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Bispecific Monoclonal Antibodies in Multiple Myeloma: Data from ASH 2022: A Podcast
The introduction of novel immunotherapies has transformed the treatment landscape in multiple myeloma (MM). The addition of these agents has significantly improved patient outcomes; however, MM remains largely incurable, with heavily pretreated patients suffering from shorter survival times. To addr...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Healthcare
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10329949/ https://www.ncbi.nlm.nih.gov/pubmed/37328635 http://dx.doi.org/10.1007/s12325-023-02551-9 |
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author | Landgren, Ola Nadeem, Omar |
author_facet | Landgren, Ola Nadeem, Omar |
author_sort | Landgren, Ola |
collection | PubMed |
description | The introduction of novel immunotherapies has transformed the treatment landscape in multiple myeloma (MM). The addition of these agents has significantly improved patient outcomes; however, MM remains largely incurable, with heavily pretreated patients suffering from shorter survival times. To address this unmet need, the focus has shifted toward novel mode of action therapies, such as bispecific antibodies (BsAb), which simultaneously bind to immune effector cells and myeloma cells. Currently, there are several T cell–redirecting BsAb being developed that target BCMA, GPRC5D, and FcRH5. These BsAb show impressive clinical activity for the relapsed/refractory population targeted and will likely become an essential part of MM treatment protocols in the future. In this podcast, the authors summarize and highlight some of the T cell–redirecting BsAb currently in development for the treatment of relapsed/refractory MM with a focus on the data reported at the oral session for BsAb at the American Society of Hematology’s 2022 meeting from clinical phase 1 and 2 studies. The six presentations reported the latest safety and efficacy data for the BsAb: talquetamab, elranatamab, teclistamab, forimtamig, and alnuctamab. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12325-023-02551-9. |
format | Online Article Text |
id | pubmed-10329949 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Healthcare |
record_format | MEDLINE/PubMed |
spelling | pubmed-103299492023-07-11 Bispecific Monoclonal Antibodies in Multiple Myeloma: Data from ASH 2022: A Podcast Landgren, Ola Nadeem, Omar Adv Ther Commentary The introduction of novel immunotherapies has transformed the treatment landscape in multiple myeloma (MM). The addition of these agents has significantly improved patient outcomes; however, MM remains largely incurable, with heavily pretreated patients suffering from shorter survival times. To address this unmet need, the focus has shifted toward novel mode of action therapies, such as bispecific antibodies (BsAb), which simultaneously bind to immune effector cells and myeloma cells. Currently, there are several T cell–redirecting BsAb being developed that target BCMA, GPRC5D, and FcRH5. These BsAb show impressive clinical activity for the relapsed/refractory population targeted and will likely become an essential part of MM treatment protocols in the future. In this podcast, the authors summarize and highlight some of the T cell–redirecting BsAb currently in development for the treatment of relapsed/refractory MM with a focus on the data reported at the oral session for BsAb at the American Society of Hematology’s 2022 meeting from clinical phase 1 and 2 studies. The six presentations reported the latest safety and efficacy data for the BsAb: talquetamab, elranatamab, teclistamab, forimtamig, and alnuctamab. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12325-023-02551-9. Springer Healthcare 2023-06-16 2023 /pmc/articles/PMC10329949/ /pubmed/37328635 http://dx.doi.org/10.1007/s12325-023-02551-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by-nc/4.0/Open Access This article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Commentary Landgren, Ola Nadeem, Omar Bispecific Monoclonal Antibodies in Multiple Myeloma: Data from ASH 2022: A Podcast |
title | Bispecific Monoclonal Antibodies in Multiple Myeloma: Data from ASH 2022: A Podcast |
title_full | Bispecific Monoclonal Antibodies in Multiple Myeloma: Data from ASH 2022: A Podcast |
title_fullStr | Bispecific Monoclonal Antibodies in Multiple Myeloma: Data from ASH 2022: A Podcast |
title_full_unstemmed | Bispecific Monoclonal Antibodies in Multiple Myeloma: Data from ASH 2022: A Podcast |
title_short | Bispecific Monoclonal Antibodies in Multiple Myeloma: Data from ASH 2022: A Podcast |
title_sort | bispecific monoclonal antibodies in multiple myeloma: data from ash 2022: a podcast |
topic | Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10329949/ https://www.ncbi.nlm.nih.gov/pubmed/37328635 http://dx.doi.org/10.1007/s12325-023-02551-9 |
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