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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

Authors
 Tudor Ciuleanu  ;  Thomas Brodowicz  ;  Christoph Zielinski  ;  Joo Hang Kim  ;  Maciej Krzakowski  ;  Eckart Laack  ;  Yi-Long Wu  ;  Isabel Bover  ;  Stephen Begbie  ;  Valentina Tzekova  ;  Branka Cucevic  ;  Jose Rodrigues Pereira  ;  Sung Hyun Yang  ;  Jayaprakash Madhavan  ;  Katherine P Sugarman  ;  Patrick Peterson  ;  William J John  ;  Kurt Krejcy  ;  Chandra P Belani 
Citation
 LANCET, Vol.374(9699) : 1432-1440, 2009 
Journal Title
 LANCET 
ISSN
 0140-6736 
Issue Date
2009
MeSH
Aged ; Antineoplastic Agents/adverse effects ; Antineoplastic Agents/therapeutic use* ; Carcinoma, Non-Small-Cell Lung/diagnosis ; Carcinoma, Non-Small-Cell Lung/drug therapy* ; Carcinoma, Non-Small-Cell Lung/mortality ; Disease-Free Survival ; Double-Blind Method ; Fatigue/chemically induced ; Female ; Glutamates/adverse effects ; Glutamates/therapeutic use* ; Guanine/adverse effects ; Guanine/analogs & derivatives* ; Guanine/therapeutic use ; Humans ; Lung Neoplasms/diagnosis ; Lung Neoplasms/drug therapy* ; Lung Neoplasms/mortality ; Male ; Middle Aged ; Neoplasm Staging ; Neutropenia/chemically induced ; Pemetrexed ; Prognosis ; Proportional Hazards Models ; Survival Rate ; Treatment Outcome
Abstract
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 (2:1 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 [11.9-15.9] 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.
Full Text
http://www.sciencedirect.com/science/article/pii/S0140673609614975
DOI
10.1016/S0140-6736(09)61497-5
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
Yonsei Authors
Kim, Joo Hang(김주항)
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/105487
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