Intensive sequential post-induction therapy for adults with acute myelogenous leukemia in first remission: long-term follow-up and results

Leuk Res. 1992 Jun-Jul;16(6-7):577-84. doi: 10.1016/0145-2126(92)90005-r.

Abstract

We designed a post-induction therapy including intensive sequential therapy with non-cross-resistant drugs in an effort to prolong disease-free survival (DFS) for adults with acute myelogenous leukemia. Forty-five patients entered this study and 33 of 35 patients entering complete remission received the post-induction therapy. With a median follow-up for survivors of 3.5 years from complete remission, the actuarial 5-year DFS was 46% +/- 19% (95% confidence interval). The five-year DFS for patients over 45 years of age was comparable to that for patients under 45 years of age (50% +/- 26% vs 47% +/- 28%). Furthermore, the actuarial 5-year DFS for patients who required two courses of induction therapy was comparable to that for patients who required only one course of induction therapy (45% +/- 29% vs 50% +/- 25%). The toxicity of post-induction therapy was tolerable and no patients died during complete remission.

MeSH terms

  • Aclarubicin / administration & dosage
  • Adolescent
  • Adult
  • Aged
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
  • Cytarabine / administration & dosage
  • Cytarabine / analogs & derivatives
  • Daunorubicin / administration & dosage
  • Etoposide / administration & dosage
  • Female
  • Follow-Up Studies
  • Humans
  • Leukemia, Myeloid, Acute / drug therapy*
  • Leukemia, Myeloid, Acute / mortality
  • Life Tables
  • Male
  • Mercaptopurine / administration & dosage
  • Middle Aged
  • Mitoxantrone / administration & dosage
  • Prednisolone / administration & dosage
  • Remission Induction
  • Survival Rate

Substances

  • Cytarabine
  • Etoposide
  • Aclarubicin
  • Prednisolone
  • Mitoxantrone
  • Mercaptopurine
  • Daunorubicin

Supplementary concepts

  • BH-AC-AMP protocol
  • DCMP protocol