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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...

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Detalles Bibliográficos
Autores principales: Sierra Morales, Fabian, Wright, Robert B., Novo, Jorge E., Arvanitis, Leonidas D., Stefoski, Dusan, Koralnik, Igor J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
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.
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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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