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Pharmacological Treatments Available for Immune-Checkpoint-Inhibitor-Induced Colitis

Immune checkpoint inhibitor treatment has shown revolutionary therapeutic effects in various carcinomas. However, immune-related adverse events (irAE) following this treatment can sometimes lead to treatment discontinuation. One such frequently encountered adverse event is immune-related colitis (ir...

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Autores principales: Ohwada, Sae, Ishigami, Keisuke, Akutsu, Noriyuki, Nakase, Hiroshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9219666/
https://www.ncbi.nlm.nih.gov/pubmed/35740355
http://dx.doi.org/10.3390/biomedicines10061334
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author Ohwada, Sae
Ishigami, Keisuke
Akutsu, Noriyuki
Nakase, Hiroshi
author_facet Ohwada, Sae
Ishigami, Keisuke
Akutsu, Noriyuki
Nakase, Hiroshi
author_sort Ohwada, Sae
collection PubMed
description Immune checkpoint inhibitor treatment has shown revolutionary therapeutic effects in various carcinomas. However, immune-related adverse events (irAE) following this treatment can sometimes lead to treatment discontinuation. One such frequently encountered adverse event is immune-related colitis (irAE colitis). Corticosteroids (CS) are the first-line treatment for irAE colitis, but we often encounter CS-refractory or -resistant cases. The application of multiple biologics has been proposed as a therapy to be administered after CS treatment; however, the efficacy and safety of biologics for patients with irAE colitis who do not respond to CS have not been established. This review summarizes the treatment regimens available for irAE colitis, focusing on the mechanism of action of corticosteroids, infliximab, vedolizumab, and other drugs.
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spelling pubmed-92196662022-06-24 Pharmacological Treatments Available for Immune-Checkpoint-Inhibitor-Induced Colitis Ohwada, Sae Ishigami, Keisuke Akutsu, Noriyuki Nakase, Hiroshi Biomedicines Review Immune checkpoint inhibitor treatment has shown revolutionary therapeutic effects in various carcinomas. However, immune-related adverse events (irAE) following this treatment can sometimes lead to treatment discontinuation. One such frequently encountered adverse event is immune-related colitis (irAE colitis). Corticosteroids (CS) are the first-line treatment for irAE colitis, but we often encounter CS-refractory or -resistant cases. The application of multiple biologics has been proposed as a therapy to be administered after CS treatment; however, the efficacy and safety of biologics for patients with irAE colitis who do not respond to CS have not been established. This review summarizes the treatment regimens available for irAE colitis, focusing on the mechanism of action of corticosteroids, infliximab, vedolizumab, and other drugs. MDPI 2022-06-06 /pmc/articles/PMC9219666/ /pubmed/35740355 http://dx.doi.org/10.3390/biomedicines10061334 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Ohwada, Sae
Ishigami, Keisuke
Akutsu, Noriyuki
Nakase, Hiroshi
Pharmacological Treatments Available for Immune-Checkpoint-Inhibitor-Induced Colitis
title Pharmacological Treatments Available for Immune-Checkpoint-Inhibitor-Induced Colitis
title_full Pharmacological Treatments Available for Immune-Checkpoint-Inhibitor-Induced Colitis
title_fullStr Pharmacological Treatments Available for Immune-Checkpoint-Inhibitor-Induced Colitis
title_full_unstemmed Pharmacological Treatments Available for Immune-Checkpoint-Inhibitor-Induced Colitis
title_short Pharmacological Treatments Available for Immune-Checkpoint-Inhibitor-Induced Colitis
title_sort pharmacological treatments available for immune-checkpoint-inhibitor-induced colitis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9219666/
https://www.ncbi.nlm.nih.gov/pubmed/35740355
http://dx.doi.org/10.3390/biomedicines10061334
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