Literature DB >> 15230299

Randomized controlled trials in systemic lupus erythematosus: what has been done and what do we need to do?

J Schiffenbauer1, L S Simon.   

Abstract

The study of systemic lupus erythematosus (SLE) is a challenging undertaking. It is difficult to assess outcomes in SLE randomized controlled trials (RCTs), and this is illustrated by the lack of new therapies approved for use in lupus. In a disease that is waxing and waning, and requires constantly changing medications, identifying treatment effects of new therapies may be difficult, and the use of potentially toxic therapies requires a rigorous understanding of the benefit to risk ratio. Some issues that need to be considered by the investigator in designing these studies include: 1) should the trial focus on patients with active or inactive disease; 2) which of the measures of disease activity should be used or should prevention of flares be examined; 3) should the study focus on defined organ specific endpoints or utilize one of the available disease activity indices to identify changes in disease activity; 4) should the trial be a superiority trial or an equivalence trial. This review summarizes the critical issues involving the design of studies in lupus and provides the reader with suggestions and recommendations for consideration before embarking on trials in this area.

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Year:  2004        PMID: 15230299     DOI: 10.1191/0961203303lu1033oa

Source DB:  PubMed          Journal:  Lupus        ISSN: 0961-2033            Impact factor:   2.911


  4 in total

Review 1.  B cell modulation in rheumatology.

Authors:  Gregg J Silverman; Sahil Khanna
Journal:  Curr Opin Pharmacol       Date:  2007-07-10       Impact factor: 5.547

2.  Down-regulated NOD2 by immunosuppressants in peripheral blood cells in patients with SLE reduces the muramyl dipeptide-induced IL-10 production.

Authors:  Shui-Lian Yu; Chun-Kwok Wong; Purple Tsz-Yan Wong; Da-Peng Chen; Cheuk-Chun Szeto; Edmund K Li; Lai-Shan Tam
Journal:  PLoS One       Date:  2011-08-19       Impact factor: 3.240

3.  CCR6+ Th cell distribution differentiates systemic lupus erythematosus patients based on anti-dsDNA antibody status.

Authors:  Wei Zhong; Zhenyu Jiang; Jiang Wu; Yanfang Jiang; Ling Zhao
Journal:  PeerJ       Date:  2018-02-09       Impact factor: 2.984

4.  Elevated levels of CCR6+ T helper 22 cells correlate with skin and renal impairment in systemic lupus erythematosus.

Authors:  Wei Zhong; Yanfang Jiang; Hongshuang Ma; Jiang Wu; Zhenyu Jiang; Ling Zhao
Journal:  Sci Rep       Date:  2017-10-11       Impact factor: 4.379

  4 in total

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