Idarubicin in combination with intermediate-dose cytarabine in the treatment of refractory or relapsed acute leukemias

Eur J Haematol. 1989 Oct;43(4):309-13. doi: 10.1111/j.1600-0609.1989.tb00304.x.

Abstract

13 patients with refractory or relapsed acute lymphoblastic leukemia (ALL) and 7 patients with acute myeloid leukemia (AML) were treated with a regimen that included idarubicin 12 mg/m2 intravenously daily for 3 d plus cytarabine 2 g/m2 by infusion over 3 hours daily for 3 d. There were 10 remissions (ALL:7; AML:3) in the 15 relapsed patients and 4 (ALL:3) in the 5 patients with primary refractory disease. Severe myelosuppression was observed in all patients. Toxicity of this regimen caused nausea and vomiting, stomatitis, infections and/or liver enzymes increase. Cardiac toxicity was not observed. 2 patients died in aplasia of Gram-negative septicemia and brain hemorrhage. In conclusion, the combination of idarubicin and intermediate-dose cytarabine (IDARA-C) seems to be highly effective and sufficiently well-tolerated for the treatment of refractory and relapsed acute leukemias.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Cytarabine / administration & dosage*
  • Cytarabine / adverse effects
  • Dose-Response Relationship, Drug
  • Female
  • Humans
  • Idarubicin / administration & dosage*
  • Idarubicin / adverse effects
  • Leukemia / drug therapy*
  • Leukemia, Myeloid, Acute / drug therapy
  • Male
  • Middle Aged
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / drug therapy

Substances

  • Cytarabine
  • Idarubicin