Shifting of erythroleukemia to myelodysplastic syndrome according to the revised WHO classification: Biologic and cytogenetic features of shifted erythroleukemia

Leuk Res. 2018 Jul:70:13-19. doi: 10.1016/j.leukres.2018.04.015. Epub 2018 Apr 30.

Abstract

The 2016 revision of the World Health Organization (WHO) classification of tumours of haematopoietic and lymphoid tissues was published. According to 2016 WHO criteria, diagnostic criteria of acute erythroid leukemia was revised. We reassessed 34 de novo acute erythroid leukemia (AEL) diagnosed by 2008 WHO criteria, according to 2016 WHO criteria. A total of 623 patients (excluding M3) with acute myeloid leukemia including 34 patients with AEL were enrolled. Among 34 patients diagnosed with AEL, diagnosis was shifted to MDS-EB in 28 patients (28/34, 82.3%) and MDS-U in 2 patients (2/34, 5.9%), while remained as AEL in 4 patients (4/34, 11.8%) according to 2016 WHO criteria. Interphase FISH for cytogenetic changes of MDS (-5/del(5q), -7/del(7q), del(20q), +8) revealed cytogenetic aberrations in 50.0% (17/34) of AEL 2008 group. AEL 2008 group showed higher frequency of complex cytogenetic abnormalities and higher MDS related cytogenetic abnormalities than AML excluding AEL group. Transformation to another AML subtype was noted in 10% in AEL shifted to MDS. Majority (88.2%) of AEL by 2008 WHO criteria was reclassified to MDS by 2016 WHO criteria. Clinical characteristics of shifted AEL were similar to those of MDS rather than de novo AML.

Keywords: 2008 WHO; 2016 WHO; Acute erythroleukemia; Cytogenetics.

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Biopsy
  • Bone Marrow / metabolism
  • Bone Marrow / pathology
  • Chromosome Aberrations
  • Chromosome Banding
  • Diagnosis, Differential
  • Disease Susceptibility
  • Female
  • Gene Duplication
  • Humans
  • In Situ Hybridization, Fluorescence
  • Leukemia, Erythroblastic, Acute / diagnosis*
  • Leukemia, Erythroblastic, Acute / etiology
  • Leukemia, Erythroblastic, Acute / mortality
  • Male
  • Middle Aged
  • Mutation
  • Myelodysplastic Syndromes / diagnosis*
  • Myelodysplastic Syndromes / etiology
  • Myelodysplastic Syndromes / mortality
  • Practice Guidelines as Topic
  • World Health Organization
  • Young Adult
  • fms-Like Tyrosine Kinase 3 / genetics

Substances

  • FLT3 protein, human
  • fms-Like Tyrosine Kinase 3