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. 2023 Dec 7;8(3):591–602. doi: 10.1182/bloodadvances.2023011721

Table 1.

Demographics and clinical characteristics

Doublet TAG-AZA
Cohort A (n = 19)
Triplet TAG-AZA-VEN
Cohort B, all patients (1L and R/R AML) (n = 37)
Triplet TAG-AZA-VEN
Cohort B, 1L AML only (n = 26)
Age (median, range) 62 (40-77) 70 (39-81) 71 (60-81)
Diagnosis
 1L AML 5 26 26
 R/R AML 9 11
 MDS 5
n (%) n (%) n (%)
Gender
 Female 7 (36.8) 15 (40.5) 10 (38.5)
 Male 12 (63.2) 22 (59.5) 16 (61.5)
Race
 White 13 (68.4) 32 (86.5) 24 (92.3)
 Other 4 (21.1) 3 (8.1) 2 (7.7)
 Asian 1 (5.3) 2 (5.4) 0 (0)
 More than 1 1 (5.3) 0 (0) 0 (0)
Ethnicity
 Non-Hispanic 14 (73.7) 33 (89.2) 24 (92.3)
 Hispanic or Latino 3 (15.8) 3 (8.1) 2 (7.7)
 Not known 2 (10.5) 1 (2.7) 0 (0)
ECOG PS
 2 3 (15.8) 7 (18.9) 2 (7.7)
 1 11 (57.9) 24 (64.9) 19 (73.1)
 0 5 (26.3) 6 (16.2) 5 (19.2)
Additional characteristics of the triplet TAG-AZA-VEN cohort B, 1L AML (n=26)
n (%)
ELN 2022 adverse risk 26 (100)
Any TP53 mutation 13 (50)
Multi-hit TP53 9/13
One TP53 mutation with 17p deletion 7/13
Two TP53 mutations 2/13
Complex karyotype 8 (30.7)
Secondary AML 8 (30.7)
Therapy-related AML 5 (19.2)
pDC-AML 2 (7.7)
Baseline bone marrow blasts (median, range) 58% (20-91)
Known extramedullary disease at screening 0

1L AML, previously untreated AML; ECOG PS, Eastern Cooperative Oncology Group Performance Status; pDC, plasmacytoid dendritic cell.