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Early Bortezomib Therapy for Refractory Anti-NMDA Receptor Encephalitis
Introduction: Anti-N-methyl-D-aspartate (NMDA) receptor encephalitis is an increasingly recognized form of immune-mediated encephalitis. Here we present a case that represents the shortest hospitalization-to-bortezomib treatment timeline (42 days), and we believe that this is reflected in the patien...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7118211/ https://www.ncbi.nlm.nih.gov/pubmed/32292386 http://dx.doi.org/10.3389/fneur.2020.00188 |
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author | Turnbull, Marion T. Siegel, Jason L. Becker, Tara L. Stephens, Alana J. Lopez-Chiriboga, A. Sebastian Freeman, William D. |
author_facet | Turnbull, Marion T. Siegel, Jason L. Becker, Tara L. Stephens, Alana J. Lopez-Chiriboga, A. Sebastian Freeman, William D. |
author_sort | Turnbull, Marion T. |
collection | PubMed |
description | Introduction: Anti-N-methyl-D-aspartate (NMDA) receptor encephalitis is an increasingly recognized form of immune-mediated encephalitis. Here we present a case that represents the shortest hospitalization-to-bortezomib treatment timeline (42 days), and we believe that this is reflected in the patient's outcome with complete independence within a short timeframe. Case Report: We describe a case of anti-NMDA receptor encephalitis in an 18-year-old African American female presenting with progressive, medically refractory disease. Despite two rounds of high-dose intravenous steroids, plasma exchange, immunoglobulin administration, and rituximab for B-cell depletion, the patient failed to respond by hospital day 42 and received off-label use of the proteasome inhibitor bortezomib. During the 15 days after the bortezomib administration, the patient showed dramatic neurologic recovery that allowed her transfer out of the intensive care unit. At follow-up after 1-month, the patient reported feeling normal cognitively and showed dramatic improvement in cognitive scores. Conclusion: This case and literature review provide preliminary evidence that early treatment of anti-NMDA receptor encephalitis with the proteasome inhibitor bortezomib appears safe and tolerable. However, randomized trials are needed to show the efficacy and the long-term benefit. |
format | Online Article Text |
id | pubmed-7118211 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71182112020-04-14 Early Bortezomib Therapy for Refractory Anti-NMDA Receptor Encephalitis Turnbull, Marion T. Siegel, Jason L. Becker, Tara L. Stephens, Alana J. Lopez-Chiriboga, A. Sebastian Freeman, William D. Front Neurol Neurology Introduction: Anti-N-methyl-D-aspartate (NMDA) receptor encephalitis is an increasingly recognized form of immune-mediated encephalitis. Here we present a case that represents the shortest hospitalization-to-bortezomib treatment timeline (42 days), and we believe that this is reflected in the patient's outcome with complete independence within a short timeframe. Case Report: We describe a case of anti-NMDA receptor encephalitis in an 18-year-old African American female presenting with progressive, medically refractory disease. Despite two rounds of high-dose intravenous steroids, plasma exchange, immunoglobulin administration, and rituximab for B-cell depletion, the patient failed to respond by hospital day 42 and received off-label use of the proteasome inhibitor bortezomib. During the 15 days after the bortezomib administration, the patient showed dramatic neurologic recovery that allowed her transfer out of the intensive care unit. At follow-up after 1-month, the patient reported feeling normal cognitively and showed dramatic improvement in cognitive scores. Conclusion: This case and literature review provide preliminary evidence that early treatment of anti-NMDA receptor encephalitis with the proteasome inhibitor bortezomib appears safe and tolerable. However, randomized trials are needed to show the efficacy and the long-term benefit. Frontiers Media S.A. 2020-03-27 /pmc/articles/PMC7118211/ /pubmed/32292386 http://dx.doi.org/10.3389/fneur.2020.00188 Text en Copyright © 2020 Turnbull, Siegel, Becker, Stephens, Lopez-Chiriboga and Freeman. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neurology Turnbull, Marion T. Siegel, Jason L. Becker, Tara L. Stephens, Alana J. Lopez-Chiriboga, A. Sebastian Freeman, William D. Early Bortezomib Therapy for Refractory Anti-NMDA Receptor Encephalitis |
title | Early Bortezomib Therapy for Refractory Anti-NMDA Receptor Encephalitis |
title_full | Early Bortezomib Therapy for Refractory Anti-NMDA Receptor Encephalitis |
title_fullStr | Early Bortezomib Therapy for Refractory Anti-NMDA Receptor Encephalitis |
title_full_unstemmed | Early Bortezomib Therapy for Refractory Anti-NMDA Receptor Encephalitis |
title_short | Early Bortezomib Therapy for Refractory Anti-NMDA Receptor Encephalitis |
title_sort | early bortezomib therapy for refractory anti-nmda receptor encephalitis |
topic | Neurology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7118211/ https://www.ncbi.nlm.nih.gov/pubmed/32292386 http://dx.doi.org/10.3389/fneur.2020.00188 |
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