Phase I study of a weekly schedule of irinotecan, high-dose leucovorin, and infusional fluorouracil as first-line chemotherapy in patients with advanced colorectal cancer

被引:74
作者
Vanhoefer, U
Harstrick, A
Köhne, CH
Achterrath, W
Rustum, YM
Seeber, S
Wilke, H
机构
[1] Univ Essen Gesamthsch, Sch Med, W German Canc Ctr, Dept Internal Med Canc Res, D-45122 Essen, Germany
[2] Humboldt Univ, Dept Hematol & Oncol, Berlin, Germany
[3] Rhone Poulenc Rorer, Dept Clin Res Oncol New Technol, Cologne, Germany
[4] Roswell Pk Canc Inst, Grace Canc Drug Ctr, Dept Pharmacol & Expt Therapeut, Buffalo, NY USA
关键词
D O I
10.1200/JCO.1999.17.3.907
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To determine the maximum-tolerated dose (MTD) of a weekly schedule of irinotecan (CPT-11), leucovorin (LV), and a 24-hour infusion of fluorouracil (5-FU24h) as first-line chemotherapy in advanced colorectal cancer and to assess preliminary data on the antitumor activity. Patients and Methods: Twenty-six patients with measurable metastatic colorectal cancer were entered onto this phase I study. In the first six dose levels, fixed doses of CPT-11 (80 mg/m(2)) and LV (500 mg/m(2)) in combination with escalated doses of 5-FU24h ranging from 1.8 to 2.6 g/m(2) were administered on a weekly-times-four (dose levels 1 to 4) or weekly-times-six (dose levers 5 to 6) schedule. The dose of CPT-11 was then increased to 100 mg/m(2) (dose level 7), Results: Seventy-nine cycles of 5-FU24h/LV with CPT-11 were administered in an outpatient setting. No dose-limiting toxicities were observed during the first cycle at dose levels 1 to 6, but diarrhea of grade 4 (National Cancer Institute common toxicity criteria) was observed in three patients after multiple treatment cycles. Of her nonhematologic and hematologic side effects, specifically alopecia and neutropenia, did not exceed grade 2, With the escalation of CPT-11 to 100 mg/m(2) (dose level 7), diarrhea of grade 3 or higher was observed in four of six patients during the first cycle; thus, the MTD was achieved. Sixteen of 25 response-assessable patients (64%; 95% confidence interval, 45% to 83%) achieved an objective response. Conclusion: The recommended doses for further studies are CPT-11 80 mg/m(2), LV 500 mg/m(2), and 5-FU24h 2.6 g/m(2) given on a weekly-times-six schedule followed by a 1-week rest period. The addition of CPT- 11 to 5-FU24h/LV seems to improve the therapeutic efficacy in terms of tumor response with manageable toxicity. (C) 1999 by American of Clinical Oncology.
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页码:907 / 913
页数:7
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