Analysis of treatment outcomes in patients with antineutrophil cytoplasmic antibody-associated vasculitis on rituximab therapy.

IF 1.1 Q4 RHEUMATOLOGY
Archives of rheumatology Pub Date : 2022-11-04 eCollection Date: 2023-09-01 DOI:10.46497/ArchRheumatol.2023.9556
Tsvetelina Yoneva, Yana Zdravkova, Georgi Kotov, Ekaterina Ivanova Todorova, Georgi Vasilev, Rasho Rashkov, Ivan Sheytanov
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Abstract

Objectives: This study aimed to analyze a group of patients with severe and refractory antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) managed with rituximab and to report on treatment outcomes.

Patients and methods: A total of 78 patients (41 females, 37 males; mean age: 50.1±13.4 years; range, 18 to 76 years) with AAV on rituximab treatment were included in the single-center, retrospective study conducted between 2009 and 2018. The diagnosis was established based on the 1990 classification criteria of the American College of Rheumatology and the definitions of vasculitis of Chapel Hill Consensus Conference. Laboratory and immunological tests were conducted. Disease activity was determined through the Birmingham Vasculitis Activity Score.

Results: Rituximab was preferred over cyclophosphamide in 37 patients and used as a second-line therapy after cyclophosphamide in 41 cases. Rituximab treatment showed favorable outcomes with regard to serum creatinine levels, proteinuria, and hematuria, as well as in cases of isolated lung involvement. Nearly half of patients with pulmonary renal syndrome also improved, with 22.2% achieving remission. ANCAs were positive in 85.9% of patients at the onset of rituximab treatment and became negative in 82% of the positive cases. Adverse events were rare and included infusion reactions (one case of reactivation of a herpes zoster infection and one case of allergic reaction).

Conclusion: Rituximab is an efficient and safe therapeutic option in patients with AAV who are difficult to treat, have insufficient response, or have not tolerated other treatments.

利妥昔单抗治疗抗中性粒细胞细胞质抗体相关血管炎的疗效分析。
目的:本研究旨在分析一组使用利妥昔单抗治疗的严重难治性抗中性粒细胞细胞质抗体(ANCA)相关血管炎(AAV)患者,并报告其治疗结果。患者与方法:共78例患者,其中女性41例,男性37例;平均年龄:50.1±13.4岁;在2009年至2018年间进行的单中心回顾性研究中,纳入了接受利妥昔单抗治疗的AAV患者,年龄在18至76岁之间。诊断依据1990年美国风湿病学会的分类标准和Chapel Hill共识会议对血管炎的定义。进行了实验室和免疫学检查。通过伯明翰血管炎活动度评分确定疾病活动度。结果:37例患者利妥昔单抗优于环磷酰胺,41例患者作为环磷酰胺后的二线治疗。利妥昔单抗治疗在血清肌酐水平、蛋白尿和血尿以及孤立肺受累病例方面显示出良好的结果。近一半的肺肾综合征患者也得到改善,22.2%的患者获得缓解。在利妥昔单抗治疗开始时,85.9%的患者anca呈阳性,82%的阳性病例变为阴性。不良事件罕见,包括输注反应(一例带状疱疹感染再激活和一例过敏反应)。结论:利妥昔单抗是一种安全有效的治疗方案,适用于难以治疗、反应不足或其他治疗方法不能耐受的AAV患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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