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Rituximabin psoriatic arthritis: An exploratory evaluation

机译:Rituximabin银屑病关节炎:探索性评估

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Background/objective: Current therapies for psoriatic arthritis (PsA) comprise synthetic drugs and tumour necrosis factor inhibitors. In contrast, other biologicals including rituximab (RTX) are available for treating rheumatoid arthritis (RA). RTX is effective in autoantibody positive RA patients, although some efficacy has been reported in seronegative individuals. RTX has not yet been assessed in PsA. Therefore, an open label study of RTX in PsA was performed. Patients and methods: Nine patients with PsA and 14 with RA received RTX at 1000 mg twice within 14 days and were evaluated over 6 months. Results: A PsA response criteria response was attained in 56% of patients. DAS28 improved from 6.2 to 4.9 (medians) in PsA and 6.4 to 5.2 in RA, and Health Assessment Questionnaire from 1.5 to 1.0 and from 2.1 to 1.4, respectively (all p≤0.05). Disease Activity index for PSoriatic Arthritis changed from 52.0 to 32.5 (p<0.05); C reactive protein and Psoriasis Area and Severity Index did not change significantly. RTX was tolerated well. Conclusions: In this exploratory open study, RTX exhibited significant efficacy in PsA patients with long-standing disease. Thus, RTX may have efficacy in PsA warranting a randomised controlled clinical trial.
机译:背景/目的:目前的银屑病关节炎(PsA)治疗方法包括合成药物和肿瘤坏死因子抑制剂。相反,包括利妥昔单抗(RTX)在内的其他生物制剂可用于治疗类风湿关节炎(RA)。 RTX在自身抗体阳性RA患者中有效,尽管据报道在血清阴性个体中有一些功效。尚未在PsA中评估RTX。因此,进行了RTS在PsA中的开放标签研究。患者和方法:9例PsA和14例RA的患者在14天内两次接受1000 mg RTX,并在6个月内进行了评估。结果:56%的患者达到了PsA反应标准反应。 DAS28在PsA中从6.2(中位数)提高到4.9(中位数),在RA中从6.4(中位数)提高到5.2(健康评估问卷),从1.5(1.0)到2.1(1.4)(所有p≤0.05)。银屑病关节炎的疾病活动指数从52.0变为32.5(p <0.05); C反应蛋白和牛皮癣面积及严重程度指数无明显变化。 RTX的耐受性很好。结论:在这项探索性开放性研究中,RTX在患有长期疾病的PsA患者中显示出显着的疗效。因此,RTX在PsA中可能具有疗效,需要进行随机对照临床试验。

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