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Encephalomyeloneuritis and arthritis after treatment with immune checkpoint inhibitors
OBJECTIVE: Immunotherapy revolutionized melanoma treatment; however, immune-related adverse events, especially neurotoxicity, may be severe and require early and correct diagnosis as well as early treatment commencement. METHODS: We report an unusual severe multiorgan manifestation of neurotoxicity...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7286649/ https://www.ncbi.nlm.nih.gov/pubmed/32461353 http://dx.doi.org/10.1212/NXI.0000000000000773 |
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author | Nowosielski, Martha Di Pauli, Franziska Iglseder, Sarah Wagner, Michaela Hoellweger, Nicole Nguyen, Van Anh Gruber, Johann Stockhammer, Günther |
author_facet | Nowosielski, Martha Di Pauli, Franziska Iglseder, Sarah Wagner, Michaela Hoellweger, Nicole Nguyen, Van Anh Gruber, Johann Stockhammer, Günther |
author_sort | Nowosielski, Martha |
collection | PubMed |
description | OBJECTIVE: Immunotherapy revolutionized melanoma treatment; however, immune-related adverse events, especially neurotoxicity, may be severe and require early and correct diagnosis as well as early treatment commencement. METHODS: We report an unusual severe multiorgan manifestation of neurotoxicity after treatment with the anti-PDL1 immune checkpoint inhibitor, nivolumab, and the anticytotoxic T-lymphocyte-associated antigen 4 immune checkpoint inhibitor, ipilimumab, in a 47-year-old male patient with metastatic melanoma. RESULTS: The patient developed immune-mediated synovitis and cranial neuritis, followed by longitudinal transverse myelitis, encephalitis, and optic neuritis. Early treatment with high-dose steroids and maintenance therapy with rituximab resulted in a favorable neurologic outcome. CONCLUSIONS: The frequency of spinal cord involvement and neuronal toxicity after cancer immunotherapy is very low and requires an extensive diagnostic workup to differentiate between disease progression and side effects. Immune checkpoint inhibitors should be discontinued and treatment with corticosteroids should be initiated early as the drug of first choice. Therapy may be escalated by other immune-modulating treatments, such as rituximab. |
format | Online Article Text |
id | pubmed-7286649 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-72866492020-06-29 Encephalomyeloneuritis and arthritis after treatment with immune checkpoint inhibitors Nowosielski, Martha Di Pauli, Franziska Iglseder, Sarah Wagner, Michaela Hoellweger, Nicole Nguyen, Van Anh Gruber, Johann Stockhammer, Günther Neurol Neuroimmunol Neuroinflamm Article OBJECTIVE: Immunotherapy revolutionized melanoma treatment; however, immune-related adverse events, especially neurotoxicity, may be severe and require early and correct diagnosis as well as early treatment commencement. METHODS: We report an unusual severe multiorgan manifestation of neurotoxicity after treatment with the anti-PDL1 immune checkpoint inhibitor, nivolumab, and the anticytotoxic T-lymphocyte-associated antigen 4 immune checkpoint inhibitor, ipilimumab, in a 47-year-old male patient with metastatic melanoma. RESULTS: The patient developed immune-mediated synovitis and cranial neuritis, followed by longitudinal transverse myelitis, encephalitis, and optic neuritis. Early treatment with high-dose steroids and maintenance therapy with rituximab resulted in a favorable neurologic outcome. CONCLUSIONS: The frequency of spinal cord involvement and neuronal toxicity after cancer immunotherapy is very low and requires an extensive diagnostic workup to differentiate between disease progression and side effects. Immune checkpoint inhibitors should be discontinued and treatment with corticosteroids should be initiated early as the drug of first choice. Therapy may be escalated by other immune-modulating treatments, such as rituximab. Lippincott Williams & Wilkins 2020-05-27 /pmc/articles/PMC7286649/ /pubmed/32461353 http://dx.doi.org/10.1212/NXI.0000000000000773 Text en Copyright © 2020 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits downloading and sharing the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. |
spellingShingle | Article Nowosielski, Martha Di Pauli, Franziska Iglseder, Sarah Wagner, Michaela Hoellweger, Nicole Nguyen, Van Anh Gruber, Johann Stockhammer, Günther Encephalomyeloneuritis and arthritis after treatment with immune checkpoint inhibitors |
title | Encephalomyeloneuritis and arthritis after treatment with immune checkpoint inhibitors |
title_full | Encephalomyeloneuritis and arthritis after treatment with immune checkpoint inhibitors |
title_fullStr | Encephalomyeloneuritis and arthritis after treatment with immune checkpoint inhibitors |
title_full_unstemmed | Encephalomyeloneuritis and arthritis after treatment with immune checkpoint inhibitors |
title_short | Encephalomyeloneuritis and arthritis after treatment with immune checkpoint inhibitors |
title_sort | encephalomyeloneuritis and arthritis after treatment with immune checkpoint inhibitors |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7286649/ https://www.ncbi.nlm.nih.gov/pubmed/32461353 http://dx.doi.org/10.1212/NXI.0000000000000773 |
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