40名患有多节性视网膜关节炎的患者的胸膜炎的应用:回顾性研究的结果

Михаил Михайлович Костик, И. А. Чикова, Е. А. Исупова, М. Ф. Дубко, В. В. Масалова, Т. С. Лихачева, Л. С. Снегирёва, Е. В. Гайдар, Ольга Владимировна Калашникова, В. Г. Часнык
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引用次数: 1

摘要

甲氨蝶呤不耐受或疗效不足的儿童特发性关节炎(JIA)的治疗问题仍然存在。目的:研究托珠单抗治疗多关节性JIA的疗效和安全性。方法。在一项回顾性研究中,我们研究了tocilizumab在对先前的甲氨蝶呤治疗或甲氨蝶呤与其他非生物疾病改善抗炎药物联合治疗有抵抗力的活动性多关节JIA(5个活动关节)患者中的应用结果。结果。对40例儿童(83%为女孩)的数据进行分析,多关节性JIA发病中位数为4.8(2.9,8.1)年,发病至开始托珠单抗治疗间隔为5.7(1.8,8.5)年。托珠单抗每4周静脉输注8mg /kg(体重30 kg)或10mg /kg(体重< 30 kg)。托珠单抗单药治疗5例(13%)儿童的持续时间为1109天(452天;1542)。根据C. Wallace, 2004年的标准,在tocilizumab治疗的6个月内,有6例(15%)患者达到非活动性疾病分期,在42个月内达到32例(80%)患者。在3例患者中,由于持续缓解,tocilizumab被取消。治疗6个月后,红细胞沉降率、c反应蛋白浓度、白细胞和血小板数量均显著下降(p < 0.001)至正常值,并持续整个给药期。达到非活动性疾病的预测因子是初始(开始托珠单抗治疗时)外周血白细胞数< 9.0X109/l[相对危险度(RR) 1.92;95%可信区间(CI) 0.9-4.6)]和缺乏既往生物治疗(RR 1.92, 95% CI 0.9-4.6)。tocilizumab治疗最常见的副作用是短暂性高胆固醇血症(13例),高甘油三酯血症(4例),短暂性II级中性粒细胞减少症(1例)。托珠单抗治疗儿童多关节性JIA的长期疗效和相对安全性已得到证实。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Применение тоцилизумаба у 40 пациентов с полиартикулярным вариантом ювенильного идиопатического артрита: результаты ретроспективного исследования
The issue of a therapy of children with juvenile idiopathic arthritis (JIA) with intolerance or insufficient effectiveness of methotrexate remains actual. Objective: Our aim was to study the efficacy and safety of tocilizumab in patients with polyarticular JIA. Methods. In a retrospective study, we studied the results of the use of tocilizumab in patients with active polyarticular JIA ( 5 active joints) resistant to prior therapy with methotrexate or a combination of methotrexate with other nonbiologic disease-modifying antiinflammatory drugs. Results. The data of 40 children (83% girls) with the onset median of polyarticular JIA of 4.8 (2.9, 8.1) years and the interval between the disease onset and the initiation of tocilizumab therapy of 5.7 (1.8, 8.5) years was analyzed. Tocilizumab was used as an intravenous infusion of 8 mg/kg (with a weight 30 kg) or 10 mg/kg (with a weight < 30 kg) every 4 weeks. The duration of tocilizumab monotherapy in 5 (13%) children was 1,109 days (452; 1,542). The stages of inactive disease (according to the criteria of C. Wallace, 2004) in 6 months of tocilizumab therapy reached 6 (15%) patients, in 42 months — 32 (80%) patients. In 3 patients, tocilizumab was canceled due to persistent remission. After 6 months of treatment, there was a marked decrease in erythrocyte sedimentation rate, C-reactive protein concentration, number of leukocytes and platelets (in all cases, p < 0.001) to normal values, which persisted throughout the whole period of drug administration. Predictors for achieving inactive disease were the initial (at the onset of tocilizumab therapy) number of peripheral blood leukocytes < 9.0X109/l [relative risk (RR) 1.92; 95% confidence interval (CI) 0.9–4.6)] and the absence of prior biological therapy (RR 1.92, 95% CI 0.9–4.6). The most frequent side effects of tocilizumab therapy were transient hypercholesterolemia (in 13), hypertriglyceridemia (in 4), transient grade II neutropenia (in 1). Conclusion. The long-term efficacy and relative safety of tocilizumab in children with polyarticular JIA have been showed.
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