Epcoritamab in relapsed/refractory large B-cell lymphoma: 2-year follow-up from the pivotal EPCORE NHL-1 trial

  • Catherine Thieblemont*
  • , Yasmin H. Karimi
  • , Herve Ghesquieres
  • , Chan Y. Cheah
  • , Michael Roost Clausen
  • , David Cunningham
  • , Wojciech Jurczak
  • , Young Rok Do
  • , Robin Gasiorowski
  • , David John Lewis
  • , Tae Min Kim
  • , Marjolein van der Poel
  • , Michelle Limei Poon
  • , Tatyana Feldman
  • , Kim M. Linton
  • , Anna Sureda
  • , Martin Hutchings
  • , Minh H. Dinh
  • , Nurgul Kilavuz
  • , David Soong
  • Thomas Mark, Mariana Sacchi, Tycel Phillips, Pieternella J. Lugtenburg
*Kontaktforfatter

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

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Abstract

Primary results (median follow-up, 10.7 months) from the pivotal EPCORE® NHL-1 study in relapsed or refractory (R/R) large B-cell lymphoma (LBCL) demonstrated deep, durable responses with epcoritamab, a CD3xCD20 bispecific antibody, when used as monotherapy. We report long-term efficacy and safety results in patients with LBCL (N = 157; 25.1-month median follow-up). As of April 21, 2023, overall response rate was 63.1% and complete response (CR) rate was 40.1%. Estimated 24-month progression-free survival (PFS) and overall survival (OS) rates were 27.8% and 44.6%, respectively. An estimated 64.2% of complete responders remained in CR at 24 months. Estimated 24-month PFS and OS rates among complete responders were 65.1% and 78.2%, respectively. Of 119 minimal residual disease (MRD)-evaluable patients, 45.4% had MRD negativity, which correlated with longer PFS and OS. CR rates were generally consistent across predefined subgroups: 36% prior chimeric antigen receptor (CAR) T-cell therapy, 32% primary refractory disease, and 37% International Prognostic Index ≥3. The most common treatment-emergent adverse events were cytokine release syndrome (51.0%), pyrexia (24.8%), fatigue (24.2%), and neutropenia (23.6%). These results underscore the long-term benefit of epcoritamab for treating R/R LBCL with deep responses across subgroups, including patients with hard-to-treat disease and expected poor prognosis (ClinicalTrials.gov Registration: NCT03625037).

OriginalsprogEngelsk
TidsskriftLeukemia
Vol/bind38
Udgave nummer12
Sider (fra-til)2653-2662
ISSN0887-6924
DOI
StatusUdgivet - dec. 2024

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Publisher Copyright:
© The Author(s) 2024.

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