AI Article Synopsis

  • Posttransplantation lymphoproliferative disease (PTLD) can be severe following organ transplants, but survival rates for a specific type (DLBCL) have improved with rituximab treatment.
  • This study presents three cases of patients with refractory EBV-negative PTLD who were successfully treated with CAR-T therapy, demonstrating positive responses and a good safety profile.
  • The findings suggest that CAR-T therapy may be beneficial for patients with EBV-negative refractory PTLD, similar to its effects on other forms of DLBCL, but more research is needed for validation.

Article Abstract

Posttransplantation lymphoproliferative disease (PTLD) is a potentially fatal disorder arising after solid organ or hematopoietic cell transplantation. Survival rates of PTLD with diffuse large B-cell lymphoma (DLBCL) phenotype have improved due to the introduction of rituximab, however, reports on curative management of refractory PTLD are scarce. Here, we describe successful management of three patients with refractory EBV-negative PTLD with chimeric antigen receptor T-cell (CAR-T) therapy. All patients continued calcineurin inhibitors throughout the whole course of treatment. T-cell immunophenotyping was performed on both the apheresed cells and CAR-T product to investigate the T-cell compartment subpopulations. All three patients responded to a single infusion of tisagenlecleucel and two of them achieved CR. Toxicity profile was similar to other patients with non-PTLD DLBCL treated with CAR-T. No transplanted graft dysfunction was observed during the course of therapy. To our knowledge, this is the first report demonstrating that patients with EBV-negative refractory PTLD may benefit from CAR-T therapy, similarly to other patients with relapse/refractory DLBCL. A larger cohort of patients is needed to further establish proof-of-concept.

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Source
http://dx.doi.org/10.1038/s41409-020-01145-1DOI Listing

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