Table 1.

Selected trials utilizing brentuximab vedotin in frontline therapy

RegimenNMedian follow-up (months)ORR/CRPFSReference
Advanced Stage  
ECHELON-1
BV-AVDx6
ABVDx6 
1334 73 BV-AVD: 86% ORR
ABVD: 83% ORR 
5-year: 82.2% BV-AVD
5-year: 75.3% ABVD 
Ansell et al
N Engl J Med 2022 
HD21
escBx4-6
BrECADDx4-6 
1500 40 escB: 80% CR
BrECADD: 82% CR 
3-year: 92.3% escB
3-year: 94.9% BrECADD 
Borchmann et al
Lancet 2024 
Early-stage  
BREACH
BV-AVDx4 + 30 Gy INRT
ABVDx4 + 30 Gy INRT 
170 45 BV-AVD: 87.6% CR
(8% missing data)
ABVD: 77.2% CR
(19% missing data) 
2-year: 97.3% BV-AVD
2-year: 92.6% ABVD 
Fornecker et al
J Clin Oncol 2023 
BV-AVDx4 +/- RT 117 46 96% CR 2-year: 94% Kumar et al
J Clin Oncol 2021 
BV-AVD  ×  4-6
Interim PET adapted 
34 14 88% CR 14-month: 90% Abramson et al
JCO 2015 (abstract) 
BV-ADx4-6
Interim PET adapted 
34 53 97% CR 5-year: 91% Abramson et al
Blood Advances 2023 
ABVDx2-6, BV  ×  6
Interim PET adapted 
41 47 95% CR 3-year: 92% Park et al
Blood Advances 2020 
Elderly or anthracycline-ineligible  
Sequential BV-AVD 48 23 95% ORR
93% CR 
2-year: 84% Evens et al
J Clin Oncol 2018 
BV-nivolumab 21 51.6 86% ORR
67% CR 
Not reached Friedberg et al
Blood 2024 
RegimenNMedian follow-up (months)ORR/CRPFSReference
Advanced Stage  
ECHELON-1
BV-AVDx6
ABVDx6 
1334 73 BV-AVD: 86% ORR
ABVD: 83% ORR 
5-year: 82.2% BV-AVD
5-year: 75.3% ABVD 
Ansell et al
N Engl J Med 2022 
HD21
escBx4-6
BrECADDx4-6 
1500 40 escB: 80% CR
BrECADD: 82% CR 
3-year: 92.3% escB
3-year: 94.9% BrECADD 
Borchmann et al
Lancet 2024 
Early-stage  
BREACH
BV-AVDx4 + 30 Gy INRT
ABVDx4 + 30 Gy INRT 
170 45 BV-AVD: 87.6% CR
(8% missing data)
ABVD: 77.2% CR
(19% missing data) 
2-year: 97.3% BV-AVD
2-year: 92.6% ABVD 
Fornecker et al
J Clin Oncol 2023 
BV-AVDx4 +/- RT 117 46 96% CR 2-year: 94% Kumar et al
J Clin Oncol 2021 
BV-AVD  ×  4-6
Interim PET adapted 
34 14 88% CR 14-month: 90% Abramson et al
JCO 2015 (abstract) 
BV-ADx4-6
Interim PET adapted 
34 53 97% CR 5-year: 91% Abramson et al
Blood Advances 2023 
ABVDx2-6, BV  ×  6
Interim PET adapted 
41 47 95% CR 3-year: 92% Park et al
Blood Advances 2020 
Elderly or anthracycline-ineligible  
Sequential BV-AVD 48 23 95% ORR
93% CR 
2-year: 84% Evens et al
J Clin Oncol 2018 
BV-nivolumab 21 51.6 86% ORR
67% CR 
Not reached Friedberg et al
Blood 2024 

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