Table 1.
Patients | N = 86 | |
---|---|---|
Sex | n | % |
Male | 55 | 64 |
Female | 31 | 36 |
Type of HSCT | n | % |
MUD | 59 | 69 |
HLA ID SIB | 18 | 21 |
HLA MM REL | 9 | 10 |
Source of stem cells | n | % |
Peripheral blood | 71 | 83 |
– after T cell depletion in vitro | 8 | 9 |
Bone marrow | 15 | 17 |
Diagnosis | n | % |
Malignant (M) | 64 | 74 |
Acute lymphoblastic leukaemia (ALL) | 33 | 38 |
Acute myeloblastic leukaemia (AML) | 17 | 20 |
Solid tumours (NBL, WT, PNET) | 6 | 7 |
Chronic myeloid leukaemia (CML) | 1 | 1 |
Hodgkin lymphoma (HL) | 2 | 2 |
Non-Hodgkin lymphoma (NHL) | 1 | 1 |
Myelodysplastic syndrome (MDS) | 3 | 3 |
Xanthogranuloma juvenile | 1 | 1 |
Non malignant (NM) | 22 | 26 |
Severe aplastic anaemia (SAA) | 4 | 5 |
Metabolic diseases (WM) | 1 | 1 |
Immune deficiencies (ID*) | 17 | 20 |
Conditionning | ||
Myeloablative (MA) | 50 | 58 |
Reduced-intensity conditioning (RIC) | 24 | 28 |
Non-myeloablative (NMA) | 8 | 10 |
None | 4 | 4 |
Graft versus host disease (GvHD) prophylaxis | ||
ATG | 50 | 58 |
CAMPATH | 13 | 15 |
None | 22 | 26 |
ATG and CAMPATH | 1 | 1 |
HLA ID SIB – HLA identical sibling; MUD – matched unrelated donor; HLA MM REL – HLA mismatched related donor; NBL – neuroblastoma; WT – Wilms tumour; PNET – primitive neuroectodermal tumour