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Immunosuppression for immune-related adverse events during checkpoint inhibition: an intricate balance
Immune checkpoint inhibitors (ICIs) have changed perspectives for patients with cancer, but come with severe immune-related adverse events (irAEs). To prevent fatality or chronicity, these irAEs are often promptly treated with high-dose immunosuppressants. Until recently, evidence on the effects of...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10182067/ https://www.ncbi.nlm.nih.gov/pubmed/37173424 http://dx.doi.org/10.1038/s41698-023-00380-1 |
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author | Verheijden, Rik J. van Eijs, Mick J. M. May, Anne M. van Wijk, Femke Suijkerbuijk, Karijn P. M. |
author_facet | Verheijden, Rik J. van Eijs, Mick J. M. May, Anne M. van Wijk, Femke Suijkerbuijk, Karijn P. M. |
author_sort | Verheijden, Rik J. |
collection | PubMed |
description | Immune checkpoint inhibitors (ICIs) have changed perspectives for patients with cancer, but come with severe immune-related adverse events (irAEs). To prevent fatality or chronicity, these irAEs are often promptly treated with high-dose immunosuppressants. Until recently, evidence on the effects of irAE management on ICI efficacy has been sparse. As a result, algorithms for irAE management are mostly expert-opinion based and barely consider possible detrimental effects of immunosuppressants on ICI efficacy. However, recent growing evidence suggests that vigorous immunosuppressive management of irAEs comes with unfavourable effects on ICI efficacy and survival. With expansion of the indications of ICIs, evidence-based treatment of irAEs without hampering tumour control becomes more and more important. In this review, we discuss novel evidence from pre-clinical and clinical studies on the effects of different irAE management regimens including corticosteroids, TNF inhibition and tocilizumab on cancer control and survival. We provide recommendations for pre-clinical research, cohort studies and clinical trials that can help clinicians in tailored irAE management, minimising patients’ burden while maintaining ICI efficacy. |
format | Online Article Text |
id | pubmed-10182067 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-101820672023-05-14 Immunosuppression for immune-related adverse events during checkpoint inhibition: an intricate balance Verheijden, Rik J. van Eijs, Mick J. M. May, Anne M. van Wijk, Femke Suijkerbuijk, Karijn P. M. NPJ Precis Oncol Review Article Immune checkpoint inhibitors (ICIs) have changed perspectives for patients with cancer, but come with severe immune-related adverse events (irAEs). To prevent fatality or chronicity, these irAEs are often promptly treated with high-dose immunosuppressants. Until recently, evidence on the effects of irAE management on ICI efficacy has been sparse. As a result, algorithms for irAE management are mostly expert-opinion based and barely consider possible detrimental effects of immunosuppressants on ICI efficacy. However, recent growing evidence suggests that vigorous immunosuppressive management of irAEs comes with unfavourable effects on ICI efficacy and survival. With expansion of the indications of ICIs, evidence-based treatment of irAEs without hampering tumour control becomes more and more important. In this review, we discuss novel evidence from pre-clinical and clinical studies on the effects of different irAE management regimens including corticosteroids, TNF inhibition and tocilizumab on cancer control and survival. We provide recommendations for pre-clinical research, cohort studies and clinical trials that can help clinicians in tailored irAE management, minimising patients’ burden while maintaining ICI efficacy. Nature Publishing Group UK 2023-05-12 /pmc/articles/PMC10182067/ /pubmed/37173424 http://dx.doi.org/10.1038/s41698-023-00380-1 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Review Article Verheijden, Rik J. van Eijs, Mick J. M. May, Anne M. van Wijk, Femke Suijkerbuijk, Karijn P. M. Immunosuppression for immune-related adverse events during checkpoint inhibition: an intricate balance |
title | Immunosuppression for immune-related adverse events during checkpoint inhibition: an intricate balance |
title_full | Immunosuppression for immune-related adverse events during checkpoint inhibition: an intricate balance |
title_fullStr | Immunosuppression for immune-related adverse events during checkpoint inhibition: an intricate balance |
title_full_unstemmed | Immunosuppression for immune-related adverse events during checkpoint inhibition: an intricate balance |
title_short | Immunosuppression for immune-related adverse events during checkpoint inhibition: an intricate balance |
title_sort | immunosuppression for immune-related adverse events during checkpoint inhibition: an intricate balance |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10182067/ https://www.ncbi.nlm.nih.gov/pubmed/37173424 http://dx.doi.org/10.1038/s41698-023-00380-1 |
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