TY - JOUR
T1 - Camidanlumab tesirine for relapsed or refractory classic Hodgkin lymphoma
T2 - a phase 2 study
AU - Herrera, Alex F.
AU - Ansell, Stephen M.
AU - Zinzani, Pier Luigi
AU - Radford, John
AU - Maddocks, Kami
AU - Pinto, Antonio
AU - Collins, Graham P.
AU - Bachanova, Veronika
AU - Bartlett, Nancy L.
AU - Bence-Bruckler, Isabelle
AU - Hamadani, Mehdi
AU - Kline, Justin
AU - Mayer, Jiří
AU - Savage, Kerry J.
AU - Advani, Ranjana H.
AU - Caimi, Paolo F.
AU - Casasnovas, René Olivier
AU - Feldman, Tatyana
AU - Hess, Brian
AU - Bastos-Oreiro, Mariana
AU - Iyengar, Sunil
AU - Szomor, Árpád
AU - Townsend, William
AU - André, Marc
AU - Dyczkowski, Jerzy
AU - Havenith, Karin
AU - Toukam, Marie
AU - Pantano, Serafino
AU - Cruz, Hans G.
AU - Wang, Luqiang
AU - Negievich, Yanina
AU - Lucero, Melanie
AU - Wuerthner, Jens
AU - Carlo-Stella, Carmelo
N1 - Publisher Copyright:
© 2025 The American Society of Hematology
PY - 2025/12/9
Y1 - 2025/12/9
N2 - Outcomes in classic Hodgkin lymphoma (cHL) have steadily improved; however, additional therapies are needed for patients who relapse or do not respond to novel agents. Here, we report the efficacy and safety of camidanlumab tesirine (Cami), an anti-CD25 antibody-drug conjugate, in patients with relapsed/refractory cHL after brentuximab vedotin/programmed cell death protein 1 inhibitor therapies from the phase 2 ADCT-301-201 study. Eligible patients were adults with cHL who had received ≥3 previous lines of systemic therapy (or ≥2 if ineligible for hematopoietic stem cell transplant). Patients received 45 μg/kg Cami (IV, once every 3 weeks) in cycles 1 to 2, followed by 30 μg/kg IV once every 3 weeks for ≤1 year. The primary end point was overall response rate (ORR) per 2014 Lugano classification. Secondary end points included complete response rate (CRR), progression-free survival (PFS), and overall survival (OS). In total, 117 patients were enrolled with a median age of 37.0 years (range, 19-87). The ORR was 70.1% (95% confidence interval [CI], 60.9-78.2), with a CRR of 33.3% (95% CI, 24.9-42.6). The median PFS was 9.13 months (95% CI, 5.3-15.0); median OS was not reached. Thirty-three (28.2%) patients discontinued treatment because of treatment-emergent adverse events; the most common reasons were skin and subcutaneous tissue disorders (n = 10 [8.5%] patients), infections and infestations (n = 5 [4.3%]), and nervous systems disorders (n = 5 [4.3%]). Guillain-Barré–type or polyradiculopathy-type events occurred in 8 (6.8%) patients. Cami was efficacious in this heavily pretreated population; however, the efficacy was overshadowed by substantial issues with the safety profile. This trial was registered at www.clinicaltrials.gov as #NCT04052997.
AB - Outcomes in classic Hodgkin lymphoma (cHL) have steadily improved; however, additional therapies are needed for patients who relapse or do not respond to novel agents. Here, we report the efficacy and safety of camidanlumab tesirine (Cami), an anti-CD25 antibody-drug conjugate, in patients with relapsed/refractory cHL after brentuximab vedotin/programmed cell death protein 1 inhibitor therapies from the phase 2 ADCT-301-201 study. Eligible patients were adults with cHL who had received ≥3 previous lines of systemic therapy (or ≥2 if ineligible for hematopoietic stem cell transplant). Patients received 45 μg/kg Cami (IV, once every 3 weeks) in cycles 1 to 2, followed by 30 μg/kg IV once every 3 weeks for ≤1 year. The primary end point was overall response rate (ORR) per 2014 Lugano classification. Secondary end points included complete response rate (CRR), progression-free survival (PFS), and overall survival (OS). In total, 117 patients were enrolled with a median age of 37.0 years (range, 19-87). The ORR was 70.1% (95% confidence interval [CI], 60.9-78.2), with a CRR of 33.3% (95% CI, 24.9-42.6). The median PFS was 9.13 months (95% CI, 5.3-15.0); median OS was not reached. Thirty-three (28.2%) patients discontinued treatment because of treatment-emergent adverse events; the most common reasons were skin and subcutaneous tissue disorders (n = 10 [8.5%] patients), infections and infestations (n = 5 [4.3%]), and nervous systems disorders (n = 5 [4.3%]). Guillain-Barré–type or polyradiculopathy-type events occurred in 8 (6.8%) patients. Cami was efficacious in this heavily pretreated population; however, the efficacy was overshadowed by substantial issues with the safety profile. This trial was registered at www.clinicaltrials.gov as #NCT04052997.
UR - https://www.scopus.com/pages/publications/105018647055
U2 - 10.1182/bloodadvances.2024015600
DO - 10.1182/bloodadvances.2024015600
M3 - Article
C2 - 40811783
AN - SCOPUS:105018647055
SN - 2473-9529
VL - 9
SP - 6205
EP - 6217
JO - Blood Advances
JF - Blood Advances
IS - 23
ER -