Table 1.

Results of adoptive immunotherapy clinical trials in Hodgkin lymphoma

TherapyReferencePhasePatients, nLymphodepletionResponseMost common toxicities
EBV-specific T cells Bollard et al38  14 None Active disease cohort: ORR 27%; PR 9%; CR 18%; SD 45%. Cohort in remission: 100% disease-free at 10- to 40-mo follow-up Transient flu-like symptoms (14%) 
LMP-1/2 specific T cells Bollard et al37  50 None Active disease cohort: ORR 62%; CR 52%; PR 10%; cohort in remission: 2 y EFS 82% No treatment-related toxicities, although 2 possible inflammatory responses 
LMP-1/2 specific T cells with DNRII Bollard et al40  None Active disease cohort: ORR 43%; PR 14%; SD 57%; patient in remission (n = 1): durable CR up to 2+ years No treatment-related toxicities 
Allogeneic LMP-1/2 specific T cells McLaughlin et al44  26 None Active disease: CR 0%; PR 28%; OS of 43% at 2 y; cohort in remission: 2 y EFS 57% at 2 y; 2-y OS 78% Grade 4 hepatic necrosis in 1/26 (4%) 
CD30 CAR T cells Wang et al52  18 Fludarabine and cyclophosphamide; gemcitabine, mustargen, and cyclophosphamide; or ab-paclitaxel and cyclophosphamide ORR: 39%; CR: 0%; PR: 39%; SD: 33%. PFS: 6 mo (range: 3-14 mo) Nausea and vomiting (28%), rash (11%), joint swelling (6%), dizziness (6%), and pneumonitis (6%) 
CD30 CAR T cells Ramos et al53  None ORR: 33%; CR: 33%; SD: 33%; PD: 33%; durable CR up to 2.5+ years No treatment-related toxicities 
CD30 CAR T cells Ramos et al54  1/2 41 Bendamustine; bendamustine and fludarabine; or cyclophosphamide and fludarabine No responses with bendamustine-alone lymphodepletion cohort; responses with fludarabine-based regimen (n = 32): ORR 72%; CR 59%; PR 13%; SD 9%; PD 19% Rash (48%); grade 1 CRS (24%); grade 3/4 leukopenia (57%), anemia (12%), neutropenia (48%), and thrombocytopenia (26%) 
CD19 CAR T cells Svoboda et al58  Early phase 1 Cyclophosphamide ORR: 50%; CR 25%; PR 25%; SD 25%; PD 25%; at 3 mo, 3/4 had PD and the remainder was taken off trial Fatigue (75%), headache (75%), confusion (50%); no grade 3 or 4 toxicities 
TherapyReferencePhasePatients, nLymphodepletionResponseMost common toxicities
EBV-specific T cells Bollard et al38  14 None Active disease cohort: ORR 27%; PR 9%; CR 18%; SD 45%. Cohort in remission: 100% disease-free at 10- to 40-mo follow-up Transient flu-like symptoms (14%) 
LMP-1/2 specific T cells Bollard et al37  50 None Active disease cohort: ORR 62%; CR 52%; PR 10%; cohort in remission: 2 y EFS 82% No treatment-related toxicities, although 2 possible inflammatory responses 
LMP-1/2 specific T cells with DNRII Bollard et al40  None Active disease cohort: ORR 43%; PR 14%; SD 57%; patient in remission (n = 1): durable CR up to 2+ years No treatment-related toxicities 
Allogeneic LMP-1/2 specific T cells McLaughlin et al44  26 None Active disease: CR 0%; PR 28%; OS of 43% at 2 y; cohort in remission: 2 y EFS 57% at 2 y; 2-y OS 78% Grade 4 hepatic necrosis in 1/26 (4%) 
CD30 CAR T cells Wang et al52  18 Fludarabine and cyclophosphamide; gemcitabine, mustargen, and cyclophosphamide; or ab-paclitaxel and cyclophosphamide ORR: 39%; CR: 0%; PR: 39%; SD: 33%. PFS: 6 mo (range: 3-14 mo) Nausea and vomiting (28%), rash (11%), joint swelling (6%), dizziness (6%), and pneumonitis (6%) 
CD30 CAR T cells Ramos et al53  None ORR: 33%; CR: 33%; SD: 33%; PD: 33%; durable CR up to 2.5+ years No treatment-related toxicities 
CD30 CAR T cells Ramos et al54  1/2 41 Bendamustine; bendamustine and fludarabine; or cyclophosphamide and fludarabine No responses with bendamustine-alone lymphodepletion cohort; responses with fludarabine-based regimen (n = 32): ORR 72%; CR 59%; PR 13%; SD 9%; PD 19% Rash (48%); grade 1 CRS (24%); grade 3/4 leukopenia (57%), anemia (12%), neutropenia (48%), and thrombocytopenia (26%) 
CD19 CAR T cells Svoboda et al58  Early phase 1 Cyclophosphamide ORR: 50%; CR 25%; PR 25%; SD 25%; PD 25%; at 3 mo, 3/4 had PD and the remainder was taken off trial Fatigue (75%), headache (75%), confusion (50%); no grade 3 or 4 toxicities 

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