Table 1

Clinical and pathologic characteristics of 29 patients with CHL studied by GEP of microdissected HRS cells

Treatment success (no progression or relapse)Treatment failure (progression or relapse)P
15 14  
Median age, y 41 35 NS 
Sex, male, % 60 72 NS 
Histology   NS 
    Nodular sclerosis 14 12  
    Mixed cellularity  
    Lymphocyte-rich  
    Lymphocyte-depleted  
    NOS (not classifiable)  
Stage, %   .082 
    I 13  
    II 60 29  
    III 20 43  
    IV 29  
B-symptoms, % 13 43 .075 
Median mass size, cm 6.6 6.6 NS 
    ≥ 10 cm, % 27 29 NS 
High risk, IPS ≥ 4, % 20 14 NS 
Primary treatment   NS 
    ABVD type ± radiation, % 93 93  
    Extended field radiation alone, %  
Treatment success (no progression or relapse)Treatment failure (progression or relapse)P
15 14  
Median age, y 41 35 NS 
Sex, male, % 60 72 NS 
Histology   NS 
    Nodular sclerosis 14 12  
    Mixed cellularity  
    Lymphocyte-rich  
    Lymphocyte-depleted  
    NOS (not classifiable)  
Stage, %   .082 
    I 13  
    II 60 29  
    III 20 43  
    IV 29  
B-symptoms, % 13 43 .075 
Median mass size, cm 6.6 6.6 NS 
    ≥ 10 cm, % 27 29 NS 
High risk, IPS ≥ 4, % 20 14 NS 
Primary treatment   NS 
    ABVD type ± radiation, % 93 93  
    Extended field radiation alone, %  

NS indicates not significant.

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