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Study to Compare Axicabtagene Ciloleucel With Standard of Care Therapy as First-line Treatment in Participants With High-risk Large B-cell Lymphoma (ZUMA-23)
EU CTIS ID: 2022-501489-24-00
What this study is testing
To compare the efficacy of axicabtagene ciloleucel versus standard of care therapy (SOCT), as measured by event-free survival (EFS).
- Therapeutic confirmatory (Phase III)
A plain-language read of the study's public EU CTIS listing. The study team confirms the details.
Who can take part
You may be able to join if
- High-risk disease defined as an IPI score of 4 or 5 at initial diagnosis
- Females of childbearing potential must have a negative serum or urine pregnancy test (females who have undergone surgical sterilization or who have been postmenopausal for at least 2 years are not considered to be of childbearing potential).
- Histologically confirmed LBCL based on 2016 World Health Organization (WHO) classification by local pathology lab assessment, including one of the following: a) Diffuse large B-cell lymphoma, NOS b) High-grade B-cell lymphoma (HGBL) (including HGBL with MYC and BCL2 and/or BCL6 rearrangements (DHL/THL) based on FISH analysis, and HGBL-NOS) Note: Transformed DLBCL from follicular lymphoma or from marginal zone lymphoma is eligible if no prior treatment with anthracycline-containing regimen.
- Ann Arbor Stage III or IV disease.
- Have received only 1 cycle of R-chemotherapy
- At least 1 measurable lesion per the Lugano Classification {Cheson 2014} on anatomical imaging such as computed tomography (CT) imaging (functional imaging such as PET may not be used to identify a measurable lesion). A measurable lesion is defined as greater than 1.5 cm LDi for lymph node and greater than 1.0 cm LDi for extranodal lesion
You likely can't join if
- Any prior treatment for LBCL other than the 1 cycle of R-chemotherapy.
- Females of childbearing potential who are pregnant or breastfeeding (due to potentially dangerous effects of the preparative chemotherapy on the fetus or infant).
- Not willing to practice birth control from the time of consent through 12 months after the last dose of axicabtagene ciloleucel or SOCT.
- The following WHO 2016 subcategories by local assessment: a) T-cell/histiocyte-rich LBCL b) Primary DLBCL of the CNS c) Primary mediastinal (thymic) LBCL d) B-cell lymphoma, unclassifiable, with features intermediate between DLBCL and classical Hodgkin lymphoma e) Burkitt lymphoma f)History of Richter’s transformation of chronic lymphocytic leukemia
- In the investigator’s judgment, the subject is unlikely to complete all study-specific visits or procedures, including follow-up visits, or comply with the study requirements for participation
- History of severe immediate hypersensitivity reaction attributed to aminoglycosides
See the full eligibility criteria
Who can join
- High-risk disease defined as an IPI score of 4 or 5 at initial diagnosis
- Females of childbearing potential must have a negative serum or urine pregnancy test (females who have undergone surgical sterilization or who have been postmenopausal for at least 2 years are not considered to be of childbearing potential).
- Histologically confirmed LBCL based on 2016 World Health Organization (WHO) classification by local pathology lab assessment, including one of the following: a) Diffuse large B-cell lymphoma, NOS b) High-grade B-cell lymphoma (HGBL) (including HGBL with MYC and BCL2 and/or BCL6 rearrangements (DHL/THL) based on FISH analysis, and HGBL-NOS) Note: Transformed DLBCL from follicular lymphoma or from marginal zone lymphoma is eligible if no prior treatment with anthracycline-containing regimen.
- Ann Arbor Stage III or IV disease.
- Have received only 1 cycle of R-chemotherapy
- At least 1 measurable lesion per the Lugano Classification {Cheson 2014} on anatomical imaging such as computed tomography (CT) imaging (functional imaging such as PET may not be used to identify a measurable lesion). A measurable lesion is defined as greater than 1.5 cm LDi for lymph node and greater than 1.0 cm LDi for extranodal lesion
- Adequate tumor biopsy specimen available for central pathology review (detailed sample collection requirement is in central pathology laboratory manual).
- Age 18 years or older.
- Eastern Cooperative Oncology Group (ECOG) performance status of 0-2 at the time of randomization. Note: ECOG > 12 at diagnosis is acceptable.
