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Bispecific antibody treatment of multiple myeloma: latest updates from the 2022 ASH annual meeting

BACKGROUND: Effective novel therapies for multiple myeloma (MM) patients who are unresponsive to conventional treatments (triple-class refractory) are an urgent need. Bispecific antibodies (BsAbs) offer a promising new approach to stimulate T cells and induce tumor cell death by targeting molecules...

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Detalles Bibliográficos
Autores principales: Yin, Xuejiao, Liu, Yi, Sun, Jianai, Tong, Hongyan, Meng, Haitao, You, Liangshun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10657518/
https://www.ncbi.nlm.nih.gov/pubmed/38028949
http://dx.doi.org/10.1177/20406223231213251
Descripción
Sumario:BACKGROUND: Effective novel therapies for multiple myeloma (MM) patients who are unresponsive to conventional treatments (triple-class refractory) are an urgent need. Bispecific antibodies (BsAbs) offer a promising new approach to stimulate T cells and induce tumor cell death by targeting molecules on the surface of malignant plasma cells and CD3 on the surface of T cells. OBJECTIVES: Addressing the issue of improving the prognosis of triple-class refractory MM patients has become a significant clinical challenge. DESIGN: This is a brief report. METHODS: This article summarizes the latest updates of BsAbs treatment of MM from the 2022 ASH annual meeting. RESULTS: BsAbs that target B-cell maturation antigen and G protein-coupled receptor family C group 5 memberD have demonstrated remarkable clinical activity and favorable safety profiles. Many potential targets for myeloma cells are currently undergoing phase I/II clinical trials, and these off-the-shelf bispecific molecules are likely to become a critical part of the MM treatment landscape. CONCLUSION: This article provides an overview of the latest advances in BsAbs immunotherapy for refractory and relapsed MM and highlights significant findings from the 2022 ASH annual meeting.