Table 1.

Characteristics of patients with AML who received IC after HMA and VEN

All (N=46)
Sex, n (%)  
Female 20 (43) 
Male 26 (57) 
Age, median (interquartile range), y 65 (50-68) 
Diagnosis, n (%)  
AML 37 (80) 
MDS/AML 9 (20) 
AML classification, n (%)  
Recurrent genetic abnormality 13 (28) 
TP53 (mutated or lost) 8 (17) 
Myelodysplasia-related gene mutation 14 (30) 
Myelodysplasia-related cytogenetic abnormality 5 (11) 
Not otherwise specified 6 (13) 
AML qualifier, n (%)  
Therapy-related 7 (15) 
Prior MDS or MDS/MPN 19 (41) 
Germ line predisposition 1 (2) 
None 19 (41) 
ELN 2022 risk classification, n (%)  
Favorable 4 (9) 
Intermediate 10 (22) 
Adverse 31 (67) 
Unknown 1 (2) 
VEN combination, n (%)  
AZA 37 (80) 
Decitabine 9 (20) 
HMA/VEN line of treatment, n (%)  
1L 24 (52) 
2L+ 22 (48) 
Prior HMA, n (%) 9 (20) 
Prior IC, n (%) 21 (46) 
Prior transplant, n (%) 15 (33) 
HMA/VEN cycles, median (interquartile range) 2 (2-4) 
HMA/VEN response, n (%)  
CR 6 (13) 
CRi 5 (11) 
MLFS 3 (7) 
PR 1 (2) 
NR 31 (67) 
All (N=46)
Sex, n (%)  
Female 20 (43) 
Male 26 (57) 
Age, median (interquartile range), y 65 (50-68) 
Diagnosis, n (%)  
AML 37 (80) 
MDS/AML 9 (20) 
AML classification, n (%)  
Recurrent genetic abnormality 13 (28) 
TP53 (mutated or lost) 8 (17) 
Myelodysplasia-related gene mutation 14 (30) 
Myelodysplasia-related cytogenetic abnormality 5 (11) 
Not otherwise specified 6 (13) 
AML qualifier, n (%)  
Therapy-related 7 (15) 
Prior MDS or MDS/MPN 19 (41) 
Germ line predisposition 1 (2) 
None 19 (41) 
ELN 2022 risk classification, n (%)  
Favorable 4 (9) 
Intermediate 10 (22) 
Adverse 31 (67) 
Unknown 1 (2) 
VEN combination, n (%)  
AZA 37 (80) 
Decitabine 9 (20) 
HMA/VEN line of treatment, n (%)  
1L 24 (52) 
2L+ 22 (48) 
Prior HMA, n (%) 9 (20) 
Prior IC, n (%) 21 (46) 
Prior transplant, n (%) 15 (33) 
HMA/VEN cycles, median (interquartile range) 2 (2-4) 
HMA/VEN response, n (%)  
CR 6 (13) 
CRi 5 (11) 
MLFS 3 (7) 
PR 1 (2) 
NR 31 (67) 

PR, partial remission; NR, no response.

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