Table 1

Patient characteristics

VariableRD/1AG-MM-GVH (n = 327)8/8 MUD (n = 452)P
Median age at transplantation, y (range) 45 (16-69) 48 (16-68) .043 
Recipient sex, n (%) 
    Male 184 (56%) 267 (59%) .434 
    Female 143 (44%) 185 (41%)  
Sex combination of donors and recipients, n (%) 
    Female to male 91 (28%) 73 (16%) < .001 
    Other combinations 236 (72%) 379 (84%)  
Performance status, n (%) 
    0/1 298 (91%) 415 (92%) .736 
    2/3/4 29 (9%) 37 (8%)  
Disease, n (%) 
    AML 167 (51%) 249 (55%) .512 
    ALL 90 (28%) 107 (24%)  
    CML 19 (6%) 21 (5%)  
    MDS 51 (16%) 75 (17%)  
Duration from diagnosis to transplantation, n (%) 
    < 6 mo 124 (38%) 102 (23%) < .001 
    ≥ 6 mo 191 (58%) 350 (77%)  
    Unknown 12 (4%) 0 (0%)  
Disease risk, n (%) 
    Standard 175 (54%) 317 (70%) < .001 
    High 133 (41%) 129 (29%)  
    Unknown 19 (6%) 6 (1%)  
Source of stem cells, n (%) 
    BM 142 (43%) 452 (100%) < .001 
    Peripheral blood 185 (57%)   
HLA compatibility in the HVG direction, n (%)* 
    Matched 36 (11%) 452 (100%) < .001 
    1-antigen mismatch 218 (67%)   
    2-antigen mismatch 65 (20%)   
    3-antigen mismatch 8 (2%)   
HLA compatibility in the GVH direction, n (%)* 
    Matched 0 (0%) 452 (100%) < .001 
    1-allele mismatch 111 (34%)   
    2-allele mismatch 36 (11%)   
    3-allele mismatch 1 (0%)   
    Uncertain/missing 179 (55%)   
Conditioning regimen, n (%) 
    Myeloablative 243 (74%) 338 (75%) .883 
    Reduced-intensity 84 (26%) 114 (25%)  
GVHD prophylaxis, n (%) 
    Cyclosporine-based 113 (35%) 108 (24%) 0.004 
    Tacrolimus-based 209 (64%) 338 (75%)  
    Others 5 (2%) 6 (1%)  
Use of ATG/alemtuzumab, n (%) 
    Yes 33 (10%) 13 (3%) < .001 
    No 294 (90%) 439 (97%)  
Median follow-up of survivors, mo (range) 36.2 (3.0-95.7) 13.5 (1.7-62.8) < .001 
VariableRD/1AG-MM-GVH (n = 327)8/8 MUD (n = 452)P
Median age at transplantation, y (range) 45 (16-69) 48 (16-68) .043 
Recipient sex, n (%) 
    Male 184 (56%) 267 (59%) .434 
    Female 143 (44%) 185 (41%)  
Sex combination of donors and recipients, n (%) 
    Female to male 91 (28%) 73 (16%) < .001 
    Other combinations 236 (72%) 379 (84%)  
Performance status, n (%) 
    0/1 298 (91%) 415 (92%) .736 
    2/3/4 29 (9%) 37 (8%)  
Disease, n (%) 
    AML 167 (51%) 249 (55%) .512 
    ALL 90 (28%) 107 (24%)  
    CML 19 (6%) 21 (5%)  
    MDS 51 (16%) 75 (17%)  
Duration from diagnosis to transplantation, n (%) 
    < 6 mo 124 (38%) 102 (23%) < .001 
    ≥ 6 mo 191 (58%) 350 (77%)  
    Unknown 12 (4%) 0 (0%)  
Disease risk, n (%) 
    Standard 175 (54%) 317 (70%) < .001 
    High 133 (41%) 129 (29%)  
    Unknown 19 (6%) 6 (1%)  
Source of stem cells, n (%) 
    BM 142 (43%) 452 (100%) < .001 
    Peripheral blood 185 (57%)   
HLA compatibility in the HVG direction, n (%)* 
    Matched 36 (11%) 452 (100%) < .001 
    1-antigen mismatch 218 (67%)   
    2-antigen mismatch 65 (20%)   
    3-antigen mismatch 8 (2%)   
HLA compatibility in the GVH direction, n (%)* 
    Matched 0 (0%) 452 (100%) < .001 
    1-allele mismatch 111 (34%)   
    2-allele mismatch 36 (11%)   
    3-allele mismatch 1 (0%)   
    Uncertain/missing 179 (55%)   
Conditioning regimen, n (%) 
    Myeloablative 243 (74%) 338 (75%) .883 
    Reduced-intensity 84 (26%) 114 (25%)  
GVHD prophylaxis, n (%) 
    Cyclosporine-based 113 (35%) 108 (24%) 0.004 
    Tacrolimus-based 209 (64%) 338 (75%)  
    Others 5 (2%) 6 (1%)  
Use of ATG/alemtuzumab, n (%) 
    Yes 33 (10%) 13 (3%) < .001 
    No 294 (90%) 439 (97%)  
Median follow-up of survivors, mo (range) 36.2 (3.0-95.7) 13.5 (1.7-62.8) < .001 
*

HLA compatibility was defined according to the HLA-A, HLA-B, and HLA-DR loci.

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