Table 2.

Patient characteristics

No. of patients 206  
Prior to progression  
Primary histology  
 Nodular sclerosis 140  (68%) 
 Mixed cellularity 46  (22%)  
 Lymphocyte depleted 11  (5%)  
 Lymphocyte predominant 5  (3%) 
 Not classified 4  (2%)  
Front-line chemotherapy  
 COPP/ABVD 111  (54%) 
 COPP/ABV/IMEP 57  (28%)  
 BEACOPP (baseline) 31  (15%)  
 BEACOPP (escalated) 7  (3%)  
Prior radiotherapy 77  (37%)  
Remission attained before progression 148  (72%)  
At progression  
Median age (range) 34  (16-71)  
Gender  
 Male 112  (54%) 
 Female 94  (46%)  
Stage  
 I 24  (11%) 
 II 64  (31%)  
 III 37  (18%)  
 IV 81  (40%)  
B symptoms 97  (47%)  
Karnofsky performance score < 90 48  (23%)  
Time of progression  
 During first-line treatment 143  (70%)  
 During 90 d after first-line treatment 63  (30%)  
Sites of progression  
 Previously involved sites only 91  (44%)  
 New sites only 15  (7%) 
 Both 97  (47%)  
 Not known 3  (2%)  
After progression  
Salvage therapy  
 Chemotherapy 153  (74%)  
 Radiotherapy 47  (23%)  
 No further salvage therapy 6  (3%)  
Sensitivity to conventional salvage chemotherapy  
 Sensitive 66  (43%)  
 Resistant 87  (57%)  
High-dose chemotherapy  
 BEAM 38  (54%) 
 CVB 22  (31%)  
 Others 10  (15%) 
No. of patients 206  
Prior to progression  
Primary histology  
 Nodular sclerosis 140  (68%) 
 Mixed cellularity 46  (22%)  
 Lymphocyte depleted 11  (5%)  
 Lymphocyte predominant 5  (3%) 
 Not classified 4  (2%)  
Front-line chemotherapy  
 COPP/ABVD 111  (54%) 
 COPP/ABV/IMEP 57  (28%)  
 BEACOPP (baseline) 31  (15%)  
 BEACOPP (escalated) 7  (3%)  
Prior radiotherapy 77  (37%)  
Remission attained before progression 148  (72%)  
At progression  
Median age (range) 34  (16-71)  
Gender  
 Male 112  (54%) 
 Female 94  (46%)  
Stage  
 I 24  (11%) 
 II 64  (31%)  
 III 37  (18%)  
 IV 81  (40%)  
B symptoms 97  (47%)  
Karnofsky performance score < 90 48  (23%)  
Time of progression  
 During first-line treatment 143  (70%)  
 During 90 d after first-line treatment 63  (30%)  
Sites of progression  
 Previously involved sites only 91  (44%)  
 New sites only 15  (7%) 
 Both 97  (47%)  
 Not known 3  (2%)  
After progression  
Salvage therapy  
 Chemotherapy 153  (74%)  
 Radiotherapy 47  (23%)  
 No further salvage therapy 6  (3%)  
Sensitivity to conventional salvage chemotherapy  
 Sensitive 66  (43%)  
 Resistant 87  (57%)  
High-dose chemotherapy  
 BEAM 38  (54%) 
 CVB 22  (31%)  
 Others 10  (15%) 
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