Optimizing Lymphodepletion to Improve Outcomes in Patients Receiving Cell Therapy With Kymriah

NCT ID: NCT06003179

Last Updated: 2024-11-12

Basic Information

• Recruitment Status: WITHDRAWN
• Clinical Phase: PHASE1
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-04-05
• Study Completion Date: 2028-11-30

Brief Summary

This is a Phase 1b study of participants with Diffuse Large B Cell Lymphoma (DLBCL). The purpose of this study is to identify an optimized lymphodepletion (LD) regimen by evaluating standard and intermediate doses of Fludarabine (Flu) / Cyclophosphamide (Cy) with or without a fixed dose of total lymphoid irradiation (TLI) in the setting of standard of care chimeric antigen receptor T (CAR T) cell therapy.

Detailed Description

Patients will be enrolled in two stages: the dose escalation stage to assess the safety and tolerability of a modified LD regimen, and once the maximum tolerated dose (MTD) is determined, a cohort expansion phase to further characterize the toxicity and efficacy profile and determine the recommended phase 2 dose (RP2D). The study will enroll approximately 20-40 patients in the dose escalation stage (Part 1), and approximately 20 further patients at cohort expansion (Part 2). There will be six dose escalation cohorts, in three study arms. There are two dosing cohorts in each study arm. Patients in Arm 1 will receive the JULIET chemotherapy LD regimen with or without TLI, and in Arms 2 and 3, intermediate doses of Cy with a fixed dose of Flu, with or without TLI, will be given.

The cohorts in Arm 1 will enroll concurrently, and enrollment into Arm 2 will begin after Arm 1 has enrolled all patients and data review by the Trial Steering Committee (TSC). Similarly, enrollment into Arm 3 will only commence once Arm 2 has accrued and relevant safety data has been reviewed.

For accrual into Cohort 2, Arm 1, there will be a 15-day staggered enrollment for the first 2 patients. Staggered enrollment with another 15-day delay may be considered for enrollment into relevant cohorts in Arms 2 and 3, after review by the TSC.

Following completion of accrual to Arm 1, a 30 day dose limiting toxicity (DLT) window will be observed, prior to review by the TSC and commencement of patient enrollment into Arm 2. The same procedure and DLT window will be followed prior to patient enrollment into Arm 3.

One DLT window will be observed during this study: 30 days post infusion of tisagenlecleucel.

Conditions

Lymphoma, Large B-Cell, Diffuse

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: SEQUENTIAL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Cyclophosphamide and fludarabine, standard dose

Fludarabine 25mg/m2 Cyclophosphamide 250mg/m2 Days -4, -3, -2

Group Type: ACTIVE_COMPARATOR

Cyclophosphamide

Intervention Type: DRUG

Conditioning chemo at different doses

Fludarabine

Intervention Type: DRUG

Fludarabine given as part of standard treatment

Cyclophosphamide and fludarabine, standard dose with radiation

Fludarabine 25mg/m2 Cyclophosphamide 250mg/m2 Days -6, -5, -4 2 Gy in 2 Fractions Days -3, -2

Group Type: EXPERIMENTAL

TLI

Intervention Type: RADIATION

radiation given with conditioning chemo

Fludarabine

Intervention Type: DRUG

Fludarabine given as part of standard treatment

Cyclophosphamide (intermediate dose) and fludarabine

Fludarabine 25mg/m2 Cyclophosphamide 500mg/m2 Days -4, -3, -2

Group Type: EXPERIMENTAL

Cyclophosphamide

Intervention Type: DRUG

Conditioning chemo at different doses

Fludarabine

Intervention Type: DRUG

Fludarabine given as part of standard treatment

Cyclophosphamide (intermediate dose) and fludarabine with radiation

Fludarabine 25mg/m2 Cyclophosphamide 500mg/m2 Days -6, -5, -4 2 Gy in 2 Fractions Days -3, -2

Group Type: EXPERIMENTAL

Cyclophosphamide

Intervention Type: DRUG

Conditioning chemo at different doses

TLI

Intervention Type: RADIATION

radiation given with conditioning chemo

Fludarabine

Intervention Type: DRUG

Fludarabine given as part of standard treatment

Cyclophosphamide (high dose) and fludarabine

Fludarabine 25mg/m2 Cyclophosphamide 750mg/m2 Days -4, -3, -2

Group Type: EXPERIMENTAL

Cyclophosphamide

Intervention Type: DRUG

Conditioning chemo at different doses

Fludarabine

Intervention Type: DRUG

Fludarabine given as part of standard treatment

Cyclophosphamide (high dose) and fludarabine with radiation

Fludarabine 25mg/m2 Cyclophosphamide 750mg/m2 Days -6, -5, -4 2 Gy in 2 Fractions Days -3, -2

Group Type: EXPERIMENTAL

Cyclophosphamide

Intervention Type: DRUG

Conditioning chemo at different doses

TLI

Intervention Type: RADIATION

radiation given with conditioning chemo

Fludarabine

Intervention Type: DRUG

Fludarabine given as part of standard treatment

Interventions

Cyclophosphamide

Conditioning chemo at different doses

Intervention Type: DRUG

TLI

radiation given with conditioning chemo

Intervention Type: RADIATION

Fludarabine

Fludarabine given as part of standard treatment

Intervention Type: DRUG

Other Intervention Names

Cytoxan, neosar

Eligibility Criteria

Inclusion Criteria

1. Age ≥ 18 years at the time of informed consent

2. Life expectancy ≥ 12 weeks

3. Biopsy-proven and histologically confirmed relapse/refractory (R/R) large B cell lymphoma, including Primary mediastinal B-cell lymphoma (PMBCL), R/R DLBCL and transformation from Follicular lymphoma (FL).

