Subcutaneous Epcoritamab in Combination with R 2 (Rituximab and Lenalidomide) in Patients with Relapsed or Refractory Follicular Lymphoma: Preliminary Results from a Phase 1/2 Trial

• Published in: BLOOD Vol. 138; no. Supplement 1; p. 3535
• Main Authors: Linton, Kim M, Wahlin, Björn, Leepä, Sirpa, Morschhauser, Franck, Elliot, Brian, Liu, Tracy, Cota Stirner, Mariana, Abbas, Aqeel, Falchi, Lorenzo
• Format: Journal Article Conference Proceeding
• Language: English
• Published: Elsevier Inc 23.11.2021
• Subjects: Medicin och hälsovetenskap
• ISSN: 0006-4971; 1528-0020
• DOI: 10.1182/blood-2021-146629

Background: Patients (pts) with relapsed or refractory (R/R) follicular lymphoma (FL) develop increasingly aggressive disease and are at increased risk for histologic transformation, death, or both. The combination of rituximab and lenalidomide (R 2) is a highly effective therapy for pts with R/R FL, but most pts eventually relapse, and better treatment options are needed. Epcoritamab (DuoBody ®-CD3×CD20) is a subcutaneously administered bispecific antibody that binds to CD3 on T cells and CD20 on B cells and induces conditional T-cell-mediated killing of malignant B cells. Single-agent epcoritamab demonstrated manageable safety and substantial antitumor activity in pts with heavily pretreated B-cell non-Hodgkin lymphoma (NHL) in the phase 1/2 EPCORE NHL-1 trial (NCT03625037). Among heavily pretreated pts with R/R FL (median, 5 prior lines of therapy) treated with epcoritamab (dose, 0.76-48 mg), the overall response rate was 90% (9/10), with 50% (5/10) achieving complete response (Hutchings, Lancet, in press). Treatment with R 2 has immunomodulatory properties that may potentiate the activity of epcoritamab, suggesting that combining R 2 with epcoritamab may be beneficial. The encouraging data from the EPCORE NHL-1 trial supported initiation of the EPCORE NHL-2 trial (NCT04663347), a phase 1/2 trial evaluating epcoritamab in combination with various standard of care therapies in pts with B-cell NHL. Herein, we present preliminary results from arm 2 of this trial, which is evaluating epcoritamab in combination with R 2 in pts with R/R FL. Methods: Adults with histologically confirmed R/R CD20+ FL received epcoritamab in a dose-escalation phase followed by an expansion phase at the recommended phase 2 dose in combination with R 2 for 12 cycles (28 days/cycle). Step-up dosing and corticosteroids during cycle 1 were used to mitigate cytokine release syndrome (CRS). Responses were evaluated by position emission tomography-computed tomography per the 2014 Lugano classification criteria. Results: As of June 29, 2021, 16 pts were treated with the combination of epcoritamab + R 2 (3 pts treated with epcoritamab 24 mg and 13 with 48 mg). Five pts completed at least 6 weeks of therapy and were evaluable for efficacy. A median of 3 cycles per pt have been administered. Fourteen (88%) pts remain on treatment. Median age was 68 years (range, 52-81), 10 (63%) pts were female, and 11 (69%) had 1 prior line of therapy (range in all 16 pts, 1-3 prior lines). All pts received prior immunochemotherapy, and 6 (38%) had disease progression ≤2 years after initial treatment (POD24). CRS occurred in 31% of pts (5/16) and all cases were of grade 1/2. The median time to onset of CRS was 15 days (study day 16; range, 5-16) and median time to resolution was 2 days; no pt required tocilizumab. Other adverse events (AEs) reported in >15% of pts were injection-site reaction (25%; 4/16), constipation (19%; 3/16), cough (19%; 3/16), diarrhea (19%; 3/16), and stomatitis (19%; 3/16), all grade 1/2. No immune effector cell-associated neurotoxicity syndrome events or fatal AEs were observed. Five (31%) pts required hospitalization due to 6 serious AEs (grade 1 CRS related to epcoritamab