Table 1.

Characteristics of patients studied for WT1 MRD and comparison of patients with and those without WT1 MRD assessment after induction chemotherapy

WT1 MRD available
(n = 314)
WT1 MRD missing
(n = 72)
P
Male, n (%) 165 (52.5) 40 (55.6) .695 
Median age, y [IQR] 46 [36-54] 48 [40-54.5] .114 
Median WBC count, 109/L [IQR] 9.8 [2.71-31.25] 10.75 [3.58-49.73] .3 
ALFA risk classification, n (%)*   .0436 
 Favorable 79 (26) 27 (39.7)  
 Intermediate 131 (43.1) 28 (41.2)  
 Unfavorable 94 (30 .9) 13 (19.1)  
ELN 2017 risk classification, n (%)   .115 
 Favorable 126 (42.4) 37 (55.2)  
 Intermediate 87 (29.3) 18 (26.9)  
 Unfavorable 84 (28.3) 12 (17.9)  
NPM1 mutation, n (%) 130 (42.2) 42 (60) .0079 
FLT3-ITD, n (%)§ 87 (28.2) 20 (28.6) .99 
FLT3-TKD, n (%)ǁ 21 (6.9) 10 (14.3) .0531 
Induction cycle to reach CR, n (%)   .192 
 1 290 (92.4) 70 (97.2)  
 2 24 (7.6) 2 (2.8)  
Postremission randomization, n (%)   .0018 
 HDAC 62 (19.7) 4 (5.6)  
 CLARA 62 (19.7) 10 (13.9)  
 Not randomized 190 (60.5) 58 (80.6)  
WT1 MRD available
(n = 314)
WT1 MRD missing
(n = 72)
P
Male, n (%) 165 (52.5) 40 (55.6) .695 
Median age, y [IQR] 46 [36-54] 48 [40-54.5] .114 
Median WBC count, 109/L [IQR] 9.8 [2.71-31.25] 10.75 [3.58-49.73] .3 
ALFA risk classification, n (%)*   .0436 
 Favorable 79 (26) 27 (39.7)  
 Intermediate 131 (43.1) 28 (41.2)  
 Unfavorable 94 (30 .9) 13 (19.1)  
ELN 2017 risk classification, n (%)   .115 
 Favorable 126 (42.4) 37 (55.2)  
 Intermediate 87 (29.3) 18 (26.9)  
 Unfavorable 84 (28.3) 12 (17.9)  
NPM1 mutation, n (%) 130 (42.2) 42 (60) .0079 
FLT3-ITD, n (%)§ 87 (28.2) 20 (28.6) .99 
FLT3-TKD, n (%)ǁ 21 (6.9) 10 (14.3) .0531 
Induction cycle to reach CR, n (%)   .192 
 1 290 (92.4) 70 (97.2)  
 2 24 (7.6) 2 (2.8)  
Postremission randomization, n (%)   .0018 
 HDAC 62 (19.7) 4 (5.6)  
 CLARA 62 (19.7) 10 (13.9)  
 Not randomized 190 (60.5) 58 (80.6)  
*

Data were not available for 14 patients.

Data were not available for 22 patients.

Data were not available for 8 patients.

§

Data were not available for 8 patients.

ǁ

Data were not available for 10 patients.

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