MRD-Directed Consolidation With Epcor-only or Epcor-R2 Post Anti-CD19 CAR TCell Therapy for Large B-Cell Lymphoma

Patients who have received CAR T-cell therapy for Relapsed/Refractory Large B-Cell Lymphoma, are in Complete Metabolic Response (CMR) or Partial Metabolic Response (PMR) and MRD positive post CAR T-cell infusion are potentially eligible. Once these patients have provided their consent, they will enter the screening phase. All events of Cytokine Release Syndrome (CRS), Haemophagocytic Lymphohistiocytosis (HLH)/Macrophage Activation Syndrome (MAS), Immune-Effector Cell Associated Neurologic Syndrome (ICANS), or infection must have completely resolved. Additionally, patients must have adequate organ and haematological function, and an ECOG performance status of up to 2.

Patients deemed eligible for the study will be randomised to receive Epcor-only (Arm A) or Epcor-R2 (Arm B) for 6 cycles. The primary endpoint is CMR by Lugano 2014 criteria at month 12 post CAR T-cell infusion.

Patients will undergo an interim response assessment after 2 cycles of treatment. Patients that complete the full 6 cycles of treatment or that discontinue treatment for any reason will have an End of Treatment visit and a Safety Follow-up visit at 60 days after Day 1 of Cycle 6. Patients with non-Progressive Disease (PD) then enter the follow-up phase of the study where they will undergo response assessments at month 12, 15, 18 and 24 after CAR T-cell infusion. Patients with PD at any time will complete a Progression visit. Patients that have completed the month 24 Follow-up visit or that they have progressed will be followed for survival and new anti-lymphoma therapy only. All patients will be followed for 2 years after the last patient randomised received the CAR T-cell infusion.

Inclusion criteria

• Age ≥ 16 years old at the time of signing the patient information and consent form (PICF)
• Eastern Cooperative Oncology Group (ECOG) performance status of 0-2
• A diagnosis of relapsed/refractory large B-cell lymphoma
• Received Therapeutic Good Administration (TGA) approved anti-CD19 CAR T-cell therapy as the most recent large B-cell lymphoma treatment.
• Partial metabolic response (PMR) or complete metabolic response (CMR) as per the Lugano criteria on the most recent PET/CT performed at any point between Day +25 and Day +100 post CAR T-cell infusion, when compared with the most recent PET/CT prior to CAR T-cell infusion.
• MRD positive by a ctDNA assay on a blood sample taken at any point between Day +25 and Day +100 post CAR T-cell infusion.
• Adequate haematological function documented within 7 days prior to randomisation
• Adequate cardiac function.
• Adequate renal function, documented within 7 days prior to randomisation
• Adequate hepatic function documented within 7 days prior to randomisation
• Complete resolution of cytokine release syndrome (CRS), macrophage-activation syndrome (MAS)/haemophagocytic lymphohistiocytosis (HLH) or immune effector cell-associated neurotoxicity syndrome (ICANS) related to prior CAR T-cell therapy.
• Female patients of childbearing potential (FCBP) must be willing to follow the contraceptive method/procedure as outline in the PICF
• Sexually active males must agree to use a condom during sexual contact with a pregnant female or a FCBP for the course of the study through to 4 months after the last dose of epcoritamab, even if he has undergone a successful vasectomy
• Women must agree not to donate eggs (ova, oocytes) for the purposes of assisted reproduction. Men must also not donate sperm during the trial and for 4 months after receiving the last dose of epcoritamab
• The patient understands the purpose of the trial and procedures required for the trial which includes compliance with the protocol requirements and restrictions listed in the PICF and in this protocol

Exclusion criteria

• A history of Grade 4 CRS or ICANS related to prior CAR T-cell therapy
• Patients whose lymphoma is known to be CD20 negative on the most recent biopsy prior to CAR T-cell therapy
• Ongoing active bacterial, viral, fungal, mycobacterial, parasitic, or other infection requiring systemic treatment
• Progression or relapse within 3 months after a regimen containing a bispecific antibody targeting CD3 and CD20
• A diagnosis of primary central nervous system (CNS) lymphoma
• Active secondary CNS involvement of lymphoma at time of screening
• A known history or current autoimmune disease or other diseases resulting in permanent immunosuppression
• Known cognitive impairment would place the patient at increased risk of complications from ICANS
• A known history of hepatitis B serology consistent with acute or chronic infection
• A known history of hepatitis C serology consistent with acute or chronic infection
• A known history of testing positive for human immunodeficiency virus (HIV)
• Any comorbidity conferring a life expectancy of < 5 years (e.g., second malignancy) or that in the opinion of the site investigator may significantly impact the ability to complete the trial therapy and follow-up or affect the interpretation of results
• Exposed to live or live attenuated vaccine within 4 weeks prior to signing the PICF.
• Women who are pregnant or lactating
• Known hypersensitivity to epcoritamab, lenalidomide, rituximab, tocilizumab or their excipients
• Presence of any psychological, social or geographical or other condition for which participation would not be in the best interest of the patient