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Glioblastoma in natalizumab‐treated multiple sclerosis patients
We present two natalizumab‐treated multiple sclerosis patients who developed glioblastoma multiforme (GBM) with variable outcomes. One patient had an isocitrate dehydrogenase (IDH)‐wildtype GBM with aggressive behavior, who declined treatment and died 13 weeks after symptoms onset. The other patient...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5497532/ https://www.ncbi.nlm.nih.gov/pubmed/28695151 http://dx.doi.org/10.1002/acn3.428 |
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author | Sierra Morales, Fabian Wright, Robert B. Novo, Jorge E. Arvanitis, Leonidas D. Stefoski, Dusan Koralnik, Igor J. |
author_facet | Sierra Morales, Fabian Wright, Robert B. Novo, Jorge E. Arvanitis, Leonidas D. Stefoski, Dusan Koralnik, Igor J. |
author_sort | Sierra Morales, Fabian |
collection | PubMed |
description | We present two natalizumab‐treated multiple sclerosis patients who developed glioblastoma multiforme (GBM) with variable outcomes. One patient had an isocitrate dehydrogenase (IDH)‐wildtype GBM with aggressive behavior, who declined treatment and died 13 weeks after symptoms onset. The other patient underwent resection of an IDH‐mutant secondary GBM that arose from a previously diagnosed grade II astrocytoma. He is still alive 5 years after the diagnosis of GBM. JC virus was not detected in either case. Whether natalizumab played a role in the development of GBM in those patients deserves further investigation. |
format | Online Article Text |
id | pubmed-5497532 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-54975322017-07-10 Glioblastoma in natalizumab‐treated multiple sclerosis patients Sierra Morales, Fabian Wright, Robert B. Novo, Jorge E. Arvanitis, Leonidas D. Stefoski, Dusan Koralnik, Igor J. Ann Clin Transl Neurol Brief Communications We present two natalizumab‐treated multiple sclerosis patients who developed glioblastoma multiforme (GBM) with variable outcomes. One patient had an isocitrate dehydrogenase (IDH)‐wildtype GBM with aggressive behavior, who declined treatment and died 13 weeks after symptoms onset. The other patient underwent resection of an IDH‐mutant secondary GBM that arose from a previously diagnosed grade II astrocytoma. He is still alive 5 years after the diagnosis of GBM. JC virus was not detected in either case. Whether natalizumab played a role in the development of GBM in those patients deserves further investigation. John Wiley and Sons Inc. 2017-06-06 /pmc/articles/PMC5497532/ /pubmed/28695151 http://dx.doi.org/10.1002/acn3.428 Text en © 2017 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals, Inc on behalf of American Neurological Association. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Brief Communications Sierra Morales, Fabian Wright, Robert B. Novo, Jorge E. Arvanitis, Leonidas D. Stefoski, Dusan Koralnik, Igor J. Glioblastoma in natalizumab‐treated multiple sclerosis patients |
title | Glioblastoma in natalizumab‐treated multiple sclerosis patients |
title_full | Glioblastoma in natalizumab‐treated multiple sclerosis patients |
title_fullStr | Glioblastoma in natalizumab‐treated multiple sclerosis patients |
title_full_unstemmed | Glioblastoma in natalizumab‐treated multiple sclerosis patients |
title_short | Glioblastoma in natalizumab‐treated multiple sclerosis patients |
title_sort | glioblastoma in natalizumab‐treated multiple sclerosis patients |
topic | Brief Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5497532/ https://www.ncbi.nlm.nih.gov/pubmed/28695151 http://dx.doi.org/10.1002/acn3.428 |
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