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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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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
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author Yin, Xuejiao
Liu, Yi
Sun, Jianai
Tong, Hongyan
Meng, Haitao
You, Liangshun
author_facet Yin, Xuejiao
Liu, Yi
Sun, Jianai
Tong, Hongyan
Meng, Haitao
You, Liangshun
author_sort Yin, Xuejiao
collection PubMed
description 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.
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spelling pubmed-106575182023-11-18 Bispecific antibody treatment of multiple myeloma: latest updates from the 2022 ASH annual meeting Yin, Xuejiao Liu, Yi Sun, Jianai Tong, Hongyan Meng, Haitao You, Liangshun Ther Adv Chronic Dis Brief Report 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. SAGE Publications 2023-11-18 /pmc/articles/PMC10657518/ /pubmed/38028949 http://dx.doi.org/10.1177/20406223231213251 Text en © The Author(s), 2023 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Brief Report
Yin, Xuejiao
Liu, Yi
Sun, Jianai
Tong, Hongyan
Meng, Haitao
You, Liangshun
Bispecific antibody treatment of multiple myeloma: latest updates from the 2022 ASH annual meeting
title Bispecific antibody treatment of multiple myeloma: latest updates from the 2022 ASH annual meeting
title_full Bispecific antibody treatment of multiple myeloma: latest updates from the 2022 ASH annual meeting
title_fullStr Bispecific antibody treatment of multiple myeloma: latest updates from the 2022 ASH annual meeting
title_full_unstemmed Bispecific antibody treatment of multiple myeloma: latest updates from the 2022 ASH annual meeting
title_short Bispecific antibody treatment of multiple myeloma: latest updates from the 2022 ASH annual meeting
title_sort bispecific antibody treatment of multiple myeloma: latest updates from the 2022 ash annual meeting
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10657518/
https://www.ncbi.nlm.nih.gov/pubmed/38028949
http://dx.doi.org/10.1177/20406223231213251
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