Allogeneic stem cell transplantation in AML with t(6;9)(p23;q34);DEK-NUP214 shows a favourable outcome when performed in first complete remission

Br J Haematol. 2020 Jun;189(5):920-925. doi: 10.1111/bjh.16433. Epub 2020 Feb 5.

Abstract

Acute myeloid leukaemia (AML) with t(6;9)(p23;q34) is a poor-risk entity, commonly associated with FLT3-ITD (internal tandem duplication). Allogeneic stem-cell tranplantation (allo-SCT) is recommended, although studies analysing the outcome of allo-SCT in this setting are lacking. We selected 195 patients with t(6;9) AML, who received a first allo-SCT between 2000 and 2016 from the EBMT (European Society for Blood and Marrow Transplantation) registry. Disease status at time of allo-SCT was the strongest independent prognostic factor, with a two-year leukaemia-free survival and relapse incidence of 57% and 19% in patients in CR1 (first complete remission), 34% and 33% in CR2 (second complete remission), and 24% and 49% in patients not in remission, respectively (P < 0·001). This study, which represents the largest one available in t(6;9) AML, supports the recommendation to submit these patients to allo-SCT in CR1.

Keywords: AML; DEK-NUP214; allo-SCT; prognosis; t(6;9) AML.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Allografts
  • Chromosomal Proteins, Non-Histone / genetics*
  • Chromosomes, Human, Pair 6 / genetics*
  • Chromosomes, Human, Pair 6 / ultrastructure
  • Chromosomes, Human, Pair 9 / genetics*
  • Chromosomes, Human, Pair 9 / ultrastructure
  • Cord Blood Stem Cell Transplantation*
  • Disease-Free Survival
  • Female
  • Gene Duplication
  • Graft vs Host Disease / etiology
  • Humans
  • Kaplan-Meier Estimate
  • Leukemia, Myeloid, Acute / genetics
  • Leukemia, Myeloid, Acute / therapy*
  • Male
  • Middle Aged
  • Nuclear Pore Complex Proteins / genetics*
  • Oncogene Proteins / genetics*
  • Oncogene Proteins, Fusion / genetics*
  • Peripheral Blood Stem Cell Transplantation*
  • Poly-ADP-Ribose Binding Proteins / genetics*
  • Proportional Hazards Models
  • Remission Induction
  • Translocation, Genetic*
  • Treatment Outcome
  • fms-Like Tyrosine Kinase 3 / genetics

Substances

  • Chromosomal Proteins, Non-Histone
  • DEK protein, human
  • NUP214 protein, human
  • Nuclear Pore Complex Proteins
  • Oncogene Proteins
  • Oncogene Proteins, Fusion
  • Poly-ADP-Ribose Binding Proteins
  • FLT3 protein, human
  • fms-Like Tyrosine Kinase 3