Treatment of neuromyelitis optica with ...
Type de document :
Article dans une revue scientifique
PMID :
URL permanente :
Titre :
Treatment of neuromyelitis optica with rituximab: a 2-year prospective multicenter study.
Auteur(s) :
Cabre, Philippe [Auteur]
Mejdoubi, M [Auteur]
Jeannin, S [Auteur]
Merle, H [Auteur]
Plumelle, Y [Auteur]
Cavillon, G [Auteur]
Smadja, D [Auteur]
Marignier, Romain [Auteur]
Vermersch, Patrick [Auteur]
Lille Inflammation Research International Center (LIRIC) - U995
Mejdoubi, M [Auteur]
Jeannin, S [Auteur]
Merle, H [Auteur]
Plumelle, Y [Auteur]
Cavillon, G [Auteur]
Smadja, D [Auteur]
Marignier, Romain [Auteur]
Vermersch, Patrick [Auteur]

Lille Inflammation Research International Center (LIRIC) - U995
Titre de la revue :
Journal of Neurology
Nom court de la revue :
J. Neurol.
Numéro :
265
Pagination :
917–925
Date de publication :
2018-04
ISSN :
1432-1459
Mot(s)-clé(s) :
Rituximab
Neuromyelitis optica
Magnetic resonance imaging
Treatment
Neuromyelitis optica
Magnetic resonance imaging
Treatment
Discipline(s) HAL :
Sciences du Vivant [q-bio]
Résumé en anglais : [en]
Objective
Neuromyelitis optica (NMO) is a very severe autoimmune disorder of the central nervous system. It affects young subjects and has a poor prognosis both on a functional and vital level. Therefore, it is imperative ...
Lire la suite >Objective Neuromyelitis optica (NMO) is a very severe autoimmune disorder of the central nervous system. It affects young subjects and has a poor prognosis both on a functional and vital level. Therefore, it is imperative to reduce the frequency of relapses. The purpose of this study was to evaluate the clinical and neuroradiological effectiveness of rituximab (RTX) on active forms of NMO. Methods We conducted a 2-year open prospective multicenter study that included 32 patients treated with RTX at a dose of 375 mg/m2/week for 1 month. When the number of circulating CD19+ B cells reached 1%, a maintenance therapy was started, consisting of two infusions of 1 g of RTX, administered at a 15-day interval. The primary objective was to reduce the annual relapse rate (ARR), in comparison to that observed in the 2 years before treatment onset. Results Rituximab administration reduced the ARR from 1.34 to 0.56 (p = 0.0005). The average Expanded Disability Status Scale (EDSS) score significantly improved by 1.1 point, from 5.9 (2–9) to 4.8 (0–9) after 2 years (p = 0.03). Anti-aquaporin-4 antibodies’ level predicted treatment failure (p = 0.03). Frequency of Gad+ lesions in spinal cord decreased from 23.3 to 14.2%. RTX treatment did not prevent the death of three patients (treatment failure in two patients and acute myeloid leukemia in a patient previously treated with mitoxantrone). Conclusion Rituximab is clinically effective in active forms of NMO, although few patients are resistant to the treatment.Lire moins >
Lire la suite >Objective Neuromyelitis optica (NMO) is a very severe autoimmune disorder of the central nervous system. It affects young subjects and has a poor prognosis both on a functional and vital level. Therefore, it is imperative to reduce the frequency of relapses. The purpose of this study was to evaluate the clinical and neuroradiological effectiveness of rituximab (RTX) on active forms of NMO. Methods We conducted a 2-year open prospective multicenter study that included 32 patients treated with RTX at a dose of 375 mg/m2/week for 1 month. When the number of circulating CD19+ B cells reached 1%, a maintenance therapy was started, consisting of two infusions of 1 g of RTX, administered at a 15-day interval. The primary objective was to reduce the annual relapse rate (ARR), in comparison to that observed in the 2 years before treatment onset. Results Rituximab administration reduced the ARR from 1.34 to 0.56 (p = 0.0005). The average Expanded Disability Status Scale (EDSS) score significantly improved by 1.1 point, from 5.9 (2–9) to 4.8 (0–9) after 2 years (p = 0.03). Anti-aquaporin-4 antibodies’ level predicted treatment failure (p = 0.03). Frequency of Gad+ lesions in spinal cord decreased from 23.3 to 14.2%. RTX treatment did not prevent the death of three patients (treatment failure in two patients and acute myeloid leukemia in a patient previously treated with mitoxantrone). Conclusion Rituximab is clinically effective in active forms of NMO, although few patients are resistant to the treatment.Lire moins >
Langue :
Anglais
Audience :
Internationale
Vulgarisation :
Non
Établissement(s) :
Inserm
Université de Lille
CHU Lille
Université de Lille
CHU Lille
Équipe(s) de recherche :
Immunity, inflammation and fibrsis in auto and allo-reactivity
Date de dépôt :
2019-03-01T14:46:27Z
2024-03-13T14:09:14Z
2024-03-13T14:09:14Z