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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2023
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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. |
format | Online Article Text |
id | pubmed-10657518 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
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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