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. 2021 Sep 23;3(4):161–168. doi: 10.2991/chi.k.210826.001

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.