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Case series: Immune checkpoint inhibitor-induced transverse myelitis

INTRODUCTION: Increasing implementation of the highly efficacious immune checkpoint inhibitors (ICIs) has raised awareness of their various complications in the form of immune-related adverse events (irAEs). Transverse myelitis following ICIs is thought to be a rare but serious neurologic irAE and k...

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Autores principales: Chatterton, Sophie, Xi, Shuo, Jia, Jessica Xi, Krause, Martin, Long, Georgina V., Atkinson, Victoria, Menzies, Alexander M., Fernando, Suran L., Boyle, Thérèse, Kwok, Samuel, Duggins, Andrew, Karikios, Deme, Parratt, John D. E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9989185/
https://www.ncbi.nlm.nih.gov/pubmed/36895912
http://dx.doi.org/10.3389/fneur.2023.1130313
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author Chatterton, Sophie
Xi, Shuo
Jia, Jessica Xi
Krause, Martin
Long, Georgina V.
Atkinson, Victoria
Menzies, Alexander M.
Fernando, Suran L.
Boyle, Thérèse
Kwok, Samuel
Duggins, Andrew
Karikios, Deme
Parratt, John D. E.
author_facet Chatterton, Sophie
Xi, Shuo
Jia, Jessica Xi
Krause, Martin
Long, Georgina V.
Atkinson, Victoria
Menzies, Alexander M.
Fernando, Suran L.
Boyle, Thérèse
Kwok, Samuel
Duggins, Andrew
Karikios, Deme
Parratt, John D. E.
author_sort Chatterton, Sophie
collection PubMed
description INTRODUCTION: Increasing implementation of the highly efficacious immune checkpoint inhibitors (ICIs) has raised awareness of their various complications in the form of immune-related adverse events (irAEs). Transverse myelitis following ICIs is thought to be a rare but serious neurologic irAE and knowledge is limited about this distinct clinical entity. CASES: We describe four patients across three tertiary centers in Australia with ICI-induced transverse myelitis. Three patients had a diagnosis of stage III–IV melanoma treated with nivolumab and one patient had stage IV non-small cell lung cancer treated with pembrolizumab. All patients had longitudinally extensive transverse myelitis on magnetic resonance imaging (MRI) spine and clinical presentation was accompanied by inflammatory cerebrospinal fluid (CSF) findings. Half of our cohort had received spinal radiotherapy, with the areas of transverse myelitis extending beyond the level of previous radiation field. Inflammatory changes on neuroimaging did not extend to the brain parenchyma or caudal nerve roots, except for one case involving the conus medullaris. All patients received high dose glucocorticoids as first-line therapy, however the majority relapsed or had a refractory state (3/4) despite this, requiring escalation of their immunomodulation, with either induction intravenous immunoglobulin (IVIg) or plasmapheresis. Patients in our cohort who relapsed had a poorer outcome with more severe disability and reduced functional independence following resolution of their myelitis. Two patients had no progression of their malignancy and two patients had malignancy progression. Of the three patients who survived, two had resolution of their neurological symptoms and one remained symptomatic. CONCLUSION: We propose that prompt intensive immunomodulation is favored for patients with ICI-transverse myelitis in an attempt to reduce associated significant morbidity and mortality. Furthermore, there is a significant risk of relapse following cessation of immunomodulatory therapy. We suggest one treatment approach of IVMP and induction IVIg for all patients presenting with ICI-induced transverse myelitis based on such findings. With the increasing use of ICIs across oncology, further studies are required to explore this neurological phenomenon in greater detail to help establish management consensus guidelines.
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spelling pubmed-99891852023-03-08 Case series: Immune checkpoint inhibitor-induced transverse myelitis Chatterton, Sophie Xi, Shuo Jia, Jessica Xi Krause, Martin Long, Georgina V. Atkinson, Victoria Menzies, Alexander M. Fernando, Suran L. Boyle, Thérèse Kwok, Samuel Duggins, Andrew Karikios, Deme Parratt, John D. E. Front Neurol Neurology INTRODUCTION: Increasing implementation of the highly efficacious immune checkpoint inhibitors (ICIs) has raised awareness of their various complications in the form of immune-related adverse events (irAEs). Transverse myelitis following ICIs is thought to be a rare but serious neurologic irAE and knowledge is limited about this distinct clinical entity. CASES: We describe four patients across three tertiary centers in Australia with ICI-induced transverse myelitis. Three patients had a diagnosis of stage III–IV melanoma treated with nivolumab and one patient had stage IV non-small cell lung cancer treated with pembrolizumab. All patients had longitudinally extensive transverse myelitis on magnetic resonance imaging (MRI) spine and clinical presentation was accompanied by inflammatory cerebrospinal fluid (CSF) findings. Half of our cohort had received spinal radiotherapy, with the areas of transverse myelitis extending beyond the level of previous radiation field. Inflammatory changes on neuroimaging did not extend to the brain parenchyma or caudal nerve roots, except for one case involving the conus medullaris. All patients received high dose glucocorticoids as first-line therapy, however the majority relapsed or had a refractory state (3/4) despite this, requiring escalation of their immunomodulation, with either induction intravenous immunoglobulin (IVIg) or plasmapheresis. Patients in our cohort who relapsed had a poorer outcome with more severe disability and reduced functional independence following resolution of their myelitis. Two patients had no progression of their malignancy and two patients had malignancy progression. Of the three patients who survived, two had resolution of their neurological symptoms and one remained symptomatic. CONCLUSION: We propose that prompt intensive immunomodulation is favored for patients with ICI-transverse myelitis in an attempt to reduce associated significant morbidity and mortality. Furthermore, there is a significant risk of relapse following cessation of immunomodulatory therapy. We suggest one treatment approach of IVMP and induction IVIg for all patients presenting with ICI-induced transverse myelitis based on such findings. With the increasing use of ICIs across oncology, further studies are required to explore this neurological phenomenon in greater detail to help establish management consensus guidelines. Frontiers Media S.A. 2023-02-21 /pmc/articles/PMC9989185/ /pubmed/36895912 http://dx.doi.org/10.3389/fneur.2023.1130313 Text en Copyright © 2023 Chatterton, Xi, Jia, Krause, Long, Atkinson, Menzies, Fernando, Boyle, Kwok, Duggins, Karikios and Parratt. https://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
Chatterton, Sophie
Xi, Shuo
Jia, Jessica Xi
Krause, Martin
Long, Georgina V.
Atkinson, Victoria
Menzies, Alexander M.
Fernando, Suran L.
Boyle, Thérèse
Kwok, Samuel
Duggins, Andrew
Karikios, Deme
Parratt, John D. E.
Case series: Immune checkpoint inhibitor-induced transverse myelitis
title Case series: Immune checkpoint inhibitor-induced transverse myelitis
title_full Case series: Immune checkpoint inhibitor-induced transverse myelitis
title_fullStr Case series: Immune checkpoint inhibitor-induced transverse myelitis
title_full_unstemmed Case series: Immune checkpoint inhibitor-induced transverse myelitis
title_short Case series: Immune checkpoint inhibitor-induced transverse myelitis
title_sort case series: immune checkpoint inhibitor-induced transverse myelitis
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9989185/
https://www.ncbi.nlm.nih.gov/pubmed/36895912
http://dx.doi.org/10.3389/fneur.2023.1130313
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