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dc.contributor.authorFisher, BAen_US
dc.contributor.authorEverett, CCen_US
dc.contributor.authorRout, Jen_US
dc.contributor.authorO'Dwyer, JLen_US
dc.contributor.authorEmery, Pen_US
dc.contributor.authorPitzalis, Cen_US
dc.contributor.authorNg, W-Fen_US
dc.contributor.authorCarr, Aen_US
dc.contributor.authorPease, CTen_US
dc.contributor.authorPrice, EJen_US
dc.contributor.authorSutcliffe, Nen_US
dc.contributor.authorMakdissi, Jen_US
dc.contributor.authorTappuni, ARen_US
dc.contributor.authorGendi, NSTen_US
dc.contributor.authorHall, FCen_US
dc.contributor.authorRuddock, SPen_US
dc.contributor.authorFernandez, Cen_US
dc.contributor.authorHulme, CTen_US
dc.contributor.authorDavies, KAen_US
dc.contributor.authorEdwards, CJen_US
dc.contributor.authorLanyon, PCen_US
dc.contributor.authorMoots, RJen_US
dc.contributor.authorRoussou, Een_US
dc.contributor.authorRichards, Aen_US
dc.contributor.authorSharples, LDen_US
dc.contributor.authorBombardieri, Men_US
dc.contributor.authorBowman, SJen_US
dc.date.accessioned2018-11-15T09:23:58Z
dc.date.available2017-12-01en_US
dc.date.issued2018-03en_US
dc.date.submitted2018-08-24T16:44:11.872Z
dc.identifier.urihttp://qmro.qmul.ac.uk/xmlui/handle/123456789/50743
dc.description.abstractOBJECTIVES: To compare the effects of rituximab versus placebo on salivary gland ultrasound (SGUS) in primary Sjögren's syndrome (PSS) in a multicentre, multiobserver phase III trial substudy. METHODS: Subjects consenting to SGUS were randomised to rituximab or placebo given at weeks 0, 2, 24 and 26, and scanned at baseline and weeks 16 and 48. Sonographers completed a 0-11 total ultrasound score (TUS) comprising domains of echogenicity, homogeneity, glandular definition, glands involved and hypoechoic foci size. Baseline-adjusted TUS values were analysed over time, modelling change from baseline at each time point. For each TUS domain, we fitted a repeated-measures logistic regression model to model the odds of a response in the rituximab arm (≥1-point improvement) as a function of the baseline score, age category, disease duration and time point. RESULTS: 52 patients (n=26 rituximab and n=26 placebo) from nine centres completed baseline and one or more follow-up visits. Estimated between-group differences (rituximab-placebo) in baseline-adjusted TUS were -1.2 (95% CI -2.1 to -0.3; P=0.0099) and -1.2 (95% CI -2.0 to -0.5; P=0.0023) at weeks 16 and 48. Glandular definition improved in the rituximab arm with an OR of 6.8 (95% CI 1.1 to 43.0; P=0.043) at week 16 and 10.3 (95% CI 1.0 to 105.9; P=0.050) at week 48. CONCLUSIONS: We demonstrated statistically significant improvement in TUS after rituximab compared with placebo. This encourages further research into both B cell depletion therapies in PSS and SGUS as an imaging biomarker. TRIAL REGISTRATION NUMBER: 65360827, 2010-021430-64; Results.en_US
dc.description.sponsorshipThis study was funded by Arthritis Research UK (18810). Rituximab was provided free of charge by Hoffman La Roche.en_US
dc.format.extent412 - 416en_US
dc.languageengen_US
dc.relation.ispartofAnn Rheum Disen_US
dc.rightsThis is an Open Access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 4.0) license, which permits others to distribute, remix, adapt and build upon this work, for commercial use, provided the original work is properly cited. See: http://creativecommons.org/licenses/by/4.0/
dc.subjectB cellsen_US
dc.subjectsjøgren’s syndromeen_US
dc.subjectultrasonographyen_US
dc.titleEffect of rituximab on a salivary gland ultrasound score in primary Sjögren's syndrome: results of the TRACTISS randomised double-blind multicentre substudy.en_US
dc.typeArticle
dc.rights.holder© Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted.
dc.identifier.doi10.1136/annrheumdis-2017-212268en_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/29275334en_US
pubs.issue3en_US
pubs.notesNot knownen_US
pubs.publication-statusPublisheden_US
pubs.volume77en_US
dcterms.dateAccepted2017-12-01en_US


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