Table 1 Baseline characteristics of the study patients (N = 1023).
Characteristic | All patients (N = 1023) |
|---|---|
Age, median (range), yr. | 72 (60–92) |
Female sex, n (%) | 433 (42) |
Ethnicity, n (%) | |
Hispanic | 23 (2) |
Non-Hispanic | 951 (93) |
Unknown | 49 (5) |
Race, n (%) | |
White | 801 (78) |
African American | 47 (5) |
Asian | 30 (3) |
Multiple or other | 78 (8) |
Unknown | 67 (7) |
Cytogenetics, n (%)b | |
Normal karyotype | 333 (36) |
Complex karyotype | 280 (30) |
Chromosome 5/5q, 7 or 17 abnormalities | 54 (6) |
Core-binding factor | 35 (4) |
KMT2A-rearrangement | 21 (2) |
inv(3) or t(3;3) or t(3q26.2;v) | 15 (2) |
t(6;9) | 2 (0.2) |
t(8;16) | 3 (0.3) |
Other | 183 (20) |
Mutation, n (%)a | |
IDH1/2d | 282 (28) |
DNMT3A | 259 (25) |
TP53 | 256 (25) |
TET2 | 241 (24) |
RUNX1 | 227 (22) |
SRSF2 | 222 (22) |
ASXL1 | 215 (21) |
FLT3c | 210 (21) |
NPM1 | 207 (20) |
NRAS | 175 (17) |
MLL2 | 146 (14) |
PTPN11 | 105 (10) |
STAG2 | 100 (10) |
BCOR | 98 (10) |
CEBPA | 85 (8) |
NF1 | 84 (8) |
U2AF1 | 80 (8) |
KRAS | 79 (8) |
SF3B1 | 66 (6) |
EZH2 | 58 (6) |
ZRSR2 | 39 (4) |