Real-world experience of ocrelizumab in multiple sclerosis patients in Latin America

Author:

ROJAS Juan Ignacio1ORCID,PATRUCCO Liliana2ORCID,FRUNS Manuel3ORCID,HORNUNG Giesela3,FLORES José4ORCID,CARNERO CONTENTTI Edgar5ORCID,LOPEZ Pablo Adrian5ORCID,PETTINICCHI Juan Pablo5ORCID,CARIDE Alejandro5ORCID,GALLEGUILLOS Lorna6ORCID,BARAHONA Jorge6ORCID,DIAZ Violeta6,HERNÁNDEZ Marianella6ORCID,ALONSO Ricardo7ORCID,CRISTIANO Edgardo8ORCID

Affiliation:

1. Hospital Universitario de CEMIC, Argentina; Centro de Esclerosis Múltiple de Buenos Aires, Argentina

2. Centro de Esclerosis Múltiple de Buenos Aires, Argentina; Hospital Italiano de Buenos Aires, Argentina

3. Clínica las Condes, Chile

4. Instituto Nacional de Neurología y Neurocirugía, México; Centro Neurológico ABC Santa Fé, México

5. Hospital Alemán, Argentina

6. Clínica Alemana de Santiago, Chile

7. Hospital Ramos Mejía, Argentina; Hospital Universitario Sanatorio Guemes, Argentina

8. Centro de Esclerosis Múltiple de Buenos Aires, Argentina

Abstract

ABSTRACT Background: Despite the abundance of information concerning ocrelizumab in phase III clinical trials, there is scarce evidence regarding real-world patient profiles. Objective: The aim of this study was to investigate patient profiles, effectiveness and persistence with treatment among patients who used ocrelizumab for treatment of multiple sclerosis in Latin America. Methods: This was a retrospective multicenter study in Argentina, Chile and Mexico. Medical record databases on patients who received ocrelizumab were analyzed. Demographic and clinical variables were described, along with effectiveness outcomes, which included the proportions of patients free from clinical relapses, from disability progression and from new or enlarging T2 or T1 gadolinium-enhancing lesions, on annual magnetic resonance imaging. Results: A total of 81 patients were included. The most frequent phenotype was relapsing-remitting MS, in 64.2% of the patients. The mean age at study entry was 41.3 ± 12.0 years and 51.8% were women. A total of 38% had had relapse activity during the 12 months before starting on ocrelizumab, with a mean relapse rate of 1.3 ± 0.6 during that period. 75% were free from clinical relapses and 91% were free from gadolinium-enhancing lesions in the relapsing-remitting course. Ocrelizumab discontinuation during the first 12 months was observed in three patients (3.7%). The mean persistence observed during the first-year follow-up was 338 ± 24 days. Conclusions: Our study is in line with previous randomized clinical trials and recent real-world studies describing patient profiles, effectiveness and persistence regarding ocrelizumab treatment in multiple sclerosis patients in Latin America.

Publisher

FapUNIFESP (SciELO)

Subject

Neurology,Neurology (clinical)

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