Table 1.

Characteristics of 94 patients with cerebral X-adrenoleukodystrophy (X-ALD) who underwent hematopoietic cell transplant (HC transplant)




Related donor (n = 42)

Unrelated donor (n = 52)

Total (n = 94)
Year of HCT, no. (%)    
   Before 1990   5 (12)   0 (0)   5 (5)  
   1991 to 1995   24 (56)   20 (38)   44 (46)  
   1996 to 1999   13 (31)   32 (62)   45 (48)  
Median age at HCT, y (range)   9.1 (5.2-15.6)   8.9 (4.9-18.6)   9.0 (4.9-18.6)  
Reason for diagnosis, no. (%)*    
   Family history   11 (29)   17 (35)   28 (33)  
   X-ALD signs and symptoms   27 (71)   31 (65)   58 (67)  
   Unknown   4   4   8  
Stem cell source and HLA matching    
   Marrow/UCB   42/0   40/12   82/12  
   Matched   33/0   27/4   60/4  
   Mismatched   9/0   13/8   22/8  
Preparative regimen, no. (%)    
   Chemotherapy only   31 (74)   17 (33)   48 (51)  
      Bu/Cy   30 (97)   17 (100)   47 (98)  
      Bu only   1 (3)   0   1 (2)  
   Chemotherapy and radiation   11 (26)   35 (67)   46 (49)  
      Cy/TBI, brain-sparing at 1400 cGy   5 (45)   13 (37)   18 (39)  
      Bu/Cy/TBI at 300-1200 cGy   1 (9)   9 (26)   10 (22)  
      Cy/TBI at 1200-1400 cGy   1 (9)   8 (23)   9 (20)  
      Bu/Cy/TLI at 150-750 cGy   2 (18)   1 (3)   3 (7)  
      Cy/TAI at 800 cGy   1 (9)   1 (3)   2 (4)  
      VP-16/Ara-C/Cy/TBI at 1200 cGy   1 (9)   1 (3)   2 (4)  
      Other   0   2 (6)   2 (4)  
GVHD prophylaxis    
   CSA/MP, no. (%)   24 (57)   29 (56)   53 (56)  
      No. with/no. without ATG   3/21   12/17   15/38  
   CSA/MTX, no. (%)   9 (21)   8 (15)   17 (18)  
      No. with/no. without ATG   2/7   6/2   8/9  
   Other, no. (%)   9 (21)   15 (29)   24 (26)  
Graft manipulation by elutriation, no. yes/no. no
 
3/39
 
15/37
 
18/76
 



Related donor (n = 42)

Unrelated donor (n = 52)

Total (n = 94)
Year of HCT, no. (%)    
   Before 1990   5 (12)   0 (0)   5 (5)  
   1991 to 1995   24 (56)   20 (38)   44 (46)  
   1996 to 1999   13 (31)   32 (62)   45 (48)  
Median age at HCT, y (range)   9.1 (5.2-15.6)   8.9 (4.9-18.6)   9.0 (4.9-18.6)  
Reason for diagnosis, no. (%)*    
   Family history   11 (29)   17 (35)   28 (33)  
   X-ALD signs and symptoms   27 (71)   31 (65)   58 (67)  
   Unknown   4   4   8  
Stem cell source and HLA matching    
   Marrow/UCB   42/0   40/12   82/12  
   Matched   33/0   27/4   60/4  
   Mismatched   9/0   13/8   22/8  
Preparative regimen, no. (%)    
   Chemotherapy only   31 (74)   17 (33)   48 (51)  
      Bu/Cy   30 (97)   17 (100)   47 (98)  
      Bu only   1 (3)   0   1 (2)  
   Chemotherapy and radiation   11 (26)   35 (67)   46 (49)  
      Cy/TBI, brain-sparing at 1400 cGy   5 (45)   13 (37)   18 (39)  
      Bu/Cy/TBI at 300-1200 cGy   1 (9)   9 (26)   10 (22)  
      Cy/TBI at 1200-1400 cGy   1 (9)   8 (23)   9 (20)  
      Bu/Cy/TLI at 150-750 cGy   2 (18)   1 (3)   3 (7)  
      Cy/TAI at 800 cGy   1 (9)   1 (3)   2 (4)  
      VP-16/Ara-C/Cy/TBI at 1200 cGy   1 (9)   1 (3)   2 (4)  
      Other   0   2 (6)   2 (4)  
GVHD prophylaxis    
   CSA/MP, no. (%)   24 (57)   29 (56)   53 (56)  
      No. with/no. without ATG   3/21   12/17   15/38  
   CSA/MTX, no. (%)   9 (21)   8 (15)   17 (18)  
      No. with/no. without ATG   2/7   6/2   8/9  
   Other, no. (%)   9 (21)   15 (29)   24 (26)  
Graft manipulation by elutriation, no. yes/no. no
 
3/39
 
15/37
 
18/76
 

UCB indicates umbilical cord blood; Bu, busulfan; Cy, cyclophosphamide; TBI, total body irradiation; TLI, total lymphoid irradiation; TAI, total abdominal irradiation; VP-16, etoposide; Ara-C, cytosine arabinoside; CSA, cyclosporin; MP, methylprednisolone; and ATG, antithymocyte globulin.

*

Percentages were calculated only for patients with a known reason

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