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

Author:

Giacchetti Sylvie1,Bjarnason Georg1,Garufi Carlo1,Genet Dominique1,Iacobelli Stefano1,Tampellini Marco1,Smaaland Rune1,Focan Christian1,Coudert Bruno1,Humblet Yves1,Canon Jean Luc1,Adenis Antoine1,Re Giovanni Lo1,Carvalho Carlos1,Schueller Johannes1,Anciaux Nicole1,Lentz Marie-Ange1,Baron Benoît1,Gorlia Thierry1,Lévi Francis1

Affiliation:

1. From the Hopital Paul Brousse and INSERM, Villejuif; Centre Hospitalier Universitaire Dupuytren, Limoges; Centre Georges-François Leclerc, Dijon; Centre Oscar Lambret, Lille, France; Toronto-Sunnybrook Regional Cancer Centre, Toronto, Ontario, Canada; Istituto Regina Elena, Roma; Universita G. d'Annunzio di Chieti, Chieti; Ospedale San Luigi Gonzaga, Orbassano-Torino; S.M. Angeli, Pordenone, Italy; Haukeland University Hospital, University of Bergen, Norway; CHC-Les Cliniques Saint-Joseph, Liège...

Abstract

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.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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