-Author name in bold denotes the presenting author
-Asterisk * with author name denotes a Non-ASH member
Clinically Relevant Abstract denotes an abstract that is clinically relevant.

PhD Trainee denotes that this is a recommended PHD Trainee Session.

Ticketed Session denotes that this is a ticketed session.

4480 3-Year Update from the Epcore NHL-1 Trial: Epcoritamab Leads to Deep and Durable Responses in Relapsed or Refractory Large B-Cell Lymphoma

Program: Oral and Poster Abstracts
Session: 627. Aggressive Lymphomas: Pharmacologic Therapies: Poster III
Hematology Disease Topics & Pathways:
Research, Clinical trials, Lymphomas, Non-Hodgkin lymphoma, Bispecific Antibody Therapy, Clinical Research, B Cell lymphoma, Diseases, Aggressive lymphoma, Treatment Considerations, Biological therapies, Lymphoid Malignancies
Monday, December 9, 2024, 6:00 PM-8:00 PM

Julie M. Vose, MD, MBA1, Chan Y. Cheah, MBBS, DMSc2*, Michael Roost Clausen, MD, PhD3*, David Cunningham, MD, FRCP, FMedSci4*, Umar Farooq, MD5, Tatyana Feldman, MD6*, Herve Ghesquieres, MD, PhD7*, Wojciech Jurczak, MD, PhD8, Kim Linton9*, Catherine Thieblemont, MD10, Tycel J. Phillips, MD11, Won Seog Kim, MD, PhD12*, Pegah Jafarinasabian, MD, PhD13*, Barbara D'Angelo Månsson, PhD14*, David Soong, PhD15*, Andrew J. Steele, PhD15*, Zhu Li, MS15*, Christian Eskelund, MD, PhD15*, Martin Hutchings, MD, PhD16 and Yasmin H. Karimi, MD17

1University of Nebraska Medical Center, Omaha, NE
2Sir Charles Gairdner Hospital and the University of Western Australia, Nedlands, Australia
3Vejle Hospital, Vejle, Denmark
4Royal Marsden NHS Foundation Trust, London, United Kingdom
5University of Iowa, Iowa City, IA
6John Theurer Cancer Center at Hackensack Meridian Health, HMH School of Medicine, Hackensack, NJ
7Hospices Civils de Lyon, Centre Hospitalier Lyon Sud, Pierre-Bénite, France
8MSC National Research Institute of Oncology, Kraków, Poland
9The Christie NHS Foundation Trust, Manchester Cancer Research Centre, and Division of Cancer Sciences, University of Manchester, Manchester, United Kingdom
10Assistance Publique & Hôpitaux de Paris (APHP), Hôpital Saint-Louis, Hémato-oncologie, Université de Paris, Paris, France
11University of Michigan Comprehensive Cancer Center (present affiliation: City of Hope, Duarte, CA), Ann Arbor, MI
12Samsung Medical Center, Seoul, Korea, Republic of (South)
13AbbVie Inc, North Chicago, IL
14Genmab, Copenhagen, Denmark
15Genmab, Plainsboro, NJ
16Rigshospitalet and University of Copenhagen, Copenhagen, Denmark
17Division of Hematology/Oncology, University of Michigan, Ann Arbor, MI

Introduction: Epcoritamab monotherapy resulted in deep, durable responses with a manageable safety profile in patients with challenging-to-treat relapsed or refractory (R/R) large B-cell lymphoma (LBCL) in the pivotal phase 2 EPCORE® NHL-1 trial (NCT03625037). Here, we report 3‑y follow-up results, including long‑term efficacy and safety.

Methods: Adults with R/R CD20+ LBCL (including diffuse LBCL [DLBCL], high-grade B‑cell lymphoma, primary mediastinal large B-cell lymphoma, and follicular lymphoma [FL] grade [G] 3B) and ≥2 prior lines of systemic therapy were enrolled in the expansion phase of the study and treated with subcutaneous epcoritamab (0.16 mg and 0.8 mg step-up doses followed by 48-mg full doses) in 28-d cycles according to the approved dosing schedule: QW, cycles 1–3; Q2W, cycles 4–9; Q4W, cycles ≥10, until progressive disease or unacceptable toxicity. Corticosteroid prophylaxis was given during cycle 1. The primary endpoint was overall response rate (ORR) per Lugano criteria. Efficacy results presented here are based on investigators’ assessment. Minimal residual disease (MRD) was assessed based on the clonoSEQ® (Adaptive Biotechnologies) ctDNA assay.

