Table 1.
Characteristics of the whole cohort of 122 patients who underwent allo-HSCT
(n = 122) | |
---|---|
Age at transplant, median (range) | 58 (20–71) |
Males, n (%) | 70 (57.3) |
Haematological disease (%) | |
AML | 63 (51.6) |
ALL | 12 (9.8) |
Lymphomas | 17 (13.9) |
MDS | 6 (4.9) |
MPNs | 16 (13.1) |
MM | 4 (3.3) |
SAA | 2 (1.6) |
CLL | 2 (1.6) |
Disease status, n (%) | |
Remission (CR1, CR2, MRD±) | 72 (59) |
Other than remission (PR1, PR2, SD) | 50 (41) |
Comorbidity | |
HCT-CI risk score, n (%) ≥ 3 | 44 (36.1) |
Donor’s compatibility, n (%) | |
Sibling donor | 34 (28) |
Haploidentical donor | 34 (28) |
Unrelated donor ≥8/8 | 40 (33) |
Unrelated donor <8/8 | 14 (11) |
Haemopoietic stem cells source, n (%) | |
PBSC | 69 (56.5) |
BM | 48 (39.4) |
PBSC + BM | 5 (4) |
Major AB0 incompatibility, n (%) | 21 (17.2) |
Conditioning regimen, n (%) | |
MAC | 85 (69.6) |
MAC + TBI | 10 (8.2) |
RIC | 28 (23) |
nMAC | 9 (7.4) |
GVHD prophylaxis, n (%) | |
CsA/FK506 + MTX | 76 (62.3) |
CsA/FK506 + ptCy | 45 (36.7) |
CsA + MMF | 1 (0.8) |
ATG | 69 (56) |
AML, acute myeloid leukemia; ALL acute lymphoid leukemia; MDS, myelodysplastic syndrome; MPNs, myeloproliferative neoplasms; MM, multiple myeloma; SAA, severe aplastic anemia; CLL, chronic lymphatic leukemia; CR, complete remission; MRD, minimal residual disease; PR, partial remission; PBSC, peripheral blood stem cell; BM, bone marrow; MAC, myeloablative conditioning; RIC, reduced-intensity conditioning; nMAC, non-myeloablative conditioning; GVHD, graft-versus-host disease; CsA, cyclosporine A; MTX, methotrexate; ptCy, post-transplant cyclophosphamide; MMF, mycophenolate mofetil; ATG, antithymocyte globulin; TBI, total body irradiation.