Table 1.
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