<HashMap><database>biostudies-literature</database><scores/><additional><submitter>McCarthy EM</submitter><funding>Medical Research Council</funding><funding>National Institute for Health Research (NIHR)</funding><funding>NIH</funding><funding>Wellcome Trust</funding><pagination>470-479</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5850287</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>57(3)</volume><pubmed_abstract>&lt;h4>Objectives&lt;/h4>To describe the baseline characteristics of SLE patients requiring biologic therapy in the UK and to explore short term efficacy and infection rates associated with rituximab (RTX) use.&lt;h4>Methods&lt;/h4>Patients commencing biologic therapy for refractory SLE and who consented to join BILAG-BR were analysed. Baseline characteristics, disease activity (BILAG 2004/SLEDAI-2K) and rates of infection over follow-up were analysed. Response was defined as loss of all A and B BILAG scores to ⩽ 1 B score with no new A/B scores in other organ systems at 6 months.&lt;h4>Results&lt;/h4>Two hundred and seventy SLE patients commenced biologic therapy from September 2010 to September 2015, most commonly RTX (n = 261). Two hundred and fifty (93%) patients were taking glucocorticoids at baseline </pubmed_abstract><journal>Rheumatology (Oxford, England)</journal><pubmed_title>Short-term efficacy and safety of rituximab therapy in refractory systemic lupus erythematosus: results from the British Isles Lupus Assessment Group Biologics Register.</pubmed_title><pmcid>PMC5850287</pmcid><funding_grant_id>NF-SI-0515-10015</funding_grant_id><funding_grant_id>NF-SI-0512-10105</funding_grant_id><funding_grant_id>NF-SI-0617-10075</funding_grant_id><funding_grant_id>MR/M01665X/1</funding_grant_id><pubmed_authors>Nesbit S</pubmed_authors><pubmed_authors>Rahman A</pubmed_authors><pubmed_authors>Edwards CJ</pubmed_authors><pubmed_authors>Bruce IN</pubmed_authors><pubmed_authors>Sutton E</pubmed_authors><pubmed_authors>Teh LS</pubmed_authors><pubmed_authors>British Isles Lupus Assessment Group Biologics Register</pubmed_authors><pubmed_authors>White J</pubmed_authors><pubmed_authors>Lanyon P</pubmed_authors><pubmed_authors>Zoma A</pubmed_authors><pubmed_authors>Yee CS</pubmed_authors><pubmed_authors>Parker B</pubmed_authors><pubmed_authors>Griffiths B</pubmed_authors><pubmed_authors>Jayne D</pubmed_authors><pubmed_authors>Vital EM</pubmed_authors><pubmed_authors>McCarthy EM</pubmed_authors><pubmed_authors>McHugh NJ</pubmed_authors><pubmed_authors>Isenberg DA</pubmed_authors><pubmed_authors>Gordon C</pubmed_authors><pubmed_authors>D'Cruz DP</pubmed_authors><pubmed_authors>Rhodes B</pubmed_authors><pubmed_authors>Akil M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Short-term efficacy and safety of rituximab therapy in refractory systemic lupus erythematosus: results from the British Isles Lupus Assessment Group Biologics Register.</name><description>&lt;h4>Objectives&lt;/h4>To describe the baseline characteristics of SLE patients requiring biologic therapy in the UK and to explore short term efficacy and infection rates associated with rituximab (RTX) use.&lt;h4>Methods&lt;/h4>Patients commencing biologic therapy for refractory SLE and who consented to join BILAG-BR were analysed. Baseline characteristics, disease activity (BILAG 2004/SLEDAI-2K) and rates of infection over follow-up were analysed. Response was defined as loss of all A and B BILAG scores to ⩽ 1 B score with no new A/B scores in other organ systems at 6 months.&lt;h4>Results&lt;/h4>Two hundred and seventy SLE patients commenced biologic therapy from September 2010 to September 2015, most commonly RTX (n = 261). Two hundred and fifty (93%) patients were taking glucocorticoids at baseline </description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Mar</publication><modification>2025-04-18T20:15:42.113Z</modification><creation>2019-03-26T23:22:56Z</creation></dates><accession>S-EPMC5850287</accession><cross_references><pubmed>29216396</pubmed><doi>10.1093/rheumatology/kex395</doi></cross_references></HashMap>