Preprint Review Version 1 This version is not peer-reviewed

Strategies for Salvage Therapy Post CAR-T Therapy Failure in Refractory/Relapsed Multiple Myeloma Patients

Version 1 : Received: 21 October 2024 / Approved: 21 October 2024 / Online: 21 October 2024 (12:37:38 CEST)

How to cite: Min, C.; Zhong, X.; Cui, Y.; Zhang, H.; Wang, Q. Strategies for Salvage Therapy Post CAR-T Therapy Failure in Refractory/Relapsed Multiple Myeloma Patients. Preprints 2024, 2024101578. https://doi.org/10.20944/preprints202410.1578.v1 Min, C.; Zhong, X.; Cui, Y.; Zhang, H.; Wang, Q. Strategies for Salvage Therapy Post CAR-T Therapy Failure in Refractory/Relapsed Multiple Myeloma Patients. Preprints 2024, 2024101578. https://doi.org/10.20944/preprints202410.1578.v1

Abstract

Over the past few decades, the landscape for multiple myeloma (MM) therapy has significantly advanced, largely due to the approval and introduction of new-generation proteasome inhibitors (PIs) and immunomodulatory drugs (IMiDs). Despite these advancements, MM remains incurable. In March 2021, the U.S. FDA approved the chimeric antigen receptor T-cell (CAR-T) therapy idecabtagene vicleucel (ide-cel) for relapsed/refractory multiple myeloma (R/R MM), heralding the advent of cellular therapies for R/R MM. However, due to factors such as the downregulation or loss of tumor antigen expression, T-cell exhaustion, and the influence of the tumor immune microenvironment, most R/R MM patients inevitably experience relapse following CAR-T cell therapy. Consequently, salvage therapy in the post-CAR-T setting has emerged as a critical area of research. This review discusses the potential factors leading to CAR-T therapy failure in R/R MM patients and discusses subsequent salvage therapeutic strategies, offering recommendations for addressing treatment failure in this context.

Keywords

Multiple Myeloma; Chimeric Antigen Receptor T-cells; Cellular Therapy Failure; Salvage Therapy

Subject

Medicine and Pharmacology, Hematology

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