Table 1.

Patient-, disease-, and transplant-related characteristics of patients with HL or NHL who underwent allo-HSCT following relapse after autologous transplantation, 1990 to 1999, reported to IBMTR


Variables

N(%)*
N   114  
Age, y, median (range)   34 (15-65) 
Male   65 (57)  
Karnofsky performance score at allo-HSCT  
   90%-100%   64 (56)  
   80%   29 (25)  
   70%   16 (14)  
   60%   2 (2)  
   50% or lower   3 (3)  
Disease type  
   NHL   79 (69)  
      Low grade   16 (20)  
      Intermediate grade   44 (56)  
      High grace   8 (10)  
      Other  11 (14)  
   HL   35 (31)  
Interval from diagnosis to first, autologous, transplantation, mo, median (range)  14 (3-130) 
   12 or less   43 (38)  
   More than 12   71 (62)  
Interval from auto-HSCT to allo-HSCT, mo, median (range)  16 (2-66) 
   12 or less   44 (39)  
   More than 12   70 (61)  
Disease status before allo-HSCT  
   Complete remission   24 (21)  
   Relapse or persistent disease, chemosensitive   39 (35)  
   Relapse or persistent disease, chemoresistant   23 (20)  
   Relapse or persistent, untreated after auto-HSCT   28 (24)  
Donor type for allo-HSCT  
   HLA-identical sibling   70 (61)  
   Haploidentical sibling   17 (14)  
   Unrelated   27 (25)  
Graft type used for allo-HSCT  
   Bone marrow   77 (68)  
   Peripheral blood   37 (32)  
TBI for allo-HSCT   45 (39)  
Posttransplantation use of growth factors, within 7 d   84 (74)  
GVHD prophylaxis  
   MTX + CSA ± others   74 (65)  
   CSA ± others   24 (21)  
   T-cell depletion ± others   16 (14)  
Years of allo-HSCT  
   1990-1996   56 (49)  
   1997-1999   58 (51)  
No. centers reporting   54  
Follow-up time of survivors, mo, median (range)  43 (3-89) 
   75th percentile   21  
   25th percentile
 
58
 

Variables

N(%)*
N   114  
Age, y, median (range)   34 (15-65) 
Male   65 (57)  
Karnofsky performance score at allo-HSCT  
   90%-100%   64 (56)  
   80%   29 (25)  
   70%   16 (14)  
   60%   2 (2)  
   50% or lower   3 (3)  
Disease type  
   NHL   79 (69)  
      Low grade   16 (20)  
      Intermediate grade   44 (56)  
      High grace   8 (10)  
      Other  11 (14)  
   HL   35 (31)  
Interval from diagnosis to first, autologous, transplantation, mo, median (range)  14 (3-130) 
   12 or less   43 (38)  
   More than 12   71 (62)  
Interval from auto-HSCT to allo-HSCT, mo, median (range)  16 (2-66) 
   12 or less   44 (39)  
   More than 12   70 (61)  
Disease status before allo-HSCT  
   Complete remission   24 (21)  
   Relapse or persistent disease, chemosensitive   39 (35)  
   Relapse or persistent disease, chemoresistant   23 (20)  
   Relapse or persistent, untreated after auto-HSCT   28 (24)  
Donor type for allo-HSCT  
   HLA-identical sibling   70 (61)  
   Haploidentical sibling   17 (14)  
   Unrelated   27 (25)  
Graft type used for allo-HSCT  
   Bone marrow   77 (68)  
   Peripheral blood   37 (32)  
TBI for allo-HSCT   45 (39)  
Posttransplantation use of growth factors, within 7 d   84 (74)  
GVHD prophylaxis  
   MTX + CSA ± others   74 (65)  
   CSA ± others   24 (21)  
   T-cell depletion ± others   16 (14)  
Years of allo-HSCT  
   1990-1996   56 (49)  
   1997-1999   58 (51)  
No. centers reporting   54  
Follow-up time of survivors, mo, median (range)  43 (3-89) 
   75th percentile   21  
   25th percentile
 
58
 

MTX indicates methotrexate; CSA, cyclosporine.

*

Categorical variable

Continuous variable

Includes NHL composite, mantle cell, and peripheral T-cell lymphomas

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