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. 2021 May 21;11(6):928. doi: 10.3390/diagnostics11060928

Table 1.

Patient characteristics.

Study Cohort (n = 63) No SOS/VOD (n = 60) SOS/VOD (n = 3)
disease type AML 28 (44.4%) 27 1
MDS 13 (20.6%) 13 0
lymphoma 7 (11.1%) 7 0
ALL 8 (12.7%) 6 0
CML 3 (4.8%) 2 1
lymphomatoid granulomatosis 1 (1.6%) 1 0
hypereosinophilic syndrome 1 (1.6%) 1 0
MM 1 (1.6%) 0 1
ET 1 (1.6%) 1 0
stem cell donor matched unrelated 47 (74.6%) 45 2
matched related 8 (12.7%) 8 0
mismatch 8 (12.7%) 6 1
conditioning regimen MAC 20 (31.7%) 17 3
RIC 43 (68.3%) 43 0
gender female 20 (31.7%) 19 1
male 43 (68.3%) 41 2
age (years) 55 54.9 48.3
baseline SWE (m/S) 1.42 1.43 1.29
baseline SWE (kPa) 6.1 6.2 4.9
baseline PV velocity (cm/S) 22.5 (n = 57) 22.4 24.7

Abbreviations: AML acute myeloid leukemia; MDS myelodysplastic syndrome; ALL acute lymphoblastic leukemia; CML chronic myeloid leukemia; MM multiple myeloma; ET essential thrombocytosis; SWE shear wave elastography; PV portal vein; MAC myeloablative conditioning with busulfan 4 × 3.2 mg/kg and 2× cyclophosphamide 60 mg/kg for AML, CML and MDS, 12 Gy and 2 × 60 mg/kg cyclophosphamide i.v. or 8 Gy and 4 × 30 mg/m2 fludarabine for ALL, TTF (3 × 12 g/m2 treosulfan, 5 × 30 mg/m2 fludarabine and 2.5 mg/kg thiotepa) for multiple myeloma; RIC = reduced conditioning with 3 × 12 g/m2 treosulfan and 5 × 30 mg/m2 fludarabine or 5 × 30 mg/m2 fludarabine and 2 × 3.2 mg/kg busulfan i.v.