Table 1

Patient characteristics

Control groupG-PBSCs groupP
Total no. of patients 28 30  
    60-70 y 20 16  
    ≥ 71 y 14 .07 
Age, y, range (median) 60-77 (65) 60-88 (68)  
Sex    
    Female, n 11 16  
    Male, n 17 14 .3 
WHO classification    
    AML with recurrent cytogenetic translocations, n  
        AML with t(8;21)(q22;q22) AML1/CBFα/ETO, n  
    AML with multilineage dysplasia, n  
        With prior MDS, n  
        Without prior MDS, n .999 
    AML with myelodysplastic syndrome, therapy related, n  
        Other types, n  
    AML not otherwise categorized, n 21 21  
        AML minimally differentiated, n  
        AML without maturation, n  
        AML with maturation, n  
        Acute myelomonocytic leukemia, n 10 11  
        Acute monocytic leukemia, n  
        Acute erythroid leukemia, n  
WBC count    
    < 50 000/L, n 25 27  
    ≥ 50 000/L, n .999 
High-risk category, n* 13 12  
Standard-risk category, n 15 18 .999 
Control groupG-PBSCs groupP
Total no. of patients 28 30  
    60-70 y 20 16  
    ≥ 71 y 14 .07 
Age, y, range (median) 60-77 (65) 60-88 (68)  
Sex    
    Female, n 11 16  
    Male, n 17 14 .3 
WHO classification    
    AML with recurrent cytogenetic translocations, n  
        AML with t(8;21)(q22;q22) AML1/CBFα/ETO, n  
    AML with multilineage dysplasia, n  
        With prior MDS, n  
        Without prior MDS, n .999 
    AML with myelodysplastic syndrome, therapy related, n  
        Other types, n  
    AML not otherwise categorized, n 21 21  
        AML minimally differentiated, n  
        AML without maturation, n  
        AML with maturation, n  
        Acute myelomonocytic leukemia, n 10 11  
        Acute monocytic leukemia, n  
        Acute erythroid leukemia, n  
WBC count    
    < 50 000/L, n 25 27  
    ≥ 50 000/L, n .999 
High-risk category, n* 13 12  
Standard-risk category, n 15 18 .999 

GDMI indicates [insert expansion]; WHO, World Health Organization; MDS, myelodysplastic syndrome; and WBC, white blood cell.

*

ETO gene expression.

Four patients exhibited complex cytogenetic abnormalities, including with ≥ 3 cytogenetic abnormalities (eg, del (7q, −5, −7), t (9,22), q(34,11.2)).

Five patients exhibited complex cytogenetic abnormalities.

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