Abstract
Objectives: Acute myeloid leukemia with myelodysplasia-related changes (AML-MRC) is a heterogeneous category with a broad range of underlying genetic abnormalities. We investigated the significance of genetic factors in a large series of AML-MRC cases. Methods: The morphologic findings, genetic data, and patient outcomes were assessed in 186 AML-MRC cases. Results: The median overall survival (OS) was dismal in AML-MRC patients (median, 7.6 months; 95% confidence interval, 5-10.6 months). Karyotypically normal cases and cytogenetically abnormal cases without myelodysplastic syndrome (MDS)-related cytogenetic abnormalities showed similar OS, significantly better than cases carrying MDS-related cytogenetic abnormalities. MDS-related cytogenetic abnormalities, monosomal or complex karyotype, and history of MDS or myelodysplastic/myeloproliferative neoplasm were all associated with dismal outcome. Conclusions: AML-MRC predicts a poor prognosis. Our study supports the finding that the genetic profile plays a key role in determining prognosis in AML-MRC as defined according to the World Health Organization revised fourth edition (2017) diagnostic criteria.
Original language | English (US) |
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Pages (from-to) | 656-663 |
Number of pages | 8 |
Journal | American journal of clinical pathology |
Volume | 153 |
Issue number | 5 |
DOIs | |
State | Published - Apr 15 2020 |
Keywords
- Acute myeloid leukemia
- Genetics
- Myelodysplasia-related changes
ASJC Scopus subject areas
- Pathology and Forensic Medicine