利妥昔单抗在儿童肾病综合征治疗中的应用

L. Vakulenko, O. Lytvynova, I.V. Posmitjuha
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引用次数: 1

摘要

背景。儿童肾病综合征的高复发率和以类固醇依赖的形式产生的后果以及皮质类固醇的高风险副作用涉及免疫抑制类固醇保存剂,这将增加长期缓解。Rituximab是一种嵌合抗cd20单克隆抗体,可抑制cd20介导的b细胞增殖和分化,已被确定为一种可能的替代治疗方法。这项研究的目的是评估使用利妥昔单抗治疗儿童肾病综合征复发的有效性和安全性,就像我们对三个临床病例所做的那样。材料和方法。根据Scopus、Web of Science、MedLine、The Cochrane Library、EMBASE、Global Health等数据库对利妥昔单抗在儿童中的应用经验进行分析,并介绍我们自己对3例类固醇敏感性肾病综合征患儿的治疗研究。结果。采用利妥昔单抗治疗3例5 ~ 7岁儿童肾病综合征。一个孩子有第二次复发,两个孩子有第一次复发。所有儿童既往肾病综合征发作均根据KDIGO 2021的建议进行治疗。所有患者均接受利妥昔单抗治疗(两次静脉注射,间隔两周),剂量为15mg /kg,持续5-6小时,之前给予甲基强的松龙,剂量为7 - 10mg /kg。1例患儿首次使用利妥昔单抗后出现低血压70/40和心动过速116-118的副作用。降低给药速度有助于消除副作用。两周后,孩子接受了第二次注射。另外两名儿童对两种利妥昔单抗注射均无副作用。此外,利妥昔单抗给药1个月后,无副作用或血液学改变。下次给药ritu-ximab计划在最后一次给药后6个月,事先控制CD20水平。结论。总的来说,对利妥昔单抗研究的回顾证实了该药对儿童肾病综合征的高疗效和长期评估的必要性。利妥昔单抗可以被认为是肾病综合征复发的一线治疗,包括在资源有限的情况下。我们自己使用利妥昔单抗治疗复发性肾病综合征的经验显示有轻微的短期副作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rituximab use in the treatment of children with nephrotic syndrome
Background. High recurrence rates of nephrotic syndrome in children and consequences in the form of steroid dependence and a high risk of side effects from corticosteroids as a result involve immunosuppressive steroid-preserving agents that would increase long-term remission. Rituximab, a chimeric anti-CD20 monoclonal antibody that inhibits CD20-mediated B-cell proliferation and differentiation, has been identified as a possible alternative treatment. The purpose of the study — to estimate the efficacy and safety of treatment recurrence of nephrotic syndrome in children using rituximab like we did it on three clinical cases. Materials and methods. The experience of rituximab in children was analyzed according to the databases of Scopus, Web of Science, MedLine, The Cochrane Library, EMBASE, Global Health and our own study of the treatment of three children with steroid-sensitive nephrotic syndrome was presented. Results. Treatment of nephrotic syndrome in three children who are 5 to 7 years with rituximab was conducted. One child had a second recurrence, two children had a first recurrence. The previous episode of nephrotic syndrome in all children was treated according to the recommendations of KDIGO 2021. All patients received rituximab (two intravenous injections two weeks apart) at a dose of 15 mg/kg for 5–6 hours with prior administration of methylprednisolone at a dose of 7–10 mg/kg. One child had side effects to the first administration of rituximab in the form of hypotension 70/40 and tachycardia 116–118. Reducing the speed of administration helped to eliminate side effects. The next injection in two weeks the child endured well. The other two children had no side effects to both rituximab injections. Moreover after 1 month of rituximab administration was without side effects or hematological changes. The next administration of ritu­ximab is scheduled in 6 months after the last administration with prior control of CD20 level. Conclusions. In general a review of studies of rituximab confirms the high efficacy of the medication in nephrotic syndrome in children and the requirement for long-term evaluation. Rituximab can be considered as a first-line treatment for recurrence of nephrotic syndrome, including in resource-limited settings. Our own experience with rituximab in recurrent nephrotic syndrome has revealed slight short-term side effects.
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