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Real-World Effectiveness of Natalizumab in Korean Patients With Multiple Sclerosis

Background and Purpose: Natalizumab is a highly efficacious disease-modifying therapy for relapsing-remitting multiple sclerosis (MS). Data on the efficacy and safety profile of natalizumab in Asian patients with MS are limited. This study assessed the efficacy and safety of natalizumab in Korean pa...

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Autores principales: Kim, Ki Hoon, Kim, Su-Hyun, Park, Na Young, Hyun, Jae-Won, Kim, Ho Jin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8299833/
https://www.ncbi.nlm.nih.gov/pubmed/34305808
http://dx.doi.org/10.3389/fneur.2021.714941
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author Kim, Ki Hoon
Kim, Su-Hyun
Park, Na Young
Hyun, Jae-Won
Kim, Ho Jin
author_facet Kim, Ki Hoon
Kim, Su-Hyun
Park, Na Young
Hyun, Jae-Won
Kim, Ho Jin
author_sort Kim, Ki Hoon
collection PubMed
description Background and Purpose: Natalizumab is a highly efficacious disease-modifying therapy for relapsing-remitting multiple sclerosis (MS). Data on the efficacy and safety profile of natalizumab in Asian patients with MS are limited. This study assessed the efficacy and safety of natalizumab in Korean patients with MS in a real-world setting. Methods: This study enrolled consecutive Korean patients with active relapsing-remitting MS who were treated with natalizumab for at least 6 months between 2015 and 2021. To evaluate the therapeutic outcome of natalizumab, we used the Expanded Disability Status Scale (EDSS) scores and brain magnetic resonance imaging; adverse events were assessed at regular intervals. No evidence of disease activity (NEDA) was defined as no clinical relapse, no worsening of EDSS score, and no radiological activities. Results: Fourteen subjects with MS were included in the study. The mean age at initiation of natalizumab therapy was 32 years. All patients were positive for anti-John Cunningham virus antibodies before natalizumab administration. The mean annual relapse rate was markedly reduced from 2.7 ± 3.2 before natalizumab therapy to 0.1 ± 0.4 during natalizumab therapy (p = 0.001). Disability was either improved or stabilized after natalizumab treatment in 13 patients (93%). During the 1st year and 2 years after initiating natalizumab, NEDA-3 was achieved in 11/12 (92%) and 9/11 (82%) patients, respectively. No progressive multifocal leukoencephalopathy or other serious adverse events leading to the discontinuation of natalizumab were observed. Conclusions: Natalizumab therapy showed high efficacy in treating Korean patients with active MS, without unexpected safety problems.
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spelling pubmed-82998332021-07-24 Real-World Effectiveness of Natalizumab in Korean Patients With Multiple Sclerosis Kim, Ki Hoon Kim, Su-Hyun Park, Na Young Hyun, Jae-Won Kim, Ho Jin Front Neurol Neurology Background and Purpose: Natalizumab is a highly efficacious disease-modifying therapy for relapsing-remitting multiple sclerosis (MS). Data on the efficacy and safety profile of natalizumab in Asian patients with MS are limited. This study assessed the efficacy and safety of natalizumab in Korean patients with MS in a real-world setting. Methods: This study enrolled consecutive Korean patients with active relapsing-remitting MS who were treated with natalizumab for at least 6 months between 2015 and 2021. To evaluate the therapeutic outcome of natalizumab, we used the Expanded Disability Status Scale (EDSS) scores and brain magnetic resonance imaging; adverse events were assessed at regular intervals. No evidence of disease activity (NEDA) was defined as no clinical relapse, no worsening of EDSS score, and no radiological activities. Results: Fourteen subjects with MS were included in the study. The mean age at initiation of natalizumab therapy was 32 years. All patients were positive for anti-John Cunningham virus antibodies before natalizumab administration. The mean annual relapse rate was markedly reduced from 2.7 ± 3.2 before natalizumab therapy to 0.1 ± 0.4 during natalizumab therapy (p = 0.001). Disability was either improved or stabilized after natalizumab treatment in 13 patients (93%). During the 1st year and 2 years after initiating natalizumab, NEDA-3 was achieved in 11/12 (92%) and 9/11 (82%) patients, respectively. No progressive multifocal leukoencephalopathy or other serious adverse events leading to the discontinuation of natalizumab were observed. Conclusions: Natalizumab therapy showed high efficacy in treating Korean patients with active MS, without unexpected safety problems. Frontiers Media S.A. 2021-07-08 /pmc/articles/PMC8299833/ /pubmed/34305808 http://dx.doi.org/10.3389/fneur.2021.714941 Text en Copyright © 2021 Kim, Kim, Park, Hyun and Kim. 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
Kim, Ki Hoon
Kim, Su-Hyun
Park, Na Young
Hyun, Jae-Won
Kim, Ho Jin
Real-World Effectiveness of Natalizumab in Korean Patients With Multiple Sclerosis
title Real-World Effectiveness of Natalizumab in Korean Patients With Multiple Sclerosis
title_full Real-World Effectiveness of Natalizumab in Korean Patients With Multiple Sclerosis
title_fullStr Real-World Effectiveness of Natalizumab in Korean Patients With Multiple Sclerosis
title_full_unstemmed Real-World Effectiveness of Natalizumab in Korean Patients With Multiple Sclerosis
title_short Real-World Effectiveness of Natalizumab in Korean Patients With Multiple Sclerosis
title_sort real-world effectiveness of natalizumab in korean patients with multiple sclerosis
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8299833/
https://www.ncbi.nlm.nih.gov/pubmed/34305808
http://dx.doi.org/10.3389/fneur.2021.714941
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