Table 3

Characteristics of patients in CR with and without residual disease at the end of induction 1

Patient characteristicsRD (n = 46)No RD (n = 142)P
Sex   .734 
    Male, n (%) 24 (52) 70 (49)  
    Female, n (%) 22 (48) 72 (51)  
Age, y    
    Median (range) 11.7 (0.2-18.3) 10.4 (0.2-20.8) .971 
    0-2, n (%) 10 (22) 37 (26) .557 
    3-10, n (%) 10 (22) 40 (28) .391 
    11-21, n (%) 26 (57) 65 (46) .205 
Cytogenetic risk groups    
    Favorable, n (%) 6 (15) 51 (38) .005 
    Unfavorable, n (%) 2 (5) 2 (2) .234 
    Intermediate, n (%) 33 (80) 81 (60) .018 
    Unknown, n (%)  
Risk class    
    Low risk (Fav. cyto, NPM, CEBPA), n (%) 10 (24) 59 (43) .029 
    High risk (Unfav. cyto, HR FLT3/ITD), n (%) 5 (12) 10 (7) .343 
    Standard risk, n (%) 26 (63) 67 (49) .112 
    Unknown, n (%)  
Median WBC count, ×103/μL (range) 21.3 (0.8-250) 22.5 (0.9-405) .360 
Median BM blasts, % (range) 70.5 (3-95) 67 (7.3-100) .578 
Median platelet count, ×103/μL (range) 53 (7-483) 37.5 (4-499) .229 
Median hemoglobin level, g/dL (range) 8.6 (3.6-14) 8 (3.1-15.2) .203 
CNS disease, n (%) 1 (2) 7 (5) .682 
FLT3/ITD+, n (%) 3 (9) 9 (7) .726 
WT1 mutation, n (%) 7 (20) 9 (7) .052 
NPM1 mutation, n (%) 0 (0) 5 (4) .586 
CEBPA mutation, n (%) 4 (12) 5 (4) .099 
Treatment outcome, 3-y % ± 2 SE %    
    OS from end course 1 56 ± 16 80 ± 8 .002 
    RFS from end course 1 30 ± 15 65 ± 9 < .001 
    RR from end of course 1 60 ± 16 29 ± 8 < .001 
Patient characteristicsRD (n = 46)No RD (n = 142)P
Sex   .734 
    Male, n (%) 24 (52) 70 (49)  
    Female, n (%) 22 (48) 72 (51)  
Age, y    
    Median (range) 11.7 (0.2-18.3) 10.4 (0.2-20.8) .971 
    0-2, n (%) 10 (22) 37 (26) .557 
    3-10, n (%) 10 (22) 40 (28) .391 
    11-21, n (%) 26 (57) 65 (46) .205 
Cytogenetic risk groups    
    Favorable, n (%) 6 (15) 51 (38) .005 
    Unfavorable, n (%) 2 (5) 2 (2) .234 
    Intermediate, n (%) 33 (80) 81 (60) .018 
    Unknown, n (%)  
Risk class    
    Low risk (Fav. cyto, NPM, CEBPA), n (%) 10 (24) 59 (43) .029 
    High risk (Unfav. cyto, HR FLT3/ITD), n (%) 5 (12) 10 (7) .343 
    Standard risk, n (%) 26 (63) 67 (49) .112 
    Unknown, n (%)  
Median WBC count, ×103/μL (range) 21.3 (0.8-250) 22.5 (0.9-405) .360 
Median BM blasts, % (range) 70.5 (3-95) 67 (7.3-100) .578 
Median platelet count, ×103/μL (range) 53 (7-483) 37.5 (4-499) .229 
Median hemoglobin level, g/dL (range) 8.6 (3.6-14) 8 (3.1-15.2) .203 
CNS disease, n (%) 1 (2) 7 (5) .682 
FLT3/ITD+, n (%) 3 (9) 9 (7) .726 
WT1 mutation, n (%) 7 (20) 9 (7) .052 
NPM1 mutation, n (%) 0 (0) 5 (4) .586 
CEBPA mutation, n (%) 4 (12) 5 (4) .099 
Treatment outcome, 3-y % ± 2 SE %    
    OS from end course 1 56 ± 16 80 ± 8 .002 
    RFS from end course 1 30 ± 15 65 ± 9 < .001 
    RR from end of course 1 60 ± 16 29 ± 8 < .001 

RD indicates residual disease; Fav, favorable; cyto, cytogenetics; Unfav, unfavorable; HR, hazard ratio; ITD, internal tandem duplication; WBC, white blood cell; OS, overall survival; RFS, relapse-free survival, and RR, relapse risk.

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