Table 1.

Patients, disease, and transplant characteristics

PatientsN = 77
Age, median (range), y 53 (19-65) 
Patient sex, n (%)  
Male/female 45 (58.4%)/32 (41.6%) 
ECOG, n (%)  
64 (83.1%) 
>0 11 (14.3%) 
Unknown 2 (2.6%) 
HCT-CI, n (%)  
0-2 64 (83.1%) 
≥3 13 (16.9%) 
Disease  
AML, n (%) 64 (83.1%) 
WHO classification, n (%)  
AML with recurrent genetic abnormalities 16 (25.0%) 
AML with myelodysplasia-related changes 15 (23.4%) 
Therapy-related myeloid neoplasm 4 (6.3%) 
AML, NOS 28 (43.8%) 
Myeloid sarcoma 1 (1.6%) 
Cytogenetic risk (ELN 2022) , n (%)  
Favorable 14 (21.9%) 
Intermediate 37 (57.8%) 
Adverse 13 (20.3%) 
Molecular markers  
FLT 3 15 
NPM1 19 
IDH1/IDH2 
ASXL1 
AML1/ETO RUNX1::RUNX1T1 
BCR::ABL1 
No CR postinduction therapy 15 (23.4%) 
≥2 CR 11 (17%) 
MRD positive at transplant, n (%)  
Molecular markers 14/64 (21%) 
NPM 11 (17%) 
AML1/ETO 2 (3%) 
bcr/abl 1 (1%) 
IF 14/64 (21%) 
MDS, n (%) 13 (16.9%) 
WHO classification, n (%)  
MDS with single lineage dysplasia 2 (15.4%) 
MDS with multilineage dysplasia 2 (15.4%) 
MDS with excess blasts 6 (46.1%) 
MDS with isolated del(5q) 1 (7.7%) 
MDS, unclassifiable 2 (15.4%) 
HSCT up-front 
Transplant and donors  
Diagnosis: transplant, median (range), d 202 (115-1482) 
Year of the transplant, n (%)  
2020 21 (27.3%) 
2021 32 (41.6%) 
2022 24 (31.2%) 
Conditioning Bu4Flu, n (%) 77 (100%) 
Donor age, median (range), y 29 (18-62) 
Donor sex, n (%)  
Male/female 51 (66.2%)/26 (33.8%) 
Donor/recipient sex mismatch, n (%)  
Male/male 31 (40.2%) 
Male/female 14 (18.2%) 
Female/male 20 (26.0%) 
Female/female 12 (15.6%) 
CMV serostatus, n (%)  
+/+ 34 (44.1%) 
–/+ 19 (24.7%) 
+/– 9 (11.7%) 
–/– 6 (7.8%) 
Missing 9 (11.7%) 
Stem cell source, n (%)  
PB 72 (93.5%) 
BM 5 (6.5%) 
Cell dose  
PB median (range), CD34+, ×106/kg 5.9 (2.2-12.2) 
BM median (range), CD34+, ×106/kg 2.3 (1.4-5.3) 
Donor HLA mismatches 7/8, n (%) 77 (100%) 
HLA class I mismatch (A, B, C) 72 (93.5%) 
HLA class II mismatch (DRB1) 3 (4%) 
Missing 2 (2.5%) 
PatientsN = 77
Age, median (range), y 53 (19-65) 
Patient sex, n (%)  
Male/female 45 (58.4%)/32 (41.6%) 
ECOG, n (%)  
64 (83.1%) 
>0 11 (14.3%) 
Unknown 2 (2.6%) 
HCT-CI, n (%)  
0-2 64 (83.1%) 
≥3 13 (16.9%) 
Disease  
AML, n (%) 64 (83.1%) 
WHO classification, n (%)  
AML with recurrent genetic abnormalities 16 (25.0%) 
AML with myelodysplasia-related changes 15 (23.4%) 
Therapy-related myeloid neoplasm 4 (6.3%) 
AML, NOS 28 (43.8%) 
Myeloid sarcoma 1 (1.6%) 
Cytogenetic risk (ELN 2022) , n (%)  
Favorable 14 (21.9%) 
Intermediate 37 (57.8%) 
Adverse 13 (20.3%) 
Molecular markers  
FLT 3 15 
NPM1 19 
IDH1/IDH2 
ASXL1 
AML1/ETO RUNX1::RUNX1T1 
BCR::ABL1 
No CR postinduction therapy 15 (23.4%) 
≥2 CR 11 (17%) 
MRD positive at transplant, n (%)  
Molecular markers 14/64 (21%) 
NPM 11 (17%) 
AML1/ETO 2 (3%) 
bcr/abl 1 (1%) 
IF 14/64 (21%) 
MDS, n (%) 13 (16.9%) 
WHO classification, n (%)  
MDS with single lineage dysplasia 2 (15.4%) 
MDS with multilineage dysplasia 2 (15.4%) 
MDS with excess blasts 6 (46.1%) 
MDS with isolated del(5q) 1 (7.7%) 
MDS, unclassifiable 2 (15.4%) 
HSCT up-front 
Transplant and donors  
Diagnosis: transplant, median (range), d 202 (115-1482) 
Year of the transplant, n (%)  
2020 21 (27.3%) 
2021 32 (41.6%) 
2022 24 (31.2%) 
Conditioning Bu4Flu, n (%) 77 (100%) 
Donor age, median (range), y 29 (18-62) 
Donor sex, n (%)  
Male/female 51 (66.2%)/26 (33.8%) 
Donor/recipient sex mismatch, n (%)  
Male/male 31 (40.2%) 
Male/female 14 (18.2%) 
Female/male 20 (26.0%) 
Female/female 12 (15.6%) 
CMV serostatus, n (%)  
+/+ 34 (44.1%) 
–/+ 19 (24.7%) 
+/– 9 (11.7%) 
–/– 6 (7.8%) 
Missing 9 (11.7%) 
Stem cell source, n (%)  
PB 72 (93.5%) 
BM 5 (6.5%) 
Cell dose  
PB median (range), CD34+, ×106/kg 5.9 (2.2-12.2) 
BM median (range), CD34+, ×106/kg 2.3 (1.4-5.3) 
Donor HLA mismatches 7/8, n (%) 77 (100%) 
HLA class I mismatch (A, B, C) 72 (93.5%) 
HLA class II mismatch (DRB1) 3 (4%) 
Missing 2 (2.5%) 

CMV, cytomegalovirus; ECOG, Eastern Cooperative Oncology Group; HCT-CI, hematopoietic cell transplantation–comorbidity index; IF, immunophenotyping; NOS, not otherwise specified; PB, peripheral blood; WHO, World Health Organization.

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