Table 2.

Patient, disease, and transplant characteristics

T-cell depleted Non-T-cell depleted P
870  998  
Median age, y (range)  24 (0.4-57) 28 (0.5-61)  .0001  
Performance score 90%, n/n eval (%) 706/869 (81%)  735/988 (74%)  .0001  
Disease and disease state, n/n eval (%)    .001   
 ALL, 1st remission  45/851 (5%)  64/987 (6%)  
 ALL, 2nd remission 162/851 (19%)  141/987 (14%)  
 ALL, not in remission 86/851 (10%)  62/987 (6%)  
 AML, 1st remission 53/851 (6%)  90/987 (9%)  
 AML, 2nd remission 51/851 (6%)  66/987 (7%)  
 AML, not in remission 101/851 (12%)  107/987 (11%)  
 CML, 1st chronic phase 203/851 (24%)  292/987 (30%)  
 CML, accelerated phase 110/851 (13%)  115/987 (12%)  
 CML, blast phase 40/851 (5%)  50/987 (5%)  
Year of transplantation, n/n eval (%)    .0001  
 1982-1987  316/870 (36%) 133/998 (14%)  
 1988-1994  554/870 (63%) 865/998 (86%)  
Median interval diagnosis-transplant, mo (range)  
 ALL, 1st remission  6 (2-21)  7 (2-19) NS  
 ALL, 2nd remission  28 (5-148)  34 (4-151)  NS 
 ALL, not in remission  18 (3-73)  13 (3-97)  NS 
 AML, 1st remission  6 (2-17)  6 (2-19)  NS  
 AML, 2nd remission  21 (7-67)  17 (5-88)  NS  
 AML, not in remission  10 (3-54)  10 (1-61)  NS  
 CML, 1st chronic phase  20 (2-124)  19 (2-123)  NS  
 CML, accelerated phase  26 (2-107)  27 (2-126)  NS  
 CML, blast phase 27 (6-123)  20 (2-116)  NS  
Median WBC at diagnosis, ×109/L (range)  
 Acute leukemia 16 (0.5-850)  16 (0.4-882)  NS  
 Chronic leukemia 164 (4-880)  158 (4-760)  NS  
Median donor age, y (range)  35 (1-81)  35 (1-75)  NS  
Donor recipient sex-match, n/n eval (%)    NS  
 Male-male 283/859 (33%)  292/987 (30%)  
 Male-female 173/859 (20%)  215/987 (22%)  
 Female-male 242/859 (28%)  282/987 (28%)  
 Female-female 161/859 (19%)  198/987 (20%)  
Donor-recipient CMV status, n/n eval (%)    .0001  
 Negative-negative 289/726 (40%)  265/912 (29%)  
 Negative-positive 151/726 (21%)  197/912 (21%)  
 Positive-negative 116/726 (16%)  152/912 (17%)  
 Positive-positive 170/726 (23%)  298/912 (33%)  
Median cell dose, ×108/kg (range)  1.1 (0.1-12)  3 (0.3-25) .0001  
Conditioning regimen*, n/n eval (%)    .0001 
 High intensity  664/863 (77%)  339/986 (34%) 
 Standard intensity  83/863 (10%)  374/986 (38%) 
 Busulfan + cyclophosphamide  25/863 (3%) 213/986 (22%)  
 Other  91/863 (10%)  60/986 (6%) 
Donor-recipient relationship and HLA-match, n/n eval (%)   .0001  
 Phenotypically matched related donor 56/870 (6%)  96/998 (10%)  
 1-Antigen mismatched related donor  180/870 (21%)  332/998 (33%)  
 2-Antigen mismatched related donor  153/870 (18%)  78/998 (8%) 
 3-Antigen mismatched related donor  98/870 (11%) 12/998 (1%)  
 Phenotypically matched unrelated donor 267/870 (31%)  408/998 (41%)  
 Mismatched unrelated donor  116/870 (13%)  72/998 (7%)  
Prophylactic use of growth factors, n/n eval (%)  79/870 (9)  103/998 (10) NS  
Posttransplant immune suppression, n/n eval (%)   —  
 Methotrexate (MTX)  39/869 (4%) 
 Cyclosporine A (CsA)  399/869 (46%)  
 CsA + MTX 40/869 (5%)  998/998 (100%)  
 CSA + Corticosteroids 120/869 (14%)  
 Corticosteroids  91/869 (10%) 
 Other  25/869 (3%)  
 None  155/869 (18%) 
T-cell depleted Non-T-cell depleted P
870  998  
Median age, y (range)  24 (0.4-57) 28 (0.5-61)  .0001  
