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

Cancer. 1991 Aug 15;68(4):744-6. doi: 10.1002/1097-0142(19910815)68:4<744::aid-cncr2820680414>3.0.co;2-r.

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.

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Oral
  • Adult
  • Aged
  • Aged, 80 and over
  • Antineoplastic Combined Chemotherapy Protocols / administration & dosage*
  • Antineoplastic Combined Chemotherapy Protocols / adverse effects
  • Dose-Response Relationship, Drug
  • Drug Evaluation
  • Female
  • Fluorouracil / administration & dosage
  • Humans
  • Hydroxyurea / administration & dosage
  • Infusion Pumps
  • Leucovorin / administration & dosage
  • Male
  • Middle Aged
  • Neoplasms / drug therapy*
  • Stomatitis / chemically induced
  • Stomatitis / prevention & control

Substances

  • Leucovorin
  • Fluorouracil
  • Hydroxyurea