دورية أكاديمية

Rituximab and glatiramer acetate in secondary progressive multiple sclerosis: A randomized clinical trial.

التفاصيل البيبلوغرافية
العنوان: Rituximab and glatiramer acetate in secondary progressive multiple sclerosis: A randomized clinical trial.
المؤلفون: Cheshmavar, Masoumeh, Mirmosayyeb, Omid, Badihian, Negin, Badihian, Shervin, Shaygannejad, Vahid
المصدر: Acta Neurologica Scandinavica; Feb2021, Vol. 143 Issue 2, p178-187, 10p
مصطلحات موضوعية: GLATIRAMER acetate, CLINICAL trials, MULTIPLE sclerosis, RITUXIMAB, DISEASE relapse
مستخلص: Background: Treatment options for secondary progressive multiple sclerosis (SPMS) are limitedly investigated. We aimed to compare the efficacy of rituximab (RTX) and glatiramer acetate (GA) in SPMS patients. Method: This open, randomized clinical trial was conducted on 84 SPMS patients, assigned to receive RTX or GA for 12 months. In RTX group, patients received 1 g intravenous RTX primarily and then every 6‐months. In GA group, patients received 40 mg of GA 3‐times/week subcutaneously. We measured EDSS as the primary outcome and neuroimaging findings, relapse rate (RR), and side effects as the secondary outcomes. Results: Seventy‐three patients completed the study (37 and 36 in RTX and GA groups, respectively). The mean EDSS increased from 3.05 ± 1.01 to 4.14 ± 0.91 in RTX group (p < 0.001) and from 3.22 ± 1.20 to 4.60 ± 0.67 in GA group (p < 0.001). No statistically significant difference was observed in EDSS between two groups (F(1, 67) = 3.377; p = 0.071). The number of active lesions in brain and cervical spine decreased with no difference between groups (p > 0.05). Also, RR decreased in both groups without significant difference between them (F(1, 67) = 0.390; p = 0.534). Non‐serious complications were observed in both groups. Conclusion: Neither RTX nor GA affects EDSS in SPMS patients. They are equally effective in the relapse control of these patients. [ABSTRACT FROM AUTHOR]
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قاعدة البيانات: Complementary Index
الوصف
تدمد:00016314
DOI:10.1111/ane.13344