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dc.creatorTsivgoulis G., Katsanos A.H., Mavridis D., Grigoriadis N., Dardiotis E., Heliopoulos I., Papathanasopoulos P., Karapanayiotides T., Kilidireas C., Hadjigeorgiou G.M., Voumvourakis K., Gravanis A., Papadimitriou A., Rompos A., Mouzaki A., Kylintireas C., Voumvourakis C., Karagogeos D., Hadjigeorgiou G., Kollias G., Helliopoulos I., Probert L., Ioannidis P., Pelidou S.-E., Tzartos S., Karapanagiotides T., Panoutsakopoulou V., HELANI (Hellenic Academy of Neuroimmunology)en
dc.date.accessioned2023-01-31T10:16:44Z
dc.date.available2023-01-31T10:16:44Z
dc.date.issued2016
dc.identifier10.1371/journal.pone.0163296
dc.identifier.issn19326203
dc.identifier.urihttp://hdl.handle.net/11615/80066
dc.description.abstractBackground: Although Fingolimod (FGD) and Natalizumab (NTZ) appear to be effective in relapsing-remitting multiple sclerosis (RRMS), they have never been directly compared in a randomized clinical trial (RCT). Methods and Findings: We evaluated the comparative efficacy of FGD vs. NTZ using a meta-analytical approach. Data from placebo-controlled RCTs was used for indirect comparisons and observational data was utilized for head-to-head comparisons. We identified 3 RCTs (2498 patients) and 5 observational studies (2576 patients). NTZ was associated with a greater reduction in the 2-year annualized relapse rate (ARR; SMDindirect = -0.24;95% CI: from -0.44 to -0.04; p = 0.005) and with the probability of no disease activity at 2 years (ORindirect:1.82, 95% CI: from 1.05 to 3.15) compared to FGD, while no differences between the two therapies were found in the proportion of patients who remained relapse-free (ORindirect= 1.20;95% CI: from 0.84 to 1.71) and those with disability progression (ORindirect = 0.76;95% CI: from 0.48 to 1.21) at 2 years. In the analysis of observational data, we found no significant differences between NTZ and FGD in the 2-year ARR (SMD = -0.05; 95% CI: from -0.26 to 0.16), and 2-year disability progression (OR:1.08;95% CI: from 0.77 to 1.52). However, NTZ-treated patients were more likely to remain relapse-free at 2-years compared to FGD (OR: 2.19;95% CI: from 1.15 to 4.18; p = z0.020). Conclusions: Indirect analyses of RCT data and head-to-head comparisons of observational findings indicate that NTZ may be more effective than FGD in terms of disease activity reduction in patients with RRMS. However, head-to-head RCTs are required to independently confirm this preliminary observation. © 2016 Tsivgoulis et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.en
dc.language.isoenen
dc.sourcePLoS ONEen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84991833410&doi=10.1371%2fjournal.pone.0163296&partnerID=40&md5=8083c9523715deebff79bce7f7d29f30
dc.subjectfingolimoden
dc.subjectnatalizumaben
dc.subjectplaceboen
dc.subjectArticleen
dc.subjectclinical effectivenessen
dc.subjectclinical evaluationen
dc.subjectdisabilityen
dc.subjectdisease associationen
dc.subjectdisease courseen
dc.subjectdrug efficacyen
dc.subjecthumanen
dc.subjectmeta analysisen
dc.subjectmultiple sclerosisen
dc.subjectobservational studyen
dc.subjectrandomized controlled trial (topic)en
dc.subjectrelapseen
dc.subjectsystematic reviewen
dc.subjecttreatment outcomeen
dc.subjecttreatment planningen
dc.subjectPublic Library of Scienceen
dc.titleThe efficacy of Natalizumab versus Fingolimod for patients with relapsing-remitting multiple sclerosis: A systematic review, indirect evidence from randomized placebo-controlled trials and meta-analysis of observational head-to-head trialsen
dc.typejournalArticleen


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