Odronextamab for the Treatment of Relapsed and Refractory Diffuse Large B-cell Lymphoma Before and After Chimeric Antigen Receptor T-cell Therapy

PRIMARY OBJECTIVE:

I. To assess anti-tumor activity of odronextamab + CAR T-cell therapy in in patients with relapsed or refractory (R/R) DLBCL.

SECONDARY OBJECTIVES:

I. To evaluate the toxicities of odronextamab + CAR T-cell therapy in patients with R/R DLBCL.

II. To further assess anti-tumor activity of odronextamab + CAR T-cell therapy in patients with R/R DLBCL.

OUTLINE:

Patients receive odronextamab intravenously (IV) over 1-4 hours on days 1, 2, 8, 9, 15, and 16 of cycle 1, on days 1, 8, and 15 of cycles 2-4 then on days 1 and 15 of subsequent cycles until achievement of durable complete response (CR). Cycles repeat every 21 days in the absence of durable CR, disease progression, or unacceptable toxicity. Patients with durable CR for ≥ 9 months may then receive odronextamab IV over 1-4 hours on day 1 of each subsequent cycle. These cycles repeat every 28 days for up to a total of 2 years in the absence of disease progression or unacceptable toxicity. Patients receive SOC CAR T-cell therapy if disease assessment shows less than a CR after cycle 4, or after cycle 5 if disease assessment shows progressive disease (PD) any time after cycle 5. Additionally, patients undergo echocardiography (ECHO) or multigated acquisition scan (MUGA) and blood sample collection, positron emission tomography (PET)/computed tomography (CT) or CT throughout the study. Patients may also undergo CT of the brain at screening.

After completion of study treatment, patients are followed up at 30 days then every 4 months for up to 2 years.

Inclusion criteria

• Aged ≥ 18 at the time of consent
• Patients must have histologically or cytologically confirmed relapsed/ refractory (R/R) diffuse large B-cell lymphoma (DLBCL); transformed follicular lymphoma patients are eligible
• Patients must have failed at least 2 prior therapies
• Life expectancy ≥ 3 months
• Candidate for any Food and Drug Administration (FDA)-approved chimeric antigen receptor (CAR) T cell therapy as per institutional guidelines
• Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2 (Karnofsky ≥ 50%)
• Leukocytes ≥ 2,500/µL
• Absolute neutrophil count ≥ 1,000/µL or > 500/µL for patients with bone marrow involvement

• A participant may not have received granulocyte colony stimulating factor within 2 days prior to first dose of odronextamab in order to meet the absolute neutrophil count (ANC) eligibility criterion
• Platelets ≥ 50,000/µL or ≥ 25,000/µL for patients with bone marrow involvement

• A patient may not have received platelet transfusion therapy within 2 days prior to first dose of odronextamab in order to meet the platelet eligibility criterion
• Total bilirubin ≤ 1.5 x institutional upper limit of normal (ULN)

• NOTE: patients with known Gilbert disease who have serum bilirubin level ≤ 3 x institutional ULN may be enrolled. Patients with known Gilbert syndrome will be excluded if the total bilirubin value is > 4 x ULN
• Irrespective of the presence of lymphoma infiltration of the liver, a participant with an aspartate aminotransferase (AST) > 3 x ULN and/or alanine aminotransferase (ALT) > 3 x ULN concurrent with a total bilirubin > 1.5 x ULN will be excluded
• AST(serum glutamic oxaloacetic transaminase [SGOT])/ALT(serum glutamic pyruvic transaminase [SGPT]) ≤ 3 x institutional ULN (AST and/or ALT ≤ 5 x ULN for patients with liver involvement)

• Irrespective of the presence of lymphoma infiltration of the liver, a participant with an AST > 3 x ULN and/or ALT > 3 x ULN concurrent with a total bilirubin > 1.5 x ULN will be excluded
• Creatinine clearance ≥ 30 mL/min/1.73 m^2 by Cockcroft-Gault
• Hemoglobin ≥ 8 g/dL or ≥ 7 g/dL for patients with bone marrow involvement

• NOTE: Growth factor or transfusion support is allowed as per treating physician's discretion
• Alkaline phosphatase 2.5 x ULN (≤ 5 x ULN for patients with documented liver involvement or bone metastases)
• International normalized ratio (INR) and activated partial thromboplastin time (aPTT) ≤ 1.5 x ULN

• NOTE: This applies only to patients who do not receive therapeutic anticoagulation; patients receiving therapeutic anticoagulation, such as low-molecular-weight heparin or warfarin, should be on a stable dose
• Cardiac ejection fraction > 50% by echocardiogram or multigated acquisition (MUGA) scan
• Serum creatinine ≤ 1.5 x ULN, or calculated creatinine clearance by Cockcroft Gault formula ≥ 50 mL/min
• For participants infected with HIV:

