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%) |