Table 1.

Patient and disease characteristics as well as incidence of 2017 ELN high-risk molecular markers by the 4 NPM1/FLT3-ITD genotypes

NPM1mut/FLT3-ITDlowNPM1mut/FLT3-ITDhighNPM1wt/FLT3-ITDlowNPM1wt/FLT3-ITDhighP
Patients, n (%) 85 (19.9) 159 (37.2) 74 (17.3) 109 (25.5)  
Age, median, y 50.6 48.1 47.2 45.7 .05 
Female, % 64.7 66.0 47.3 48.6 .0065 
WBCs, median (range), ×109/L 23.6 (1.4-253.2) 45.3 (1.4-329.8) 23.6 (0.6-207.4) 44.6 (0.8-236.0) <.0001 
Median BM blasts, % 72 80 72 77 .0019 
Incidence of 2017 ELN high-risk mutations, n (%)      
RUNX1 1/73 (1.4) 1/140 (0.7) 16/53 (30.2) 24/92 (26.1) .0005 
ASXL1 4/73 (5.5) 9/140 (6.4) 6/53 (11.3) 12/92 (13.0) .23 
TP53 0/73 (0) 1/140 (0.7) 1/53 (1.9) 0/92 (0) .50 
Karyotype, n (%)      
 Normal 52 (89.7) 101 (90.2) 32 (52.5) 54 (58.1) .0005 
 Abnormal 6 (10.3) 11 (9.8) 29 (47.5) 39 (41.9)  
 Missing 27 47 13 16  
NPM1mut/FLT3-ITDlowNPM1mut/FLT3-ITDhighNPM1wt/FLT3-ITDlowNPM1wt/FLT3-ITDhighP
Patients, n (%) 85 (19.9) 159 (37.2) 74 (17.3) 109 (25.5)  
Age, median, y 50.6 48.1 47.2 45.7 .05 
Female, % 64.7 66.0 47.3 48.6 .0065 
WBCs, median (range), ×109/L 23.6 (1.4-253.2) 45.3 (1.4-329.8) 23.6 (0.6-207.4) 44.6 (0.8-236.0) <.0001 
Median BM blasts, % 72 80 72 77 .0019 
Incidence of 2017 ELN high-risk mutations, n (%)      
RUNX1 1/73 (1.4) 1/140 (0.7) 16/53 (30.2) 24/92 (26.1) .0005 
ASXL1 4/73 (5.5) 9/140 (6.4) 6/53 (11.3) 12/92 (13.0) .23 
TP53 0/73 (0) 1/140 (0.7) 1/53 (1.9) 0/92 (0) .50 
Karyotype, n (%)      
 Normal 52 (89.7) 101 (90.2) 32 (52.5) 54 (58.1) .0005 
 Abnormal 6 (10.3) 11 (9.8) 29 (47.5) 39 (41.9)  
 Missing 27 47 13 16  

The Fisher’s exact test was used for categorical variables, and the Kruskal-Wallis test was used for continuous variables.

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