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:80
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
相关论文
共 34 条
[1]  
[Anonymous], 1997, AJCC CANC STAGING MA
[2]  
[Anonymous], 2006, Cancer Therapy Evaluation Program, Common Terminology Criteria for Adverse Events, Version 3.0
[3]   Cisplatin-versus carboplatin-based chemotherapy in first-line treatment of advanced non-small-cell lung cancer: An individual patient data meta-analysis [J].
Ardizzoni, Andrea ;
Boni, Luca ;
Tiseo, Marcello ;
Fossella, Frank V. ;
Schiller, Joan H. ;
Paesmans, Marianne ;
Radosavljevic, Davorin ;
Paccagnella, Adriano ;
Zatloukal, Petr ;
Mazzanti, Paola ;
Bisset, Donald ;
Rosell, Rafael .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2007, 99 (11) :847-857
[4]   American Society of Clinical Oncology Clinical Practice Guideline Update on Chemotherapy for Stage IV Non-Small-Cell Lung Cancer [J].
Azzoli, Christopher G. ;
Baker, Sherman, Jr. ;
Temin, Sarah ;
Pao, William ;
Aliff, Timothy ;
Brahmer, Julie ;
Johnson, David H. ;
Laskin, Janessa L. ;
Masters, Gregory ;
Milton, Daniel ;
Nordquist, Luke ;
Pfister, David G. ;
Piantadosi, Steven ;
Schiller, Joan H. ;
Smith, Reily ;
Smith, Thomas J. ;
Strawn, John R. ;
Trent, David ;
Giaccone, Giuseppe .
JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (36) :6251-6266
[5]   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 [J].
Ciuleanu, Tudor ;
Brodowicz, Thomas ;
Zielinski, Christoph ;
Kim, Joo Hang ;
Krzakowski, Maciej ;
Laack, Eckart ;
Wu, Yi-Long ;
Bover, Isabel ;
Begbie, Stephen ;
Tzekova, Valentina ;
Cucevic, Branka ;
Pereira, Jose Rodrigues ;
Yang, Sung Hyun ;
Madhavan, Jayaprakash ;
Sugarman, Katherine P. ;
Peterson, Patrick ;
John, William J. ;
Krejcy, Kurt ;
Belani, Chandra P. .
LANCET, 2009, 374 (9699) :1432-1440
[6]   FDA drug approval summary:: Pemetrexed for injection (Alimta®) for the treatment of non-small cell lung cancer [J].
Cohen, MH ;
Johnson, JR ;
Wang, YC ;
Sridhara, R ;
Pazdur, R .
ONCOLOGIST, 2005, 10 (06) :363-368
[7]   Early stage and locally advanced (non-metastatic) non-small-cell lung cancer: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up [J].
Crino, L. ;
Weder, W. ;
van Meerbeeck, J. ;
Felip, E. .
ANNALS OF ONCOLOGY, 2010, 21 :v103-v115
[8]  
*CTR DRUG EV RES, 2010, COMM CARB DOS
[9]   Metastatic non-small-cell lung cancer: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up [J].
D'Addario, G. ;
Frueh, M. ;
Reck, M. ;
Baumann, P. ;
Klepetko, W. ;
Felip, E. .
ANNALS OF ONCOLOGY, 2010, 21 :v116-v119
[10]   Randomized, multinational, phase III study of docetaxel plus platinum combinations versus vinorelbine plus cisplatin for advanced non-small-cell lung cancer: The TAX 326 study group [J].
Fossella, F ;
Pereira, JR ;
von Pawel, J ;
Pluzanska, A ;
Gorbounova, V ;
Kaukel, E ;
Mattson, KV ;
Ramlau, R ;
Szczesna, A ;
Fidias, P ;
Millward, M ;
Belani, CP .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (16) :3016-3024