IDI-Istituto Dermopatico dell'Immacolata, Rome, Italy.
Oncol Rep. 2010 Jun;23(6):1635-40. doi: 10.3892/or_00000805.
A weekly administration of alternating irinotecan or oxaliplatin associated to 5-Fluorouracil in advanced colorectal cancer was planned in order to evaluate a new schedule maintaining dose intensities of each drug as in double combinations and tolerability of the triplet association. The following weekly schedule was administered: irinotecan, days 1 and 15; oxaliplatin, days 8 and 22; 5-fluorouracil (5-FU) over 12-h (from 10:00 p.m. to 10:00 a.m.) timed flat infusion, days 1-2, 8-9, 15-16 and 22-23, every 4 weeks. Dose- finding and phase II study were planned. Thirteen patients were enrolled in the dose-finding study and 23 in the phase II study. The recommended doses of our study are: irinotecan 160 mg/m(2); oxaliplatin 80 mg/m(2); 5-FU 900 mg/m(2). The dose-limiting toxicity was diarrhea (35% of patients) but no cases of febrile neutropenia were observed. In 30 patients assessable for response two complete (6.7%) and 18 partial (60%) responses were observed, for an overall response rate of 66.7% (alpha 0.05, CI+/-17). The triplet association using this weekly alternating schedule is an active and well-tolerated outpatient regimen. Surgical removal of residual disease was considered in 5 patients and a radical resection was performed in 5 patients (147 %).
在晚期结直肠癌患者中,计划每周交替给予伊立替康或奥沙利铂联合 5-氟尿嘧啶,以评估一种新的方案,该方案保持两种药物的剂量强度,并评估三联疗法的耐受性。每周的方案如下:伊立替康,第 1 天和第 15 天;奥沙利铂,第 8 天和第 22 天;5-氟尿嘧啶(5-FU)持续 12 小时输注(从晚上 10 点到早上 10 点),第 1-2 天、第 8-9 天、第 15-16 天和第 22-23 天,每 4 周一次。计划进行剂量探索和 II 期研究。在剂量探索研究中,共入组 13 例患者,在 II 期研究中,共入组 23 例患者。我们研究的推荐剂量为:伊立替康 160mg/m(2);奥沙利铂 80mg/m(2);5-FU 900mg/m(2)。剂量限制性毒性是腹泻(35%的患者),但未观察到发热性中性粒细胞减少症。在可评估疗效的 30 例患者中,观察到 2 例完全缓解(6.7%)和 18 例部分缓解(60%),总缓解率为 66.7%(alpha 0.05,置信区间+/-17)。该三联疗法使用这种每周交替方案是一种有效的、耐受性良好的门诊治疗方案。5 例患者考虑手术切除残留疾病,5 例患者(147%)行根治性切除术。