Factor | Â | Â |
---|---|---|
Age (range) | 48.5 (21–65) |  |
Sex, n | Â | Â |
 Male | 49 (54.4%) |  |
 Female | 41 (45.6%) |  |
FAB classification, n | Â | Â |
 M0 | 8 (8.9%) |  |
 M1 | 27 (30.0%) |  |
 M2 | 25 (27.8%) |  |
 M4 | 19 (21.1%) |  |
 M5 | 10 (11.1%) |  |
 M6 | 1 (1.1%) |  |
Cytogenetic abnormality, n | Â | Â |
 Normal karyotype | 43 (47.8%) |  |
 RUNX1::RUNX1T1 | 6 (6.7%) |  |
 CBFB::MYH11 | 8 (8.9%) |  |
 MLL translocation, t(9;11) | 1 (1.1%) |  |
 Other intermediate risk cytogenetic abnormality | 9 (10.0%) |  |
 MLL translocation, otherwise | 4 (4.4%) |  |
 BCR::ABL1 | 2 (2.2%) |  |
 Other poor risk cytogenetic abnormality | 7 (7.8%) |  |
 Complex cytogenetics | 8 (8.9%) |  |
 Data not available | 2 (2.2%) |  |
NCCN2017 risk stratification, n | Â | Â |
 Good | 14 (15.6%) |  |
 Intermediate | 49 (54.4%) |  |
 Poor | 25 (27.8%) |  |
 Data not available | 2 (2.2%) |  |
Upfront allo-HCT, n | Â | Â |
 Performed | 33 (36.7%) |  |
 Not performed | 57 (63.3%) |  |
 | Total n = 90 |  |