首页> 外文期刊>Annals of the Rheumatic Diseases: A Journal of Clinical Rheumatology and Connective Tissue Research >Reduction of fatigue in Sjogren syndrome with rituximab: results of a randomised, double-blind, placebo-controlled pilot study.
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Reduction of fatigue in Sjogren syndrome with rituximab: results of a randomised, double-blind, placebo-controlled pilot study.

机译:利妥昔单抗减轻Sjogren综合征的疲劳:一项随机,双盲,安慰剂对照试验研究的结果。

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OBJECTIVE: Primary Sjogren syndrome (pSS) causes significant systemic symptoms including fatigue as well as glandular dysfunction. There are currently no effective systemic therapies; however, open label series have suggested that rituximab may be beneficial for systemic and glandular manifestations. Therefore, we performed a double blind, placebo-controlled, randomised pilot study of the efficacy of rituximab in reducing fatigue in pSS. METHODS: A total of 17 patients with pSS and a score on fatigue visual analogue scale (VAS) >50 were randomised to receive either 2 infusions of rituximab 1 g or placebo; patients also received oral and intravenous steroids. Outcome measures included: the proportion of patients with >20% reduction in fatigue VAS, changes in pSS related symptoms, health related quality of life and immunological parameters of pSS. These were measured 6 months after therapy. RESULTS: There was significant improvement from baseline in fatigue VAS in the rituximab group (p<0.001) in contrast to the placebo group (p = 0.147). There was a significant difference between the groups at 6 months in the social functioning score of SF-36 (p = 0.01) and a trend to significant difference in the mental health domain score of SF-36 (p = 0.06). There was one episode of serum sickness in the rituximab treated group. CONCLUSIONS: This is the first double blind study of rituximab in pSS to show benefit; further studies are justified.
机译:目的:原发性干燥综合征(pSS)引起明显的全身症状,包括疲劳和腺体功能障碍。目前尚无有效的全身疗法。然而,开放标签系列提示利妥昔单抗可能对全身和腺体表现有益。因此,我们对利妥昔单抗减轻pSS疲劳的功效进行了双盲,安慰剂对照,随机先导研究。方法:将17例pSS和疲劳视觉模拟量表(VAS)得分> 50的患者随机分为两组,分别接受1 g利妥昔单抗或安慰剂输注。患者还接受了口服和静脉内的类固醇治疗。结果指标包括:疲劳VAS降低> 20%的患者比例,pSS相关症状的变化,健康相关的生活质量以及pSS的免疫学参数。在治疗后6个月进行测量。结果:与安慰剂组(p = 0.147)相比,利妥昔单抗组的疲劳VAS较基线有显着改善(p <0.001)。 SF-36的社交功能评分在6个月时两组之间存在显着差异(p = 0.01),而SF-36的心理健康领域评分则存在显着差异(p = 0.06)。利妥昔单抗治疗组有1次血清病发作。结论:这是利妥昔单抗在pSS中首次显示出益处的双盲研究。进一步的研究是合理的。

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