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Ustekinumab, TNF Inhibitors Exhibit Similar Remission, Disease Activity Responses in PsA

机译:Ustekinumab, TNF抑制剂表现出相似的在PsA缓解、疾病活动的反应

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Both ustekinumab and TNF inhibitors demonstrate significant improvement in psoriatic arthritis disease activity, with similar positive results in minimal and low disease activity and remission after 6 months, according to data. “The interleukin (IL)-12 and IL-23/ IL-17 axes are implicated as significant pathways in disease pathogenesis,” Josef S. Smolen, MD, of the Medical University of Vienna, and colleagues wrote in the Annals of the Rheumatic Diseases. “A number of [biologic disease-modifying antirheumatic drugs (bDMARDs)] directed against IL-12/IL-23, IL-17 or IL-23 are now available to treat PsA, alongside TNF inhibitors. “Treatment decisions are challenging in PsA, given the wide array of available drugs, and the scarcity of head-to-head trials of biologies,” they added. To assess the effectiveness of Stelara (ustekinumab, Janssen) compared with TNF inhibitors and analyze the predictors of low disease activity and remission in patients with PsA, Smolen and colleagues conducted the PsABio study. According to the researchers, PsABio is an international, prospective, observational, cohort study of adults with PsA at 92 sites across eight European countries. Participants received either ustekinumab or a TNF inhibitor as a first-, second- or third-line treatment and are followed biannually for up to 3 years. The first analysis was performed once all patients reached the 6-month milestone.
机译:ustekinumab和TNF抑制剂演示银屑病关节炎的重要改进疾病活动,类似的积极成果在最小和低疾病活动和缓解6个月后,根据数据。白介素(IL) -12和IL-23 / IL-17轴与疾病的重要途径发病机理,”约瑟夫·s . Smolen博士的维也纳医科大学,和他的同事们风湿性疾病的年报中写道。(生物疾病修饰(bDMARDs)]针对治疗风湿病的药物il - 12 / IL-23 IL-17或IL-23现在可用治疗前列腺特异性抗原,与肿瘤坏死因子抑制剂。决定在PsA具有挑战性,考虑到宽阵列可用的药物,和稀缺的一对一的生物学试验,”他们补充说。评估的有效性Stelara (ustekinumab詹森)与肿瘤坏死因子抑制剂和分析低疾病活动和预测缓解患者的PsA, Smolen和同事进行PsABio研究。研究人员、PsABio是国际前瞻性观察性队列研究在八个欧洲成人PsA在92网站国家。ustekinumab或TNF抑制剂作为第—,第二或三线治疗和遵循每3年。执行一次所有的病人达到了吗6个月的里程碑。

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