Outcome of allogeneic stem cell transplantation for patients transformed to myelodysplastic syndrome or leukemia from severe aplastic anemia: a report from the MDS Subcommittee of the Chronic Malignancies Working Party and the Severe Aplastic Anemia Working Party of the European Group for Blood and Marrow Transplantation

Biol Blood Marrow Transplant. 2014 Sep;20(9):1448-50. doi: 10.1016/j.bbmt.2014.05.028. Epub 2014 Jun 6.

Abstract

One hundred and forty patients who had undergone hematopoietic stem cell transplantation (HSCT) for myelodysplastic syndrome (MDS) or acute myelogenous leukemia (AML) transformation after treatment of severe aplastic anemia (SAA) were identified in the European Group for Blood and Marrow Transplantation (EBMT) database. The median age at HSCT was 29 years (range, 1 to 66 years). The transplant donor was related in 49% cases and unrelated in 51% cases. The 5-year probability of relapse was 17%, and that of nonrelapse mortality was 41%. The 5-year overall survival was 45% ± 9%, better for patients untreated and patients in remission compared with patients with refractory disease. Our data indicate that allogeneic HSCT leads to prolonged survival in close to one-half of the patients transforming to MDS or AML from SAA.

Keywords: Acute myelogenous leukemia; Hematopoietic stem cell transplantation; Myelodysplastic syndrome; Severe aplastic anemia.

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Anemia, Aplastic / therapy*
  • Child
  • Child, Preschool
  • Europe
  • Female
  • Hematopoietic Stem Cell Transplantation / adverse effects*
  • Humans
  • Infant
  • Leukemia
  • Male
  • Middle Aged
  • Myelodysplastic Syndromes
  • Neoplasm Recurrence, Local
  • Transplantation Conditioning / adverse effects*
  • Transplantation, Homologous / adverse effects*
  • Treatment Outcome
  • Young Adult