First-Line Pemetrexed plus Cisplatin followed by Gefitinib Maintenance Therapy versus Gefitinib Monotherapy in East Asian Never-Smoker Patients with Locally Advanced or Metastatic Nonsquamous Non-Small Cell Lung Cancer: Final Overall Survival Results from a Randomized Phase 3 Study

被引:20
|
作者
Yang, James Chih-Hsin [1 ]
Srimuninnimit, Vichien [2 ]
Ahn, Myung-Ju [3 ]
Lin, Chia-Chi [1 ]
Kim, Sang-We [4 ]
Tsai, Chun-Ming [5 ,6 ]
Mok, Tony [7 ]
Orlando, Mauro [8 ]
Puri, Tarun [9 ]
Wang, Xin [10 ]
Park, Keunchil [3 ]
机构
[1] Natl Taiwan Univ Hosp, Taipei 100, Taiwan
[2] Mahidol Univ, Siriraj Hosp, Bangkok 10700, Thailand
[3] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Seoul, South Korea
[4] Univ Ulsan, Asan Med Ctr, Coll Med, Seoul, South Korea
[5] Taipei Vet Gen Hosp, Taipei, Taiwan
[6] Natl Yang Ming Univ, Taipei 112, Taiwan
[7] Prince Wales Hosp, Sha Tin, Hong Kong, Peoples R China
[8] Eli Lilly Interamer Inc, Buenos Aires, DF, Argentina
[9] Eli Lilly & Co, Gurgaon, Haryana, India
[10] Eli Lilly & Co, Shanghai, Peoples R China
关键词
Non-small cell lung cancer; East Asia; Gefitinib; Pemetrexed; Overall survival; GROWTH-FACTOR RECEPTOR; GENE-MUTATIONS; CARBOPLATIN-PACLITAXEL; OPEN-LABEL; EGFR; ADENOCARCINOMA; ERLOTINIB; TRIAL; CHEMOTHERAPY; EXON-19;
D O I
10.1016/j.jtho.2015.11.008
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: The primary analysis of this open-label, randomized, multicenter phase 3 study revealed no significant difference in progression-free survival between pemetrexed plus cisplatin followed by maintenance gefitinib. (PC/G) and gefitinib monotherapy (G) in patients with advanced nonsquamous non-small cell lung cancer (NSCLC) and unknown epidermal growth factor receptor gene (EGFR) mutation status; however, the hazard ratio favored PC/G. This report describes the final overall survival (OS) results. Methods: Chemonaive, East Asian light ex-smokers/never-smokers with advanced nonsquamous NSCLC and unknown EGFR mutation status were randomized (1:1) to PC/G (n = 118) or G (n = 118). EGFR mutation status was retrospectively determined for 76 patients, 52 (68.4%) of whom had EGFR-mutated tumors (exon 19 deletions in 26 and L858R point mutation in 24). OS was analyzed by the Kaplan-Meier method. The study was registered at ClinicalTrials.gov (NCT01017874). Results: Median OS was similar in the PC/G (26.9 months) and G (27.9 months) groups (hazard ratio = 0.94, 95% confidence interval: 0.68-1.31, p = 0.717). Median OS was longer with PC/G than with G in patients with EGFR wild type tumors (28.4 versus 8.9 months) and longer with G than with PC/G in patients with EGFR-mutated tumors (45.7 versus 32.4 months), especially those with exon 19 deletions. Second-line postdiscontinuation therapy was common and included chemotherapy (PC/G, 41 of 118 [34.7%]; G, 73 of 118 [61.9%]) and rechallenge with an EGFR tyrosine kinase inhibitor (PC/G, 27 of 118 [22.9%]; G, 9 of 118 [7.6%]). Conclusions: The progression-free survival and OS results from this study further demonstrate the importance of determining EGFR mutation status to select the most appropriate first-line treatment for patients with advanced NSCLC. (C) 2015 International Association for the Study of Lung Cancer. Published by Elsevier Inc.
引用
收藏
页码:370 / 379
页数:10
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