Table 1

Patient and transplantation characteristics according to initial presentation

CharacteristicAcute onset (n = 352)Chronic onset (n = 388)
Patient median age, y (range) 37.2 (0.8-67.0) 41.8 (1.4-66.4) 
Disease at transplantation, no. (%)   
    Myelodysplastic syndrome 48 (14) 67 (17) 
    Acute myeloid leukemia 71 (20) 72 (19) 
    Chronic myeloid leukemia 146 (41) 151 (39) 
    Acute lymphoid leukemia 52 (15) 42 (11) 
    Chronic lymphoid leukemia 4 (1) 6 (2) 
    Non-Hodgkin lymphoma or Hodgkin disease 10 (3) 34 (9) 
    Multiple myeloma 4 (1) 7 (2) 
    Other* 17 (5) 9 (2) 
Pretransplantation risk category, no. (%)   
    Low 142 (40) 143 (37) 
    Intermediate 150 (43) 171 (44) 
    High 60 (17) 74 (19) 
Donor median age, y (range) 40.0 (0.0-81.7) 39.0 (0.0-70.9) 
Donor/recipient sex, no. (%)   
    Male/male 122 (35) 122 (31) 
    Male/female 73 (21) 87 (22) 
    Female/male 90 (26) 107 (28) 
    Female/female 67 (19) 72 (19) 
Donor type, no. (%)   
    HLA-identical related 152 (43) 176 (45) 
    HLA-mismatched related 35 (10) 24 (6) 
    HLA-matched unrelated 83 (24) 101 (26) 
    HLA-mismatched unrelated 82 (23) 87 (22) 
No. of mismatched HLA loci (%)   
    0 243 (69) 282 (73) 
    1 64 (18) 65 (17) 
    2 42 (12) 29 (7) 
    More than 2 3 (1) 12 (3) 
Conditioning regimen, no. (%)   
    Cyclophosphamide and TBI 196 (56) 215 (55) 
    Busulfan and cyclophosphamide 114 (32) 127 (33) 
    Busulfan and TBI 16 (5) 26 (7) 
    Other 26 (7) 20 (5) 
Source of stem cells, no. (%)   
    Bone marrow 289 (82) 302 (78) 
    Mobilized blood 59 (17) 85 (22) 
    Cord blood 4 (1) 1 (< 1) 
GVHD prophylaxis, no. (%)   
    Cyclosporine plus methotrexate 297 (84) 329 (85) 
    Tacrolimus plus methotrexate 12 (3) 11 (3) 
    Other 43 (12) 48 (12) 
Year of transplantation, no. (%)   
    1994-1997 203 (58) 217 (56) 
    1998-2000 149 (42) 171 (44) 
Prior acute GVHD before day 100, no. (%)   
    Grade 0-I 34 (10) 69 (18) 
    Grade II 222 (63) 229 (59) 
    Grades III-IV 96 (27) 90 (23) 
CharacteristicAcute onset (n = 352)Chronic onset (n = 388)
Patient median age, y (range) 37.2 (0.8-67.0) 41.8 (1.4-66.4) 
Disease at transplantation, no. (%)   
    Myelodysplastic syndrome 48 (14) 67 (17) 
    Acute myeloid leukemia 71 (20) 72 (19) 
    Chronic myeloid leukemia 146 (41) 151 (39) 
    Acute lymphoid leukemia 52 (15) 42 (11) 
    Chronic lymphoid leukemia 4 (1) 6 (2) 
    Non-Hodgkin lymphoma or Hodgkin disease 10 (3) 34 (9) 
    Multiple myeloma 4 (1) 7 (2) 
    Other* 17 (5) 9 (2) 
Pretransplantation risk category, no. (%)   
    Low 142 (40) 143 (37) 
    Intermediate 150 (43) 171 (44) 
    High 60 (17) 74 (19) 
Donor median age, y (range) 40.0 (0.0-81.7) 39.0 (0.0-70.9) 
Donor/recipient sex, no. (%)   
    Male/male 122 (35) 122 (31) 
    Male/female 73 (21) 87 (22) 
    Female/male 90 (26) 107 (28) 
    Female/female 67 (19) 72 (19) 
Donor type, no. (%)   
    HLA-identical related 152 (43) 176 (45) 
    HLA-mismatched related 35 (10) 24 (6) 
    HLA-matched unrelated 83 (24) 101 (26) 
    HLA-mismatched unrelated 82 (23) 87 (22) 
No. of mismatched HLA loci (%)   
    0 243 (69) 282 (73) 
    1 64 (18) 65 (17) 
    2 42 (12) 29 (7) 
    More than 2 3 (1) 12 (3) 
Conditioning regimen, no. (%)   
    Cyclophosphamide and TBI 196 (56) 215 (55) 
    Busulfan and cyclophosphamide 114 (32) 127 (33) 
    Busulfan and TBI 16 (5) 26 (7) 
    Other 26 (7) 20 (5) 
Source of stem cells, no. (%)   
    Bone marrow 289 (82) 302 (78) 
    Mobilized blood 59 (17) 85 (22) 
    Cord blood 4 (1) 1 (< 1) 
GVHD prophylaxis, no. (%)   
    Cyclosporine plus methotrexate 297 (84) 329 (85) 
    Tacrolimus plus methotrexate 12 (3) 11 (3) 
    Other 43 (12) 48 (12) 
Year of transplantation, no. (%)   
    1994-1997 203 (58) 217 (56) 
    1998-2000 149 (42) 171 (44) 
Prior acute GVHD before day 100, no. (%)   
    Grade 0-I 34 (10) 69 (18) 
    Grade II 222 (63) 229 (59) 
    Grades III-IV 96 (27) 90 (23) 
*

Twenty-four patients had diseases other than hematologic malignancies.

The low-risk category included chronic myeloid leukemia in chronic phase and aplastic anemia. The high-risk category included chronic myeloid leukemia in blast crisis, acute leukemia or lymphoma in relapse, refractory anemia with excess blasts in transformation, and myeloma. The intermediate-risk category included all other diseases.

HLA-C and -DQ typing was not available for 3 cord blood donors. HLA-C and -DQ typing was not available for one marrow donor at each locus.

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