Exclusion of persistent mutations in splicing factor genes and isocitrate dehydrogenase 2 improves the prognostic power of molecular measurable residual disease assessment in acute myeloid leukemia

Haematologica. 2024 Feb 1;109(2):671-675. doi: 10.3324/haematol.2023.283510.
No abstract available

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Humans
  • Isocitrate Dehydrogenase* / genetics
  • Leukemia, Myeloid, Acute* / diagnosis
  • Leukemia, Myeloid, Acute* / genetics
  • Mutation
  • Neoplasm, Residual / diagnosis
  • Neoplasm, Residual / genetics
  • Prognosis
  • RNA Splicing Factors / genetics

Substances

  • RNA Splicing Factors
  • Isocitrate Dehydrogenase

Grants and funding

Funding: This work was supported by a Collaborative Personalized Cancer Medicine Team Grant from the Princess Margaret Cancer Foundation and an Acute Leukemia Translational Research Initiative Grant from the Ontario Institute for Cancer Research.