Department of Pediatric Nephrology and Rheumatology, the First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Pediatr Res. 2023 Dec;94(6):2040-2046. doi: 10.1038/s41390-023-02747-3. Epub 2023 Jul 24.
To analyze the efficacy and safety of multi-target therapy in children with lupus nephritis (LN).
In our retrospective study from January 2009 to December 2021, the multi-target therapy of glucocorticoids, MMF and tacrolimus was adopted as induction therapy or re-induction therapy for 36 LN children who had combined proliferative and membranous LN or for who were ineffective to combination therapy of glucocorticoids with IV-CYC or MMF for at least 6 months. The clinical and pathological data were collected and analyzed.
The levels of 24-h urinary protein, anti-dsDNA antibody and SLE disease activity index were decreased, while the levels of albumin and complement 3 were increased after multi-target therapy. More than 90% of LN children achieved partial or complete remission within 6 months. In terms of adverse effects, there was no significant difference between the level of eGFR before and after multi-target therapy. During the follow-up period, four children had infection, two children had hyperuricemia, and one child had liver dysfunction. All of them improved after symptomatic therapy.
Multi-target therapy could be an effective treatment option with minimal adverse effects for LN children who are refractory to initial first-line induction therapies or had combined proliferative and membranous LN.
The multi-target therapy of glucocorticoids, mycophenolate mofetil and tacrolimus was adopted in 36 children with lupus nephritis. Multi-target therapy could be an effective treatment option for lupus nephritis children who are refractory to initial first-line induction therapies or had combined proliferative and membranous lupus nephritis. Adverse effects of multi-target therapy were infrequent and minimal that can be improved by symptomatic therapy.
分析多靶点治疗儿童狼疮性肾炎(LN)的疗效和安全性。
在我们 2009 年 1 月至 2021 年 12 月的回顾性研究中,采用糖皮质激素、MMF 和他克莫司的多靶点治疗作为诱导或再诱导治疗,用于 36 例 LN 儿童,这些儿童合并增殖性和膜性 LN,或对糖皮质激素联合 IV-CYC 或 MMF 的联合治疗至少 6 个月无效。收集和分析临床和病理数据。
多靶点治疗后,24 小时尿蛋白、抗 dsDNA 抗体和 SLE 疾病活动指数水平降低,白蛋白和补体 3 水平升高。90%以上的 LN 儿童在 6 个月内达到部分或完全缓解。在不良反应方面,多靶点治疗前后 eGFR 水平无显著差异。在随访期间,4 例患儿发生感染,2 例患儿出现高尿酸血症,1 例患儿出现肝功能异常,经对症治疗后均有所改善。
对于初始一线诱导治疗无效或合并增殖性和膜性 LN 的 LN 儿童,多靶点治疗可能是一种有效且不良反应最小的治疗选择。
36 例狼疮性肾炎儿童采用糖皮质激素、霉酚酸酯和他克莫司的多靶点治疗。多靶点治疗可能是一种有效的治疗选择,用于对初始一线诱导治疗无效或合并增殖性和膜性狼疮性肾炎的狼疮性肾炎儿童。多靶点治疗的不良反应罕见且轻微,可通过对症治疗改善。