Table 2.
M | V | M | V | M | V | |||
---|---|---|---|---|---|---|---|---|
% | % | Diagnosis | % | % | HSCT | % | % | |
Age at HSCT, years | ||||||||
0→1 | 16 | 19 | Immunodeficiencies | 43 | 40 | 1st | 85 | 88 |
1→2 | 21 | 16 | SCID | 26 | 24 | 2nd | 13 | 11 |
2→5 | 23 | 21 | Wiskott‐Aldrich | 4 | 7 | 3rd | 1 | 1 |
5→10 | 24 | 31 | CGD | 4 | 8 | GvHD | ||
10→ | 16 | 13 | Leukemia | 30 | 23 | Reported | 32 | 60 |
Sex | ALL | 14 | 11 | I | 12 | 33 | ||
Male | 37 | 32 | AML | 11 | 11 | II | 12 | 20 |
Female | 63 | 68 | HLH | 11 | 7 | III | 6 | 5 |
Stem cells | Anemia | 7 | 0 | IV | 2 | 1 | ||
Bone marrow | 47 | 36 | Autoimmune | 3 | 0 | Conditioning | ||
Peripheral blood | 38 | 37 | Lymphomas | 2 | 0 | Fludarabine | 21 | 73 |
Cord blood | 15 | 27 | Viruses | Cyclophosphamide | 44 | 16 | ||
Combinations | 1 | 0 | Cytomegalovirus | Melphalan | 30 | 23 | ||
Donor type | Positive | 32 | 16 | Busulphan | 24 | 41 | ||
Matched | 63 | 52 | Negative | 67 | 81 | Treosulphan | 21 | 24 |
Sibling | 27 | 19 | Unknown | 1 | 3 | Alemtuzumab | 50 | 40 |
Family | 5 | 7 | Epstein‐Barr virus | ATG | 3 | 16 | ||
Unrelated | 31 | 27 | Positive | 26 | 16 | Anti‐CD45 | 4 | 3 |
Mismatched | 32 | 37 | Negative | 38 | 64 | Total body irradiation | 14 | 8 |
Sibling | 1 | 0 | Unknown | 37 | 3 | None | 13 | 5 |
Family | 2 | 1 | Adenovirus | Prophylaxis | ||||
Unrelated | 29 | 36 | Positive | 33 | – | Cyclosporine | 88 | 88 |
Haploidentical | 4 | 3 | Negative | 67 | – | Methotrexate | 21 | 16 |
Autologous | 1 | 8 | Mycophenolate | 50 | 68 |
ALL, acute lymphoblastic leukemia; AML, acute myeloblastic leukemia; ATG, antithymocyte globulin; CGD, chronic granulomatous disease; GvHD, graft‐vs.‐host disease; HLH, hemophagocytic lymphohistiocytosis; SCT, stem cell transplantation; M, model‐building dataset (n = 319), used for model building and covariate analysis; SCID, severe combined immunodeficiency syndrome; V, validation dataset (n = 75), used for assessing the predictive ability of the model.
Positive for cytomegalovirus, Epstein‐Barr virus, or adenovirus was defined as detectable virus post‐transplant.