4. Radiographically documented measurable disease as per Lugano response criteria (i.e. longest transverse diameter of a lesion (LDi) > 1.5 cm that is [18F] fluorodeoxyglucose (FDG) avid).

5. At least 2 weeks or 5 half-lives, whichever is shorter, must have elapsed since any prior systemic cancer therapy at the time the subject provides consent

6. Eligible for standard of care CAR T cell therapy, specifically, relapsed or refractory large B cell lymphoma after two or more lines of systemic therapy, and subjects must have received adequate first-line therapy including at a minimum:

7. Patient is sufficiently stable to facilitate planned CAR T-cell therapy (e.g. not rapidly progressing on temporizing therapy, no significant compromise of vital organ functions (intubation, dialysis, requiring Intensive care unit (ICU)/vasopressor support)) and has good performance status

8. Patient does not have active central nervous system (CNS) disease

9. Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1 at enrollment

10. Patient has not received prior adoptive T-cell immunotherapy

11. Patient is not human immunodeficiency virus (HIV) positive

12. Patient did not receive prior allogeneic stem cell transplant

13. Adequate bone marrow, renal, hepatic, pulmonary and cardiac function

14. 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)

15. Sexually active males who accept to use a condom during intercourse during treatment and for 12 months after treatment as they should not father a child in this period. A condom is required to be used also by vasectomized men (as well as during intercourse with a male partner) in order to prevent delivery of the drug via seminal fluid

16. Must have an apheresis product of non-mobilized cells accepted for manufacturing.

Exclusion Criteria

1. Persisting disease bulk (defined as ≥10 cm) on restaging imaging following bridging therapy.

2. History of malignancy other than nonmelanoma skin cancer or carcinoma in situ (e.g. cervix, bladder, breast) unless disease free for at least 3 years

3. History of Richter's transformation of chronic lymphocytic leukemia (CLL)

4. History of allogeneic stem cell transplant

5. Received < 2 lines of therapy for large B cell lymphoma

6. Prior CD19 targeted therapy

7. Subject has received or undergone the protocol defined treatments/therapies

8. Prior chimeric antigen receptor therapy or other genetically modified T-cell therapy

9. Presence of fungal, bacterial, viral, or other infection that is uncontrolled or requiring intravenous (IV) antimicrobials for management. Simple urinary tract infection (UTI) and uncomplicated bacterial pharyngitis are permitted if responding to active treatment.

10. Known history of infection with human immunodeficiency virus (HIV) or hepatitis B (HBsAg positive) or hepatitis C virus (anti-HCV positive). 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.

11. Active tuberculosis

12. Subjects with detectable cerebrospinal fluid malignant cells or known CNS involvement; a history of prior treated CNS lymphoma which is not active at the time of relapse is permitted

13. History or presence of significant non-malignant CNS disorder such as seizure disorder, cerebrovascular ischemia/hemorrhage, dementia, cerebellar disease, or any autoimmune disease with CNS involvement

14. Subjects with cardiac atrial or cardiac ventricular lymphoma involvement

15. 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 of enrollment

16. Requirement for urgent therapy due to tumor mass effects such as bowel obstruction or blood vessel compression

17. History of autoimmune disease, requiring systemic immunosuppression and/or systemic disease modifying agents within the last 2 years.

18. History of idiopathic pulmonary fibrosis, organizing pneumonia (e.g., bronchiolitis obliterans), drug-induced pneumonitis, idiopathic pneumonitis, or evidence of active pneumonitis per chest computed tomography (CT) scan at screening. History of radiation pneumonitis in the radiation field (fibrosis) is allowed.

19. History of symptomatic deep vein thrombosis or pulmonary embolism within 6 months of enrollment

20. Any medical condition likely to interfere with assessment of safety or efficacy of study treatment

21. History of severe immediate hypersensitivity reaction to tocilizumab or any of the agents used in this study

22. Treatment with a live, attenuated vaccine within 6 weeks prior to initiation of study treatment, or anticipation of need for such a vaccine during the course of the study

23. Women of childbearing potential who are pregnant or breastfeeding because of the potentially dangerous effects of chemotherapy on the fetus or infant.

24. Subjects of either sex who are not willing to practice birth control from the time of consent and at least 6 months after tisagenlecleucel infusion

25. In the investigators judgment, the subject is unlikely to complete all protocol-required study visits or procedures, including follow-up visits, or comply with the study requirements for participation.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University Health Network, Toronto

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

John G Kuruvilla

Role: PRINCIPAL_INVESTIGATOR

Princess Margaret Cancer Centre - University Health Network

Locations

Princess Margaret Cancer Centre

Toronto, Ontario, Canada

Countries

Canada

Other Identifiers

OZM-123

Identifier Type: -

Identifier Source: org_study_id