Résumé
Patients and methods: LMCRC patients were randomized to receive every 14 days, FA, 400 mg/m(2) infused over 2 h, followed by 5-FU as a 400 mg/m(2) i.v. bolus, followed by continuous 5-FU infusion, 2400 mg/m(2) over 46 h (LV5FUs) with or without irinotecan: 180 mg/m(2) infusion (FOLFIRI). The primary end point was disease-free survival (DFS); secondary end points included overall survival (OS) and safety.
Results: Treated patients (n = 306) were balanced for critical prognostic factors in each arm. Median DFS in patients receiving LV5FUs was 21.6 versus 24.7 months for FOLFIRI [hazard ratio (HR) 0.89, log-rank P = 0.44]. No significant differences were found in OS. A trend was observed for improved DFS in patients receiving FOLFIRI within 42 days of surgery (HR 0.75, P = 0.17). Grade 3/4 toxic effects were more common in patients treated with FOLFIRI versus LV5FUs (47% versus 30%) with neutropenia being most common (23% versus 7%).
Conclusion: FOLFIRI in the adjuvant treatment of LMCRC showed no significant improvement in DFS compared with LV5FUs.