Table 1.
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).