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. Author manuscript; available in PMC: 2023 Jul 19.
Published in final edited form as: Lancet Haematol. 2019 Dec 11;7(2):e122–e133. doi: 10.1016/S2352-3026(19)30203-0

Table 1:

Patient Characteristics

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.