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How we treat neurological toxicity from immune checkpoint inhibitors

Neurological adverse events from immune checkpoint inhibition are increasingly recognised, especially with combination anti-cytotoxic T-lymphocyte antigen 4 (CTLA4) and anti-programmed death receptor 1 (anti-PD-1) therapies. Their presenting symptoms and signs are often subacute and highly variable,...

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Autores principales: Spain, Lavinia, Tippu, Zayd, Larkin, James M, Carr, Aisling, Turajlic, Samra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6678012/
https://www.ncbi.nlm.nih.gov/pubmed/31423344
http://dx.doi.org/10.1136/esmoopen-2019-000540
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author Spain, Lavinia
Tippu, Zayd
Larkin, James M
Carr, Aisling
Turajlic, Samra
author_facet Spain, Lavinia
Tippu, Zayd
Larkin, James M
Carr, Aisling
Turajlic, Samra
author_sort Spain, Lavinia
collection PubMed
description Neurological adverse events from immune checkpoint inhibition are increasingly recognised, especially with combination anti-cytotoxic T-lymphocyte antigen 4 (CTLA4) and anti-programmed death receptor 1 (anti-PD-1) therapies. Their presenting symptoms and signs are often subacute and highly variable, reflecting the numerous components of the nervous system. Given the risk of substantial morbidity and mortality, it is important to inform patients of symptoms that may be of concern, and to assess any suspected toxicity promptly. As with other immune-related adverse events, the cornerstone of management is administration of corticosteroids. Specialist neurology input is vital in this group of patients to guide appropriate investigations and tailor treatment strategies.
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spelling pubmed-66780122019-08-16 How we treat neurological toxicity from immune checkpoint inhibitors Spain, Lavinia Tippu, Zayd Larkin, James M Carr, Aisling Turajlic, Samra ESMO Open Review Neurological adverse events from immune checkpoint inhibition are increasingly recognised, especially with combination anti-cytotoxic T-lymphocyte antigen 4 (CTLA4) and anti-programmed death receptor 1 (anti-PD-1) therapies. Their presenting symptoms and signs are often subacute and highly variable, reflecting the numerous components of the nervous system. Given the risk of substantial morbidity and mortality, it is important to inform patients of symptoms that may be of concern, and to assess any suspected toxicity promptly. As with other immune-related adverse events, the cornerstone of management is administration of corticosteroids. Specialist neurology input is vital in this group of patients to guide appropriate investigations and tailor treatment strategies. BMJ Publishing Group 2019-07-31 /pmc/articles/PMC6678012/ /pubmed/31423344 http://dx.doi.org/10.1136/esmoopen-2019-000540 Text en © Author (s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. Published by BMJ on behalf of the European Society for Medical Oncology. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, any changes made are indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Review
Spain, Lavinia
Tippu, Zayd
Larkin, James M
Carr, Aisling
Turajlic, Samra
How we treat neurological toxicity from immune checkpoint inhibitors
title How we treat neurological toxicity from immune checkpoint inhibitors
title_full How we treat neurological toxicity from immune checkpoint inhibitors
title_fullStr How we treat neurological toxicity from immune checkpoint inhibitors
title_full_unstemmed How we treat neurological toxicity from immune checkpoint inhibitors
title_short How we treat neurological toxicity from immune checkpoint inhibitors
title_sort how we treat neurological toxicity from immune checkpoint inhibitors
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6678012/
https://www.ncbi.nlm.nih.gov/pubmed/31423344
http://dx.doi.org/10.1136/esmoopen-2019-000540
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