Phase I study of intravenous 4-hydroxyanisole

Eur J Cancer. 1992;28A(8-9):1362-4. doi: 10.1016/0959-8049(92)90520-c.

Abstract

4-Hydroxyanisole is a depigmenting agent which has been shown to have activity against malignant melanoma when given intra-arterially in man. An intravenous dose escalation study has been carried out with the aim of obtaining maximum plasma concentrations in a 5 day schedule. 8 patients entered this study which was stopped because of drug toxicity after 3 patients had been treated at the third dose escalation of 15 g/m2. 2 patients had WHO grade 4 liver and one also grade 4 renal toxicity and another had grade 4 haemoglobin toxicity. Extrapolated plateau plasma levels between 112 and 860 mumol/l were obtained, which in vitro studies suggested would be cytotoxic. Hopefully, newer analogues will have a greater specificity for the melanin pathway with less toxicity.

Publication types

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

MeSH terms

  • Anisoles / pharmacokinetics
  • Anisoles / therapeutic use*
  • Antineoplastic Agents / pharmacokinetics
  • Antineoplastic Agents / therapeutic use*
  • Drug Administration Schedule
  • Drug Evaluation
  • Evaluation Studies as Topic
  • Humans
  • Infusions, Intravenous
  • Lymphatic Metastasis
  • Melanoma / blood
  • Melanoma / drug therapy*
  • Pigmentation / drug effects*
  • Skin Neoplasms / blood
  • Skin Neoplasms / drug therapy*

Substances

  • Anisoles
  • Antineoplastic Agents
  • mequinol