Literature DB >> 1855174

Dual modulation of 5-fluorouracil using leucovorin and hydroxyurea. A phase I trial.

J Lokich1, N Anderson, M Bern, F Coco, T Zipoli, C Moore, L Gonsalves.   

Abstract

Oral hydroxyurea (HU) was added to a regimen of 5-fluorouracil (5-FU) plus leucovorin (LCV) administered as a continuous 24-hour infusion for 14 days. A previous report of the 5-FU plus LCV infusion established optimal dosages of 200 mg/m2/d and 5 mg/m2/d, respectively, for each agent. Oral HU was added to the regimen in total dosages of 0.5 g/d, 1.0 g/d, 1.5 g/d, or 2.0 g/d. Twenty-two patients received a total of 45 courses of treatment. Stomatitis was the dose-limiting side effect; it occurred in 3 of 14 courses with HU at 0.5 g/d (21%) and 9 of 17 courses with HU at 1.0 g/d (53%). Dosage escalation to 1.5 g/d or 2.0 g/d was possible in only 3 of 22 patients (17%). The median time to stomatitis was 10 days (range, 7 to 12 days). One response was observed in this heavily pretreated population. Phase II trials of HU plus LCV dual modulation of infusional 5-FU should use initial HU dosages of 0.5 g/d for the 14-day regimen described, with dose escalation as tolerated. Variable oral absorption presumably accounts for the small group of patients who can tolerate the higher doses of HU.

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Year:  1991        PMID: 1855174     DOI: 10.1002/1097-0142(19910815)68:4<744::aid-cncr2820680414>3.0.co;2-r

Source DB:  PubMed          Journal:  Cancer        ISSN: 0008-543X            Impact factor:   6.860


  1 in total

1.  An unwanted side effect of hydroxyurea in a patient with idiopathic myelofibrosis.

Authors:  M J Starmans-Kool; M M Fickers; M A Pannebakker
Journal:  Ann Hematol       Date:  1995-05       Impact factor: 3.673

  1 in total

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