Efficacy of rituximab therapy in patients with non-systemic juvenile idiopathic arthritis

Q3 Medicine
N. Kondratieva, T. Dvoryakovskaya, T. Kriulina, K. Isaeva, A. Chomakhidze, O. Lomakina, K. Chibisova, I. Kriulin, E. Krekhova, I. Tsulukiya, M.S. Botova, M. Shingarova, Marta Kokina, E. Alexeeva
{"title":"Efficacy of rituximab therapy in patients with non-systemic juvenile idiopathic arthritis","authors":"N. Kondratieva, T. Dvoryakovskaya, T. Kriulina, K. Isaeva, A. Chomakhidze, O. Lomakina, K. Chibisova, I. Kriulin, E. Krekhova, I. Tsulukiya, M.S. Botova, M. Shingarova, Marta Kokina, E. Alexeeva","doi":"10.20953/1817-7646-2023-3-56-66","DOIUrl":null,"url":null,"abstract":"Juvenile idiopathic arthritis (JIA) is arthritis of unknown cause lasting more than 6 weeks, which starts in children under 16 years old with the exclusion of other joint disorder. According to the recommendations for the treatment of JIA, patients who does not responded to with antirheumatic therapy, we prescribe biological therapy, primarily TNF-alpha inhibitors. Despite their high effectiveness, in some patients, the TNF-alpha inhibitors has no proper therapeutic effect, which requires studying the possibility of using other therapy, in particular- rituximab. Objective. To evaluate the efficacy and safety of rituximab in patients with JIA without systemic manifestations Patients and methods. Retrospective cohort study included 33 patients who received rituximab. Treatment was initiated in the Department of Rheumatology, National Medical Research Center for Children's Health (Moscow) between December 2006 and April 2022. All patients were treated with non-steroid anti-inflammatory drugs (NSAIDs), non-biologic disease-modifying antirheumatic drugs (DMARDs), corticosteroids, biological agents with other mechanism of action. There was ineffectiveness of previous antirheumatic therapy in all patients. Patients were divided into two groups: with RF-positive polyarthritis (n = 30) and other non-systemic JIA (n = 13). Efficacy was evaluated in 1, 3, 6, 9, 12 months after first rituximab infusion and every 6 months till discontinuation or 18 years old achievement. Inactive disease/remission was registered according to Juvenile Arthritis Disease Activity Score (JADAS71) <1, С.Wallace criteria (2011) and The American College of Rheumatology (ACR) Pediatric criteria for assessing joint status (ACR Pedi 30, 50, 70, and 90). Results. Among 16 patients with RF-positive JIA 8 (50%) achieved 90% improvement according to ACR Pedi, inactive disease/remission according to С.Wallace was registered in 12 (75%) 12 months after rituximab initiation. In patients with other nonsystemic JIA (n = 13) 90% improvement according to ACR Pedi was registered in 5 (45%) patients, inactive disease/remission according to С.Wallace was registered in 6 (54, 5%) patients. Conclusion. Rituximab is highly effective in patients with JIA without systemic manifestation, who failed to previous treatment with NSAIDs, DMARDs and biological agents with other mechanism of action and it could be considered as next escalation therapy. Key words: rituximab, juvenile idiopathic arthritis, efficiency of therapy","PeriodicalId":38157,"journal":{"name":"Voprosy Prakticheskoi Pediatrii","volume":"1 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Voprosy Prakticheskoi Pediatrii","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.20953/1817-7646-2023-3-56-66","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