- Adequate bone marrow, renal, hepatic, pulmonary, and cardiac function as indicated by: a) Absolute neutrophil count (ANC) ≥ 1000/μL b) Platelet count ≥ 75,000/μL c) Absolute lymphocyte count ≥ 100/μL d) Creatinine clearance (as estimated by any local institutional method) ≥ 60 mL/minute e) Serum alanine aminotransferase (ALT)/aspartate aminotransferase (AST) levels ≤ 2.5 × upper limit of normal (ULN) or ≤ 5 x ULN if documented liver involvement of lymphoma f) Total bilirubin ≤ 1.5 mg/dL, except in subjects with Gilbert’s Syndrome or documented LBCL liver or pancreatic involvement where ≤ 3.0 times the ULN g) Left ventricular ejection fraction (LVEF) ≥ 50% and no evidence of clinically significant pericardial effusion, and no clinically significant abnormal electrocardiogram (ECG) findings h) No evidence of Grade 2 (per Common Terminology Criteria for Adverse Events [CTCAE] 5.0) or greater pleural effusion or ascites (subjects with Grade 1 ascites or pleural effusion are eligible) i) Baseline oxygen saturation > 92% on room air
What rules you out
- Any prior treatment for LBCL other than the 1 cycle of R-chemotherapy.
- Females of childbearing potential who are pregnant or breastfeeding (due to potentially dangerous effects of the preparative chemotherapy on the fetus or infant).
- Not willing to practice birth control from the time of consent through 12 months after the last dose of axicabtagene ciloleucel or SOCT.
- The following WHO 2016 subcategories by local assessment: a) T-cell/histiocyte-rich LBCL b) Primary DLBCL of the CNS c) Primary mediastinal (thymic) LBCL d) B-cell lymphoma, unclassifiable, with features intermediate between DLBCL and classical Hodgkin lymphoma e) Burkitt lymphoma f)History of Richter’s transformation of chronic lymphocytic leukemia
- In the investigator’s judgment, the subject is unlikely to complete all study-specific visits or procedures, including follow-up visits, or comply with the study requirements for participation
- History of severe immediate hypersensitivity reaction attributed to aminoglycosides
- Presence or suspicion of fungal, bacterial, viral, or other infection that is uncontrolled or requiring IV antimicrobials for management. Simple bacterial infections are permitted if responding to active treatment. Discussion with the Kite medical monitor is encouraged.
- History of acute or chronic active hepatitis B or C infection. If there is a positive history of treated hepatitis B or hepatitis C, the viral load must be undetectable per quantitative polymerase chain reaction (PCR) and/or nucleic acid testing.
- Positive for human immunodeficiency virus (HIV) unless taking appropriate anti-HIV medications, with an undetectable viral load by PCR and with a CD4 count > 200 cells/uL. Note: HIV-positive subjects in Australia are not permitted regardless of active anti-retroviral therapy or undetectable blood viral load (Refer to 12.4.4).
- Presence of any indwelling line or drain (eg, percutaneous nephrostomy tube, indwelling Foley catheter, biliary drain, or pleural/peritoneal/pericardial catheter). Dedicated central venous access catheters, such as a Port-a-Cath or Hickman catheter, are permitted.
- Presence of detectable cerebrospinal fluid (CSF)-malignant cells, brain metastases, or a history of central nervous system (CNS) involvement of lymphoma.
- Presence of cardiac atrial or ventricular lymphoma involvement.
- Presence of CNS disorder such as dementia, autoimmune disease with CNS involvement, cerebral edema with confirmed structural defects by appropriate imaging, or seizure disorders requiring active anticonvulsive medication. History of stroke, transient ischemic attack, or posterior reversible encephalopathy syndrome (PRES) within 12 months prior to enrollment.
- History of malignancy other than non-melanoma skin cancer or carcinoma in situ (eg, cervix, bladder, breast) unless disease free for at least 3 years
- History of autologous or allogeneic stem cell transplant (SCT)
- History of myocardial infarction, cardiac angioplasty or stenting, unstable angina, New York Heart Association Class II or greater congestive heart failure, or other clinically significant cardiac disease within 12 months before enrolment.
- Presence of primary immunodeficiency.
- History of any medical condition including but not limited to autoimmune disease (eg, Crohn’s disease, rheumatoid arthritis, systemic lupus) requiring maintenance systemic immunosuppression/systemic disease modifying agents within the last 2 years. Endocrine conditions that require maintenance with physiologic dose steroids are allowed.
- History of non-line associated, clinically significant (CTCAE 5.0 Grade 2 or greater) deep vein thrombosis or pulmonary embolism requiring therapeutic anticoagulation within 6 months of randomization.
- Any medical condition or residual toxicities from prior therapies per investigator assessment likely to interfere with assessment of safety or efficacy of study treatment
- History of severe immediate hypersensitivity reaction to any of the agents used in this study, including the lymphodepletion chemotherapy (cyclophosphamide or fludarabine).
- Receipt of live vaccine ≤ 6 weeks before randomization and/or anticipation of need for such a vaccine during the subject’s participation in the study.
The study team makes the final eligibility decision.
Where it's taking place
- Canada
- United States
- United Kingdom
- Australia
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 65+ years, 18-64 years. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Canada; United States; United Kingdom; Australia. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from EU CTIS; the study team decides eligibility.