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Atezolizumab (programmed cell death-ligand 1 antibody)-induced inflammation of actinic keratosis: A case report
Atezolizumab is a programmed cell death-ligand 1 antibody that modulates the immune system response and has shown great promise in treating malignancies. Cutaneous toxicities from immune checkpoint inhibitors are the most commonly reported immune-related adverse events, although toxicities related t...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9661553/ https://www.ncbi.nlm.nih.gov/pubmed/36388634 http://dx.doi.org/10.1177/2050313X221131863 |
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author | Spitz, Kathleen E Chu, Lena Swerlick, Robert A |
author_facet | Spitz, Kathleen E Chu, Lena Swerlick, Robert A |
author_sort | Spitz, Kathleen E |
collection | PubMed |
description | Atezolizumab is a programmed cell death-ligand 1 antibody that modulates the immune system response and has shown great promise in treating malignancies. Cutaneous toxicities from immune checkpoint inhibitors are the most commonly reported immune-related adverse events, although toxicities related to immunotherapy are still being characterized. Herein, we present a novel case of inflamed actinic keratoses in a patient after receiving atezolizumab therapy that resolved without requirement of dose adjustment or discontinuation of treatment. |
format | Online Article Text |
id | pubmed-9661553 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-96615532022-11-15 Atezolizumab (programmed cell death-ligand 1 antibody)-induced inflammation of actinic keratosis: A case report Spitz, Kathleen E Chu, Lena Swerlick, Robert A SAGE Open Med Case Rep JCMS Case Report Atezolizumab is a programmed cell death-ligand 1 antibody that modulates the immune system response and has shown great promise in treating malignancies. Cutaneous toxicities from immune checkpoint inhibitors are the most commonly reported immune-related adverse events, although toxicities related to immunotherapy are still being characterized. Herein, we present a novel case of inflamed actinic keratoses in a patient after receiving atezolizumab therapy that resolved without requirement of dose adjustment or discontinuation of treatment. SAGE Publications 2022-11-11 /pmc/articles/PMC9661553/ /pubmed/36388634 http://dx.doi.org/10.1177/2050313X221131863 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | JCMS Case Report Spitz, Kathleen E Chu, Lena Swerlick, Robert A Atezolizumab (programmed cell death-ligand 1 antibody)-induced inflammation of actinic keratosis: A case report |
title | Atezolizumab (programmed cell death-ligand 1 antibody)-induced inflammation of actinic keratosis: A case report |
title_full | Atezolizumab (programmed cell death-ligand 1 antibody)-induced inflammation of actinic keratosis: A case report |
title_fullStr | Atezolizumab (programmed cell death-ligand 1 antibody)-induced inflammation of actinic keratosis: A case report |
title_full_unstemmed | Atezolizumab (programmed cell death-ligand 1 antibody)-induced inflammation of actinic keratosis: A case report |
title_short | Atezolizumab (programmed cell death-ligand 1 antibody)-induced inflammation of actinic keratosis: A case report |
title_sort | atezolizumab (programmed cell death-ligand 1 antibody)-induced inflammation of actinic keratosis: a case report |
topic | JCMS Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9661553/ https://www.ncbi.nlm.nih.gov/pubmed/36388634 http://dx.doi.org/10.1177/2050313X221131863 |
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