in 3 pts; unrelated grade 2 mania in 1 pt; unrelated grade 3 pneumonia in 1 pt; and unrelated grade 3 atrial flutter). All 5 response-evaluable pts achieved an objective response by week 7, with 4 achieving complete metabolic response. All 5 responders had stage IV disease at baseline, 3 had an FL International Prognostic Index of 4/5, 3 had received >2 prior lines of therapy, and 2 had POD24 with first-line therapy. Conclusions: These data from a small population of pts suggest that epcoritamab can be safely combined with R 2 with a manageable toxicity profile, with no new safety signals or unexpected AEs. The novel chemotherapy-free combination showed encouraging preliminary activity with early responses in all evaluable pts by week 7, including a majority of pts with high-risk features. Enrollment is ongoing. Additional data will be presented. Linton: Blood Cancer UK: Research Funding; Genmab: Consultancy, Research Funding; Roche: Consultancy, Honoraria, Research Funding, Speakers Bureau; Celgene: Membership on an entity's Board of Directors or advisory committees, Other: Travel support, Research Funding; Beigene: Research Funding; Aptitude Health: Honoraria, Speakers Bureau; Hartley Taylor: Honoraria, Speakers Bureau; Kite: Membership on an entity's Board of Directors or advisory committees; Karyopharm: Membership on an entity's Board of Directors or advisory committees; Roy Castle Lung Cancer Foundation: Research Funding; Janssen: Other: Travel support. Wahlin: Roche: Consultancy, Research Funding; Gilead Sciences: Research Funding. Leepä: MSD: Membership on an entity's Board of Directors or advisory committees; Roche: Membership on an entity's Board of Directors or advisory committees, Research Funding; Incyte: Honoraria, Membership on an entity's Board of Directors or advisory committees, Speakers Bureau; Gilead: Honoraria, Membership on an entity's Board of Directors or advisory committees, Speakers Bureau; Novartis: Honoraria, Membership on an entity's Board of Directors or advisory committees, Research Funding, Speakers Bureau; CHO Pharma USA: Consultancy; Orion: Consultancy; Genmab: Research Funding; University of Helsinki and Helsinki University Hospital: Current Employment; Takeda: Research Funding; Bayer: Research Funding; Celgene: Membership on an entity's Board of Directors or advisory committees, Research Funding; Nordic Nanovector: Research Funding; Finnish Cancer Organizations: Membership on an entity's Board of Directors or advisory committees. Morschhauser: Chugai: Honoraria; Epizyme: Consultancy, Membership on an entity's Board of Directors or advisory committees; Genentech, Inc.: Consultancy; Celgene: Membership on an entity's Board of Directors or advisory committees; Novartis: Consultancy, Membership on an entity's Board of Directors or advisory committees; Gilead: Consultancy, Membership on an entity's Board of Directors or advisory committees; Janssen: Honoraria; Incyte: Membership on an entity's Board of Directors or advisory committees; AstraZenenca: Membership on an entity's Board of Directors or advisory committees; BMS: Consultancy, Membership on an entity's Board of Directors or advisory committees; Genmab: Membership on an entity's Board of Directors or advisory committees; Roche: Consultancy, Speakers Bureau; AbbVie: Consultancy, Membership on an entity's Board of Directors or advisory committees; Servier: Consultancy; F. Hoffmann-La Roche Ltd: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees. Elliot: Genmab: Current Employment, Patents & Royalties: P158-US-PSP3 . Liu: Genmab: Current Employment. Cota Stirner: AbbVie: Current Employment. Abbas: Genmab: Current Employment. Falchi: Abbvie: Consultancy, Research Funding; Genetech: Research Funding; Roche: Research Funding; Genmab: Consultancy, Research Funding.