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. Author manuscript; available in PMC: 2020 Jan 3.
Published in final edited form as: Bone Marrow Transplant. 2019 Sep 2;55(1):165–171. doi: 10.1038/s41409-019-0651-9

Table 1.

Patient and transplant characteristics

Factors N (%)

Total 370
Year of transplant
 1990–1995 119 (32%)
 1996–2000 106 (29%)
 2001–2005 69 (19%)
 2006–2010 30 (8%)
 2011–2016 46 (12%)
Age
 <2 years 67 (18%)
 2–9 years 168 (45%)
 10–17 years 135 (36%)
 Median, years (range) 7 (0.2–17.95)
Gender
 Male 244 (66%)
 Female 126 (34%)
Disease
 Acute lymphoblastic leukemia 91 (25%)
 Acute myelogenous leukemia 60 (16%)
 CML/JMML 19 (5%)
 Myelodsyplastic syndrome 19 (5%)
 Hodgkins lymphoma/Non-Hodgkins lymphoma 8 (2%)
 Inborn error of metabolism 94 (25%)
 Fanconi anemia 27 (7%)
 Aplastic anemia 21 (6%)
 Immune deficiency 27 (7%)
 Epidermolysis bullosa 4 (1%)
Disease risk
 Standard risk malignancy 132 (36%)
 High risk malignancy 65 (18%)
 Nonmalignant disease 173 (47%)
CMV serostatus
 Recipient negative, donor negative 167 (45%)
 Recipient negative and/or donor positive 203 (55%)
Donor type
 HLA-matched sibling 61 (16%)
 HLA-mismatched sibling 8 (2%)
 Well matched URD 48 (13%)
 Partial matched URD 56 (15%)
 HLA-mismatched URD 65 (18%)
 Single UCB 97 (26%)
 Double UCB 35 (9%)
Conditioning
 Myeloablative 351 (95%)
 Reduced intensity 19 (5%)
GVHD prophylaxis
 Cyclosporine or tacrolimus containing 290 (78%)
 T-cell depletion 65 (18%)
 Methotrexate alone 14 (4%)
 Sirolimus and mycophenolate mofetil 1 (0.3%)

Standard risk = acute leukemia in CR1 or CR2, CML in first chronic phase, MDS without excess blasts or nonmalignant diseases. High risk malignancy = all others

CML chronic myelogenous leukemia, JMML juvenile myelomonocytic leukemia