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中国临床药理学与治疗学 ›› 2025, Vol. 30 ›› Issue (5): 657-664.doi: 10.12092/j.issn.1009-2501.2025.05.009

• 药物治疗学 • 上一篇    下一篇

对比环磷酰胺和利妥昔单抗在特发性膜性肾病中的疗效及安全性分析

吴姗1,余琦1,杨覃2,王文婧1,张洋洋1,刘燕1,杨沿浪1   

  1. 1皖南医学院第一附属医院弋矶山医院肾脏内科,芜湖  241000,安徽;2南昌大学,南昌  330031,江西
  • 收稿日期:2024-11-04 修回日期:2025-02-11 出版日期:2025-05-26 发布日期:2025-05-13
  • 通讯作者: 杨沿浪,男,博士,主任医师,硕导,研究方向:免疫相关性肾病。 E-mail: yangyanlang@126.com
  • 作者简介:吴姗,女,硕士,医师,研究方向:免疫相关性肾病。 E-mail: wushan1232024@163.com 余琦,共同第一作者,女,博士,主治医师,研究方向:免疫相关性肾病。 E-mail: Christinayuqi@163.com
  • 基金资助:
    皖南医学院横向课题(622202504003,662202404013)

Comparing the efficacy and safety of cyclophosphamide and rituximab in idiopathic membranous nephropathy

WU Shan1, YU Qi1, YANG Qin2, WANG Wenjing1, ZHANG Yangyang1, LIU Yan1, YANG Yanlang1   

  1. 1Department of Nephrology, The First Affiliated Hospital of Wannan Medical College, Yijishan Hospital, Wuhu 241000, Anhui, China; 2Nanchang University, Nanchang 330031, Jiangxi, China
  • Received:2024-11-04 Revised:2025-02-11 Online:2025-05-26 Published:2025-05-13

摘要:

目的:比较环磷酰胺和利妥昔单抗对初诊特发性膜性肾病(idiopathic membranous nephropathy,IMN)患者的疗效和安全性。方法:回顾性研究2019年11月至2024年7月于皖南医学院弋矶山医院肾脏内科经肾活检或PLA2R抗体阳性诊断为IMN的113例患者,其中55例接受环磷酰胺治疗,58例接受利妥昔单抗治疗,并且随访≥6个月。结果:6个月时,环磷酰胺治疗组有38例(69.09%)得到复合缓解(完全缓解或部分缓解),利妥昔单抗治疗组有36例(62.07%)得到复合缓解。12个月和18个月时,两组复合缓解率无统计学差异(70.83% vs. 83.87%,P=0.186和73.68% vs. 73.68%,P=1.000),但在12个月时,利妥昔单抗组的复合缓解率高于环磷酰胺组。对于eGFR<60 mL/(min·1.73 m2)的IMN患者,利妥昔单抗能显著改善肾功能(P=0.008)。在整个随访期间,环磷酰胺组的不良事件总数高于利妥昔单抗组(57例vs. 45例),并且非严重不良事件发生率高于利妥昔单抗组(P=0.039)。结论:利妥昔单抗治疗IMN的疗效不劣于环磷酰胺,具有更好的安全性;利妥昔单抗改善eGFR<60 mL/(min·1.73 m2)IMN患者肾功能的效果优于环磷酰胺。

关键词: 膜性肾病, 利妥昔单抗, 环磷酰胺, 估算肾小球滤过率  

Abstract:

AIM: To explore the efficacy and safety of two drugs in diagnosed idiopathic membranous nephropathy (IMN). METHODS: A retrospective study was conducted on 113 patients diagnosed with IMN by renal biopsy or PLA2R antibody positive at the department of nephrology, yijishan hospital, wannan medical college from november 2019 to July 2024, of whom 55 received cyclophosphamide treatment and 58 received rituximab treatment, and follow-up was ≥6 months. RESULTS: At 6 months, 38 patients (69.09%) in the cyclophosphamide treatment group and 36 patients (62.07%) in the rituximab treatment group had achieved a combined response (complete or partial response). At 12 and 18 months, there was no statistical difference in the combined response rate between the two groups (70.83% vs. 83.87%, P=0.186 and 73.68% vs. 73.68%, P=1.000), but at 12 months, the combined response rate in the rituximab group was higher than that in the cyclophosphamide group. In IMN patients with eGFR<60 mL/(min·1.73 m2), rituximab significantly improved renal function (P=0.008). Over the entire follow-up period, the total number of adverse events was higher in the cyclophosphamide group than in the rituximab group (57 vs.. 45), and the incidence of non-serious adverse events was higher than in the rituximab group (P=0.039). CONCLUSION:The efficacy of rituximab in the treatment of IMN is not inferior to that of cyclophosphamide, and it has better safety. Rituximab improved renal function better than cyclophosphamide in patients with eGFR<60 mL/(min·1.73 m2) IMN.

Key words: membranous nephropathy, rituximab, cyclophosphamide, eGFR ,   

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