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dc.creatorTsivgoulis G., Katsanos A.H., Grigoriadis N., Hadjigeorgiou G.M., Heliopoulos I., Papathanasopoulos P., Kilidireas C., Voumvourakis K., Dardiotis E., Helani (Hellenic Academy Of Neuroimmunology)en
dc.date.accessioned2023-01-31T10:16:40Z
dc.date.available2023-01-31T10:16:40Z
dc.date.issued2015
dc.identifier10.1371/journal.pone.0144538
dc.identifier.issn19326203
dc.identifier.urihttp://hdl.handle.net/11615/80063
dc.description.abstractImportance: A number of officially approved disease-modifying drugs (DMD) are currently available for the early intervention in patients with relapsing-remitting multiple sclerosis (RRMS). The aim of the present study was to systematically evaluate the effect of DMDs on disability progression in RRMS Methods: We performed a systematic review on MEDLINE and SCOPUS databases to include all available placebo-controlled randomized clinical trials (RCTs) of RRMS patients that reported absolute numbers or percentages of disability progression during each study period. Observational studies, case series, case reports, RCTs without placebo subgroups and studies reporting the use of RRMS therapies that are not still officially approved were excluded. Risk ratios (RRs) were calculated in each study protocol to express the comparison of disability progression in RRMS patients treated with a DMD and those RRMS patients receiving placebo. The mixed-effects model was used to calculate both the pooled point estimate in each subgroup and the overall estimates. Results: DMDs for RRMS were found to have a significantly lower risk of disability progression compared to placebo (RR = 0.72, 95%CI: 0.66-0.79; p < 0.001), with no evidence of heterogeneity or publication bias. In subsequent subgroup analyses, neither dichotomization of DMDs as "first" and "second" line RRMS therapies [(RR = 0.72, 95% CI = 0.65-0.80) vs. (RR = 0.72, 95% = 0.57-0.91); p = 0.96] nor the route of administration (injectable or oral) [RR = 0.75 (95% CI = 0.64-0.87) vs. RR = 0.74 (95% CI = 0.66-0.83); p = 0.92] had a differential effect on the risk of disability progression. Either considerable (5-20%) or significant (>20%) rates of loss to follow-up were reported in many study protocols, while financial and/ or other support from pharmaceutical industries with a clear conflict of interest on the study outcomes was documented in all included studies. Conclusions: Available DMD are effective in reducing disability progression in patients with RRMS, independently of the route of administration and their classification as "first" or "second" line therapies. Attrition bias needs to be taken into account in the interpretation of these findings. © 2015 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-s2.0-84947035139&doi=10.1371%2fjournal.pone.0144538&partnerID=40&md5=fc7a5921eb3c85040ee0b82c3a023b2a
dc.subjectbeta1a interferonen
dc.subjectfingolimoden
dc.subjectfumaric acid dimethyl esteren
dc.subjectglatirameren
dc.subjectinterferon beta serineen
dc.subjectnatalizumaben
dc.subjectpeginterferon beta1aen
dc.subjectteriflunomideen
dc.subjectimmunosuppressive agenten
dc.subjectArticleen
dc.subjectdisease courseen
dc.subjectdrug efficacyen
dc.subjectdrug responseen
dc.subjecthumanen
dc.subjectmeta analysisen
dc.subjectmultiple sclerosisen
dc.subjectoutcome assessmenten
dc.subjectprimary health careen
dc.subjectrandomized controlled trial (topic)en
dc.subjectrisk assessmenten
dc.subjectsystematic reviewen
dc.subjectMultiple Sclerosis, Relapsing-Remittingen
dc.subjecttreatment outcomeen
dc.subjectHumansen
dc.subjectImmunosuppressive Agentsen
dc.subjectMultiple Sclerosis, Relapsing-Remittingen
dc.subjectRandomized Controlled Trials as Topicen
dc.subjectTreatment Outcomeen
dc.subjectPublic Library of Scienceen
dc.titleThe Effect of Disease Modifying Therapies on Disease Progression in Patients with Relapsing-Remitting Multiple Sclerosis: A Systematic Review and Meta-Analysisen
dc.typejournalArticleen


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