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Update of the literature review on treatment with biologics as a basis for the first update of the ASAS/EULAR management recommendations of ankylosing spondylitis

机译:有关使用生物制剂治疗的文献综述的更新,作为首次更新强直性脊柱炎的ASAS / EULAR管理建议的基础

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Objective: To perform a literature review as basis for the update of the Assessment in SpondyloArthritis international Society/European League Against Rheumatism (ASAS/EULAR) treatment recommendations with biologics in AS.Methods: A literature search of all publications found in MedLine, Embase and Cochrane database between 2005 and 2009 and in the EULAR/ACR meetings between 2007 and 2009 was performed. The research evidence and strength of recommendation (SOR) for biologics were provided.Results: Out of 247 reports on AS treatment with biologics, 98 contained efficacy data and 25 had complete data for analysis. The treatment effect sizes (95% CI) for anti-TNF vs placebo varied between 0.34 (0.08, 0.6) and 1.5 (0.45, 2.5) for BASDAI and 0.33 (0.07, 0.59) and 2.5 (1.3, 3.7) for BASFI. The calculation of the numbers needed to treat all the different outcomes varied between 2.3 and 3.0 patients for all ASAS outcomes and between 2.7 and 6.5 patients for ASAS partial remission. Data on biologics other than anti-TNF and for TNF blockers on juvenile SpA were limited. The incidence rates of uveitis during anti-TNF treatment varied between 4.4/100 patient-years (pys) and 15.6/100 pys during placebo (P < 0.05). The incidence rates of IBD flares were significantly less during infliximab treatment (0.2/100 pys). The rate of infections was higher in patients treated with anti-TNF as compared with placebo, but there was no difference in the incidence of serious infections for treatment with anti-TNF vs placebo.Conclusions: The overall evidence was very high for anti-TNF treatment (1b, SOR: A) with respect to efficacy and safety, while it was low for biologic treatment other than anti-TNF (3, SOR: C).
机译:目的:进行文献综述,作为更新脊柱关节炎国际协会/欧洲抗风湿病联盟(ASAS / EULAR)的AS中使用生物制剂治疗建议的评估方法。方法:对MedLine,Embase和进行了2005年至2009年之间的Cochrane数据库以及2007年至2009年之间的EULAR / ACR会议。结果:在247份有关生物制剂AS治疗的报告中,有98份包含功效数据,而25份具有完整的分析数据。抗TNF和安慰剂的治疗效果大小(95%CI)在BASDAI的0.34(0.08,0.6)和1.5(0.45,2.5)之间以及BASFI的0.33(0.07,0.59)和2.5(1.3,3.7)之间变化。对于所有ASAS结局,治疗所有不同结局所需的数字的计算结果在2.3至3.0例患者之间,对于ASAS部分缓解在2.7至6.5例患者之间。除抗TNF以外的其他生物制剂以及针对青少年SpA的TNF阻滞剂的数据有限。抗TNF治疗期间葡萄膜炎的发生率在4.4 / 100患者年(pys)和安慰剂期间的15.6 / 100pys之间变化(P <0.05)。在英夫利昔单抗治疗期间,IBD耀斑的发生率显着降低(0.2 / 100 pys)。与安慰剂相比,接受抗TNF治疗的患者的感染率更高,但接受抗TNF治疗的严重感染的发生率与安慰剂没有差异。结论:抗TNF的总体证据非常高疗效和安全性方面的治疗(1b,SOR:A),而抗TNF以外的生物治疗的治疗率较低(3,SOR:C)。

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