Lymphodepletion With Low Dose Total Body Irradiation Before Standard of Care Tisagenlecleucel for the Treatment of Relapsed and Recurrent Large B-cell Lymphoma

Trial statusNot yet recruiting
Trial phasePhase 1
Trial typeInterventional
Biological sexAll
Age18+
SponsorNathan Denlinger

About this trial

This phase I trial tests the safety, side effects, and best dose of total body irradiation (TBI) in combination with standard of care lymphodepletion with cyclophosphamide and fludarabine before tisagenlecleucel (Tisa-cel) and how well the combination works in patients with large B-cell lymphoma (LBCL) that has come back after a period of improvement (relapsed) or that has not responded to previous treatment (refractory). TBI is a common treatment that sends radiation (for example, through x-rays) to the entire body. Lymphodepleting chemotherapy, such as cyclophosphamide and fludarabine, along with TBI helps kill cancer cells in the body and helps prepare the body for the Tisa-cel infusion. Tisagenlecleucel is made using a patient's T cells (a type of immune system cell). A gene for a special receptor called chimeric antigen receptor (CAR) is added to the T cells in the laboratory. These changed T cells called CAR T cells are grown in large numbers in the laboratory and given to the patient by infusion. Tisa-cel binds to a protein called CD19, which is found on some leukemia and lymphoma cells. This helps the body's immune system kill cancer cells. Tisa-cel is a type of CAR T-cell therapy. Giving low dose TBI in combination with standard of care lymphodepletion therapy and Tisa-cel may be safe, tolerable, and/or effective in treating patients with relapsed or refractory (R/R) LBCL.

Eligibility criteria

Qualifiers

Eligible for standard of care anti-CD19 CAR-T treatment with Tisa-cel

Age ≥ 18 years

Biopsy-confirmed relapsed or refractory large B-cell lymphoma after 2 lines of prior therapy

Qualitative CD19 expression by either immunohistochemistry (IHC) or flow cytometry

Disqualifiers

Active central nervous system (CNS) disease at screening or prior to lymphodepletion

Prior therapy with autologous or allogenic CAR-T or CAR-natural killer (NK) cell therapy

Prior anti-CD19 therapies (such as, but not limited to tafasitamab or loncastuximab)

Prior allogeneic stem cell transplant

Trial design

Treatments tested in this trial

  • Biospecimen Collection
  • Computed Tomography
  • Cyclophosphamide
  • Fludarabine
  • Leukapheresis
  • Positron Emission Tomography
  • Tisagenlecleucel
  • Total-Body Irradiation

Treatment groups

18 Participants
are divided into 1 treatment group

Sponsors and collaborators

Nathan Denlinger

Lead sponsor

Ohio State University Comprehensive Cancer Center

Sponsor institution

Novartis

Collaborator