Table 2.

Demographic characteristics of all patients by intensity of the preparative regimen


Characteristic

Myeloablative

Nonmyeloablative

P
No. of patients   240   95   
Median age, y (range)   8 (0.2-53)   50 (18-69)   < .01  
Median weight, kg (range)   30 (4-120)   78 (50-134)   < .01  
CMV-positive recipients, no. (%)   108 (45)   47 (49)   .46  
HLA match, no. (%)    .02  
   6 of 6   28 (12)   6 (6)   
   5 of 6   109 (45)   29 (31)   
   3-4 of 6   103 (43)   60 (63)   
No. treated with ATG (%)   174 (73)   30 (32)   < .01  
No. of UCB recipients (%)    < .01  
   Single unit   192 (80)   17 (18)   
   Double unit   48 (20)   78 (82)   
Median infused nucleated cell dose, × 107/kg (range)   4.1 (0.7-28.1)   3.6 (1.1-6.8)   < .01  
Median infused CD34+ cell dose × 105/kg (range)   4.3 (0.4-96.7)   4.5 (0.7-18.8)   .57  
No. with malignant diagnosis (%)   157 (65)   93 (98)   .09  
Median time to follow-up, y (range)
 
1.5 (0.-9.2)
 
1.2 (0.3-3.5)
 
.02
 

Characteristic

Myeloablative

Nonmyeloablative

P
No. of patients   240   95   
Median age, y (range)   8 (0.2-53)   50 (18-69)   < .01  
Median weight, kg (range)   30 (4-120)   78 (50-134)   < .01  
CMV-positive recipients, no. (%)   108 (45)   47 (49)   .46  
HLA match, no. (%)    .02  
   6 of 6   28 (12)   6 (6)   
   5 of 6   109 (45)   29 (31)   
   3-4 of 6   103 (43)   60 (63)   
No. treated with ATG (%)   174 (73)   30 (32)   < .01  
No. of UCB recipients (%)    < .01  
   Single unit   192 (80)   17 (18)   
   Double unit   48 (20)   78 (82)   
Median infused nucleated cell dose, × 107/kg (range)   4.1 (0.7-28.1)   3.6 (1.1-6.8)   < .01  
Median infused CD34+ cell dose × 105/kg (range)   4.3 (0.4-96.7)   4.5 (0.7-18.8)   .57  
No. with malignant diagnosis (%)   157 (65)   93 (98)   .09  
Median time to follow-up, y (range)
 
1.5 (0.-9.2)
 
1.2 (0.3-3.5)
 
.02
 

CMV indicates cytomegalovirus; HLA, human major histocompatibility complex; ATG, antithymocyte globulin; and UCB, umbilical cord blood

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