Phase I and pharmacokinetic study of two different schedules of oxaliplatin, irinotecan, fluorouracil, and leucovorin in patients with solid tumors

被引:40
作者
Goetz, MP
Erlichman, C
Windebank, AJ
Reid, JM
Sloan, JA
Atherton, P
Adiei, AA
Rubin, J
Pitot, H
Galanis, E
Ames, MM
Goldberg, RM
机构
[1] Mayo Clin & Mayo Fdn, Dept Oncol, Div Med Oncol, Rochester, MN 55905 USA
[2] Mayo Clin & Mayo Fdn, Div Oncol Res, Rochester, MN 55905 USA
[3] Mayo Clin & Mayo Fdn, Dept Neurol, Rochester, MN 55905 USA
关键词
D O I
10.1200/JCO.2003.01.238
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: We sought to determine the maximum-tolerated dose (MTD) and evaluate the toxicities and clinical activity of two irinotecon (CPT-11), fluorouracil (FU), leucovorin (LV), and oxaliplatin schedules in patients with advanced solid tumors. Additionally, we investigated the effect of CPT-11 on oxaliplatin pharmacokinetics. Patients and Methods: Thirteen patients (cohort 1) received intravenous CPT-11 (infusion) and FU/LV (bolus) on days 1, 8, 15, and 22 and oxaliplatin (infusion) on days 1 and 15 every 6 weeks for a total 37 courses (median, three courses) at three dose levels. Twenty-two cohort 2 patients received intravenous CPT-11/oxaliplatin (infusion, day 1) and FU/LV (90-minute bolus infusion, days 2 to 5) every 3 weeks for a total of 122 courses (median, four courses) at three dose levels. Pharmacokinetic and neurotoxicity assessments were performed at the cohort 2 MTD. Results: Dose-limiting toxicity (DLT) seen in both cohorts at the starting dose required dose de-escalation. Cohort 1 DLT included diarrhea and neutropenia. In cohort 2, diarrhea, vomiting, dehydration, neutropenia, febrile neutropenia, and paresthesias were DLTs. Antitumor activity was seen in both cohorts. In cohort 2, the total platinum area under the curve of patients increased 17% in cycle 2 (P = .048), but objective neurotoxicity was not seen. Conclusion: The toxicities resulting from the addition of oxaliplatin to CPT-11/FU/LV are significant but manageable. The MTDs for the weekly schedule are CPT-11 (75 mg/m(2)), oxaliplatin (50 mg/m(2)), FU (320 mg/m(2)), and LV (20 mg/m(2)); and, for the 3-weekly schedule, the MTDs are CPT-11 (175 mg/m(2)), oxaliplatin (85 mg/m(2)), FU (240 mg/m(2)), and LV (20 mg/m(2)). Second-cycle platinum accumulation raises the possibility for enhanced cumulative neurotoxicity with CPT-11/oxaliplatin combinations. (C) 2003 by American Society of Clinical Oncology.
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收藏
页码:3761 / 3769
页数:9
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