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Effect of Rituximab Compared with Natalizumab and Fingolimod in Patients with Relapsing–Remitting Multiple Sclerosis: A Cohort Study

The objective of this study was to evaluate the clinical files of patients with RRMS who started rituximab (RTX) compared with a second-line treatment (natalizumab (NTZ) or fingolimod (FTY)). This was a historical cohort study. We compared the effect according to the Expanded Disability Status Scale...

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Detalles Bibliográficos
Autores principales: Hernández-Preciado, Martha Rocio, Marquez-Pedroza, Jazmin, Sánchez-Rosales, Nayeli Alejandra, García-Rivera, José de Jesús, Kobayashi-Gutiérrez, Antonio, Torres-Mendoza, Blanca Miriam, Chavarría-Avila, Efraín, Montaño-Serrano, Raúl Alejandro, Cortes-Enriquez, Fernando, Mireles-Ramírez, Mario Alberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9267823/
https://www.ncbi.nlm.nih.gov/pubmed/35806869
http://dx.doi.org/10.3390/jcm11133584
Descripción
Sumario:The objective of this study was to evaluate the clinical files of patients with RRMS who started rituximab (RTX) compared with a second-line treatment (natalizumab (NTZ) or fingolimod (FTY)). This was a historical cohort study. We compared the effect according to the Expanded Disability Status Scale (EDSS) and the number of relapses in RRMS patients receiving these treatments after a mean period of 12 months. We found a statistically significant difference (p < 0.001) when comparing the EDSS scores and the annual relapse rates of patients receiving RTX with those receiving NTZ or FTY. This study is essential for our clinical practice, since patients with limited treatment options represent a challenge with regard to the management of their medical care. However, clinical trials and prospective studies with long follow-up periods are necessary to provide sufficient evidence on the efficacy of RTX and thus include this treatment in the therapeutic profile of patients with MS.