Skip to main content
. 2016 Oct 30;8(1):13–20. doi: 10.1177/2040620716676256

Table 1.

Patient characteristics.

All patients
(n = 167)
Typical NS
(n = 124)
SV
(n = 43)
Age, years 31 30 31
Median, range 17–75 17–75 20–53
Male 85 (50%) 60 (58%) 25 (48%)
ECOG 0–1 161 (96%) 119 (97%) 42 (96%)
Stage (III/IV) 65 (39%) 48 (38%) 17 (41%)
>3 node site 44 (26%) 34 (27%) 10 (23%)
⩽3 78 (47%) 59 (48%) 19 (44%)
N/A 45 (27%) 31 (25%) 14 (33%)
B symptoms 82 (49%) 57 (46%) 26 (60%)
Bulky 41 (25%) 31 (25%) 10 (23%)
Nonbulky 91 (55%) 70 (56%) 21 (49%)
N/A 35 (20%) 23 (19%) 12 (28%)
Treatment
 ABVD 152 (91%) 113 (91%) 39 (91%)
 Stanford V 4 (2.5%) 3 (2.5%) 1 (2%)
 COPP/ABV 6 (3.5%) 3 (2.5%) 3 (7%)
 Other* 5 (3%) 5 (4%)
 XRT 62 (38%) 45 (36.8%) 17 (43%)
 HDT/ASCT 44 (27%) 28 (23%) 16 (37%)
 No ASCT 114 (68%) 93 (75%) 21 (49%)
 N/A 9 (5%) 3 (2%) 6 (14%)
*

Other, ABV, AVD, COPP and MOPP/ABV.

p = 0.07; p = 0.016.

ABV, doxorubicin, bleomycin and vinblastine; ABVD, adriamycin, bleomycin, vinblastine, dacarbazine; ASCT, autologous stem cell transplant; AVD, doxorubicin, vinblastine and dacarbazine; COPP, cyclophosphamide, vincristine, procarbazine and prednisone; HDT, high dose therapy; MOPP, mechlorethamine, vincristine, procarbazine and prednisone; N/A, not available; NS, nodular sclerosis; Stanford V, doxorubicin, vinblastine, mechlorethamine, vincristine, bleomycin, etoposide, and prednisone; SV, syncytial variant; XRT, radiation.