Performance score 90%, n/n eval (%) 706/869 (81%)  735/988 (74%)  .0001  
Disease and disease state, n/n eval (%)    .001   
 ALL, 1st remission  45/851 (5%)  64/987 (6%)  
 ALL, 2nd remission 162/851 (19%)  141/987 (14%)  
 ALL, not in remission 86/851 (10%)  62/987 (6%)  
 AML, 1st remission 53/851 (6%)  90/987 (9%)  
 AML, 2nd remission 51/851 (6%)  66/987 (7%)  
 AML, not in remission 101/851 (12%)  107/987 (11%)  
 CML, 1st chronic phase 203/851 (24%)  292/987 (30%)  
 CML, accelerated phase 110/851 (13%)  115/987 (12%)  
 CML, blast phase 40/851 (5%)  50/987 (5%)  
Year of transplantation, n/n eval (%)    .0001  
 1982-1987  316/870 (36%) 133/998 (14%)  
 1988-1994  554/870 (63%) 865/998 (86%)  
Median interval diagnosis-transplant, mo (range)  
 ALL, 1st remission  6 (2-21)  7 (2-19) NS  
 ALL, 2nd remission  28 (5-148)  34 (4-151)  NS 
 ALL, not in remission  18 (3-73)  13 (3-97)  NS 
 AML, 1st remission  6 (2-17)  6 (2-19)  NS  
 AML, 2nd remission  21 (7-67)  17 (5-88)  NS  
 AML, not in remission  10 (3-54)  10 (1-61)  NS  
 CML, 1st chronic phase  20 (2-124)  19 (2-123)  NS  
 CML, accelerated phase  26 (2-107)  27 (2-126)  NS  
 CML, blast phase 27 (6-123)  20 (2-116)  NS  
Median WBC at diagnosis, ×109/L (range)  
 Acute leukemia 16 (0.5-850)  16 (0.4-882)  NS  
 Chronic leukemia 164 (4-880)  158 (4-760)  NS  
Median donor age, y (range)  35 (1-81)  35 (1-75)  NS  
Donor recipient sex-match, n/n eval (%)    NS  
 Male-male 283/859 (33%)  292/987 (30%)  
 Male-female 173/859 (20%)  215/987 (22%)  
 Female-male 242/859 (28%)  282/987 (28%)  
 Female-female 161/859 (19%)  198/987 (20%)  
Donor-recipient CMV status, n/n eval (%)    .0001  
 Negative-negative 289/726 (40%)  265/912 (29%)  
 Negative-positive 151/726 (21%)  197/912 (21%)  
 Positive-negative 116/726 (16%)  152/912 (17%)  
 Positive-positive 170/726 (23%)  298/912 (33%)  
Median cell dose, ×108/kg (range)  1.1 (0.1-12)  3 (0.3-25) .0001  
Conditioning regimen*, n/n eval (%)    .0001 
 High intensity  664/863 (77%)  339/986 (34%) 
 Standard intensity  83/863 (10%)  374/986 (38%) 
 Busulfan + cyclophosphamide  25/863 (3%) 213/986 (22%)  
 Other  91/863 (10%)  60/986 (6%) 
Donor-recipient relationship and HLA-match, n/n eval (%)   .0001  
 Phenotypically matched related donor 56/870 (6%)  96/998 (10%)  
 1-Antigen mismatched related donor  180/870 (21%)  332/998 (33%)  
 2-Antigen mismatched related donor  153/870 (18%)  78/998 (8%) 
 3-Antigen mismatched related donor  98/870 (11%) 12/998 (1%)  
 Phenotypically matched unrelated donor 267/870 (31%)  408/998 (41%)  
 Mismatched unrelated donor  116/870 (13%)  72/998 (7%)  
Prophylactic use of growth factors, n/n eval (%)  79/870 (9)  103/998 (10) NS  
Posttransplant immune suppression, n/n eval (%)   —  
 Methotrexate (MTX)  39/869 (4%) 
 Cyclosporine A (CsA)  399/869 (46%)  
 CsA + MTX 40/869 (5%)  998/998 (100%)  
 CSA + Corticosteroids 120/869 (14%)  
 Corticosteroids  91/869 (10%) 
 Other  25/869 (3%)  
 None  155/869 (18%) 
*

Standard intensity: cyclophosphamide + 12 Gy fractionated or 10 Gy unfractionated total body irradiation.

High intensity: >12 Gy total body irradiation or cyclophosphamide, total body irradiation and other drugs.

G-CSF or GM-CSF started within 1 week of transplantation.

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