Zhu Yu, Chen Junyi, Zhang Yao, Wang Xiaoai, Wang Jingjing
Department of Traditional Chinese Medicine, Children's Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, Zhejiang, Hangzhou, China.
Department of Nephrology, Children's Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, Zhejiang, Hangzhou, China.
Front Immunol. 2024 Feb 23;15:1310032. doi: 10.3389/fimmu.2024.1310032. eCollection 2024.
This study aimed to systematically compare the efficacy of various immunosuppressive agents in treating pediatric frequently relapsing or steroid-dependent nephrotic syndrome (FRSDNS).
We conducted systematic searches of PubMed, Embase, the Cochrane Library, and the Web of Science up to May 23, 2023. Outcome measures included relapses within 1 year, mean cumulative exposure to corticosteroids, patients with treatment failure at 1 year, relapse-free survival during 1 year, and adverse events. The quality of the included studies was evaluated using the modified Jadad scale, the Methodological Index for Non-Randomized Studies (MINORS), and the modified Newcastle-Ottawa Scale (NOS).
Rituximab was found to be the most likely (92.44%) to be associated with the fewest relapses within 1 year and was also most likely (99.99%) to result in the lowest mean cumulative exposure to corticosteroids. Rituximab had the highest likelihood (45.98%) of being associated with the smallest number of patients experiencing treatment failure at 1 year. CsA was most likely (57.93%) to achieve the highest relapse-free survival during 1 year, followed by tacrolimus (26.47%) and rituximab (30.48%). Rituximab showed no association with serious side effects and had comparable adverse effects to ofatumumab and tacrolimus.
Rituximab may be the most favorable immunosuppressive agent for treating pediatric FRSDNS. Nephrologists should consider this drug, along with their clinical experience, patient characteristics, and cost considerations, when choosing a treatment approach.
本研究旨在系统比较各种免疫抑制剂治疗儿童频繁复发或激素依赖型肾病综合征(FRSDNS)的疗效。
我们对截至2023年5月23日的PubMed、Embase、Cochrane图书馆和科学网进行了系统检索。观察指标包括1年内的复发情况、皮质类固醇的平均累积暴露量、1年时治疗失败的患者、1年内的无复发生存率以及不良事件。采用改良的Jadad量表、非随机研究方法学指数(MINORS)和改良的纽卡斯尔-渥太华量表(NOS)对纳入研究的质量进行评估。
发现利妥昔单抗最有可能(92.44%)与1年内最少的复发相关,也最有可能(99.99%)导致皮质类固醇的平均累积暴露量最低。利妥昔单抗在1年时与最少数量的治疗失败患者相关的可能性最高(45.98%)。环孢素最有可能(57.93%)在1年内实现最高的无复发生存率,其次是他克莫司(26.47%)和利妥昔单抗(30.48%)。利妥昔单抗与严重副作用无关,其不良反应与奥法木单抗和他克莫司相当。
利妥昔单抗可能是治疗儿童FRSDNS最有利的免疫抑制剂。肾病学家在选择治疗方法时,应结合临床经验、患者特征和成本考虑等因素,考虑使用这种药物。