Clinical and biological characteristics of acute myeloid leukemia with 20-29% blasts: a retrospective single-center study

Leuk Lymphoma. 2019 May;60(5):1136-1145. doi: 10.1080/10428194.2018.1515938. Epub 2018 Oct 10.

Abstract

It is controversial whether acute myeloid leukemia (AML) patients with 20-29% bone marrow (BM) blasts should be considered AML or myelodysplastic syndromes (MDS). We retrospectively studied 382 patients, including 108 AML with 20-29% BM blasts (AML20-29), 210 AML with ≥30% BM blasts (AML ≥ 30), and 64 MDS with 10-19% BM blasts (MDS-EB2). We found that AML20-29 were more similar to MDS-EB2 in terms of advanced age, less blood count, the increased presence of poor-risk cytogenetics. The frequency of mutated genes in AML20-29 had both the characters of AML and MDS. Median overall survival of AML20-29 and MDS-EB2 were similar and shorter than those of AML ≥ 30 (p = .045). Multivariate analysis showed inferior survival with increased age, low platelet count and FLT3 mutations. Our findings suggest that AML20-29 have clinical features more similar to MDS than AML.

Keywords: AML; BM blast; MDS.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Antineoplastic Combined Chemotherapy Protocols / adverse effects
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Biomarkers, Tumor
  • Blast Crisis / diagnosis
  • Blast Crisis / etiology
  • Blast Crisis / therapy
  • Bone Marrow / pathology*
  • Disease Management
  • Disease Progression
  • Disease Susceptibility
  • Female
  • Gene Frequency
  • Humans
  • Kaplan-Meier Estimate
  • Leukemia, Myeloid, Acute / diagnosis*
  • Leukemia, Myeloid, Acute / etiology*
  • Leukemia, Myeloid, Acute / mortality
  • Leukemia, Myeloid, Acute / therapy
  • Male
  • Middle Aged
  • Mutation
  • Myelodysplastic Syndromes / drug therapy
  • Myelodysplastic Syndromes / etiology
  • Myelodysplastic Syndromes / pathology
  • Prognosis

Substances

  • Biomarkers, Tumor