KW-2149-induced pulmonary toxicity is not prevented by corticosteroids: a phase I and pharmacokinetic study

Anticancer Drugs. 1999 Aug;10(7):633-9. doi: 10.1097/00001813-199908000-00002.

Abstract

KW-2149 is a new, semisynthetic, C-7-N-Substituted, mitomycin C analog showing antitumor activity both in vitro and in vivo, equal or superior to mitomycin C. In a phase I study, KW-2149 was administered as an i.v. bolus injection every 21 days and at a dose of 100 mg/m2 pulmonary toxicity was dose limiting. Animal studies have indicated since that KW-2149-induced pulmonary toxicity can be prevented by pretreatment with corticosteroids. This paper presents the results of a further phase I study of KW-2149 with corticosteroid pretreatment. Patients were treated with oral dexamethasone 8 mg every 12 h, starting 24 h before KW-2149 administration, for 5 days. KW-2149 was given as an i.v. bolus injection every 21 days. Seventeen patients were treated with a total of 48 courses. Six patients received 60 mg/m2 and 11 patients 75 mg/m2. Two courses were not evaluable for toxicity. Significant lung toxicity was observed in at least three patients treated with a dose of 75 mg/m2 KW-2149 and pulmonary toxicity was therefore considered the dose-limiting toxicity at 75 mg/m2. No other important side effects were noted. One partial response was observed in a patient with colorectal cancer. Pretreatment with dexamethasone failed to suppress KW-2149-induced lung toxicity.

Publication types

  • Clinical Trial
  • Clinical Trial, Phase I

MeSH terms

  • Adrenal Cortex Hormones / therapeutic use*
  • Adult
  • Aged
  • Antibiotics, Antineoplastic / adverse effects*
  • Digestive System / drug effects
  • Female
  • Humans
  • Kidney / drug effects
  • Liver / drug effects
  • Lung / drug effects*
  • Male
  • Middle Aged
  • Mitomycins / adverse effects*
  • Mitomycins / pharmacokinetics
  • Neoplasms / drug therapy*

Substances

  • Adrenal Cortex Hormones
  • Antibiotics, Antineoplastic
  • Mitomycins
  • KW 2149