Table 1.

Patient characteristics

CharacteristicEntire cohortTCD HCTT-replete–TDUCB-T
N (%)n (%)n (%)n (%)
Total N = 267Total n = 119Total n = 96Total n = 52
Age     
Median (range), y 53.6 (21.1-73.9) 55.7 (21.4-70.8) 54.3 (24-73.9) 50.8 (21.1-69.9) 
Gender     
Female 103 (38.6%) 47 (39.5%) 31 (32.3%) 25 (48.1%) 
Male 164 (61.4%) 72 (60.5%) 65 (67.7%) 27 (51.9%) 
CMV serostatus (recipient [R]/donor [D])     
R+/D+ 73 (27.3%) 32 (26.9%) 41 (42.7%) 0 (0%) 
R+/D− 93 (34.8%) 38 (31.9%) 20 (20.8%) 34 (65.4%) 
R−/D+ 25 (9.4%) 14 (11.8%) 12 (12.5%) 0 (0%) 
R−/D− 76 (28.5%) 35 (29.4%) 23 (24%) 18 (34.6%) 
CMV reactivation     
Yes 129 (48.3%) 57 (47.9%) 47 (49%) 25 (48.1%) 
No 138 (51.7%) 62 (52.1%) 49 (51%) 27 (51.9%) 
Underlying disease     
Acute leukemia 123 (46.1%) 58 (48.7%) 33 (34.4%) 32 (61.5%) 
Chronic leukemia 20 (7.5%) 5 (4.2%) 9 (9.4%) 5 (9.6%) 
Myelodysplastic syndrome 34 (12.7%) 26 (21.8%) 7 (7.3%) 1 (1.9%) 
Multiple myeloma 24 (9%) 23 (19.3%) 1 (1%) 0 (0%) 
Hodgkin disease 7 (2.6%) 0 (0%) 5 (5.2%) 2 (3.8%) 
Non-Hodgkin lymphoma 44 (16.5%) 1 (0.8%) 32 (33.3%) 11 (21.2%) 
Other  15 (5.6%) 6 (5%) 9 (9.4%) 1 (1.9%) 
Conditioning regimen     
Busulfan based 107 (40.1%) 86 (72.3%) 21 (21.9%) 0 (0%) 
Carmustine/etoposide/cytarabine/melphalan 1 (0.4%) 0 (0%) 1 (1%) 0 (0%) 
Clofarabine/thio-TEPA/melphalan 10 (3.7%) 6 (5%) 4 (4.2%) 0 (0%) 
Cyclophosphamide/fludarabine/TBI 46 (17.2%) 0 (0%) 30 (31.3%) 16 (30.8%) 
Cyclophosphamide/fludarabine/thio-TEPA/TBI 40 (15%) 0 (0%) 5 (5.2%) 35 (67.3%) 
Fludarabine/melphalan 27 (10.1%) 0 (0%) 26 (27.1%) 1 (1.9%) 
Fludarabine/TBI 1 (0.4%) 0 (0%) 1 (1%) 0 (0%) 
High-dose TBI based 35 (13.1%) 27 (22.7%) 8 (8.3%) 0 (0%) 
GVHD prophylaxis     
Calcineurin inhibitor/methotrexate with/without sirolimus 96 (35.9%) 96 (100%) 
CSA/MMF 52 (19.5%) 52 (100%) 
Donor type     
Matched related 79 (29.6%) 44 (37%) 35 (36.5%) 0 (0%) 
Matched unrelated  99 (37.1%) 45 (37.8%) 54 (56.3%) 0 (0%) 
Mismatched 89 (33.3%) 30 (25.2%) 7 (7.3%) 52 (100%) 
CharacteristicEntire cohortTCD HCTT-replete–TDUCB-T
N (%)n (%)n (%)n (%)
Total N = 267Total n = 119Total n = 96Total n = 52
Age     
Median (range), y 53.6 (21.1-73.9) 55.7 (21.4-70.8) 54.3 (24-73.9) 50.8 (21.1-69.9) 
Gender     
Female 103 (38.6%) 47 (39.5%) 31 (32.3%) 25 (48.1%) 
Male 164 (61.4%) 72 (60.5%) 65 (67.7%) 27 (51.9%) 
CMV serostatus (recipient [R]/donor [D])     
R+/D+ 73 (27.3%) 32 (26.9%) 41 (42.7%) 0 (0%) 
R+/D− 93 (34.8%) 38 (31.9%) 20 (20.8%) 34 (65.4%) 
R−/D+ 25 (9.4%) 14 (11.8%) 12 (12.5%) 0 (0%) 
R−/D− 76 (28.5%) 35 (29.4%) 23 (24%) 18 (34.6%) 
CMV reactivation     
Yes 129 (48.3%) 57 (47.9%) 47 (49%) 25 (48.1%) 
No 138 (51.7%) 62 (52.1%) 49 (51%) 27 (51.9%) 
Underlying disease     
Acute leukemia 123 (46.1%) 58 (48.7%) 33 (34.4%) 32 (61.5%) 
Chronic leukemia 20 (7.5%) 5 (4.2%) 9 (9.4%) 5 (9.6%) 
Myelodysplastic syndrome 34 (12.7%) 26 (21.8%) 7 (7.3%) 1 (1.9%) 
Multiple myeloma 24 (9%) 23 (19.3%) 1 (1%) 0 (0%) 
Hodgkin disease 7 (2.6%) 0 (0%) 5 (5.2%) 2 (3.8%) 
Non-Hodgkin lymphoma 44 (16.5%) 1 (0.8%) 32 (33.3%) 11 (21.2%) 
Other  15 (5.6%) 6 (5%) 9 (9.4%) 1 (1.9%) 
Conditioning regimen     
Busulfan based 107 (40.1%) 86 (72.3%) 21 (21.9%) 0 (0%) 
Carmustine/etoposide/cytarabine/melphalan 1 (0.4%) 0 (0%) 1 (1%) 0 (0%) 
Clofarabine/thio-TEPA/melphalan 10 (3.7%) 6 (5%) 4 (4.2%) 0 (0%) 
Cyclophosphamide/fludarabine/TBI 46 (17.2%) 0 (0%) 30 (31.3%) 16 (30.8%) 
Cyclophosphamide/fludarabine/thio-TEPA/TBI 40 (15%) 0 (0%) 5 (5.2%) 35 (67.3%) 
Fludarabine/melphalan 27 (10.1%) 0 (0%) 26 (27.1%) 1 (1.9%) 
Fludarabine/TBI 1 (0.4%) 0 (0%) 1 (1%) 0 (0%) 
High-dose TBI based 35 (13.1%) 27 (22.7%) 8 (8.3%) 0 (0%) 
GVHD prophylaxis     
Calcineurin inhibitor/methotrexate with/without sirolimus 96 (35.9%) 96 (100%) 
CSA/MMF 52 (19.5%) 52 (100%) 
Donor type     
Matched related 79 (29.6%) 44 (37%) 35 (36.5%) 0 (0%) 
Matched unrelated  99 (37.1%) 45 (37.8%) 54 (56.3%) 0 (0%) 
Mismatched 89 (33.3%) 30 (25.2%) 7 (7.3%) 52 (100%) 

CSA, cyclosporine A; MMF, mycophenolate mofetil; TBI, total body irradiation; thio-TEPA, N,N’N’-triethylenethiophosphoramide.

Nonmalignant hematologic disorder, myeloproliferative disorder, Waldenström macroglobulinemia, or aplastic anemia.

9/10 or 10/10 HLA–matched unrelated donor.

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