Studies of hydroxyurea administered by continuous infusion: toxicity, pharmacokinetics, and cell synchronization

Cancer. 1980 Aug 1;46(3):455-62. doi: 10.1002/1097-0142(19800801)46:3<455::aid-cncr2820460306>3.0.co;2-n.

Abstract

Hydroxyurea was administered by means of two schedules designed to provide continuous 72-hour exposure of tumor cells to therapeutic drug levels. Toxicity and pharmacokinetics were determined for both an oral pulse dose schedule (every 4 hours x 18 doses) and continuous intravenous (IV) infusion for 72 hours. The maximal tolerated dose (MTD) was 800 mg/m2 every 4 hours for the oral route and 3.0 mg/m2/min x 72 hours for IV infusion. Granulocytopenia was dose-limiting for both schedules and correlated well with plasma-HU levels. Serial sampling of normal bone marrow (10 patients) and tumor tissue (3 patients) showed a modest degree of synchronization induced by continuous IV infusion of hydroxyurea. Interindividual pharmacokinetic variations severely limit the usefulness of the oral pulse schedule as a potential means of synchronizing cells. Hydroxyurea administered by continuous IV infusion may be useful as a synchronizing agent in humans.

Publication types

  • Comparative Study
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Administration, Oral
  • Bone Marrow / drug effects
  • Bone Marrow / pathology
  • Drug Administration Schedule
  • Half-Life
  • Humans
  • Hydroxyurea / administration & dosage*
  • Hydroxyurea / adverse effects
  • Hydroxyurea / metabolism
  • Infusions, Parenteral
  • Mitotic Index
  • Neoplasms / drug therapy*
  • Thrombocytopenia / chemically induced
  • Time Factors

Substances

  • Hydroxyurea