Treatment of multiple sclerosis with rituximab: A Spanish multicenter experience
INTRODUCTION: Rituximab (RTX) is considered a potential therapeutic option for relapsing-remitting (RRMS) and progressive forms (PMS) of multiple sclerosis (MS). The main objective of this work was to investigate the effectiveness and safety of rituximab in MS. PATIENTS AND METHODS: Observational mu...
| Autores: | , , , , , , , , , , , , , , , , , , , , , |
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| Tipo de recurso: | artículo |
| Fecha de publicación: | 2023 |
| País: | España |
| Institución: | Conselleria de Salut i Consum del Govern de les Illes Balears |
| Repositorio: | Docusalut |
| Idioma: | inglés |
| OAI Identifier: | oai:docusalut.com:20.500.13003/25433 |
| Acceso en línea: | https://hdl.handle.net/20.500.13003/25433 |
| Access Level: | acceso abierto |
| Palabra clave: | Antibodies, Monoclonal Multiple Sclerosis Multiple Sclerosis, Chronic Progressive Multiple Sclerosis, Relapsing-Remitting Rituximab Anticuerpos Monoclonales Esclerosis Múltiple Esclerosis Múltiple Crónica Progresiva Esclerosis Múltiple Recurrente-Remitente anti-CD20 monoclonal antibody multiple sclerosis progressive multiple sclerosis relapsing-remitting multiple sclerosis rituximab treatment |
| Sumario: | INTRODUCTION: Rituximab (RTX) is considered a potential therapeutic option for relapsing-remitting (RRMS) and progressive forms (PMS) of multiple sclerosis (MS). The main objective of this work was to investigate the effectiveness and safety of rituximab in MS. PATIENTS AND METHODS: Observational multicenter study of clinical and radiological effectiveness and safety of rituximab in RRMS and PMS. RESULTS: A total of 479 rituximab-treated patients were included in 12 Spanish centers, 188 RRMS (39.3%) and 291 (60.7%) PMS. Despite standard treatment, the annualized relapse rate (ARR) the year before RTX was 0.63 (: 0.8) and 156 patients (41%) had at least one gadolinium-enhanced lesion (GEL) on baseline MRI. Mean EDSS had increased from 4.3 ( 1.9) to 4.8 (: 1.7) and almost half of the patients (41%) had worsened at least one point. After a median follow-up of 14.2 months ( 6.5-27.2), ARR decreased by 85.7% ( < 0.001) and GEL by 82.9%, from 0.41 to 0.07 ( < 0.001). A significant decrease in EDSS to 4.7 ( = 0.046) was observed after 1 year of treatment and this variable remained stable during the second year of therapy. There was no evidence of disease activity in 68% of patients. Infusion-related symptoms were the most frequent side effect (19.6%) and most were mild. Relevant infections were reported only in 18 patients (including one case of probable progressive multifocal leukoencephalopathy). CONCLUSION: Rituximab could be an effective and safe treatment in RRMS, including aggressive forms of the disease. Some selected PMS patients could also benefit from this treatment. |
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