Table 3.

Detailed information of 12 patients who underwent alloHSCT after mAb2

CharacteristicN = 12
Median age at transplantation (IQR, y) 49 (17-42) 
Disease status at the time of transplantation 
 MRDnegative CR 9 (75.0) 
 MRDpositive CR 3 (25.0) 
Graft source 
 Bone marrow 2 (16.7) 
 Peripheral blood 8 (66.7) 
 Cord blood 2 (16.7) 
Donor 
 Related 3 (25.0) 
  HLA matched sibling 1 (8.3) 
  HLA haploidentical 2 (16.7) 
 Unrelated 7 (58.3) 
 Umbilical cord blood or haploidentical-umbilical cord 2 (16.7) 
Recipient–donor gender relation 
 Male–male 3 (25.0) 
 Male–female 2 (16.7) 
 Female–male 3 (25.0) 
 Female–female 3 (25.0) 
 NA* 1 (8.3) 
Histocompatibility 
 10/10 (fully HLA matched) 6 (50.0) 
 9/10 (one HLA locus mismatched) 2 (16.7) 
 ≤8/10 (2 or more loci mismatched including haploidentical HLA) 4 (33.3) 
Conditioning regimens 
 Myeloablative  
  Clofarabine, busulfan 16 mg/kg 2 (16.7) 
  Cyclophosphamide, thiotepa, TBI 2 (16.7) 
  Fludarabine, cyclophosphamide, thiotepa, TBI 1 (8.3) 
  Clofarabine, melphalan, thiotepa 2 (16.7) 
 Reduced intensity or non-myeloablative  
  Fludarabine, cyclophosphamide, TBI-200 2 (16.7) 
  Fludarabine, melphalan 3 (25.0) 
GVHD prophylaxis 
 Ex vivo T-cell depletion (CD34 selection) 5 (41.7) 
 Posttransplant cyclophosphamide 3 (25.0) 
 Methotrexate, calcineurin inhibitor 3 (25.0) 
 Calcineurin inhibitor, mycophenolate mofetil 1 (8.3) 
Median number of CD34+ dose (IQR, ×106 cells/kg) 5.02 (4.7-7.4) 
Median time from infusion to neutrophil engraftment (IQR, d) 12 (11-24) 
GVHD 6/12 (50) 
 Grade 1 1/6 (16.7) 
 Grade 2 2/6 (33.3) 
 Grade 3 1/6 (16.7) 
 Grade 4 2/6 (33.3) 
SOS 4 (33.3) 
Relapse after alloHSCT 5 (41.7) 
Death after alloHSCT 9 (75.0) 
 Died of progressive disease 4/9 (44.4) 
 Died in remission 5/9 (55.6) 
CharacteristicN = 12
Median age at transplantation (IQR, y) 49 (17-42) 
Disease status at the time of transplantation 
 MRDnegative CR 9 (75.0) 
 MRDpositive CR 3 (25.0) 
Graft source 
 Bone marrow 2 (16.7) 
 Peripheral blood 8 (66.7) 
 Cord blood 2 (16.7) 
Donor 
 Related 3 (25.0) 
  HLA matched sibling 1 (8.3) 
  HLA haploidentical 2 (16.7) 
 Unrelated 7 (58.3) 
 Umbilical cord blood or haploidentical-umbilical cord 2 (16.7) 
Recipient–donor gender relation 
 Male–male 3 (25.0) 
 Male–female 2 (16.7) 
 Female–male 3 (25.0) 
 Female–female 3 (25.0) 
 NA* 1 (8.3) 
Histocompatibility 
 10/10 (fully HLA matched) 6 (50.0) 
 9/10 (one HLA locus mismatched) 2 (16.7) 
 ≤8/10 (2 or more loci mismatched including haploidentical HLA) 4 (33.3) 
Conditioning regimens 
 Myeloablative  
  Clofarabine, busulfan 16 mg/kg 2 (16.7) 
  Cyclophosphamide, thiotepa, TBI 2 (16.7) 
  Fludarabine, cyclophosphamide, thiotepa, TBI 1 (8.3) 
  Clofarabine, melphalan, thiotepa 2 (16.7) 
 Reduced intensity or non-myeloablative  
  Fludarabine, cyclophosphamide, TBI-200 2 (16.7) 
  Fludarabine, melphalan 3 (25.0) 
GVHD prophylaxis 
 Ex vivo T-cell depletion (CD34 selection) 5 (41.7) 
 Posttransplant cyclophosphamide 3 (25.0) 
 Methotrexate, calcineurin inhibitor 3 (25.0) 
 Calcineurin inhibitor, mycophenolate mofetil 1 (8.3) 
Median number of CD34+ dose (IQR, ×106 cells/kg) 5.02 (4.7-7.4) 
Median time from infusion to neutrophil engraftment (IQR, d) 12 (11-24) 
GVHD 6/12 (50) 
 Grade 1 1/6 (16.7) 
 Grade 2 2/6 (33.3) 
 Grade 3 1/6 (16.7) 
 Grade 4 2/6 (33.3) 
SOS 4 (33.3) 
Relapse after alloHSCT 5 (41.7) 
Death after alloHSCT 9 (75.0) 
 Died of progressive disease 4/9 (44.4) 
 Died in remission 5/9 (55.6) 

Data are presented as no. (%) unless otherwise indicated.

NA, not applicable; TBI, total body irradiation.

*

Patients who received single cord blood transplantation, HLA match 4/6, no available data on sex of the cord unit.

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