A Randomized Phase 3 Trial Comparing Pemetrexed/Carboplatin and Docetaxel/Carboplatin as First-Line Treatment for Advanced, Nonsquamous Non-small Cell Lung Cancer

被引:79
|
作者
Rodrigues-Pereira, Jose [2 ]
Kim, Joo-Hang [3 ]
Magallanes, Manuel [4 ]
Lee, Dae Ho [5 ]
Wang, Jie [6 ,7 ]
Ganju, Vinod [8 ]
Martinez-Barrera, Luis [9 ]
Barraclough, Helen [10 ]
van Kooten, Maximiliano [10 ]
Orlando, Mauro [1 ]
机构
[1] Eli Lilly Interamer Inc, Buenos Aires, DF, Argentina
[2] Inst Canc Arnaldo Vieira de Carvalho, Sao Paulo, Brazil
[3] Yonsei Univ Hlth Syst, Yonsei Canc Ctr, Seoul, South Korea
[4] Mil Hosp Mexico, Dept Med Oncol, Mexico City, DF, Mexico
[5] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Oncol, Seoul, South Korea
[6] Peking Univ, Sch Oncol, Dept Thorac Med Oncol, Beijing 100871, Peoples R China
[7] Beijing Canc Hosp & Inst, Beijing, Peoples R China
[8] Frankston Private, Peninsula Oncol Ctr, Dept Oncol, Frankston, Vic, Australia
[9] INER, Dept Med Oncol, Mexico City, DF, Mexico
[10] Eli Lilly Australia Pty Ltd, Sydney, NSW, Australia
关键词
Carboplatin; Docetaxel; First-line therapy; Non-small cell lung carcinoma; Nonsquamous; Pemetrexed; CLINICAL-PRACTICE GUIDELINES; CISPLATIN PLUS GEMCITABINE; STAGE-IV; CARBOPLATIN; DOCETAXEL; CHEMOTHERAPY; TOXICITY; MULTICENTER; DIAGNOSIS; SURVIVAL;
D O I
10.1097/JTO.0b013e318226b5fa
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: This study compared survival without toxicity in patients with advanced, nonsquamous non-small cell lung cancer who were treated with first-line pemetrexed/carboplatin or docetaxel/carboplatin. Methods: This multicenter, open-label, parallel-group, phase 3 trial comprised patients randomized (1:1) to pemetrexed/carboplatin (n = 128) or docetaxel/carboplatin (n = 132). Patients received treatment on day 1 of each 21-day cycle (maximum of six cycles). Treatment included carboplatin (area under the curve = 5 mg/ml x min) and pemetrexed (500 mg/m(2)) or docetaxel (75 mg/m(2)). The primary outcome measure, survival without treatment-emergent grade 3/4 toxicity, was defined as the time from randomization to the first treatment-emergent grade 3/4 adverse event or death and was analyzed using a log-rank test. The analysis population included 106 patients in the pemetrexed/carboplatin (Pem/Carb) group and 105 patients in the docetaxel/carboplatin (Doc/Carb) group. Results: Survival without treatment-emergent grade 3/4 toxicity was significantly longer in the Pem/Carb versus the Doc/Carb group (log-rank p < 0.001; median survival without treatment-emergent grade 3/4 toxicity: 3.2 versus 0.7 months; adjusted hazard ratio = 0.45 [95% confidence interval: 0.34-0.61]). Overall survival was similar in the Pem/Carb versus the Doc/Carb group (log-rank p = 0.934; median survival: 14.9 versus 14.7 months; adjusted hazard ratio = 0.93 [95% confidence interval: 0.66-1.32]). Compared with the Doc/Carb group, fewer patients in the Pem/Carb group experienced grade 3/4 drug-related, treatment-emergent neutropenia, leukopenia, or febrile neutropenia, and more patients experienced anemia and thrombocytopenia. There were three study drug-related deaths during treatment in each group. Conclusions: The favorable benefit-to-risk profile of pemetrexed/ carboplatin suggests that pemetrexed/carboplatin is an appropriate first-line treatment option for chemona ve patients with advanced, nonsquamous non-small cell lung cancer.
引用
收藏
页码:1907 / 1914
页数:8
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