Abstract
We have studied a mitoxantrone, 5-fluorouracil (5-FU) and leucovorin chemotherapy regimen in metastatic breast cancer. 8 patients received mitoxantrone 10 mg/m2 on day 1, leucovorin 200 mg/m2 and 5-FU 300 mg/m2 on days 1-5 by intravenous bolus every 28 days in a pilot study. Grades 3-4 granulocytopenia followed 55% of the courses, with 2 patients admitted for febrile neutropenia. Only a 29% objective response rate was seen in a subsequent phase II trial using reduced mitoxantrone doses. Comparison with other trials suggested that 5-day bolus 5-FU administration adversely affects the combination's therapeutic index.
Publication types
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Clinical Trial
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Clinical Trial, Phase II
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Research Support, Non-U.S. Gov't
MeSH terms
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Adenocarcinoma / drug therapy*
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Adenocarcinoma / secondary*
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Antineoplastic Combined Chemotherapy Protocols / adverse effects
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Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
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Breast Neoplasms*
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Drug Administration Schedule
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Female
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Fluorouracil / administration & dosage
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Fluorouracil / adverse effects
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Humans
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Leucovorin / administration & dosage
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Leucovorin / adverse effects
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Mitoxantrone / administration & dosage
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Mitoxantrone / adverse effects
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Pilot Projects
Substances
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Mitoxantrone
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Leucovorin
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Fluorouracil