GHSG trials, cHL patient characteristics, and association with serum Gal1 levels
. | Patients . | (%) . | Gal1 (ng/mL)* . | P value . |
---|---|---|---|---|
All patients | 293 | (100) | 93.0 ± 56.5 | |
Trial/risk group | .0002 | |||
HD13/favorable | 80 | (27.3) | 71.6 ± 39.7 | |
HD14/intermediate | 89 | (30.4) | 97.4 ± 54.3 | |
HD18/unfavorable | 124 | (42.3) | 103.7 ± 63.4 | |
Age | NS | |||
≥45 y | 65 | (22.2) | 62.8 ± 43.0 | |
<45 y | 228 | (77.8) | 90.4 ± 55.9 | |
Gender | NS | |||
Male | 156 | (53.2) | 92.8 ± 57.1 | |
Female | 137 | (46.8) | 89.6 ± 53.6 | |
Histologic type | NS | |||
Nodular sclerosis | 151 | (51.5) | 95.9 ± 55.9 | |
Mixed cellularity | 64 | (21.8) | 96.2 ± 60.9 | |
Lymphocyte rich | 12 | (4.1) | 79.1 ± 43.3 | |
Unclassified | 66 | (22.5) | 76.7 ± 43.8 | |
Ann Arbor stage | .012 | |||
I | 32 | (10.9) | 72.7 ± 42.0 | |
II | 151 | (51.5) | 88.9 ± 53.7 | |
III | 53 | (18.1) | 96.5 ± 45.8 | |
IV | 46 | (15.7) | 116.4 ± 76.5 | |
Unknown† | 11 | (3.8) | ||
B symptoms | .047 | |||
Absence | 168 | (57.3) | 85.3 ± 47.1 | |
Presence | 114 | (38.9) | 104.1 ± 67.1 | |
Unknown† | 11 | (3.8) | ||
IPS | .019 | |||
0 or 1 | 134 | (45.7) | 82.4 ± 44.0 | |
2-7 | 128 | (43.7) | 103.7 ± 66.0 | |
Unknown† | 31 | (10.6) | ||
Individual IPS risk factors | ||||
Extranodal involvement (stage IV) | .011 | |||
Absence | 249 | (85.0) | 89.2 ± 54.3 | |
Presence | 35 | (11.9) | 116.3 ± 67.2 | |
Unknown† | 9 | (3.1) | ||
Lymphocyte count, <600/mm3 or <8% of total white-cell count | .036 | |||
Absence | 269 | (91.8) | 91.2 ± 56.2 | |
Presence | 13 | (4.4) | 124.9 ± 62.9 | |
Unknown† | 11 | (3.8) | ||
Additional prognostic factors | ||||
Number of involved lymph node sites ≥3 | <.0001 | |||
Absence | 120 | (41.0) | 78.6 ± 49.0 | |
Presence | 165 | (56.3) | 102.7 ± 59.6 | |
Unknown† | 8 | (2.7) | ||
Elevated erythrocyte sedimentation rate (ESR) | .007 | |||
Absence | 148 | (50.5) | 82.1 ± 45.3 | |
Presence | 134 | (45.7) | 104.1 ± 65.6 | |
Unknown† | 11 | (3.8) |
. | Patients . | (%) . | Gal1 (ng/mL)* . | P value . |
---|---|---|---|---|
All patients | 293 | (100) | 93.0 ± 56.5 | |
Trial/risk group | .0002 | |||
HD13/favorable | 80 | (27.3) | 71.6 ± 39.7 | |
HD14/intermediate | 89 | (30.4) | 97.4 ± 54.3 | |
HD18/unfavorable | 124 | (42.3) | 103.7 ± 63.4 | |
Age | NS | |||
≥45 y | 65 | (22.2) | 62.8 ± 43.0 | |
<45 y | 228 | (77.8) | 90.4 ± 55.9 | |
Gender | NS | |||
Male | 156 | (53.2) | 92.8 ± 57.1 | |
Female | 137 | (46.8) | 89.6 ± 53.6 | |
Histologic type | NS | |||
Nodular sclerosis | 151 | (51.5) | 95.9 ± 55.9 | |
Mixed cellularity | 64 | (21.8) | 96.2 ± 60.9 | |
Lymphocyte rich | 12 | (4.1) | 79.1 ± 43.3 | |
Unclassified | 66 | (22.5) | 76.7 ± 43.8 | |
Ann Arbor stage | .012 | |||
I | 32 | (10.9) | 72.7 ± 42.0 | |
II | 151 | (51.5) | 88.9 ± 53.7 | |
III | 53 | (18.1) | 96.5 ± 45.8 | |
IV | 46 | (15.7) | 116.4 ± 76.5 | |
Unknown† | 11 | (3.8) | ||
B symptoms | .047 | |||
Absence | 168 | (57.3) | 85.3 ± 47.1 | |
Presence | 114 | (38.9) | 104.1 ± 67.1 | |
Unknown† | 11 | (3.8) | ||
IPS | .019 | |||
0 or 1 | 134 | (45.7) | 82.4 ± 44.0 | |
2-7 | 128 | (43.7) | 103.7 ± 66.0 | |
Unknown† | 31 | (10.6) | ||
Individual IPS risk factors | ||||
Extranodal involvement (stage IV) | .011 | |||
Absence | 249 | (85.0) | 89.2 ± 54.3 | |
Presence | 35 | (11.9) | 116.3 ± 67.2 | |
Unknown† | 9 | (3.1) | ||
Lymphocyte count, <600/mm3 or <8% of total white-cell count | .036 | |||
Absence | 269 | (91.8) | 91.2 ± 56.2 | |
Presence | 13 | (4.4) | 124.9 ± 62.9 | |
Unknown† | 11 | (3.8) | ||
Additional prognostic factors | ||||
Number of involved lymph node sites ≥3 | <.0001 | |||
Absence | 120 | (41.0) | 78.6 ± 49.0 | |
Presence | 165 | (56.3) | 102.7 ± 59.6 | |
Unknown† | 8 | (2.7) | ||
Elevated erythrocyte sedimentation rate (ESR) | .007 | |||
Absence | 148 | (50.5) | 82.1 ± 45.3 | |
Presence | 134 | (45.7) | 104.1 ± 65.6 | |
Unknown† | 11 | (3.8) |