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. 2021 Oct 4;11(10):164. doi: 10.1038/s41408-021-00558-5

Table 1.

Patient characteristics (n = 188).

Characteristics n %
Age, years (median, range) 65 (26–80)
Gender
 Female 70 37
 Male 118 63
Karnofsky (n = 165)
 ≥80 135 82
 <80 30 18
HCT-CI (n = 155)
 Low 29 18
 Intermediate 55 35
 High 74 47
AML subtype (n = 186)
 AML-MRC 131 70
 t-AML 53 29
 Othera 2 1
2017 ELN genetic risk (n = 179)
 Favorable 12 7
 Intermediate 59 33
 Adverse 108 60
Karyotype (n = 179)
 Normal 63 35
 Abnormal 116 65
 Complex 44 25
 Non-complex 72 40
Molecular genetics
 NPM1/n.d. 18/11 10/6
 FLT3-ITD/n.d. 13/13 7/7
 ASXL1/n.d. 31/24 16/13
 TP53/n.d. 14/26 7/14
 RUNX1/n.d. 24/20 13/11
BM blast count at diagnosis (median, range) 38 (7–99)
PB blast count at diagnosis (median, range) 10 (0–92)
WBC at diagnosis, ×103/µl (median, range) 3.8 (0.6–330)
No treatment prior CPX 169 90
Pretreatment with HMA 19 10

AML acute myeloid leukemia, AML-MRC AML with myelodysplasia-related changes, BM bone marrow, ELN European Leukemia Net, HCT-CI hematopoietic cell transplantation-specific comorbidity index, HMA hypomethylating agents, n.d. not done, n number, PB peripheral blood, t-AML therapy-related AML, WBC white blood cells.

Numbers in parentheses display patients with available information.

aSecondary AML evolving from systemic mastocytosis (n = 1) and blastic plasmacytoid dendritic cell neoplasm (BPDCN) with antecedent history of chronic myelomonocytic leukemia (CMML) (n = 1).