Phase III trial comparing 4-day chronomodulated therapy versus 2-day conventional delivery of fluorouracil, leucovorin, and oxaliplatin as first-line chemotherapy of metastatic colorectal cancer:: The European Organisation for Research and Treatment of Cancer Chronotherapy group

被引:186
作者
Giacchetti, Sylvie
Bjarnason, Georg
Garufi, Carlo
Genet, Dominique
Iacobelli, Stefano
Tampellini, Marco
Smaaland, Rune
Focan, Christian
Coudert, Bruno
Humblet, Yves
Canon, Jean Luc
Adenis, Antoine
Lo Re, Giovanni
Carvalho, Carlos
Schueller, Johannes
Anciaux, Nicole
Lentz, Marie-Ange
Baron, Benoit
Gorlia, Thierry
Levi, Francis
机构
[1] Hop Paul Brousse, INSERM, Canc Chronotherapeut E0354, F-94807 Villejuif, France
[2] CHU Dupuytren, Limoges, France
[3] Ctr Georges Francois Leclerc, Dijon, France
[4] Ctr Oscar Lambret, F-59020 Lille, France
[5] Toronto Sunnybrook Reg Canc Ctr, Toronto, ON, Canada
[6] Ist Regina Elena, I-00161 Rome, Italy
[7] Univ G DAnnunzio, Chieti, Italy
[8] Osped San Luigi Gonzaga, Orbassano, Italy
[9] SM Angeli, Pordenone, Italy
[10] Univ Bergen, Haukeland Univ Hosp, N-5020 Bergen, Norway
[11] Liege Clin Univ St Luc, CHC Les Clin St Joseph, Liege, Belgium
[12] European Org Res & Treatment Canc Data Ctr, Brussels, Belgium
[13] Clin Notre Dame, Charleroi, Belgium
[14] Clin Ste Elisabeth, Namur, Belgium
[15] Hop F Fonseca, Amadora, Portugal
[16] Krankenanstalt Rudolfstiftung Wien, Vienna, Austria
关键词
D O I
10.1200/JCO.2006.06.1440
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose In two previous randomized trials, the adjustment of chemotherapy delivery to circadian rhythms improved tolerability and anticancer activity compared with constant-rate infusion during 5 days in patients with metastatic colorectal cancer. Patients and Methods For this multicenter randomized trial, it was hypothesized that a chronomodulated infusion of fluorouracil, leucovorin, and oxaliplatin for 4 days (chronoFLO4) would improve survival by 10% compared with conventional 2-day delivery of the same drugs (FOLFOX2). Patients were treated every 2 weeks with intrapatient dose escalation. Results Baseline characteristics were similar in both arms for the 564 patients (36 institutions, 10 countries). Median survival was 19.6 months (95% confidence limit [CL] 18.2, 21.2) with chronoFLO4 and 18.7 months with FOLFOX2 (95% CL = 17.7, 21.0; P = .55). The main dose-limiting toxicities were diarrhea for chronoFLO4 and neutropenia for FOLFOX2. The analysis of survival predictors showed that sex was the single most important factor (P = .001). In women, the risk of an earlier death with chronoFLO4 was increased by 38% compared with FOLFOX2, with median survival times of 16.3 and 19.1 months (P = .03), respectively. In men, the risk of death was decreased by 25% with chronoFLO4 compared with FOLFOX2, with median survival times of 21.4 and 18.3 months (P = .02), respectively. Conclusion Both regimens achieved similar median survival times more than 18 months with an acceptable toxicity. The chronomodulated schedule produced a survival advantage over FOLFOX in men. The strong sex dependency of optimal scheduling of fluorouracil, leucovorin, and oxaliplatin calls for translational investigations of determinants related to the patient's molecular clock.
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收藏
页码:3562 / 3569
页数:8
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