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Современная терапия ювенильного артрита с применением генно-инженерных препаратов в региональном центре 3 уровня - результаты и проблемы

机译:在第3级区域中心使用基因工程药物对青少年关节炎进行现代治疗-结果和问题

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Background. Juvenile idiopathic arthritis is accompanied by severe functional disabilities refractory to standard treatment with methotrexate. Recently introduced genetic engineering has significantly improved the functional state of the patients with persistent disease and stopped the progressive destruction of joints. However, the risk of adverse reactions against the background of this type of therapy requires further study. Aims: to analyze the efficiency of the genetically engineered drugs applied at juvenile arthritis and undesirable effects of this treatment. Materials and methods. Long-term (7 years) observations of 141 patients aged from 8 months to 18 with juvenile idiopathic arthritis. Results. The article summarizes the experience of successful application of genetically engineered biological preparations (tocilizumab, abatacept, etanercept, adalimumab) in 33 patients out of 141 patients with juvenile arthritis observed in Irkutsk. Serious infections were not registered, but we detected cases of managed neutropenia in 2 out of 12 patients receiving tocilizumab. In one case (3 %) out of 33 patients receiving genetically engineered drugs, the drug was withdrawn because of the risk of tuberculosis. Rare cases of secondary inefficiency of such drugs as abatacept, etanercept, adalimumab have been revealed. The tactics of treating children with undesirable reactions to genetically engineered drugs is described. Conclusions. Genetic engineering therapy has shown a good effect in improving clinical and functional indices and stopping joint destructive damage. However, when using genetically engineered drugs in treatment, the safety issues should be evaluated. Nevertheless, in our study there were no serious adverse events.
机译:背景。幼年特发性关节炎伴有甲氨蝶呤标准治疗难以治疗的严重功能障碍。最近引进的基因工程技术已大大改善了患有持续性疾病的患者的功能状态,并停止了关节的进行性破坏。然而,在这种疗法的背景下发生不良反应的风险需要进一步研究。目的:分析应用于青少年关节炎的基因工程药物的效率以及该治疗的不良影响。材料和方法。 141例年龄在8个月至18岁之间的青少年特发性关节炎的长期观察(7年)。结果。文章总结了在伊尔库茨克观察到的141例青少年关节炎患者中,有33例成功应用了基因工程生物制剂(托西珠单抗,阿巴西普,依那西普,阿达木单抗)。未记录严重感染,但我们在接受tocilizumab的12例患者中有2例检测到中性粒细胞减少的病例。在接受基因工程药物治疗的33例患者中,有1例(3%)由于存在结核病风险而停用了该药物。已经发现罕见的继发无效的药物如abatacept,etanercept,adalimumab。描述了治疗儿童对基因工程药物产生不良反应的策略。结论。基因工程疗法在改善临床和功能指标以及阻止关节破坏性破坏方面显示出良好的效果。但是,在治疗过程中使用基因工程药物时,应评估安全性问题。然而,在我们的研究中没有严重的不良事件。

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