefitinib and Docetaxel in Previously Treated Non-Small-Cell Lung Cancer: Data From the Randomized Phase III INTEREST Trial [J].
Douillard, Jean-Yves ;
Shepherd, Frances A. ;
Hirsh, Vera ;
Mok, Tony ;
Socinski, Mark A. ;
Gervais, Radj ;
Liao, Mei-Lin ;
Bischoff, Helge ;
Reck, Martin ;
Sellers, Mark V. ;
Watkins, Claire L. ;
Speake, Georgina ;
Armour, Alison A. ;
Kim, Edward S. .
JOURNAL OF CLINICAL ONCOLOGY, 2010, 28 (05) :744-752
[7]   A comparison of ARMS and DNA sequencing for mutation analysis in clinical biopsy samples [J].
Ellison, Gillian ;
Donald, Emma ;
McWalter, Gael ;
Knight, Lucy ;
Fletcher, Lynn ;
Sherwood, James ;
Cantarini, Mireille ;
Orr, Maria ;
Speake, Georgina .
JOURNAL OF EXPERIMENTAL & CLINICAL CANCER RESEARCH, 2010, 29
[8]   Non-Small Cell Lung Cancer, Version 2.2013 Featured Updates to the NCCN Guidelines [J].
Ettinger, David S. ;
Akerley, Wallace ;
Borghaei, Hossein ;
Chang, Andrew C. ;
Cheney, Richard T. ;
Chirieac, Lucian R. ;
D'Amico, Thomas A. ;
Demmy, Todd L. ;
Govindan, Ramaswamy ;
Grannis, Frederic W., Jr. ;
Grant, Stefan C. ;
Horn, Leora ;
Jahan, Thierry M. ;
Komaki, Ritsuko ;
Kong, Feng-Ming ;
Kris, Mark G. ;
Krug, Lee M. ;
Lackner, Rudy P. ;
Lennes, Inga T. ;
Loo, Billy W., Jr. ;
Martins, Renato ;
Otterson, Gregory A. ;
Patel, Jyoti D. ;
Pinder-Schenck, Mary C. ;
Pisters, Katherine M. ;
Reckamp, Karen ;
Riely, Gregory J. ;
Rohren, Eric ;
Shapiro, Theresa A. ;
Swanson, Scott J. ;
Tauer, Kurt ;
Wood, Douglas E. ;
Yang, Stephen C. ;
Gregory, Kristina ;
Hughes, Miranda .
JOURNAL OF THE NATIONAL COMPREHENSIVE CANCER NETWORK, 2013, 11 (06) :645-653
[9]  
Fan X, 2001, INT J ONCOL, V18, P1023
[10]   Erlotinib versus docetaxel as second-line treatment of patients with advanced non-small-cell lung cancer and wild-type EGFR tumours (TAILOR): a randomised controlled trial [J].
Garassino, Marina Chiara ;
Martelli, Olga ;
Broggini, Massimo ;
Farina, Gabriella ;
Veronese, Silvio ;
Rulli, Eliana ;
Bianchi, Filippo ;
Bettini, Anna ;
Longo, Flavia ;
Moscetti, Luca ;
Tomirotti, Maurizio ;
Marabese, Mirko ;
Ganzinelli, Monica ;
Lauricella, Calogero ;
Labianca, Roberto ;
Floriani, Irene ;
Giaccone, Giuseppe ;
Torri, Valter ;
Scanni, Alberto ;
Marsoni, Silvia .
LANCET ONCOLOGY, 2013, 14 (10) :981-988