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Epcoritamab With R‑CHOP Cuts Progression Risk 51% in First‑Line DLBCL Trial

The phase 3 result could prompt regulatory submissions that reshape frontline treatment for patients with aggressive lymphoma

Test tubes are seen in front of a displayed Abbvie logo in this illustration taken, May 21, 2021. REUTERS/Dado Ruvic/Illustration/File Photo

Overview

  • Genmab and AbbVie reported that adding epcoritamab to standard R‑CHOP reduced the risk of disease progression or death by 51% versus R‑CHOP alone in a randomized phase 3 study of newly diagnosed diffuse large B‑cell lymphoma.
  • The trial met its primary goal in the higher‑risk group and showed the same 51% PFS benefit in the broader enrolled population, suggesting a consistent effect across patients with International Prognostic Index scores in the study range.
  • Epcoritamab is a bispecific, T‑cell engaging antibody that redirects a patient’s T cells to attack lymphoma cells and is jointly developed by Genmab and AbbVie.
  • The companies said the combination’s safety profile was generally consistent with known effects of epcoritamab and R‑CHOP, but detailed adverse‑event data were not included in the topline announcement.
  • Investors reacted quickly with Genmab shares jumping about 11% and AbbVie shares rising about 1.5%, and the companies said they will present the data at a future medical meeting and share results with health authorities, which could influence first‑line care if regulators review the full data.