A phase I-II study of high-dose cyclophosphamide, thiotepa and escalating doses of mitoxantrone with autologous stem cell rescue in patients with refractory malignancies

Bone Marrow Transplant. 1990 Dec;6(6):439-42.

Abstract

Twenty-five patients with refractory solid tumors were treated with high-dose cyclophosphamide, thiotepa and mitoxantrone followed by autologous stem cell rescue in a phase I dose escalation study. The dose-limiting toxic effect was mucositis at 60 mg/m2 of mitoxantrone in combination with cyclophosphamide and thiotepa. The early death rate due to toxic effects was 24%; all deaths were attributed to infections. Hematopoietic recovery was quite prolonged with median times to granulocyte (greater than 500 x 10(6)/l) and platelet (greater than 50 x 10(9)/l) recovery at 58 and 148 days, respectively. The overall response rate was 56%. The median time to progression was 14 weeks. Thus, this regimen has activity against refractory malignancies although early and prohibitive toxicity occurs when mitoxantrone is escalated in this setting.

Publication types

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

MeSH terms

  • Actuarial Analysis
  • Chicago / epidemiology
  • Cyclophosphamide / administration & dosage
  • Cyclophosphamide / therapeutic use*
  • Drug Evaluation
  • Heart Failure / chemically induced
  • Hematopoietic Stem Cell Transplantation*
  • Humans
  • Mitoxantrone / administration & dosage
  • Mitoxantrone / adverse effects
  • Mitoxantrone / therapeutic use*
  • Neoplasms / surgery*
  • Preoperative Care
  • Survival Rate
  • Thiotepa / administration & dosage
  • Thiotepa / therapeutic use*
  • Transplantation, Autologous / mortality

Substances

  • Cyclophosphamide
  • Thiotepa
  • Mitoxantrone