Table 3

Gene polymorphisms in the Hodgkin's lymphoma patients and in control subjects

GeneGenotype/phenotypeHodgkin patients
Controls
P
N%N%
UGT1A1 Missing or rare*   .18 
 66 148 48 71 39  
 67 130 42 89 49  
 77 31 10 21 12  
CYP3A4 Missing   1.00 
 AA 278 90 166 90  
 AG 29 17  
 GG  
GTPIE5 Missing   .99 
 AA 130 42 79 42  
 AG 141 45 85 45  
 GG 40 13 23 12  
GTT1 Missing   .67 
 48 15 31 17  
 264 85 153 83  
GSTM1 Missing   .35 
 164 53 105 57  
 148 47 79 43  
GeneGenotype/phenotypeHodgkin patients
Controls
P
N%N%
UGT1A1 Missing or rare*   .18 
 66 148 48 71 39  
 67 130 42 89 49  
 77 31 10 21 12  
CYP3A4 Missing   1.00 
 AA 278 90 166 90  
 AG 29 17  
 GG  
GTPIE5 Missing   .99 
 AA 130 42 79 42  
 AG 141 45 85 45  
 GG 40 13 23 12  
GTT1 Missing   .67 
 48 15 31 17  
 264 85 153 83  
GSTM1 Missing   .35 
 164 53 105 57  
 148 47 79 43  

Patients with rare or missing phenotypes were not included in the prognostic analyses. For GSTT1 and GSTM1, genotype is not available; the information 0 or 1 refers to the presence or the absence of gene expression.

*

Two missing and 2 rare phenotypes for UGT1A1 (1 phenotype 65, and 1 phenotype 75) in HD patients, 3 missing and 2 rare phenotypes (2 phenotypes 65, and 1 phenotype 86) in controls.

Comparison of the proportions of between Hodgkin patients and controls, Fisher exact test, patients with missing or rare genotypes/phenotypes excluded.

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