Was ist die beste Relapstherapie bei der ANCA-assoziierten Vaskulitis?

Karger Kompass Pub Date : 2023-10-12 DOI:10.1159/000534353
Sibylle von Vietinghoff
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Abstract

Objective: Following induction of remission with rituximab in anti-neutrophil cytoplasmic antibody-associated vasculitis (AAV) relapse rates are high, especially in patients with history of relapse. Relapses are associated with increased exposure to immunosuppressive medications, the accrual of damage and increased morbidity and mortality. The RITAZAREM trial compared the efficacy of repeat-dose rituximab to daily oral azathioprine for prevention of relapse in patients with relapsing AAV in whom remission was reinduced with rituximab. Methods: RITAZAREM was an international randomized controlled, open-label, superiority trial that recruited 188 patients at the time of an AAV relapse from 29 centres in seven countries between April 2013 and November 2016. All patients received rituximab and glucocorticoids to reinduce remission. Patients achieving remission by 4 months were randomised to receive rituximab intravenously (1000 mg every 4 months, through month 20) (85 patients) or azathioprine (2 mg/kg/day, tapered after month 24) (85 patients) and followed for a minimum of 36 months. The primary outcome was time to disease relapse (either major or minor relapse). Results: Rituximab was superior to azathioprine in preventing relapse: HR 0.41; 95% CI 0.27 to 0.61, p&#x3c;0.001. 19/85 (22%) patients in the rituximab group and 31/85 (36%) in the azathioprine group experienced at least one serious adverse event during the treatment period. There were no differences in rates of hypogammaglobulinaemia or infection between groups.
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在anca共济病毒中,最好的放松疗法是什么?
& lt; b>目的:& lt; / b>在抗中性粒细胞细胞质抗体相关血管炎(AAV)诱导缓解后,复发率很高,特别是在有复发史的患者中。复发与免疫抑制药物暴露增加、损害累积以及发病率和死亡率增加有关。RITAZAREM试验比较了重复剂量的利妥昔单抗与每日口服硫唑嘌呤对预防复发性AAV患者复发的疗效,这些患者使用利妥昔单抗再次诱导缓解。& lt; b>方法:& lt; / b>RITAZAREM是一项国际随机对照、开放标签、优势试验,在2013年4月至2016年11月期间,从7个国家的29个中心招募了188名AAV复发患者。所有患者均接受利妥昔单抗和糖皮质激素治疗以缓解病情。4个月达到缓解的患者随机接受静脉注射利妥昔单抗(每4个月1000毫克,直到第20个月)(85例患者)或硫唑嘌呤(2毫克/公斤/天,第24个月后逐渐减少)(85例患者),并随访至少36个月。主要终点是疾病复发的时间(主要或轻微复发)。& lt; b>结果:& lt; / b>利妥昔单抗在预防复发方面优于硫唑嘌呤:HR 0.41;95% CI 0.27 ~ 0.61, p<0.001。利妥昔单抗组19/85(22%)患者和硫唑嘌呤组31/85(36%)患者在治疗期间至少发生一次严重不良事件。两组之间的低丙种球蛋白血症和感染率没有差异。
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