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Patient selection for CAR T or BiTE therapy in multiple myeloma: Which treatment for each patient?
Multiple myeloma (MM) is a plasma cell malignancy that affects an increasing number of patients worldwide. Despite all the efforts to understand its pathogenesis and develop new treatment modalities, MM remains an incurable disease. Novel immunotherapies, such as CAR T cell therapy (CAR) and bispeci...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9171942/ https://www.ncbi.nlm.nih.gov/pubmed/35672793 http://dx.doi.org/10.1186/s13045-022-01296-2 |
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author | Kegyes, David Constantinescu, Catalin Vrancken, Louise Rasche, Leo Gregoire, Celine Tigu, Bogdan Gulei, Diana Dima, Delia Tanase, Alina Einsele, Hermann Ciurea, Stefan Tomuleasa, Ciprian Caers, Jo |
author_facet | Kegyes, David Constantinescu, Catalin Vrancken, Louise Rasche, Leo Gregoire, Celine Tigu, Bogdan Gulei, Diana Dima, Delia Tanase, Alina Einsele, Hermann Ciurea, Stefan Tomuleasa, Ciprian Caers, Jo |
author_sort | Kegyes, David |
collection | PubMed |
description | Multiple myeloma (MM) is a plasma cell malignancy that affects an increasing number of patients worldwide. Despite all the efforts to understand its pathogenesis and develop new treatment modalities, MM remains an incurable disease. Novel immunotherapies, such as CAR T cell therapy (CAR) and bispecific T cell engagers (BiTE), are intensively targeting different surface antigens, such as BMCA, SLAMF7 (CS1), GPRC5D, FCRH5 or CD38. However, stem cell transplantation is still indispensable in transplant-eligible patients. Studies suggest that the early use of immunotherapy may improve outcomes significantly. In this review, we summarize the currently available clinical literature on CAR and BiTE in MM. Furthermore, we will compare these two T cell-based immunotherapies and discuss potential therapeutic approaches to promote development of new clinical trials, using T cell-based immunotherapies, even as bridging therapies to a transplant. |
format | Online Article Text |
id | pubmed-9171942 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-91719422022-06-08 Patient selection for CAR T or BiTE therapy in multiple myeloma: Which treatment for each patient? Kegyes, David Constantinescu, Catalin Vrancken, Louise Rasche, Leo Gregoire, Celine Tigu, Bogdan Gulei, Diana Dima, Delia Tanase, Alina Einsele, Hermann Ciurea, Stefan Tomuleasa, Ciprian Caers, Jo J Hematol Oncol Review Multiple myeloma (MM) is a plasma cell malignancy that affects an increasing number of patients worldwide. Despite all the efforts to understand its pathogenesis and develop new treatment modalities, MM remains an incurable disease. Novel immunotherapies, such as CAR T cell therapy (CAR) and bispecific T cell engagers (BiTE), are intensively targeting different surface antigens, such as BMCA, SLAMF7 (CS1), GPRC5D, FCRH5 or CD38. However, stem cell transplantation is still indispensable in transplant-eligible patients. Studies suggest that the early use of immunotherapy may improve outcomes significantly. In this review, we summarize the currently available clinical literature on CAR and BiTE in MM. Furthermore, we will compare these two T cell-based immunotherapies and discuss potential therapeutic approaches to promote development of new clinical trials, using T cell-based immunotherapies, even as bridging therapies to a transplant. BioMed Central 2022-06-07 /pmc/articles/PMC9171942/ /pubmed/35672793 http://dx.doi.org/10.1186/s13045-022-01296-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits 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/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Review Kegyes, David Constantinescu, Catalin Vrancken, Louise Rasche, Leo Gregoire, Celine Tigu, Bogdan Gulei, Diana Dima, Delia Tanase, Alina Einsele, Hermann Ciurea, Stefan Tomuleasa, Ciprian Caers, Jo Patient selection for CAR T or BiTE therapy in multiple myeloma: Which treatment for each patient? |
title | Patient selection for CAR T or BiTE therapy in multiple myeloma: Which treatment for each patient? |
title_full | Patient selection for CAR T or BiTE therapy in multiple myeloma: Which treatment for each patient? |
title_fullStr | Patient selection for CAR T or BiTE therapy in multiple myeloma: Which treatment for each patient? |
title_full_unstemmed | Patient selection for CAR T or BiTE therapy in multiple myeloma: Which treatment for each patient? |
title_short | Patient selection for CAR T or BiTE therapy in multiple myeloma: Which treatment for each patient? |
title_sort | patient selection for car t or bite therapy in multiple myeloma: which treatment for each patient? |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9171942/ https://www.ncbi.nlm.nih.gov/pubmed/35672793 http://dx.doi.org/10.1186/s13045-022-01296-2 |
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