Fludarabine and cytarabine in patients with relapsed acute myeloid leukemia refractory to initial salvage therapy

Int J Hematol. 2012 Dec;96(6):743-7. doi: 10.1007/s12185-012-1192-9. Epub 2012 Nov 7.

Abstract

The most effective regimen for relapsed acute myeloid leukemia (AML) patients who do not achieve complete remission (CR) after a course of salvage therapy has not been established. We evaluated the efficacy and toxicity of fludarabine and cytarabine in patients with AML in first relapse who did not respond to a course of salvage chemotherapy with mitoxantrone and etoposide. CR was achieved in 39 % of treated patients, and in 47 % of patients with a favorable/intermediate-risk karyotype. The median overall survival was 4.75 months. The median survival for patients achieving CR with fludarabine-cytarabine was significantly higher than for those who did not respond to therapy (9.6 vs. 4.5 months, P = 0.04). Our data suggest that the fludarabine-cytarabine regimen merits further investigation in relapsed AML patients with favorable or intermediate-risk karyotype with persistent leukemia after a course of salvage therapy.

Publication types

  • Clinical Trial

MeSH terms

  • Adult
  • Aged
  • Antineoplastic Combined Chemotherapy Protocols / adverse effects
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
  • Chemical and Drug Induced Liver Injury / etiology
  • Cytarabine / administration & dosage
  • Cytarabine / adverse effects
  • Etoposide / administration & dosage
  • Female
  • Gastrointestinal Diseases / chemically induced
  • Hematologic Diseases / chemically induced
  • Humans
  • Karyotype
  • Leukemia, Myeloid, Acute / drug therapy*
  • Leukemia, Myeloid, Acute / genetics
  • Male
  • Middle Aged
  • Mitoxantrone / administration & dosage
  • Neoplasms, Second Primary / drug therapy
  • Neoplasms, Second Primary / genetics
  • Recurrence
  • Remission Induction
  • Salvage Therapy*
  • Vidarabine / administration & dosage
  • Vidarabine / adverse effects
  • Vidarabine / analogs & derivatives

Substances

  • Cytarabine
  • Etoposide
  • Mitoxantrone
  • Vidarabine
  • fludarabine