Table 1.
Characteristic | Value |
Number of patients | 45 |
Age, yr, median (range) | 32 (15-63) |
Age >50 yr, n (%) | 14 (31.1) |
Males/females, n | 28/17 |
Etiology of aplasia, n (%) | |
Idiopathic | 41 (91.2) |
Posthepatitic (seronegative) | 2 (4.4) |
Eosinophilic fasciitis | 1 (2.2) |
Celiac disease | 1 (2.2) |
Type of donor, n (%) | |
Matched sibling | 12 (26.6) |
Unrelated | 33 (73.4) |
9/10 unrelated | 8 of 33 (24.2) |
Previous immunosuppressive therapy, n/N (%) | |
Matched sibling donor | 6/12 (50) |
Unrelated donor | 27/33 (81.8); P = .055 |
Time to transplantation, d, median (range) | |
Matched sibling donor | 5.9 (2.7-34.7) |
Unrelated donor | 8.4 (2.1-178.9); P = .095 |
HLA alloimmunization, n (%) | 11 (24.4) |
Stem cell source, n (%) | |
Bone marrow | 7 (15.5) |
Peripheral blood stem cells | 38 (84.5) |
PNH clone, n (%) | 21 (46.6) |
PNH clone size, % median (range) | |
Granulocytes | 2 (0.02-40) |
Monocytes | 2.85 (0.01-32) |
Red cells | Not available |
Alemtuzumab dose, mg, median (range) | 70 (45-100) |
CD34+ stem cell dose, × 106/kg, median (range) | 6.55 (1.97-12.40) |
Follow-up after HSCT, mo, median (range) | 31.4 (3-93) |
HSCT indicates hematopoietic stem cell transplantation; PNH, paroxysmal nocturnal hemoglobinuria.