Capecitabine plus oxaliplatin (XELOX) versus 5-fluorouracil/leucovorin plus oxaliplatin (FOLFOX-6) as first-line treatment for metastatic colorectal cancer

被引:126
作者
Ducreux, Michel [1 ]
Bennouna, Jaafar [2 ]
Hebbar, Mohamed [3 ]
Ychou, Marc [4 ]
Lledo, Gerard [5 ]
Conroy, Thierry [6 ,7 ]
Adenis, Antoine [8 ]
Faroux, Roger [9 ]
Rebischung, Christine [10 ]
Bergougnoux, Loic [11 ]
Kockler, Leila [11 ]
Douillard, Jean-Yves [2 ]
机构
[1] Inst Gustave Roussy, Dept Med, F-94805 Villejuif, France
[2] Ctr Rene Gauducheau, Dept Med, St Herblain, France
[3] CHU Lille, Oncol Unit, F-59037 Lille, France
[4] Ctr Val Aurelle, Dept Med, Montpellier, France
[5] Clin St Jean, Gastroenterol Unit, Lyon, France
[6] Ctr Alexis Vautrin, Dept Med, Vandoeuvre Les Nancy, France
[7] Nancy Univ, Vandoeuvre Les Nancy, France
[8] Ctr Oscar Lambret, Dept Med, F-59020 Lille, France
[9] Ctr Hosp Dept Les Oudairies, Gastroenterol Unit, La Roche Sur Yon, France
[10] Hop Michallon, Oncol Unit, La Tronche, France
[11] Labs Roche, Neuilly Sur Seine, France
关键词
5-fluorouracil/leucovorin; capecitabine; metastatic colorectal cancer; oxaliplatin; RANDOMIZED PHASE-III; HIGH-DOSE LEUCOVORIN; SIMPLIFIED BIMONTHLY LEUCOVORIN; CONTINUOUS-INFUSION; ORAL CAPECITABINE; 2ND-LINE THERAPY; SOLID TUMORS; FINAL REPORT; FLUOROURACIL; SURVIVAL;
D O I
10.1002/ijc.25369
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A regimen consisting of 5-fluorouracil/leucovorin plus oxaliplatin (FOLFOX-6) is widely used in France in the first-line treatment of metastatic colorectal cancer (MCRC). The aim of our study was to demonstrate the non-inferiority of capecitabine plus oxaliplatin (XELOX) versus FOLFOX-6 for this indication. Patients were randomly assigned to receive XELOX or FOLFOX-6 for 6 months. The primary endpoint was overall response rate (ORR) in the per-protocol (PP) population; however, progression-free and overall survival (OS), time to response and response duration were also assessed. A total of 306 patients were enrolled (XELOX n = 156; FOLFOX-6 n = 150). ORR was 42 and 46% with XELOX and FOLFOX-6, respectively, in the PP population. The difference between groups was 4.7%; the upper limit of the unilateral 95% confidence interval (14.4%) was below the non-inferiority margin of 15%. In the intent-to-treat population, median progression-free survival was 8.8 months with XELOX and 9.3 months with FOLFOX-6, and median OS was 19.9 and 20.5 months, respectively. XELOX patients had significantly more grade 3/4 thrombocytopenia (12% vs. 5%) and diarrhoea (14% vs. 7%), but significantly less grade 3/4 neutropenia (5% vs. 47%), febrile neutropenia (0% vs. 6%) and neuropathy (11% vs. 26%) than FOLFOX-6 patients. We conclude that XELOX is non-inferior in terms of efficacy to FOLFOX-6 in the first-line treatment of MCRC, but has a different toxicity profile.
引用
收藏
页码:682 / 690
页数:9
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