XELOX vs FOLFOX-4 as first-line therapy for metastatic colorectal cancer: NO16966 updated results

被引:193
|
作者
Cassidy, J. [1 ]
Clarke, S. [2 ,3 ]
Diaz-Rubio, E. [4 ]
Scheithauer, W. [5 ]
Figer, A. [6 ]
Wong, R. [7 ]
Koski, S. [8 ]
Rittweger, K. [9 ]
Gilberg, F. [10 ]
Saltz, L. [11 ]
机构
[1] Beatson Oncol Ctr, Inst Canc Sci, Glasgow G12 0YN, Lanark, Scotland
[2] Univ Sydney, Sydney Med Sch, Sydney, NSW 2006, Australia
[3] Royal N Shore Hosp, Sydney Canc Ctr, Sydney, NSW 2006, Australia
[4] Hosp Clin San Carlos, Med Oncol Serv, Madrid 28040, Spain
[5] Univ Vienna, Sch Med, Dept Internal Med, A-1090 Vienna, Austria
[6] Tel Aviv Sourasky Med Ctr, Dept Med Oncol, IL-64239 Tel Aviv, Israel
[7] St Boniface Gen Hosp, Dept Med Oncol Canc Care Manitoba, Winnipeg, MB R2N 2A6, Canada
[8] Cross Canc Inst, Dept Oncol, Edmonton, AB T6G 1Z2, Canada
[9] Hoffmann La Roche Inc, Dept Clin Sci, Nutley, NJ 07110 USA
[10] F Hoffmann La Roche, Dept Stat, CH-4070 Basel, Switzerland
[11] Mem Sloan Kettering Canc Ctr, Dept Med, New York, NY 10065 USA
关键词
5-fluorouracil/folinic acid; capecitabine; colorectal cancer; overall survival; oxaliplatin; RANDOMIZED PHASE-III; FLUOROURACIL PLUS LEUCOVORIN; ORAL CAPECITABINE; OXALIPLATIN XELOX; FINAL REPORT; TRIALS;
D O I
10.1038/bjc.2011.201
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: We report updated overall survival (OS) data from study NO16966, which compared capecitabine plus oxaliplatin (XELOX) vs 5-fluorouracil/folinic acid plus oxaliplatin (FOLFOX4) as first-line therapy in metastatic colorectal cancer. METHODS: NO16966 was a randomised, two-arm, non-inferiority, phase III comparison of XELOX vs FOLFOX4, which was subsequently amended to a 2 x 2 factorial design with further randomisation to bevacizumab or placebo. A planned follow-up exploratory analysis of OS was performed. RESULTS: The intent-to-treat (ITT) population comprised 2034 patients (two-arm portion, n = 634; 2 x 2 factorial portion, n 1400). For the whole NO16966 study population, median OS was 19.8 months in the pooled XELOX/XELOX-placebo/XELOX-bevacizumab arms vs 19.5 months in the pooled FOLFOX4/FOLFOX4-placebo/FOLFOX4-bevacizumab arms (hazard ratio 0.95 (97.5% CI 0.85-1.06)). In the pooled XELOX/XELOX-placebo arms, median OS was 19.0 vs 18.9 months in the pooled FOLFOX4/FOLFOX4-placebo arms (hazard ratio 0.95 (97.5% CI 0.83-1.09)). FOLFOX4 was associated with more grade 3/4 neutropenia/granulocytopenia and febrile neutropenia than XELOX, and XELOX with more grade 3 diarrhoea and grade 3 hand-foot syndrome than FOLFOX4. CONCLUSION: Updated survival data from study NO16966 show that XELOX is similar to FOLFOX4, confirming the primary analysis of progression-free survival. XELOX can be considered as a routine first-line treatment option for patients with metastatic colorectal cancer. British Journal of Cancer (2011) 105, 58-64. doi: 10.1038/bjc.2011.201 www.bjcancer.com Published online 14 June 2011 (C) 2011 Cancer Research UK
引用
收藏
页码:58 / 64
页数:7
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