Table 1.

Patient characteristics


N  

41  
Median age, y (range)   42 (19-62)  
Sex, n, M/F   26/15  
Stem cell source, n (%)   
    Bone marrow   41 (100)  
Donor,* n (%)   
    Histocompatible unrelated donor   26 (68)  
    5 of 6 unrelated donor   8 (20)  
    5 of 6 matched family member   5 (12)  
Diagnosis   
    CML, n (%)   12 (29)  
        Stable phase   8  
        Accelerated phase or second stable phase   2  
        Blast crisis   2  
    ALL, n (%)   9 (22)  
        First remission   4 
        Second remission   4  
        Resistant relapse   1  
    AML, n (%)   10 (24)  
        Second remission   1  
        Resistant relapse   8  
        Untreated relapse   1  
    Myelodysplasia, n (%)   7 (17)  
    Non-Hodgkin lymphoma, n (%)
 
2 (5)
 

N  

41  
Median age, y (range)   42 (19-62)  
Sex, n, M/F   26/15  
Stem cell source, n (%)   
    Bone marrow   41 (100)  
Donor,* n (%)   
    Histocompatible unrelated donor   26 (68)  
    5 of 6 unrelated donor   8 (20)  
    5 of 6 matched family member   5 (12)  
Diagnosis   
    CML, n (%)   12 (29)  
        Stable phase   8  
        Accelerated phase or second stable phase   2  
        Blast crisis   2  
    ALL, n (%)   9 (22)  
        First remission   4 
        Second remission   4  
        Resistant relapse   1  
    AML, n (%)   10 (24)  
        Second remission   1  
        Resistant relapse   8  
        Untreated relapse   1  
    Myelodysplasia, n (%)   7 (17)  
    Non-Hodgkin lymphoma, n (%)
 
2 (5)
 

CML indicates chronic myeloid leukemia; ALL, acute lymphoblastic leukemia; AML, acute myeloid leukemia.

*

Mismatch locus: Unrelated donor disparity: HLA-A (n = 4), HLA-B (n = 3), HLA-DR (n = 1). Related donor disparity: HLA-A (n = 4), HLA-DR (n = 1). Donor-recipient disparity at HLA-C (n = 8), HLA-DRB3 (n = 1), and HLA-DQ (n = 3) were not considered to be mismatched. Two unrelated donors were mismatched at both HLA-B and HLA-C, and one was mismatched at HLA-A and HLA-C. These were counted as single antigen mismatches.

All 4 patients had high-risk cytogenetics or clinical features.

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