Results: A total of 157 patients were treated with epcoritamab monotherapy. Median age was 64 y, 60% of patients were male, median number of prior lines of therapy was 3 (range, 2–11), and 61% had primary refractory disease; additional baseline characteristics have been presented previously. At data cutoff (May 3, 2024), 19 patients (12%) remained on treatment. Primary reasons for treatment discontinuation included progressive disease in 91 patients (58%) and adverse events (AEs) in 26 patients (17%); few patients who remained on epcoritamab ≥1 y progressed: 5/47 patients from >12 to ≤24 mo and 2/29 patients beyond 24 mo. The ORR and complete response (CR) rate per investigators were 59% and 41%; median follow-up was 37.1 mo (range, 0.3+ to 45.5). Median duration of response was 20.8 mo (95% CI, 13.0–32.0). Median duration of CR was 36.1 mo (95% CI, 20.2 to not reached [NR]). Median progression-free survival (PFS) was 4.2 mo (95% CI, 2.8–5.5); among complete responders, it was 37.3 mo (95% CI, 26.0–NR). Median overall survival (OS) was 18.5 mo (95% CI, 11.7–27.7); among complete responders, it was NR (95% CI, 36.4–NR). At 36 mo, an estimated 63% of complete responders remained alive. For patients with FL G3B (n=5) and patients with DLBCL transformed from FL (n=32), ORR/CR rates were 60%/60% and 50%/44%, respectively. Of the 119 overall patients who were MRD evaluable, 54 (45%) were MRD negative. In a cycle 3 day 1 landmark analysis, 36-mo rates of PFS/OS were 52%/55% among MRD-negative patients, and 18%/30% among MRD-positive patients. In an exploratory cycle 13 day 1 evaluation, 98% (40/41) of MRD-evaluable patients were MRD negative. There were 15 patients with CR who had a temporary epcoritamab hold for >6 wk (primarily due to AEs; median, 70.5 d, range, 48–257 d); all maintained their response at their next imaging assessment following treatment reinitiation. Of these patients, 6 had post-reinitiation MRD samples available, all of which were MRD negative. The most common treatment-emergent AEs (TEAEs) remained CRS (51%; 32% G1, 16% G2, 3% G3), fatigue (25%), and pyrexia (25%); CRS rates remained unchanged since prior reports. Fatal TEAEs were reported in 20 patients; 10 patients had G5 COVID-19 (including COVID-19 pneumonia). Rates of G≥3 infections were stable over time with rates within 3%–17% for 12-wk study intervals up to wk 144. Incidence of G≥3 cytopenias was highest (27%) during the first 8 wks of treatment and rates were within 0%–13% in subsequent 12‑wk time periods up to wk 144. Immunoglobulin G levels decreased by a median of ~20% after the start of epcoritamab treatment (baseline median, 540.0 mg/dL) and remained stable over time.

Conclusions: With a 3-year follow-up, epcoritamab continued to show deep and durable responses, with more than half of complete responders remaining in remission at 3 years: median duration of CR, 36.1 mo. Sustained MRD negativity was observed. Long-term safety was consistent with prior reports. These results with extended follow-up support the value of epcoritamab monotherapy as an effective and potentially curative therapy for patients with challenging-to-treat R/R LBCL.

