Maintenance pemetrexed plus best supportive care versus placebo plus best supportive care for non-small-cell lung cancer: a randomised, double-blind, phase 3 study

被引:1199
作者
Ciuleanu, Tudor [3 ,4 ]
Brodowicz, Thomas [4 ,5 ]
Zielinski, Christoph [4 ,5 ]
Kim, Joo Hang [6 ]
Krzakowski, Maciej [4 ,7 ,8 ]
Laack, Eckart [9 ]
Wu, Yi-Long [10 ]
Bover, Isabel [11 ]
Begbie, Stephen [12 ]
Tzekova, Valentina [4 ,13 ]
Cucevic, Branka [4 ,14 ]
Pereira, Jose Rodrigues [15 ]
Yang, Sung Hyun [16 ]
Madhavan, Jayaprakash [17 ]
Sugarman, Katherine P. [18 ]
Peterson, Patrick [18 ]
John, William J. [18 ]
Krejcy, Kurt [2 ]
Belani, Chandra P. [1 ]
机构
[1] Penn State Hershey Canc Inst, Hershey, PA 17033 USA
[2] Lilly Reg Operat, Vienna, Austria
[3] Oncol Inst Ion Chiricuta, Cluj Napoca, Romania
[4] CECOG, Vienna, Austria
[5] Med Univ Vienna Gen Hosp, Dept Med 1, Div Clin Oncol, Vienna, Austria
[6] Yonsei Canc Ctr, Seoul, South Korea
[7] Maria Sklodowska Curie Mem Canc Ctr, Warsaw, Poland
[8] Inst Oncol, Warsaw, Poland
[9] Univ Hosp Hamburg Eppendorf, Univ Canc Ctr Hamburg, Hamburg, Germany
[10] Guangdong Gen Hosp, Guangzhou, Guangdong, Peoples R China
[11] Fdn Hosp Son Llatzer Ctra Manacor, Manacor, Spain
[12] N Coast Canc Inst, Port Macquarie, NSW, Australia
[13] Univ Hosp Queen Joanna, Sofia, Bulgaria
[14] Hosp Lung Dis, Jordanovac, Croatia
[15] Inst Canc Arnaldo Vieira de Carvalho, Sao Paulo, Brazil
[16] Korea Canc Ctr Hosp, Seoul, South Korea
[17] Reg Canc Ctr, Trivandrum 695011, Kerala, India
[18] Eli Lilly & Co, Indianapolis, IN 46285 USA
关键词
III TRIAL; LINE THERAPY; CHEMOTHERAPY; CISPLATIN; GEMCITABINE; COMBINATION; NSCLC; CARBOPLATIN; DURATION; DOCETAXEL;
D O I
10.1016/S0140-6736(09)61497-5
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Background Several studies have shown the efficacy, tolerability, and ease of administration of pemetrexed-an antifolate antineoplastic agent-in patients with advanced non-small-cell lung cancer. We assessed pemetrexed as maintenance therapy in patients with this disease. Methods This randomised double-blind study was undertaken in 83 centres in 20 countries. 663 patients with stage IIIB or IV disease who had not progressed on four cycles of platinum-based chemotherapy were randomly assigned (21 ratio) to receive pemetrexed (500 mg/m(2), day 1) plus best supportive care (n=441) or placebo plus best supportive care (n=222) in 21-day cycles until disease progression. Treatment was randomised with the Simon and Pocock minimisation method. Patients and investigators were masked to treatment. All patients received vitamin B-12, folic acid, and dexamethasone. The primary endpoint of progression-free survival and the secondary endpoint of overall survival were analysed by intention to treat. This study is registered with ClinicalTrials.gov, number NCT00102804. Findings All randomly assigned participants were analysed. Pemetrexed significantly improved progression-free survival (4.3 months [95% CI 4.1-4.7] vs 2.6 months [1.7-2.8]; hazard ratio [HR] 0.50, 95% CI 0.42-0.61, p<0.0001) and overall survival (13.4 months [11.9-15.91 vs 10.6 months [8.7-12.0]; HR 0.79, 0.65-0.95, p=0.012) compared with placebo. Treatment discontinuations due to drug-related toxic effects were higher in the pemetrexed group than in the placebo group (21 [5%] vs three [1%]). Drug-related grade three or higher toxic effects were higher with pemetrexed than with placebo (70 [16%] vs nine [4%]; p<0.0001), specifically fatigue (22 [5%] vs one [1%], p=0.001) and neutropenia (13 [3%] vs 0, p=0.006). No pemetrexed-related deaths occurred. Relatively fewer patients in the pemetrexed group than in the placebo group received systemic post-discontinuation therapy (227 [51%] vs 149 [67%]; p=0.0001). Interpretation Maintenance therapy with pemetrexed is well tolerated and offers improved progression-free and overall survival compared with placebo in patients with advanced non-small-cell lung cancer. Funding Eli Lilly.
引用
收藏
页码:1432 / 1440
页数:9
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