Table 1.

Patient characteristics

UMC/PMC (n = 276)MSK (n = 315)
Median (range) age at transplantation, y 7.06 (0.16-22.74) 10.4 (0.1-35.6) 
Sex, n   
 Male 159 188 
 Female 117 127 
HCT source, n   
 BM (T-cell replete) 100 61 
 Unrelated cord blood 172 40 
 PBSCs 
 TCD PBSCs 169 
 TCD BM 39 
Diagnosis, n   
 Malignancy 139 220 
 Metabolic inborn error 51 
 Hemoglobinopathy 11 
 Primary immune deficiency 52 42 
 BM failure 29 40 
 Autoimmune disease 
aGVHD incidence by grade, n   
 2 44 38 
 3 19 23 
 4 10 
Chronic (all) GvHD, n 31 18 
 Extensive 11 
Conditioning regimen, n   
 TBI based 26 112 
 Chemotherapy based* 250 203 
Serotherapy in conditioning, n (%) 198 (72) 227 (72) 
Median (range) time to grade 2-4 aGVHD, d 34 (6-205) 55 (14-303) 
Median (range) follow-up, d 1293 (14-5017) 750 (11-3780) 
UMC/PMC (n = 276)MSK (n = 315)
Median (range) age at transplantation, y 7.06 (0.16-22.74) 10.4 (0.1-35.6) 
Sex, n   
 Male 159 188 
 Female 117 127 
HCT source, n   
 BM (T-cell replete) 100 61 
 Unrelated cord blood 172 40 
 PBSCs 
 TCD PBSCs 169 
 TCD BM 39 
Diagnosis, n   
 Malignancy 139 220 
 Metabolic inborn error 51 
 Hemoglobinopathy 11 
 Primary immune deficiency 52 42 
 BM failure 29 40 
 Autoimmune disease 
aGVHD incidence by grade, n   
 2 44 38 
 3 19 23 
 4 10 
Chronic (all) GvHD, n 31 18 
 Extensive 11 
Conditioning regimen, n   
 TBI based 26 112 
 Chemotherapy based* 250 203 
Serotherapy in conditioning, n (%) 198 (72) 227 (72) 
Median (range) time to grade 2-4 aGVHD, d 34 (6-205) 55 (14-303) 
Median (range) follow-up, d 1293 (14-5017) 750 (11-3780) 

BM, bone marrow; PBSC, peripheral blood stem cell.

*

Clofarabine, fludarabine, and busulfan.

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