[Phase I study of bestrabucil (KM 2210)]

Gan To Kagaku Ryoho. 1986 Jun;13(6):2208-15.
[Article in Japanese]

Abstract

A phase I study was performed on a newly developed antitumor agent, Bestrabucil (KM 2210). The study was started at an initial dose of 1 n 25 mg/body, and gradually increased up to 32n 800 mg/body. With single (35 patients) and five-consecutive-day (36 patients) administration, the dose-limiting factor was found to be tarry stool, remarkable decrease in hemoglobin content, and strong nipple and breast pain. The maximum tolerated dose (MTD) was concluded to be around 700 to 800 mg/body. With long-term administration (the longest term, 20 weeks, 36 patients), the dose-limiting factor was concluded to be a decrease in the peripheral leukocyte count when the total amount administered reached about 10 g. Side effects on the alimentary system due to this agent, such as vomiting, nausea and anorexia, were observed. In addition, mastalgia and genital bleeding due to released estrogen were also seen, especially in the case of long-term administration.

Publication types

  • English Abstract

MeSH terms

  • Adult
  • Aged
  • Animals
  • Anorexia / chemically induced
  • Chlorambucil / administration & dosage
  • Chlorambucil / adverse effects
  • Chlorambucil / analogs & derivatives*
  • Chlorambucil / therapeutic use
  • Dose-Response Relationship, Drug
  • Drug Administration Schedule
  • Drug Evaluation
  • Estradiol / administration & dosage
  • Estradiol / adverse effects
  • Estradiol / analogs & derivatives*
  • Estradiol / therapeutic use
  • Female
  • Humans
  • Leukocyte Count
  • Leukopenia / chemically induced
  • Male
  • Middle Aged
  • Neoplasms / drug therapy*
  • Pain / chemically induced
  • Rats

Substances

  • Chlorambucil
  • Estradiol
  • bestrabucil