Table 1:
N (%) | |
---|---|
Number Enrolled | 39 |
Median age (IQR, range) | 67 (8, 33–83) |
Male | 25 (64%) |
Caucasian | 38 (97%) |
Median WBC (x10 3 ) (IQR, range) | 3.6 (7.15, 0.4–59.7) |
Secondary AML | 19 (49%) |
Prior MDS | 16 (41%) |
Prior CMML | 2 (5%) |
Prior MPN | 1 (3%) |
Therapy-related AML | 3 (8%) |
Cytogenetic Risk | |
High | 13 (33%) |
Intermediate | 26 (67%) |
Normal Karyotype | 17 (44%) |
ELN 2017 Risk Category | |
Favorable* | 5 (13%) |
Intermediate | 9 (23%) |
Adverse | 25 (64%) |
Mutation Profile | |
ASXL1 | 12 (31%) |
DNMT3A | 12 (31%) |
RUNX1 | 8 (21%) |
TET2 | 7 (18%) |
NPM1 | 7 (18%) |
SRSF2 | 7 (18%) |
NRAS | 6 (15%) |
FLT3 ITD | 5 (13%) |
FLT3 TKD | 3 (8%) |
IDH1 | 5 (13%) |
IDH2 | 5 (13%) |
STAG2 | 5 (13%) |
TP53 | 4 (10%) |
PTPN11 | 4 (10%) |
BCOR | 4 (10%) |
EZH2 | 4 (10%) |
SF3B1 | 3 (8%) |
BCORL1 | 3 (8%) |
CEBPA | 3 (8%) |
CBL | 3 (8%) |
ZRSR2 | 1 (3%) |
RIT1 | 1 (3%) |
KRAS | 1 (3%) |
ETV6 | 1 (3%) |
Other | 7 (18%) |
All favorable risk patients were 65 or older at the time of induction, and none had core binding factor-altered AML.