4-Demethoxydaunorubicin (Idarubicin) in refractory or relapsed acute leukemias. A pilot study

Cancer. 1985 Apr 1;55(7):1452-4. doi: 10.1002/1097-0142(19850401)55:7<1452::aid-cncr2820550705>3.0.co;2-d.

Abstract

Twenty-five adults with previously treated acute leukemia were treated with 4-demethoxydaunorubicin (Idarubicin) with a daily dose of 8 mg/m2 for 3 days intravenously. Complete remission was achieved in 3 of 18 patients with acute nonlymphoblastic leukemia (ANLL) and 2 of 6 with lymphoblastic leukemia. Complete remissions were observed in two of eight ANLL patients refractory to cytarabine, anthracycline, and m-Amsa (amsacrine), indicating a lack of cross-resistance between these drugs and Idarubicin. The median duration of remission was 8 weeks. The main major toxicity of Idarubicin therapy, severe myelosuppression, cannot be considered a toxic effect because it was desired in this case list. Our preliminary results indicate that Idarubicin has significant activity against refractory adult acute leukemia.

MeSH terms

  • Acute Disease
  • Adolescent
  • Adult
  • Daunorubicin / analogs & derivatives*
  • Daunorubicin / therapeutic use
  • Drug Evaluation
  • Drug Resistance
  • Female
  • Humans
  • Idarubicin
  • Leukemia / drug therapy*
  • Leukemia, Lymphoid / drug therapy
  • Male
  • Middle Aged
  • Pilot Projects

Substances

  • Idarubicin
  • Daunorubicin