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Use of glucocorticoids in the management of immunotherapy‐related adverse effects

Immune checkpoint inhibitors (ICIs) activate host antitumor immunity to kill tumor cells. However, ICI therapy may be accompanied by a series of immunotherapy‐related adverse effects (irAEs) caused by activated autoreactive T cells. Glucocorticoids are the mainstream therapy for irAEs. However, the...

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Detalles Bibliográficos
Autores principales: Wang, Hanping, Zhou, Jiaxin, Guo, Xiaoxiao, Li, Yue, Duan, Lian, SI, Xiaoyan, Zhang, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons Australia, Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7529549/
https://www.ncbi.nlm.nih.gov/pubmed/32893490
http://dx.doi.org/10.1111/1759-7714.13589
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author Wang, Hanping
Zhou, Jiaxin
Guo, Xiaoxiao
Li, Yue
Duan, Lian
SI, Xiaoyan
Zhang, Li
author_facet Wang, Hanping
Zhou, Jiaxin
Guo, Xiaoxiao
Li, Yue
Duan, Lian
SI, Xiaoyan
Zhang, Li
author_sort Wang, Hanping
collection PubMed
description Immune checkpoint inhibitors (ICIs) activate host antitumor immunity to kill tumor cells. However, ICI therapy may be accompanied by a series of immunotherapy‐related adverse effects (irAEs) caused by activated autoreactive T cells. Glucocorticoids are the mainstream therapy for irAEs. However, the usage, dosage and course of treatment of irAEs with glucocorticoids differs from those used in classic autoimmune diseases. Furthermore, the long‐term use of large doses of glucocorticoids may cause serious adverse effects. In this article, the mechanism, dosage forms, adverse effects and management of glucocorticoids are described in detail, providing references and suggestions for oncologists to use glucocorticoids in the treatment of irAEs.
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spelling pubmed-75295492020-10-05 Use of glucocorticoids in the management of immunotherapy‐related adverse effects Wang, Hanping Zhou, Jiaxin Guo, Xiaoxiao Li, Yue Duan, Lian SI, Xiaoyan Zhang, Li Thorac Cancer Clinical Guideline Immune checkpoint inhibitors (ICIs) activate host antitumor immunity to kill tumor cells. However, ICI therapy may be accompanied by a series of immunotherapy‐related adverse effects (irAEs) caused by activated autoreactive T cells. Glucocorticoids are the mainstream therapy for irAEs. However, the usage, dosage and course of treatment of irAEs with glucocorticoids differs from those used in classic autoimmune diseases. Furthermore, the long‐term use of large doses of glucocorticoids may cause serious adverse effects. In this article, the mechanism, dosage forms, adverse effects and management of glucocorticoids are described in detail, providing references and suggestions for oncologists to use glucocorticoids in the treatment of irAEs. John Wiley & Sons Australia, Ltd 2020-09-06 2020-10 /pmc/articles/PMC7529549/ /pubmed/32893490 http://dx.doi.org/10.1111/1759-7714.13589 Text en © 2020 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Guideline
Wang, Hanping
Zhou, Jiaxin
Guo, Xiaoxiao
Li, Yue
Duan, Lian
SI, Xiaoyan
Zhang, Li
Use of glucocorticoids in the management of immunotherapy‐related adverse effects
title Use of glucocorticoids in the management of immunotherapy‐related adverse effects
title_full Use of glucocorticoids in the management of immunotherapy‐related adverse effects
title_fullStr Use of glucocorticoids in the management of immunotherapy‐related adverse effects
title_full_unstemmed Use of glucocorticoids in the management of immunotherapy‐related adverse effects
title_short Use of glucocorticoids in the management of immunotherapy‐related adverse effects
title_sort use of glucocorticoids in the management of immunotherapy‐related adverse effects
topic Clinical Guideline
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7529549/
https://www.ncbi.nlm.nih.gov/pubmed/32893490
http://dx.doi.org/10.1111/1759-7714.13589
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