[Phase II study on oral administration of MCNU (ranomustine) tablet. Hanshin Cooperative Study Group on Hematological Disorders]

Gan To Kagaku Ryoho. 1986 May;13(5):1915-20.
[Article in Japanese]

Abstract

A phase II study of MCNU tablet has been performed on 70 patients with hematological disorders including mostly myeloproliferative disorders. MCNU tablet was given p.o. at a dose of 50 mg daily for 2-6 days (total 100-300mg) as one course with average intervals of 3 to 5 months or more for patients responding to this drug. The effective rates were 72% in 18 patients with chronic myelogenous leukemia, 88% in 25 patients with polycythemia vera and 68.5% in 19 patients with essential thrombocythemia. Side effects of MCNU tablet were nausea and vomiting (31%) which had a dose-dependent relationship, mild liver dysfunction (5%) and elevation of BUN and creatinine (2%) which were not serious. The results were almost comparable to those of the phase II study of MCNU given intravenously.

Publication types

  • English Abstract

MeSH terms

  • Administration, Oral
  • Adult
  • Aged
  • Antineoplastic Agents / therapeutic use*
  • Drug Administration Schedule
  • Female
  • Hematologic Diseases / drug therapy*
  • Humans
  • Leukemia, Myeloid / drug therapy
  • Male
  • Middle Aged
  • Nitrosourea Compounds / therapeutic use*
  • Polycythemia / drug therapy
  • Tablets
  • Thrombocytosis / drug therapy

Substances

  • Antineoplastic Agents
  • Nitrosourea Compounds
  • Tablets
  • ranimustine