Management of aggressive lymphoma after CAR T-cell therapy failure.

Hematology Am Soc Hematol Educ Program

City of Hope National Medical Center, Department of Hematology & Hematopoietic Cell Transplantation, Duarte, CA.

Published: December 2023

AI Article Synopsis

  • Advances in CAR T-cell therapy have changed how we treat diffuse large B-cell lymphoma, especially for patients who don’t respond to traditional chemotherapy.
  • Two new studies have shown that CAR T-cell therapy can now be given earlier, even in the second line of treatment, for some patients.
  • However, many patients still relapse after CAR T-cell therapy, and there’s a need for more research on effective treatments for these high-risk individuals, particularly with promising new options like bispecific antibodies.

Article Abstract

Several recent advances have affected the treatment landscape of diffuse large B-cell lymphoma. Chimeric antigen receptor (CAR) T-cell therapy has transformed the management of chemorefractory disease. Two randomized studies in early relapse disease have expanded the label to provide access to CAR T-cell therapy as early as second line for some patients. Despite the durable remissions that have been achieved, many patients will experience relapse. There is a growing population of patients previously treated with CAR T-cell therapy facing dismal outcomes. We review the prospective studies that inform treatment options in later lines and highlight the limited data examining outcomes with novel therapies after CAR T-cell failure. The treatment landscape is anticipated to continue to evolve with the emergence of bispecific antibodies that appear to be a promising approach, particularly after CAR T-cell therapy, although little is known about overlapping mechanisms of resistance. Enrichment for patients who have received prior CAR T-cell therapy on prospective trials is a critical unmet need to inform the preferred management for these high-risk patients.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10727106PMC
http://dx.doi.org/10.1182/hematology.2023000437DOI Listing

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