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Multicenter retrospective analysis of the effectiveness and safety of rituximab in Korean patients with refractory systemic lupus erythematosus

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dc.contributor.authorBang, S.-Y.-
dc.contributor.authorLee, C.K.-
dc.contributor.authorKang, Y.M.-
dc.contributor.authorKim, H.-A.-
dc.contributor.authorSuh, C.-H.-
dc.contributor.authorChung, W.T.-
dc.contributor.authorPark, Y.-B.-
dc.contributor.authorChoe, J.-Y.-
dc.contributor.authorKim, T.-J.-
dc.contributor.authorPark, Y.-W.-
dc.contributor.authorYoo, D.-H.-
dc.contributor.authorBae, S.-C.-
dc.contributor.authorLee, H.-S.-
dc.date.accessioned2021-08-02T19:26:19Z-
dc.date.available2021-08-02T19:26:19Z-
dc.date.created2021-05-13-
dc.date.issued2012-12-
dc.identifier.issn2090-0422-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/27416-
dc.description.abstractObjective. Although two recent randomized placebo-controlled trials of rituximab (RTX) failed to demonstrate efficacy in systemic lupus erythematosus (SLE), clinicians continue to use off-label RTX for cases refractory to current treatments. We evaluated the effectiveness and safety of rituximab for patients with refractory SLE in Korea. Methods. We retrospectively analyzed multicenter patients treated with RTX in Korea. Results. 39 SLE patients treated with RTX were included in the following manner: lupus nephritis 43.6%, hematologic 33.3%, arthritis 7.8%, myositis 7.8%, and others 7.7%. All patients had responded poorly to at least one conventional immunosuppressive agent (mean 2.5 ± 1.1, cyclophosphamide 43.6%, mycophenolate mofetil 48.7%, and other drugs) before RTX. Clinical improvements (complete or partial remission) occurred in patients with renal disease, hematologic disease, arthritis, myositis, and other manifestations at 6 months after RTX. The SLEDAI score was significantly decreased from 10.8 ± 7.1 at baseline to 6.7 ± 4.0 at 6 months, 6.2 ± 4.1 at 12 months, and 5.5 ± 3.6 at 24 months after RTX (P < 0.05). Among 28 clinical responders, 4 patients experienced a relapse of disease at 25 ± 4 months. Infections were noted in 3 patients (7.7%). Conclusion. RTX could be an effective and relatively safe therapeutic option in patients with severe refractory SLE until novel B-cell depletion therapy is available. © 2012 So-Young Bang et al.-
dc.language영어-
dc.language.isoen-
dc.titleMulticenter retrospective analysis of the effectiveness and safety of rituximab in Korean patients with refractory systemic lupus erythematosus-
dc.typeArticle-
dc.contributor.affiliatedAuthorBang, S.-Y.-
dc.contributor.affiliatedAuthorBae, S.-C.-
dc.contributor.affiliatedAuthorLee, H.-S.-
dc.identifier.doi10.1155/2012/565039-
dc.identifier.scopusid2-s2.0-84872125016-
dc.identifier.bibliographicCitationAutoimmune Diseases, v.1, no.1, pp.1 - 7-
dc.relation.isPartOfAutoimmune Diseases-
dc.citation.titleAutoimmune Diseases-
dc.citation.volume1-
dc.citation.number1-
dc.citation.startPage1-
dc.citation.endPage7-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscopus-
dc.subject.keywordPlusazathioprine-
dc.subject.keywordPluscyclophosphamide-
dc.subject.keywordPluscyclosporin-
dc.subject.keywordPlushydroxychloroquine-
dc.subject.keywordPlusimmunoglobulin-
dc.subject.keywordPlusmethotrexate-
dc.subject.keywordPlusmycophenolic acid-
dc.subject.keywordPlusprednisone-
dc.subject.keywordPlusrituximab-
dc.subject.keywordPlustacrolimus-
dc.subject.keywordPlusabscess-
dc.subject.keywordPlusadult-
dc.subject.keywordPlusarthritis-
dc.subject.keywordPlusarticle-
dc.subject.keywordPlusclinical article-
dc.subject.keywordPlusclinical feature-
dc.subject.keywordPlusdrug efficacy-
dc.subject.keywordPlusdrug safety-
dc.subject.keywordPlusfemale-
dc.subject.keywordPlusfever-
dc.subject.keywordPlushematologic disease-
dc.subject.keywordPlushuman-
dc.subject.keywordPlusimmunosuppressive treatment-
dc.subject.keywordPluskidney disease-
dc.subject.keywordPlusKorea-
dc.subject.keywordPluslupus erythematosus nephritis-
dc.subject.keywordPlusmale-
dc.subject.keywordPlusmulticenter study-
dc.subject.keywordPlusmyalgia-
dc.subject.keywordPlusmyositis-
dc.subject.keywordPluspneumonia-
dc.subject.keywordPluspriority journal-
dc.subject.keywordPlusrash-
dc.subject.keywordPlusremission-
dc.subject.keywordPlusretrospective study-
dc.subject.keywordPlussystemic lupus erythematosus-
dc.subject.keywordPlustreatment duration-
dc.subject.keywordPlustreatment response-
dc.subject.keywordPlustuberculosis-
dc.identifier.urlhttps://www.hindawi.com/journals/ad/2012/565039/-
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