AI Article Synopsis

  • - Since the launch of first-generation proteasome inhibitors and immunomodulatory agents, treatments for multiple myeloma have significantly advanced, particularly with new immunotherapies targeting B cell maturation antigen (BCMA).
  • - Various BCMA-targeted therapies, including antibody-drug conjugates, bispecific antibodies, and CAR-T/NK cell therapies, are now approved or in clinical trials, enhancing treatment options for patients.
  • - The growing number of BCMA-targeting therapies presents challenges in clinical decision-making, which this review addresses by providing updates on clinical trial outcomes and discussing patient selection criteria for these new treatments.

Article Abstract

Since the introduction of first-generation proteasome inhibitors and immunomodulatory agents, the multiple myeloma (MM) treatment landscape has undergone a remarkable development. Most recently, immunotherapeutic strategies targeting the B cell maturation antigen (BCMA) entered the clinical stage providing access to highly anticipated novel treatment strategies. At present, numerous different approaches investigate BCMA as an effective multi-modal target. Currently, BCMA-directed antibody-drug conjugates, bispecific and trispecific antibodies, autologous and allogeneic CAR-T cell as well as CAR-NK cell constructs are either approved or in different stages of clinical and preclinical development for the treatment of MM. This armamentarium of treatment choices raises several challenges for clinical decision making, particularly in the absence of head-to-head comparisons. In this review, we provide a comprehensive overview of BCMA-targeting therapeutics, deliver latest updates on clinical trial data, and focus on potential patient selection criteria for different BCMA-targeting immunotherapeutic strategies.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8471156PMC
http://dx.doi.org/10.3390/cancers13184701DOI Listing

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