Phase I and pharmacokinetic study of a water-soluble etoposide prodrug, etoposide phosphate (BMY-40481)

Eur J Cancer. 1995 Dec;31A(13-14):2409-11. doi: 10.1016/0959-8049(95)00331-2.

Abstract

Etoposide phosphate is a water-soluble prodrug of etoposide. A phase I and pharmacokinetic study has been performed over the dose range 25-110 mg/m2/day for 5 days (etoposide equivalent doses). The maximum tolerated dose (MTD) was 110 mg/m2/day for 5 days every 3 weeks and the dose-limiting toxicity was neutropenia. Other toxicities were mild, with the exception of 2 patients who displayed significant hypersensitivity reactions. The etoposide phosphate:etoposide area under the plasma concentration versus time curve (AUC) ratio was < 1% and the pharmacokinetic parameters for etoposide were within previously reported ranges. Pharmacodynamic analyses demonstrated that etoposide AUC and baseline white blood cell count were significant determinants of leucopenia (model r2 = 0.51).

Publication types

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

MeSH terms

  • Adult
  • Aged
  • Antineoplastic Agents / administration & dosage*
  • Antineoplastic Agents / pharmacokinetics
  • Drug Administration Schedule
  • Drug Resistance, Neoplasm
  • Etoposide / administration & dosage
  • Etoposide / analogs & derivatives*
  • Etoposide / pharmacokinetics
  • Female
  • Humans
  • Male
  • Middle Aged
  • Neoplasms / drug therapy*
  • Organophosphorus Compounds / administration & dosage*
  • Organophosphorus Compounds / pharmacokinetics
  • Ovarian Neoplasms / drug therapy
  • Prodrugs / administration & dosage*
  • Prodrugs / pharmacokinetics

Substances

  • Antineoplastic Agents
  • Organophosphorus Compounds
  • Prodrugs
  • etoposide phosphate
  • Etoposide