Combination therapy with venetoclax and azacitidine for the treatment of myelodysplastic syndromes with DDX41 mutations

Hematology. 2024 Dec;29(1):2338509. doi: 10.1080/16078454.2024.2338509. Epub 2024 Apr 10.

Abstract

Myelodysplastic syndromes (MDS) patients with DEAD-box helicase 41 (DDX41) mutations have been reported to be treated effectively with lenalidomide; however, there are no randomized studies to prove it. Venetoclax and azacitidine are safe and effective in high-risk MDS/AML. In this study, we evaluated the efficacy of venetoclax and azacitidine combination therapy in eight consecutive MDS patients with DDX41 mutations at our centre from March 2021 to November 2023. We retrospectively analyzed the genetic features and clinical characteristics of these patients. Our findings suggest that MDS patients with DDX41 mutation may benefit from the therapy, for six subjects received this regimen as initial therapy and five of the six subjects achieved complete remission.

Keywords: DDX41; Myelodysplastic syndromes; azacitidine; venetoclax.

MeSH terms

  • Azacitidine / therapeutic use
  • Bridged Bicyclo Compounds, Heterocyclic*
  • DEAD-box RNA Helicases
  • Humans
  • Mutation
  • Myelodysplastic Syndromes* / drug therapy
  • Myelodysplastic Syndromes* / genetics
  • Retrospective Studies
  • Sulfonamides*

Substances

  • venetoclax
  • Azacitidine
  • DDX41 protein, human
  • DEAD-box RNA Helicases
  • Sulfonamides
  • Bridged Bicyclo Compounds, Heterocyclic