Abstract

Juvenile idiopathic arthritis (JIA) is arthritis of unknown cause lasting more than 6 weeks, which starts in children under 16 years old with the exclusion of other joint disorder. According to the recommendations for the treatment of JIA, patients who does not responded to with antirheumatic therapy, we prescribe biological therapy, primarily TNF-alpha inhibitors. Despite their high effectiveness, in some patients, the TNF-alpha inhibitors has no proper therapeutic effect, which requires studying the possibility of using other therapy, in particular- rituximab. Objective. To evaluate the efficacy and safety of rituximab in patients with JIA without systemic manifestations Patients and methods. Retrospective cohort study included 33 patients who received rituximab. Treatment was initiated in the Department of Rheumatology, National Medical Research Center for Children's Health (Moscow) between December 2006 and April 2022. All patients were treated with non-steroid anti-inflammatory drugs (NSAIDs), non-biologic disease-modifying antirheumatic drugs (DMARDs), corticosteroids, biological agents with other mechanism of action. There was ineffectiveness of previous antirheumatic therapy in all patients. Patients were divided into two groups: with RF-positive polyarthritis (n = 30) and other non-systemic JIA (n = 13). Efficacy was evaluated in 1, 3, 6, 9, 12 months after first rituximab infusion and every 6 months till discontinuation or 18 years old achievement. Inactive disease/remission was registered according to Juvenile Arthritis Disease Activity Score (JADAS71) <1, С.Wallace criteria (2011) and The American College of Rheumatology (ACR) Pediatric criteria for assessing joint status (ACR Pedi 30, 50, 70, and 90). Results. Among 16 patients with RF-positive JIA 8 (50%) achieved 90% improvement according to ACR Pedi, inactive disease/remission according to С.Wallace was registered in 12 (75%) 12 months after rituximab initiation. In patients with other nonsystemic JIA (n = 13) 90% improvement according to ACR Pedi was registered in 5 (45%) patients, inactive disease/remission according to С.Wallace was registered in 6 (54, 5%) patients. Conclusion. Rituximab is highly effective in patients with JIA without systemic manifestation, who failed to previous treatment with NSAIDs, DMARDs and biological agents with other mechanism of action and it could be considered as next escalation therapy. Key words: rituximab, juvenile idiopathic arthritis, efficiency of therapy
利妥昔单抗治疗非系统性青少年特发性关节炎的疗效
青少年特发性关节炎(JIA)是一种不明原因的关节炎,持续时间超过6周,始于16岁以下的儿童,排除其他关节疾病。根据治疗JIA的建议,对抗风湿治疗无反应的患者,我们开生物治疗,主要是tnf - α抑制剂。尽管它们的疗效很高,但在一些患者中,tnf - α抑制剂没有适当的治疗效果,这需要研究使用其他治疗方法的可能性,特别是利妥昔单抗。目标。评价利妥昔单抗治疗无全身性表现的JIA患者的疗效和安全性。回顾性队列研究包括33例接受利妥昔单抗治疗的患者。2006年12月至2022年4月,在国家儿童健康医学研究中心(莫斯科)风湿病学系开始治疗。所有患者均接受非甾体抗炎药(NSAIDs)、非生物疾病缓解类抗风湿药(DMARDs)、皮质类固醇及其他作用机制的生物制剂治疗。所有患者既往抗风湿治疗无效。患者分为两组:rf阳性多发性关节炎(n = 30)和其他非系统性JIA (n = 13)。在首次输注利妥昔单抗后1、3、6、9、12个月及每6个月评估一次疗效,直至停药或18岁成功。根据青少年关节炎疾病活动评分(JADAS71) <1, С登记非活动性疾病/缓解。华莱士标准(2011)和美国风湿病学会(ACR)评估关节状态的儿科标准(ACR Pedi 30,50,70和90)。结果。在16例rf阳性的JIA 8患者中(50%),根据ACR Pedi达到90%的改善,根据С达到非活动性疾病/缓解。Wallace在利妥昔单抗启动后12个月(75%)注册。在其他非全身性JIA患者(n = 13)中,根据ACR Pedi, 5例(45%)患者有90%的改善,根据С,疾病不活跃/缓解。Wallace在6例(54,5%)患者中登记。结论。利妥昔单抗对既往非甾体抗炎药、dmard及其他作用机制的生物制剂治疗失败的无全身性表现的JIA患者疗效显著,可考虑作为下一个升级治疗。关键词:利妥昔单抗;青少年特发性关节炎;疗效
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Voprosy Prakticheskoi Pediatrii
Voprosy Prakticheskoi Pediatrii Medicine-Pediatrics, Perinatology and Child Health
CiteScore
1.20
自引率
0.00%
发文量
50
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信