• No history of AIDS-defining conditions other than lymphoma or history of CD4+ T-cells below 200/mm^3 prior to beginning combination antiretroviral therapy (ART)
• Human immunodeficiency virus (HIV)-infected patients on effective anti-retroviral therapy with undetectable viral load within 6 months are eligible for this trial
• At time of study entry CD4+ T-cells must have recovered from prior lymphoma therapy to ≥ 250/mm^3
• At the time of study entry, the HIV viral load must be undetectable by standard laboratory assay
• During prior lymphoma therapy, patients must not have experienced documented infections attributed to the HIV+ status
• No history of non-adherence to ART and willing to adhere to ART while on study
• Antiretroviral drugs with overlapping or similar toxicity profiles as study agents not allowed
• People with hepatitis B or C on suppressive therapy with a negative viral load and no evidence of hepatic damage are eligible
• People of child-bearing potential and reproductive partners must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry, for the duration of study participation, and for 6 months (180 days) after the last dose of study agent. Egg and sperm donation is prohibited during the study and for 6 months after the last dose of study agent
• Willing and able to provide informed consent

Exclusion criteria

• Any condition, including the presence of laboratory abnormalities, which places the subject at unacceptable risk if he/she/they were to participate in the study or confounds the ability to interpret data from the study as determined by the study principal investigator (PI) or enrolling physician
• Known involvement by primary central nervous system (CNS) lymphoma or known uncontrolled involvement by non-primary CNS non-Hodgkin lymphoma (NHL) at the time of study entry
• Known history (within last 12 months) of or current relevant CNS pathology, such as:

• Epilepsy, seizure, paresis, aphasia, apoplexy, severe brain injury, cerebellar disease, organic brain syndrome, psychosis, cerebrovascular stroke or
• Evidence for presence of inflammatory lesions and/or vasculitis on cerebral magnetic resonance imaging (MRI)
• Another active malignancy (aside from B-cell NHL) in the past 5 years, with the following exceptions: non-melanoma skin cancer that has undergone potentially curative therapy, in situ cervical carcinoma, or any other tumor that has been deemed to be effectively treated with definitive local control and with curative intent as per treating investigator
• Evidence of any active infection (bacterial, viral, fungal, mycobacterial, parasitic, or other) at study enrollment or within 2 weeks of study enrollment, if requiring ongoing treatment and/or has the potential to cause disseminated disease or severe infection upon immunosuppression. There should be evidence that the infection has cleared or is well controlled by start of study therapy
• Active COVID-19 infection
• Uncontrolled infection with human immunodeficiency virus (HIV), hepatitis B virus (HBV), or hepatitis C virus (HCV)

• Participants with HIV who have controlled infection (undetectable viral load and CD4 count above 350 cells/µL either spontaneously or on a stable antiviral regimen) are permitted.
• Participants who are hepatitis B surface antigen positive or who are hepatitis B core antibody positive should undergo evaluation by a specialist and be considered to have controlled infection (serum hepatitis B virus deoxyribonucleic acid [DNA] polymerase chain reaction [PCR] that is below the limit of detection AND receiving anti-viral therapy for hepatitis B) before they are permitted onto study
• Participants who are HCV antibody positive who have controlled infection (undetectable HCV ribonucleic acid [RNA] by PCR either spontaneously or in response to a successful prior course of anti-HCV therapy) are permitted
• Cytomegalovirus (CMV) infection as noted by detectable levels on peripheral blood polymerase chain reaction (PCR) assay. Patients who show detectable levels of CMV at screening will need to be treated with appropriate antiviral therapy and demonstrate at least 2 undetectable levels of CMV by PCR assay (at least 7 days apart) before being re-considered for eligibility
• Continuous systemic corticosteroid treatment with more than 10 mg per day of prednisone/prednisolone or anti-inflammatory equivalent within 72 hours of start of assigned treatment
• Recent major surgery (within 4 weeks prior to the start of study treatment)
• Standard radiotherapy within 14 days of first administration of study treatment
• Prior organ transplantation
• Administration of live vaccination within 28 days of study first dose
• Use of any other experimental drug or therapy within 28 days (or 5 half-lives of the drug, whichever is shorter) of initiating study treatment
• Concurrent use of other anti-cancer treatments except for certain therapeutics (e.g., maintenance hormonal-based therapy) per the treating physician's discretion
• Uncontrolled systemic fungal, bacterial, or viral infection (defined as ongoing signs/symptoms related to the infection without improvement despite appropriate antibiotics, antiviral therapy and/or other treatment)
• Pregnancy or lactation
• Known allergic reactions or hypersensitivity to allopurinol, rasburicase, or compounds of similar chemical or biological components