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Neurological management and work-up of neurotoxicity associated with CAR T cell therapy
INTRODUCTION: Treatment with CD19 chimeric antigen receptor (CAR) T cells is an innovative therapeutic approach for patients with relapsed/refractory diffuse large B cell lymphoma (r/rDLBCL) and B-lineage acute lymphoblastic leukemia (r/rALL). However, convincing therapeutic response rates can be ac...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8744256/ https://www.ncbi.nlm.nih.gov/pubmed/35000613 http://dx.doi.org/10.1186/s42466-021-00166-5 |
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author | Möhn, Nora Bonda, Viktoria Grote-Levi, Lea Panagiota, Victoria Fröhlich, Tabea Schultze-Florey, Christian Wattjes, Mike P. Beutel, Gernot Eder, Matthias David, Sascha Körner, Sonja Höglinger, Günter Stangel, Martin Ganser, Arnold Koenecke, Christian Skripuletz, Thomas |
author_facet | Möhn, Nora Bonda, Viktoria Grote-Levi, Lea Panagiota, Victoria Fröhlich, Tabea Schultze-Florey, Christian Wattjes, Mike P. Beutel, Gernot Eder, Matthias David, Sascha Körner, Sonja Höglinger, Günter Stangel, Martin Ganser, Arnold Koenecke, Christian Skripuletz, Thomas |
author_sort | Möhn, Nora |
collection | PubMed |
description | INTRODUCTION: Treatment with CD19 chimeric antigen receptor (CAR) T cells is an innovative therapeutic approach for patients with relapsed/refractory diffuse large B cell lymphoma (r/rDLBCL) and B-lineage acute lymphoblastic leukemia (r/rALL). However, convincing therapeutic response rates can be accompanied by cytokine release syndrome (CRS) and severe neurotoxicity termed immune effector cell-associated neurotoxicity syndrome (ICANS). METHODS: Single center, prospective observational study of fifteen consecutive r/r DLBCL patients treated with Tisagenlecleucel within 1 year at Hannover Medical School. Extensive neurological work-up prior to CAR T cell infusion included clinical examination, cognitive testing (Montreal-Cognitive-Assessment), brain MRI, electroencephalogram, electroneurography, and analysis of cerebrospinal fluid. After CAR T cell infusion, patients were neurologically examined for 10 consecutive days. Afterwards, all patients were assessed at least once a week. RESULTS: ICANS occurred in 4/15 patients (27%) within 6 days (4–6 days) after CAR T cell infusion. Patients with ICANS grade 2 (n = 3) exhibited similar neurological symptoms including apraxia, expressive aphasia, disorientation, and hallucinations, while brain MRI was inconspicuous in either case. Treatment with dexamethasone rapidly resolved the clinical symptoms in all three patients. Regarding baseline parameters prior to CAR T cell treatment, patients with and without ICANS did not differ. CONCLUSIONS: In our cohort, ICANS occurred in only every fourth patient and rather low grade neurotoxicity was found during daily examination. Our results demonstrate that a structured neurological baseline examination and close monitoring are helpful to detect CAR T cell related neurotoxicity already at an early stage and to potentially prevent higher grade neurotoxicity. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s42466-021-00166-5. |
format | Online Article Text |
id | pubmed-8744256 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-87442562022-02-01 Neurological management and work-up of neurotoxicity associated with CAR T cell therapy Möhn, Nora Bonda, Viktoria Grote-Levi, Lea Panagiota, Victoria Fröhlich, Tabea Schultze-Florey, Christian Wattjes, Mike P. Beutel, Gernot Eder, Matthias David, Sascha Körner, Sonja Höglinger, Günter Stangel, Martin Ganser, Arnold Koenecke, Christian Skripuletz, Thomas Neurol Res Pract Research Article INTRODUCTION: Treatment with CD19 chimeric antigen receptor (CAR) T cells is an innovative therapeutic approach for patients with relapsed/refractory diffuse large B cell lymphoma (r/rDLBCL) and B-lineage acute lymphoblastic leukemia (r/rALL). However, convincing therapeutic response rates can be accompanied by cytokine release syndrome (CRS) and severe neurotoxicity termed immune effector cell-associated neurotoxicity syndrome (ICANS). METHODS: Single center, prospective observational study of fifteen consecutive r/r DLBCL patients treated with Tisagenlecleucel within 1 year at Hannover Medical School. Extensive neurological work-up prior to CAR T cell infusion included clinical examination, cognitive testing (Montreal-Cognitive-Assessment), brain MRI, electroencephalogram, electroneurography, and analysis of cerebrospinal fluid. After CAR T cell infusion, patients were neurologically examined for 10 consecutive days. Afterwards, all patients were assessed at least once a week. RESULTS: ICANS occurred in 4/15 patients (27%) within 6 days (4–6 days) after CAR T cell infusion. Patients with ICANS grade 2 (n = 3) exhibited similar neurological symptoms including apraxia, expressive aphasia, disorientation, and hallucinations, while brain MRI was inconspicuous in either case. Treatment with dexamethasone rapidly resolved the clinical symptoms in all three patients. Regarding baseline parameters prior to CAR T cell treatment, patients with and without ICANS did not differ. CONCLUSIONS: In our cohort, ICANS occurred in only every fourth patient and rather low grade neurotoxicity was found during daily examination. Our results demonstrate that a structured neurological baseline examination and close monitoring are helpful to detect CAR T cell related neurotoxicity already at an early stage and to potentially prevent higher grade neurotoxicity. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s42466-021-00166-5. BioMed Central 2022-01-10 /pmc/articles/PMC8744256/ /pubmed/35000613 http://dx.doi.org/10.1186/s42466-021-00166-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article Möhn, Nora Bonda, Viktoria Grote-Levi, Lea Panagiota, Victoria Fröhlich, Tabea Schultze-Florey, Christian Wattjes, Mike P. Beutel, Gernot Eder, Matthias David, Sascha Körner, Sonja Höglinger, Günter Stangel, Martin Ganser, Arnold Koenecke, Christian Skripuletz, Thomas Neurological management and work-up of neurotoxicity associated with CAR T cell therapy |
title | Neurological management and work-up of neurotoxicity associated with CAR T cell therapy |
title_full | Neurological management and work-up of neurotoxicity associated with CAR T cell therapy |
title_fullStr | Neurological management and work-up of neurotoxicity associated with CAR T cell therapy |
title_full_unstemmed | Neurological management and work-up of neurotoxicity associated with CAR T cell therapy |
title_short | Neurological management and work-up of neurotoxicity associated with CAR T cell therapy |
title_sort | neurological management and work-up of neurotoxicity associated with car t cell therapy |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8744256/ https://www.ncbi.nlm.nih.gov/pubmed/35000613 http://dx.doi.org/10.1186/s42466-021-00166-5 |
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