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利妥昔单抗治疗特发性膜性肾病疗效的初步研究:单中心经验。

Preliminary study on the efficacy of rituximab in the treatment of idiopathic membranous nephropathy: A single-centre experience.

机构信息

Department of Nephrology, Fifth Hospital of Shanxi Medical University (Shanxi Provincial People's Hospital), Taiyuan, China.

Shanxi Genetic Engineering Center for Experimental Animal Models, Taiyuan, China.

出版信息

Front Endocrinol (Lausanne). 2023 Feb 15;14:1044782. doi: 10.3389/fendo.2023.1044782. eCollection 2023.

Abstract

OBJECTIVE

To investigate the efficacy of rituximab in the treatment of idiopathic membranous nephropathy (IMN).

METHODS

A total of 77 patients with IMN diagnosed in both our hospital and other hospitals were included in this study; the patients were divided into two groups: a treatment-naïve group ( = 19) and a refractory/relapsed group ( = 58). The clinical data of the patients, including urine examination, blood test, safety evaluation and efficacy evaluation results, were analysed retrospectively. The changes in clinical biochemical indexes and adverse reactions were compared between the two groups before and after treatment, and the clinical efficacy of rituximab (RTX) in the treatment of primary IMN and refractory recurrent membranous nephropathy was evaluated.

RESULTS

Of the 77 patients included in this study, the average age was 48 years, and there was a male-to-female ratio of 61:16. There were 19 cases in the initial treatment group and 58 cases in the refractory/relapse group. The 24-hour urine protein quantification, cholesterol, B cell count and M-type phospholipase A2 receptor (PLA2R) results in the 77 patients with IMN after treatment were all lower than those before treatment, and the differences were statistically significant ( < 0.05). Serum albumin was higher than before treatment, and the difference was statistically significant ( < 0.05). The total remission rate in the initial and refractory/relapsed treatment groups was 84.21% and 82.76%, respectively. There was no statistical difference in the total remission rate between the two groups ( > 0.05). During treatment, nine patients (11.69%) experienced infusion-related adverse reactions, which were relieved rapidly after symptomatic treatment. The anti-PLA2R antibody titre of the refractory/relapsed group was significantly negatively correlated with serum creatinine ( = -0.187, = 0.045) and significantly correlated with 24-hour urine protein ( = -0.490, < 0.001). There was a positive correlation and a significant negative correlation with serum albumin ( = -0.558, < 0.001).

CONCLUSIONS

Regardless of whether RTX is used as an initial therapy or refractory/relapsed membranous nephropathy, most patients with IMN have complete or partial remission after RTX treatment, with mild adverse reactions.

摘要

目的

探究利妥昔单抗治疗特发性膜性肾病(IMN)的疗效。

方法

本研究纳入我院及外院确诊的特发性膜性肾病患者 77 例,分为初治组(n=19)和复发/难治组(n=58)。回顾性分析患者的临床资料,包括尿检查、血化验、安全性评估及疗效评估结果。比较两组治疗前后临床生化指标变化及不良反应发生情况,并评价利妥昔单抗(RTX)治疗原发性 IMN 及复发/难治性膜性肾病的临床疗效。

结果

本研究共纳入 77 例患者,平均年龄 48 岁,男女比为 61:16。初治组 19 例,复发/难治组 58 例。77 例 IMN 患者治疗后 24 h 尿蛋白定量、胆固醇、B 细胞计数、M 型磷脂酶 A2 受体(PLA2R)均低于治疗前,差异有统计学意义(<0.05);血清白蛋白高于治疗前,差异有统计学意义(<0.05)。初治组与复发/难治组总缓解率分别为 84.21%、82.76%,两组总缓解率比较差异无统计学意义(>0.05)。治疗期间,9 例(11.69%)患者出现与输注相关的不良反应,经对症治疗后迅速缓解。复发/难治组抗 PLA2R 抗体滴度与血肌酐呈显著负相关(r=-0.187,P=0.045),与 24 h 尿蛋白呈显著正相关(r=-0.490,P<0.001),与血清白蛋白呈显著正相关(r=-0.558,P<0.001)。

结论

无论 RTX 作为初始治疗还是复发/难治性膜性肾病,大多数 IMN 患者在接受 RTX 治疗后完全或部分缓解,不良反应轻微。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5cb0/9974647/2f78b5a3f948/fendo-14-1044782-g001.jpg

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