NPM1 mutation but not RUNX1 mutation or multilineage dysplasia defines a prognostic subgroup within de novo acute myeloid leukemia lacking recurrent cytogenetic abnormalities in the revised 2016 WHO classification

MeSH terms

• Chromosome Aberrations*
• Core Binding Factor Alpha 2 Subunit / genetics*
• Female
• Humans
• Leukemia, Myeloid, Acute* / classification
• Leukemia, Myeloid, Acute* / genetics
• Male
• Neoplasm Proteins / genetics*
• Nuclear Proteins / genetics*
• Nucleophosmin
• Retrospective Studies
• World Health Organization