TABLE 1.
Non‐CBF‐AML (n = 74) | CBF‐AML (n = 75) | p | |
---|---|---|---|
ELN risk classification | |||
Favorable | 50 (67.5%) | 57 (76%) | 0.121 |
Intermediate | 17 (22.9%) | 8 (10.6%) | |
High | 7 (9.4%) | 10 (13.3%) | |
Sex | |||
Male | 47 (63.5%) | 47 (62.6%) | 0.915 |
Female | 27 (36.4%) | 28 (37.3%) | |
Age (years) | 44 (16–75) | 38 (14–77) | 0.162 |
Specific mutations | |||
CEBPA | 27 (36.4%) | 1 (1.3%) | |
NPM1 | 33 (44.5%) | 2 (2.6%) | |
FLT3 | 14 (18.9%) | 10 (13.3%) | |
TP53 | 1 (1.3%) | 1 (1.3%) | |
IDH | 5 (6.7%) | 2 (2.6%) | |
Induction therapy | |||
IA | 39 (52.7%) | 30 (40%) | 0.120 |
Others | 35 (47.2%) | 45 (60%) | |
Consolidation therapy | |||
Chemotherapy | 16 (21.6%) | 27 (36%) | 0.072 |
Auto‐HSCT | 5 (6.7%) | 10 (13.3%) | |
Allo‐HSCT | 52 (70.2%) | 37 (49.3%) | |
UCBT | 1 (1.3%) | 1 (1.3%) | |
ECOG | 1 (0–4) | 1 (0–4) | 0.270 |
Type of AML | 0.067 | ||
De novo | 65 (87.8%) | 72 (96%) | |
Secondary | 9 (12.1%) | 3 (4%) | |
Cytogenetic categories | |||
Autosomal abnormalities | 5 (6.7%) | 12 (16%) | 0.129 |
Sex chromosome abnormalities | 3 (4.1%) | 11 (14.7%) | 0.031 |
Complex karyotype | 0 | 10 (13.3%) | 0.001 |
WBC (×109/L) | 12.29 (0.67–311.28) | 12.79 (0.95–391.60) | 0.522 |
HGB (g/L) | 88.5 (35–158) | 80 (35–139) | 0.086 |
PLT (×109/L) | 38 (5–430) | 25 (5–424) | 0.018 |
BM blasts (%) | 61.5 (14–99) | 52.5 (20–96.5) | 0.434 |
Extramedullary involvement | 3 (4%) | 1 (1.3%) | 0.603 |
CNS leukemia | 4 (5.4%) | 8 (10.6%) | 0.370 |
Abbreviations: Allo‐HSCT, allogeneic stem cell transplantation; auto‐HSCT, autologous stem cell transplantation; BM, bone marrow; CNS, central nervous system; ELN, European Leukemia Net; HGB, hemoglobin; Mut, mutation; Others induction therapy contains DA, VA, MA, HA, HAE, HAA, CAG, DCAG, AZA‐HAG, Priming; PLT, palatelete; UCBT, umbilical cord blood transplantation; WBC, white blood cell.