Table 1

Demographic and biologic characteristics of 84 elderly adults with newly diagnosed AML treated with T + E

Arm A (n = 63)Arm B (n = 21)Total (n = 84)
Sex, no. (%)    
    Male 39 (63) 14 (67) 53 (63) 
    Female 24 (38) 7 (33) 31 (37) 
Median age, y (range) 76 (70-90) 78 (71-90) 76 (70-90) 
Biologic disease features, no. (%)    
    Secondary AML 36 (57) 10 (48) 46 (55) 
        MDS/AML 24 31 
        t-AML 12 12 
        Prior therapy* 10 (28) 5 (50) 15 (33) 
    Adverse cytogenetics 38 (60) 14 (67) 52 (62) 
        Single 10 14 
        Complex (> 3 lesions) 19 26 
        Other 12 
    No. with > 1 poor risk feature 47 (75) 15 (71) 62 (74) 
Host comorbidities, no. (%)    
    1 comorbidity 61 (97) 19 (90) 80 (95) 
    3 comorbidities 36 (57) 13 (62) 49 (58) 
Arm A (n = 63)Arm B (n = 21)Total (n = 84)
Sex, no. (%)    
    Male 39 (63) 14 (67) 53 (63) 
    Female 24 (38) 7 (33) 31 (37) 
Median age, y (range) 76 (70-90) 78 (71-90) 76 (70-90) 
Biologic disease features, no. (%)    
    Secondary AML 36 (57) 10 (48) 46 (55) 
        MDS/AML 24 31 
        t-AML 12 12 
        Prior therapy* 10 (28) 5 (50) 15 (33) 
    Adverse cytogenetics 38 (60) 14 (67) 52 (62) 
        Single 10 14 
        Complex (> 3 lesions) 19 26 
        Other 12 
    No. with > 1 poor risk feature 47 (75) 15 (71) 62 (74) 
Host comorbidities, no. (%)    
    1 comorbidity 61 (97) 19 (90) 80 (95) 
    3 comorbidities 36 (57) 13 (62) 49 (58) 

t-AML indicates treatment-related AML.

*

Includes previous therapy for MDS and t-MDS with growth factors, demethylating agents, thalidomide, or lenalidomide individually or in combinations.

Adverse cytogenetics: −5/5q, −7/7q, abnormal 3/3q, abnormal 11q23, abnormal 17p, −20q, +13, t(6;9), t(9;22), complex (> 3 abnormalities).

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