Table 4

Clinical characteristics of patients classified as high- or low-risk based on a comprehensive risk assessment, including baseline cytogenetics/genetics and status of MRD after consolidation*

High-risk (n = 97)Low-risk (n = 32)P
Postconsolidation MRD    
    Positive 96 < .001 
    Negative 32  
Age    
    Older than 60 y 32 .059 
    Younger than 60 y 65 27  
FLT3 status    
    Wild-type 78 32 .006 
    ITD 19  
Cytogenetics    
    Good-risk 10 .001 
    Intermediate-risk 75 22  
    Poor-risk  
Postconsolidation therapy    
    Chemotherapy 15 .039 
    AuSCT 30 22  
    ASCT 17 (1 MRD 
Reason for not giving postconsolidation therapy    
    Relapse 31 .025 
    Toxicity  
    Medical decision  
    Too early  
High-risk (n = 97)Low-risk (n = 32)P
Postconsolidation MRD    
    Positive 96 < .001 
    Negative 32  
Age    
    Older than 60 y 32 .059 
    Younger than 60 y 65 27  
FLT3 status    
    Wild-type 78 32 .006 
    ITD 19  
Cytogenetics    
    Good-risk 10 .001 
    Intermediate-risk 75 22  
    Poor-risk  
Postconsolidation therapy    
    Chemotherapy 15 .039 
    AuSCT 30 22  
    ASCT 17 (1 MRD 
Reason for not giving postconsolidation therapy    
    Relapse 31 .025 
    Toxicity  
    Medical decision  
    Too early  
*

Patients were stratified according to refined MRC classification of cytogenetic risk, as follows: “favorable” risk, cases with t(8;21), t(15;17), or inv(16)/t(16;16); “adverse” risk, cases with complex cytogenetic changes (> 3 unrelated abnormalities), −5, add(5q)/del(5q), −7/add(7q), t(6;11), t(10;11), t(9;22), −17, abn(17p) with other changes, 3q abnormalities excluding t(3;5), inv(3)/t(3;3); and “intermediate” risk, cases with normal karyotype and other noncomplex.

MRD indicates minimal residual disease; ITD, internal tandem duplication; AuSCT, autologous stem cell transplantation; and ASCT, allogeneic stem cell transplantation.

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