Skip to main content
. Author manuscript; available in PMC: 2022 Aug 1.
Published in final edited form as: Lancet Haematol. 2021 Aug;8(8):e562–e571. doi: 10.1016/S2352-3026(21)00170-8

Table 1.

Patient characteristics

Characteristic N = 45

Age, median (range) 31 (20–60)

Male, n (%) 16 (36%)

Stage at Diagnosis, n (%)
I 3 (7%)
II 24 (53%)
III 6 (13%)
IV 12 (27%)

Stage at Enrollment, n (%)
I 6 (13%)
II 22 (49%)
III 6 (13%)
IV 11 (24%)

Primary therapy received, n (%)
ABVD/AVD 43 (96%)
ABVE-PC 1 (2%)
Stanford V 1 (2%)

Prior consolidative radiotherapy, n (%) 8 (18%)

Baseline disease characteristics, n (%)
B symptoms at diagnosis 18 (40%)
Extranodal disease at diagnosis 12 (27%)
Spleen involved at diagnosis 7 (16%)

Response to frontline therapy, n (%)
Primary Refractory* 29 (64%)
Relapse 3–12 months after treatment completion 8 (18%)
Relapse > 12 months after treatment completions 8 (18%)

Relapse disease characteristics, n (%)
B symptoms at relapse 1 (2%)
Extranodal involvement at relapse 11 (24%)
Spleen involvement at relapse 4 (9%)
*

For patients with progression within 3 months, best response (including interim PET) to frontline therapy for patients with primary refractory disease includes: PD (1 patient), PR (14 patients), and CR (14 patients)

ABVD: Doxorubicin, bleomycin, vinblastine, dacarbazine

AVD: Doxorubicin, vinblastine, dacarbazine

ABVD/AVD: No patient received AVD alone. However, this group includes patients who received ABVD alone as well as those who initiated ABVD and subsequently omitted bleomycin and finished their primary treatment with AVD

ABVE-PC: doxorubicin, bleomycin, vincristine, etoposide, prednisone, cyclophosphamide