Table 1.

Patient characteristics

CharacteristicN = 55
Age, median (range), y 36 (19-79) 
Male, n (%) 24 (43.6) 
White, n (%) 46 (83.6) 
ECOG status, n (%)  
 0 36 (65.5) 
 1 18 (32.7) 
 2 1 (1.8) 
Months since HL diagnosis, median (range) 13.8 (3-98) 
Disease stage at diagnosis, n (%)  
 I 3 (5.5) 
 II 23 (41.8) 
 III 14 (25.5) 
 IV 15 (27.3) 
Frontline therapy received, n (%)*  
 ABVD 50 (90.9) 
 Stanford V 3 (5.5) 
 AVD 1 (1.8) 
 VAMP 1 (1.8) 
Response to frontline therapy, n (%)  
 Primary refractory 28 (50.9) 
 Relapsed 27 (49.1) 
  CR > 1 y 17 
  CR ≤ 1 y 10 
Prior cancer-related radiotherapy, n (%) 15 (27.3) 
Baseline disease characteristics, n (%)  
 B symptoms 12 (21.8) 
 Bulky disease§ 5 (9.1) 
 Extranodal disease 17 (30.9) 
 Bone marrow involvement 9 (16.4) 
CharacteristicN = 55
Age, median (range), y 36 (19-79) 
Male, n (%) 24 (43.6) 
White, n (%) 46 (83.6) 
ECOG status, n (%)  
 0 36 (65.5) 
 1 18 (32.7) 
 2 1 (1.8) 
Months since HL diagnosis, median (range) 13.8 (3-98) 
Disease stage at diagnosis, n (%)  
 I 3 (5.5) 
 II 23 (41.8) 
 III 14 (25.5) 
 IV 15 (27.3) 
Frontline therapy received, n (%)*  
 ABVD 50 (90.9) 
 Stanford V 3 (5.5) 
 AVD 1 (1.8) 
 VAMP 1 (1.8) 
Response to frontline therapy, n (%)  
 Primary refractory 28 (50.9) 
 Relapsed 27 (49.1) 
  CR > 1 y 17 
  CR ≤ 1 y 10 
Prior cancer-related radiotherapy, n (%) 15 (27.3) 
Baseline disease characteristics, n (%)  
 B symptoms 12 (21.8) 
 Bulky disease§ 5 (9.1) 
 Extranodal disease 17 (30.9) 
 Bone marrow involvement 9 (16.4) 

ABVD, adriamycin, bleomycin, vinblastine, dacarbazine; AVD, adriamycin, vinblastine, dacarbacine; BEACOPP, bleomycin, etoposide, adriamycin, cyclophosphamide, vincristine, procarbazine, prednisone; CHOP, cyclophosphamide, adriamycin, vincristine, predinsone; GVD, gemcitabine, vinorelbine, doxorubicin; PD, progressive disease; PR, partial remission; SD, stable disease; VAMP, vinblastine, adriamycin, methotrexate, prednisone.

*

Number of cycles of frontline therapy was not determined.

One patient received GVD following ABVD, 1 patient received BEACOPP following ABVD, and 1 patient received ABVD following CHOP.

Response to frontline therapy among patients with primary refractory disease included PR (15 patients), PD (10 patients), SD (2 patients), and CR (1 patient).

§

As assessed per investigator.

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