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Enhanced effect of high-dose leukocytapheresis using a large filter in rheumatoid arthritis.

机译:使用大型过滤器在类风湿关节炎中增强大剂量白细胞清除的效果。

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To evaluate the efficacy of high-dose leukocytapheresis (LCAP) using a large filter in patients with refractory rheumatoid arthritis (RA), we conducted a multicenter, nonrandomized, open-label clinical study. Thirty patients with highly active RA were treated with high-dose LCAP performed 3-5 sessions at 1-week intervals using a CS-180S filter (CS-180S group); the treatment involves the removal of leukocytes from a higher blood volume per body weight (100;Sml/kg). The clinical response was evaluated at 4 and 8 weeks after a series of LCAP using the 28-joint disease activity score (DAS28). Similar data of 53 patients treated with conventional LCAP (60;Sml/kg) using a standard filter, CS-100, were compared as a control (CS-100 group). The CS-180S filter demonstrated a higher adsorption capacity for leukocytes, particularly lymphocytes. The CS-180S group exhibited significant improvements in each item of DAS28 after treatment although the CS-100 group did not demonstrate such improvements in the CRP leveland the ESR. Compared to the CS-100 group, the patients of the CS-180S group exhibited a tendency toward improvement with respect to the CRP level and ESR (P = 0.057 and 0.041, respectively). According to the EULAR improvement criteria based on DAS28, 60% and 45% of the patients from CS-180S and CS-100 groups achieved moderate or more responses, respectively, at 4 weeks after treatment. These results suggest that compared to conventional LCAP, high-dose LCAP may enhance the suppression of RA disease activity.
机译:为了评估使用大容量滤器对难治性类风湿关节炎(RA)患者进行大剂量白细胞清除术(LCAP)的疗效,我们进行了一项多中心,非随机,开放标签的临床研究。使用CS-180S滤器(CS-180S组),以1周的间隔对3-5例高活性RA患者进行了3-5次大剂量LCAP治疗;该治疗包括从每体重较高的血容量(100; Sml / kg)中去除白细胞。在一系列LCAP后第4周和第8周,使用28关节疾病活动评分(DAS28)评估临床反应。比较了使用标准过滤器CS-100接受常规LCAP(60; Sml / kg)治疗的53例患者的相似数据,作为对照组(CS-100组)。 CS-180S过滤器对白细胞特别是淋巴细胞具有更高的吸附能力。 CS-180S组在治疗后的DAS28的各个项目上均表现出显着改善,尽管CS-100组在CRP水平和ESR方面未显示出这种改善。与CS-100组相比,CS-180S组的患者CRP水平和ESR均有改善的趋势(分别为P = 0.057和0.041)。根据基于DAS28的EULAR改善标准,来自CS-180S和CS-100组的60%和45%的患者在治疗后4周分别达到中度或更高反应。这些结果表明,与常规LCAP相比,大剂量LCAP可能会增强对RA疾病活性的抑制。

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