Irinotecan Combined With Bolus Fluorouracil, Continuous Infusion Fluorouracil, and High-Dose Leucovorin Every Two Weeks (LV5FU2 Regimen): A Clinical Dose-Finding and Pharmacokinetic Study in Patients With Pretreated Metastatic Colorectal Cancer

Author:

Ducreux Michel1,Ychou Marc1,Seitz Jean-François1,Bonnay Marc1,Bexon Alice1,Armand Jean-Pierre1,Mahjoubi Monder1,Méry-Mignard Dominique1,Rougier Philippe1

Affiliation:

1. From the Institut Gustave Roussy, Villejuif; Centre du Val d'Aurelle, Montpellier; Institut Paoli Calmettes, Marseille; and Laboratoires Rhône-Poulenc Rorer, Montrouge, France.

Abstract

PURPOSE: To determine the maximum-tolerated dose (MTD) and recommended dose of irinotecan (CPT-11) in combination with fluorouracil (5-FU) and leucovorin (LV), using a biweekly LV5FU2 regimen and increasing doses of CPT-11, and to assess the efficacy of this combination in pretreated patients with colorectal cancer (CRC). PATIENTS AND METHODS: All patients had metastatic CRC and a World Health Organization performance status of 0 or 1. CPT-11 was administered over a 90-minute infusion every 2 weeks at a range of dose levels (100, 120, 150, 180, 200, 220, and 260 mg/m2). LV5FU2 was started 1 hour after the end of the biweekly CPT-11 infusion and was also administered on day 2. RESULTS: Fifty-five patients were entered onto this trial; 549 cycles were administered. The MTD was not reached at 260 mg/m2, and a dose level of 300 mg/m2 was added. The MTD as defined in the protocol was not reached at this dose level either, but all patients had cycles delayed and/or required a dose reduction. This dose was deemed to be the MTD. To take into account both the toxicity of and compliance with the biweekly schedule, the recommended CPT-11 dose was established at 180 to 200 mg/m2. Antitumor activity was observed at almost all dose levels, with an objective response rate of 22%. Median time to progression was 6.3 months and overall survival was 15 months. CONCLUSION: The biweekly CPT-11/LV5FU2 combination is feasible and safe, without overlapping toxicity. CPT-11 at 180 to 200 mg/m2 in combination with LV5FU2 has been selected as the recommended dose for further studies.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

Reference35 articles.

1. Kunimoto T, Nitta K, Kanaka T, et al: Antitumor activity of 7-ethyl-10 (4 -(1-piperidino)-1-piperidino)-1-carbonyloxy-camptothecin, a novel water-soluble derivative of camptothecin, against murine tumors. Cancer Res 47:5944,1987-5947,

2. On the mechanism of topoisomerase I inhibition by camptothecin: evidence for binding to an enzyme-DNA complex

3. Hsiang YH, Liu LF: Identification of mammalian DNA topoisomerase as an intracellular target of the anticancer drug camptothecin. Cancer Res 48:1722,1988-1726,

4. Eng WK, Faucette L, Johnson RK, et al: Evidence that DNA topoisomerase I is necessary for the cytotoxic effects of camptothecin. Mol Pharmacol 34:755,1988-760,

5. DNA Topoisomerases-Enzymes that Catalyse the Breaking and Rejoining of DNA

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