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Dual contribution of the gut microbiome to immunotherapy efficacy and toxicity: supportive care implications and recommendations

The efficacy of immune checkpoint inhibitors (immunotherapy) is increasingly recognized to be linked to the composition the gut microbiome. Given the high rates of resistance, interventions targeting the gut microbiome are now being investigated for its ability to improve the efficacy of immunothera...

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Autores principales: Wardill, Hannah R., Chan, Raymond J., Chan, Alexandre, Keefe, Dorothy, Costello, Samuel P., Hart, Nicolas H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9213341/
https://www.ncbi.nlm.nih.gov/pubmed/35266052
http://dx.doi.org/10.1007/s00520-022-06948-0
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author Wardill, Hannah R.
Chan, Raymond J.
Chan, Alexandre
Keefe, Dorothy
Costello, Samuel P.
Hart, Nicolas H.
author_facet Wardill, Hannah R.
Chan, Raymond J.
Chan, Alexandre
Keefe, Dorothy
Costello, Samuel P.
Hart, Nicolas H.
author_sort Wardill, Hannah R.
collection PubMed
description The efficacy of immune checkpoint inhibitors (immunotherapy) is increasingly recognized to be linked to the composition the gut microbiome. Given the high rates of resistance, interventions targeting the gut microbiome are now being investigated for its ability to improve the efficacy of immunotherapy. In light of recently published data demonstrating a strong correlation between the efficacy and toxicity of immunotherapy, there is a risk that efforts to enhance immunotherapy efficacy may be undermined by increases in immune-related adverse events (IrAEs) This is particularly important for microbial interventions aimed at increasing immunotherapy efficacy, with many microbes implicated in tumour response also linked to IrAEs, especially colitis. IrAEs have a profound impact on patient quality of life, causing physical, psychosocial, and financial distress. Here, we outline strategies at the discovery, translational, and clinical research phases to ensure the impact of augmenting immunotherapy efficacy is approached in a manner that considers adverse implications. Adopting these strategies will ensure that our ongoing efforts to overcome immunotherapy resistance are not impacted by unacceptable toxicity.
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spelling pubmed-92133412022-06-23 Dual contribution of the gut microbiome to immunotherapy efficacy and toxicity: supportive care implications and recommendations Wardill, Hannah R. Chan, Raymond J. Chan, Alexandre Keefe, Dorothy Costello, Samuel P. Hart, Nicolas H. Support Care Cancer Commentary The efficacy of immune checkpoint inhibitors (immunotherapy) is increasingly recognized to be linked to the composition the gut microbiome. Given the high rates of resistance, interventions targeting the gut microbiome are now being investigated for its ability to improve the efficacy of immunotherapy. In light of recently published data demonstrating a strong correlation between the efficacy and toxicity of immunotherapy, there is a risk that efforts to enhance immunotherapy efficacy may be undermined by increases in immune-related adverse events (IrAEs) This is particularly important for microbial interventions aimed at increasing immunotherapy efficacy, with many microbes implicated in tumour response also linked to IrAEs, especially colitis. IrAEs have a profound impact on patient quality of life, causing physical, psychosocial, and financial distress. Here, we outline strategies at the discovery, translational, and clinical research phases to ensure the impact of augmenting immunotherapy efficacy is approached in a manner that considers adverse implications. Adopting these strategies will ensure that our ongoing efforts to overcome immunotherapy resistance are not impacted by unacceptable toxicity. Springer Berlin Heidelberg 2022-03-10 2022 /pmc/articles/PMC9213341/ /pubmed/35266052 http://dx.doi.org/10.1007/s00520-022-06948-0 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/) .
spellingShingle Commentary
Wardill, Hannah R.
Chan, Raymond J.
Chan, Alexandre
Keefe, Dorothy
Costello, Samuel P.
Hart, Nicolas H.
Dual contribution of the gut microbiome to immunotherapy efficacy and toxicity: supportive care implications and recommendations
title Dual contribution of the gut microbiome to immunotherapy efficacy and toxicity: supportive care implications and recommendations
title_full Dual contribution of the gut microbiome to immunotherapy efficacy and toxicity: supportive care implications and recommendations
title_fullStr Dual contribution of the gut microbiome to immunotherapy efficacy and toxicity: supportive care implications and recommendations
title_full_unstemmed Dual contribution of the gut microbiome to immunotherapy efficacy and toxicity: supportive care implications and recommendations
title_short Dual contribution of the gut microbiome to immunotherapy efficacy and toxicity: supportive care implications and recommendations
title_sort dual contribution of the gut microbiome to immunotherapy efficacy and toxicity: supportive care implications and recommendations
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9213341/
https://www.ncbi.nlm.nih.gov/pubmed/35266052
http://dx.doi.org/10.1007/s00520-022-06948-0
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