Maintenance azacitidine after myeloablative allogeneic hematopoietic cell transplantation for myeloid malignancies

Leuk Lymphoma. 2018 Dec;59(12):2836-2841. doi: 10.1080/10428194.2018.1443334. Epub 2018 Apr 4.

Abstract

Allogeneic hematopoietic cell transplantation (HCT) is a curative option for patients with acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS), but carries a high risk of relapse. This retrospective review evaluates the effectiveness of maintenance azacitidine in high-risk AML and MDS patients to reduce the probability of relapse. Twenty-five patients who received maintenance azacitidine were matched to historical controls in a two-to-one ratio based on diagnosis, donor type, conditioning regimen intensity, and age. Over 90% of patients received myeloablative conditioning. There was no difference in time to hematologic relapse, overall survival, or non-relapse mortality. Maintenance therapy was stopped early in 72% of patients due to graft-versus-host-disease, relapse, infection, and intolerance (13 of 25 patients received less than 4 cycles). There was a trend towards higher toxicity in the azacitidine group. The use of prophylactic azacitidine following myeloablative allogeneic HCT outside a clinical trial cannot be recommended at this time.

Keywords: Acute myeloid leukemia; allogeneic transplantation; azacitidine; maintenance chemotherapy; myelodysplastic syndrome.

Publication types

  • Evaluation Study
  • Research Support, N.I.H., Extramural

MeSH terms

  • Adult
  • Aged
  • Antimetabolites, Antineoplastic / therapeutic use*
  • Azacitidine / therapeutic use*
  • Case-Control Studies
  • Female
  • Hematopoietic Stem Cell Transplantation / adverse effects*
  • Humans
  • Leukemia, Myeloid, Acute / mortality
  • Leukemia, Myeloid, Acute / therapy*
  • Maintenance Chemotherapy / adverse effects
  • Maintenance Chemotherapy / methods
  • Male
  • Middle Aged
  • Myeloablative Agonists / administration & dosage
  • Myelodysplastic Syndromes / mortality
  • Myelodysplastic Syndromes / therapy*
  • Neoplasm Recurrence, Local / epidemiology
  • Neoplasm Recurrence, Local / prevention & control*
  • Retrospective Studies
  • Time Factors
  • Transplantation Conditioning / methods
  • Transplantation, Homologous / adverse effects
  • Young Adult

Substances

  • Antimetabolites, Antineoplastic
  • Myeloablative Agonists
  • Azacitidine