Disclosures: Vose: Novartis: Honoraria; GenMab: Honoraria, Research Funding; Abbvie: Honoraria, Research Funding; Pfizer: Research Funding. Cheah: Roche: Other: Travel Expenses; BMS, Roche, AbbVie: Research Funding; Roche, Janssen, MSD, Gilead, Ascentage Pharma, AstraZeneca, Lilly, TG Therapeutics, BeiGene, Novartis, BMS: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees. Clausen: Genmab: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees, Other: Travel Expenses; Incyte: Consultancy, Honoraria; AstraZeneca: Consultancy, Honoraria, Other: Travel Expenses; Gilead: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees; Janssen: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees, Other: Travel Expenses; AbbVie: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees, Other: Travel Expenses; Roche: Consultancy, Honoraria, Other: Travel Expenses; Pfizer: Other: Travel Expenses. Cunningham: Clovis, Eli Lilly, 4SC, Bayer, Celgene, Roche: Research Funding. Farooq: Caribou, Gilead/Kite: Honoraria; Caribou, MorphoSys: Consultancy; Regeneron: Research Funding. Feldman: AbbVie, AstraZeneca, Epizyme, Genmab, Gilead/Kite, Karyopharm, Takeda: Consultancy; Seagen: Consultancy, Speakers Bureau. Ghesquieres: Gilead, Roche, BMS, Abbvie, Takeda: Honoraria; Roche, BMS, Takeda: Consultancy. Jurczak: BeiGene: Consultancy, Research Funding; Regeneron: Consultancy, Research Funding; Janssen Cilag: Consultancy, Research Funding; AstraZeneca: Consultancy, Research Funding; Lilly: Consultancy, Research Funding; AbbVie: Consultancy, Research Funding; Roche: Consultancy, Research Funding; Takeda: Consultancy, Research Funding; MSD: Research Funding; Merck: Research Funding. Linton: Kite/Gilead: Consultancy, Research Funding; Genmab: Consultancy, Other: Member of the Epcoritamab Global Council, Research Funding; Roche: Consultancy, Research Funding; AbbVie: Consultancy, Research Funding, Speakers Bureau; BeiGene: Consultancy, Research Funding; BMS: Consultancy, Other: Travel Expenses, Research Funding, Speakers Bureau; ADC Therapeutics: Research Funding; AstraZeneca: Research Funding; CellCentric: Research Funding; Janssen: Research Funding; MorphoSys: Research Funding; MSD: Research Funding; Nurix: Research Funding; Regeneron: Research Funding; Step Pharma: Research Funding; Viracta: Research Funding; Celgene: Consultancy, Other: Travel Expenses, Research Funding, Speakers Bureau. Thieblemont: AstraZeneca: Honoraria; ADC Therapeutics: Honoraria; Incyte Corporation: Consultancy, Honoraria, Speakers Bureau; Sanofi: Honoraria; Novartis: Consultancy, Honoraria, Other: Travel and accommodation, Speakers Bureau; Cellectis: Honoraria; Janssen: Consultancy, Honoraria, Other: Travel and accommodation, Research Funding, Speakers Bureau; Bayer: Consultancy, Honoraria, Other: Travel and accommodation, Speakers Bureau; Roche: Consultancy, Honoraria, Other: Travel and accommodation, Research Funding, Speakers Bureau; BeiGene: Consultancy, Honoraria; AbbVie: Consultancy, Honoraria, Other: Travel and accommodations, Research Funding, Speakers Bureau; Bristol Myers Squibb/Celgene: Consultancy, Honoraria, Other: Travel and accommodation, Speakers Bureau; Takeda: Consultancy, Honoraria, Other: Travel and Accommodation, Speakers Bureau; Kite/Gilead: Consultancy, Honoraria, Other: Travel and accommodation, Research Funding, Speakers Bureau; Amgen: Consultancy, Honoraria, Other: Travel and accommodation, Speakers Bureau; University of Paris: Current Employment, Ended employment in the past 24 months; Regeneron: Consultancy, Honoraria. Phillips: AbbVie, Pharmacyclics/Janssen, Bayer: Other: Scholar in Clinical Research of The Leukemia & Lymphoma Society, Research Funding; Genentech, a member of the Roche Group.: Membership on an entity's Board of Directors or advisory committees; Seattle Genetics, Lymphoma & Myeloma Connect: Honoraria; AbbVie Inc, Genentech, a member of the Roche Grou: Research Funding; AbbVie Inc, ADC Therapeutics, AstraZeneca Pharmaceuticals LP, Bayer HealthCare Pharmaceuticals, BeiGene Ltd, Bristol Myers Squibb, Epizyme Inc, Genentech, a member of the Roche Group, Genmab US Inc, Gilead Sciences Inc, Incyte Corporation, Lilly, Pharmacy: Consultancy; AbbVie Inc, Genentech, a member of the Roche Group, Genmab US Inc, Merc: Membership on an entity's Board of Directors or advisory committees. Kim: Sanofi, BeiGene, Boryung, F. Hoffmann-La Roche Ltd, Kyowa Kirin, Dong-A: Research Funding. Jafarinasabian: AbbVie: Current Employment, Other: stockholder of AbbVie. D'Angelo Månsson: Genmab: Current Employment. Soong: Genmab: Current Employment, Current equity holder in publicly-traded company. Steele: Genmab: Current Employment, Other: owns Genmab stock; Janssen: Other: owns Janssen stock; AbbVie: Other: owns AbbVie stock. Li: Genmab: Current Employment. Eskelund: Genmab: Current Employment. Hutchings: BMS/Celgene: Honoraria, Membership on an entity's Board of Directors or advisory committees, Research Funding; AstraZeneca: Membership on an entity's Board of Directors or advisory committees, Research Funding; Takeda: Honoraria, Membership on an entity's Board of Directors or advisory committees, Research Funding; AbbVie: Honoraria, Membership on an entity's Board of Directors or advisory committees, Research Funding; Genmab: Honoraria, Membership on an entity's Board of Directors or advisory committees, Research Funding; Genentech: Research Funding; Incyte: Research Funding; Janssen/J&J: Honoraria, Membership on an entity's Board of Directors or advisory committees, Research Funding; Merck: Honoraria, Membership on an entity's Board of Directors or advisory committees; Novartis: Research Funding. Karimi: Merck: Research Funding; AstraZeneca: Research Funding; Xencor: Research Funding; Roche/Genentech: Other: Travel Expenses, Research Funding; AbbVie: Consultancy, Honoraria, Research Funding; ADC Therapeutics: Consultancy, Honoraria; Lilly/Loxo: Research Funding.

*signifies non-member of ASH