Pouransiri Zhara, Assadi Farahnak, Mohkam Masoumeh, Hooman Nakysa, Rostami Zahra, Mazaheri Mojgan, Azarfar Anoush, Sharbaf Fatemeh Ghane
Pediatric Nephrology Research Center (ZP, MaM), Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Department of Pediatrics, Division of Nephrology (FA), Rush University of Medical Center, Chicago, IL, USA.
J Pediatr Pharmacol Ther. 2023;28(4):308-315. doi: 10.5863/1551-6776-28.4.308. Epub 2023 Aug 9.
This systematic review and meta-analysis aimed to explore rituximab (RTX) associated infectious complications in children with glomerular disease.
We performed an electronic search of PubMed, International Scientific Information (ISI), Scopus, and EMBASE between January 2010 and July 2021. Infection rates and total drug-related adverse events were the outcomes. Statistical heterogeneity was evaluated by using the statistic. When there was statistical evidence of heterogeneity ( > 50%, p > 0.1), a random-effect model was adopted. Data analysis was performed with Stata17.0 software.
A total of 7 studies with 668 patients (136 with lupus nephritis [LN] and 532 with nephrotic syndrome were included in the meta-analysis. The pooled risk ratio showed that the administration of RTX was significantly associated with lower risk of infectious complications in patients with LN and nephrotic syndrome (0.72 [95% CI 0.58, 0.85]) when compared with population data of patients without glomerular disease (p = 0.2). There was no significant difference between the LN and nephrotic syndrome groups in terms of total serious adverse events or the occurrence of infections. There was significant heterogeneity among the reported studies (Q = 42.39, p < 0.001, = 81%).
Administration of RTX in children with glomerular disease is associated with a lower rate of infections when compared with population data of patients without LN or nephrotic syndrome. Additional high-quality randomized controlled trials with long-term follow-up are needed to identify the long-term potential complications. Trial registration PROPERO ID: CRD42021274869 (https://www.crd.york.ac/prospero/display_record.php?).
本系统评价和荟萃分析旨在探讨利妥昔单抗(RTX)与肾小球疾病患儿感染并发症之间的关系。
我们于2010年1月至2021年7月期间在PubMed、国际科学信息(ISI)、Scopus和EMBASE数据库进行了电子检索。以感染率和药物相关不良事件总数作为观察指标。采用 统计量评估统计异质性。当存在异质性的统计学证据(>50%,p>0.1)时,采用随机效应模型。使用Stata17.0软件进行数据分析。
共有7项研究纳入荟萃分析,涉及668例患者(136例狼疮性肾炎[LN]患者和532例肾病综合征患者)。汇总风险比显示,与无肾小球疾病患者的总体数据相比,RTX给药与LN和肾病综合征患者感染并发症风险较低显著相关(0.72[95%置信区间0.58,0.85])(p = 0.2)。LN组和肾病综合征组在严重不良事件总数或感染发生率方面无显著差异。报告的研究之间存在显著异质性(Q = 42.39,p < 0.001, = 81%)。
与无LN或肾病综合征患者的总体数据相比,肾小球疾病患儿使用RTX与较低的感染率相关。需要更多高质量的长期随访随机对照试验来确定长期潜在并发症。试验注册号:PROPERO ID:CRD42021274869(https://www.crd.york.ac/prospero/display_record.php?)