Table 2

Clinical characteristics of the 29 ML-DS patients at induction failure or at relapse

No%
Disease status   
    Refractory AML 10.3 
    Relapsed AML 26 89.7 
Duration from initial diagnosis to relapse, mo (n = 26)   
    Median (range) 8.6 (2.4-71.8)  
    < 6 30.8 
    ≤ 6 to < 12 13 50.0 
    ≤ 12 19.2 
Site of relapse (n = 26)   
    Bone marrow 25 96.2 
    Extramedullary (skin) 3.8 
FAB classification at relapse (n = 26)   
    M1 1* 3.8 
    M7 23 88.5 
    Not available 2 7.7 
Karyotype at relapse (n = 26)   
    Same as before 10 38.5 
    Additional abnormalities 12 46.1 
    Not available 15.4 
No%
Disease status   
    Refractory AML 10.3 
    Relapsed AML 26 89.7 
Duration from initial diagnosis to relapse, mo (n = 26)   
    Median (range) 8.6 (2.4-71.8)  
    < 6 30.8 
    ≤ 6 to < 12 13 50.0 
    ≤ 12 19.2 
Site of relapse (n = 26)   
    Bone marrow 25 96.2 
    Extramedullary (skin) 3.8 
FAB classification at relapse (n = 26)   
    M1 1* 3.8 
    M7 23 88.5 
    Not available 2 7.7 
Karyotype at relapse (n = 26)   
    Same as before 10 38.5 
    Additional abnormalities 12 46.1 
    Not available 15.4 

AML indicates acute myeloid leukemia; FAB, French-American-British; and MDS, myelodysplastic syndrome.

*

This patient was M7 at initial diagnosis.

A total of 18 patients were M7, 1 was M1, 3 were MDS, and 1 unknown at initial diagnosis.

One patient was M5a, and 1 was M7 at initial diagnosis.

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