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Hypophysitis induced by immune checkpoint inhibitors in a Scottish melanoma population

AIM: This study aims to determine the incidence of all immune-mediated adverse events (IMAEs) with a focus on hypophysitis in patients with metastatic melanoma receiving immune checkpoint inhibitors (ICI). METHODS: 51 patients with metastatic melanoma who received immune checkpoint inhibitors (ipili...

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Autores principales: Wei, Khor Zhong, Baxter, Mark, Casasola, Richard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Future Medicine Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6582457/
https://www.ncbi.nlm.nih.gov/pubmed/31236205
http://dx.doi.org/10.2217/mmt-2018-0009
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author Wei, Khor Zhong
Baxter, Mark
Casasola, Richard
author_facet Wei, Khor Zhong
Baxter, Mark
Casasola, Richard
author_sort Wei, Khor Zhong
collection PubMed
description AIM: This study aims to determine the incidence of all immune-mediated adverse events (IMAEs) with a focus on hypophysitis in patients with metastatic melanoma receiving immune checkpoint inhibitors (ICI). METHODS: 51 patients with metastatic melanoma who received immune checkpoint inhibitors (ipilimumab, pembrolizumab and nivolumab) in Ninewells Hospital, Dundee between 2014 and 2018 were identified. Patient demographic data and outcomes were recorded retrospectively. RESULTS: A total of 6 patients (11.7%) developed hypophysitis, while 15 patients (29.4%) developed IMAEs. A significant improvement in overall survival (p = 0.03) and progression-free survival (p = 0.041) was seen in patients who developed IMAEs compared with those who did not. CONCLUSION: This study demonstrates a high rate of hypophysitis in melanoma patients receiving ipilimumab. Careful monitoring of symptoms is crucial to detect and appropriately manage IMAEs.
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spelling pubmed-65824572019-06-24 Hypophysitis induced by immune checkpoint inhibitors in a Scottish melanoma population Wei, Khor Zhong Baxter, Mark Casasola, Richard Melanoma Manag Research Article AIM: This study aims to determine the incidence of all immune-mediated adverse events (IMAEs) with a focus on hypophysitis in patients with metastatic melanoma receiving immune checkpoint inhibitors (ICI). METHODS: 51 patients with metastatic melanoma who received immune checkpoint inhibitors (ipilimumab, pembrolizumab and nivolumab) in Ninewells Hospital, Dundee between 2014 and 2018 were identified. Patient demographic data and outcomes were recorded retrospectively. RESULTS: A total of 6 patients (11.7%) developed hypophysitis, while 15 patients (29.4%) developed IMAEs. A significant improvement in overall survival (p = 0.03) and progression-free survival (p = 0.041) was seen in patients who developed IMAEs compared with those who did not. CONCLUSION: This study demonstrates a high rate of hypophysitis in melanoma patients receiving ipilimumab. Careful monitoring of symptoms is crucial to detect and appropriately manage IMAEs. Future Medicine Ltd 2019-04-15 /pmc/articles/PMC6582457/ /pubmed/31236205 http://dx.doi.org/10.2217/mmt-2018-0009 Text en © 2019 Khor Zhong Wei This work is licensed under the Attribution-NonCommercial-NoDerivatives 4.0 Unported License (http://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Research Article
Wei, Khor Zhong
Baxter, Mark
Casasola, Richard
Hypophysitis induced by immune checkpoint inhibitors in a Scottish melanoma population
title Hypophysitis induced by immune checkpoint inhibitors in a Scottish melanoma population
title_full Hypophysitis induced by immune checkpoint inhibitors in a Scottish melanoma population
title_fullStr Hypophysitis induced by immune checkpoint inhibitors in a Scottish melanoma population
title_full_unstemmed Hypophysitis induced by immune checkpoint inhibitors in a Scottish melanoma population
title_short Hypophysitis induced by immune checkpoint inhibitors in a Scottish melanoma population
title_sort hypophysitis induced by immune checkpoint inhibitors in a scottish melanoma population
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6582457/
https://www.ncbi.nlm.nih.gov/pubmed/31236205
http://dx.doi.org/10.2217/mmt-2018-0009
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