Table 1.

Baseline patient and disease characteristics

All patients
N = 198
Age, y  
Median (range) 56.0 (18.9-81.5) 
>60, n (%) 75 (37.9) 
Sex, n (%)  
Male 109 (55.05) 
Female 89 (44.95) 
AML etiology, n (%)  
De novo 185 (93.4) 
Secondary 13 (6.6) 
WBC, ×10⁹/L  
Median (range) 25.7 (0.6-191.3) 
>50, n (%) 56 (28.3) 
NA, n (%) 2 (1.0) 
FAB category, n (%)  
M0 4 (2.0) 
M1 46 (23.2) 
M2 43 (21.7) 
M3 0 (0) 
M4 51 (25.8) 
M5 35 (17.7) 
M6 4 (2.0) 
M7 0 (0) 
NA 15 (7.6) 
PB blasts, %  
Mean (SD) 50.4 (32.9) 
ELN classification, n (%)  
Favorable 79 (39.9) 
Intermediate 119 (60.1) 
CBF mutation, n (%) 24 (12.1) 
CEBPA mutation, n (%) 20 (13.5) 
NPM1 mutation, n (%) 92 (53.8) 
FLT3 mutation, n (%) 58 (34.1) 
Vγ9Vδ2 (% of LC) 
Mean (SD) 2.5 (4.3) 
30-d mortality, n (%) 3 (1.5) 
60-d mortality, n (%) 11 (5.6) 
CR after induction, n (%) 161 (81.3) 
HSCT, n (%) 32 (16.3) 
All patients
N = 198
Age, y  
Median (range) 56.0 (18.9-81.5) 
>60, n (%) 75 (37.9) 
Sex, n (%)  
Male 109 (55.05) 
Female 89 (44.95) 
AML etiology, n (%)  
De novo 185 (93.4) 
Secondary 13 (6.6) 
WBC, ×10⁹/L  
Median (range) 25.7 (0.6-191.3) 
>50, n (%) 56 (28.3) 
NA, n (%) 2 (1.0) 
FAB category, n (%)  
M0 4 (2.0) 
M1 46 (23.2) 
M2 43 (21.7) 
M3 0 (0) 
M4 51 (25.8) 
M5 35 (17.7) 
M6 4 (2.0) 
M7 0 (0) 
NA 15 (7.6) 
PB blasts, %  
Mean (SD) 50.4 (32.9) 
ELN classification, n (%)  
Favorable 79 (39.9) 
Intermediate 119 (60.1) 
CBF mutation, n (%) 24 (12.1) 
CEBPA mutation, n (%) 20 (13.5) 
NPM1 mutation, n (%) 92 (53.8) 
FLT3 mutation, n (%) 58 (34.1) 
Vγ9Vδ2 (% of LC) 
Mean (SD) 2.5 (4.3) 
30-d mortality, n (%) 3 (1.5) 
60-d mortality, n (%) 11 (5.6) 
CR after induction, n (%) 161 (81.3) 
HSCT, n (%) 32 (16.3) 

CBF, core-bing factor; CEBPA, CCAAT enhancer binding protein alpha; FAB, French-American-British classification; FLT3, fms-like tyrosine kinase 3; LC, lymphocyte; NPM1, nucleophosmin 1; WBC, white blood cell; SD, standard deviation.

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