Evaluating Efficacy and Safety of Tacrolimus Treatment in Membranous Nephropathy: Results of a Retrospective Study of 182 Patients.

IF 2.3 3区 医学 Q2 HEALTH CARE SCIENCES & SERVICES Therapeutics and Clinical Risk Management Pub Date : 2023-01-01 DOI:10.2147/TCRM.S399218
Shuang Liang, Yan-Jun Liang, Zhao Li, Yong Wang, Xin-Ru Guo, Chao-Yang Zhang, Chun Zhang, Jie Wu, Xiao-Long Wang, Yi-Sha Li, Guang-Yan Cai, Xiang-Mei Chen
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Abstract

Purpose: Tacrolimus is recommended by KDIGO Clinical Practice Guidelines as an initial therapy for the treatment of membranous nephropathy (MN). However, little is known about the factors that influence response and recurrence of the disease after tacrolimus therapy, and there are limited data regarding the duration of tacrolimus treatment. Here, we present a real-world retrospective cohort study of 182 MN patients treated with tacrolimus, aiming to assess the efficacy and safety of tacrolimus in the treatment of MN.

Patients and methods: The clinical data of 182 patients with MN treated with tacrolimus and followed up for at least one year were analyzed retrospectively for the efficacy and safety of tacrolimus.

Results: The mean follow-up period was 27.3 (19.3-41.6) months. A total of 154 patients (84.6%) achieved complete or partial remission, and 28 patients (15.4%) did not. Multivariate Cox regression analysis showed that male and higher baseline BMI were independently associated with lower, while higher serum albumin was associated with higher probability of remission. Among the responders, 56 patients (36.4%) relapsed. After adjustments for age and sex, Cox regression analysis revealed that the longer period of full-dose tacrolimus was administered, the lower the incidence of relapse. However, high levels of serum creatinine and proteinuria at the onset of tacrolimus discontinuation were risk factors for relapse. During the treatment of tacrolimus, a decline in renal function (≥50% increase in serum creatinine after the onset of tacrolimus treatment) was the most common adverse reaction, observed in 20 (11.0%) patients, followed by elevated blood glucose and infection, but the latter two occurred mostly during treatment with tacrolimus plus corticosteroids.

Conclusion: Tacrolimus is effective in the treatment of MN, but the relapse rate is high. Clinical studies with larger sample sizes are needed to further explore the use of tacrolimus in the treatment of membranous nephropathy.

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评价他克莫司治疗膜性肾病的疗效和安全性:182例患者的回顾性研究结果。
目的:KDIGO临床实践指南推荐他克莫司作为膜性肾病(MN)的初始治疗。然而,对影响他克莫司治疗后反应和疾病复发的因素知之甚少,关于他克莫司治疗持续时间的数据有限。在此,我们对182例接受他克莫司治疗的MN患者进行了一项真实世界的回顾性队列研究,旨在评估他克莫司治疗MN的有效性和安全性。患者和方法:回顾性分析182例接受他克莫司治疗并随访1年以上的MN患者的临床资料,探讨他克莫司的疗效和安全性。结果:平均随访时间27.3(19.3 ~ 41.6)个月。154例患者(84.6%)达到完全或部分缓解,28例患者(15.4%)没有。多因素Cox回归分析显示,男性和较高的基线BMI与较低的血清白蛋白独立相关,而较高的血清白蛋白与较高的缓解概率相关。在应答者中,56例(36.4%)复发。在调整年龄和性别后,Cox回归分析显示,全剂量他克莫司给药时间越长,复发率越低。然而,他克莫司停药时血清肌酐和蛋白尿水平高是复发的危险因素。在他克莫司治疗期间,肾功能下降(他克莫司治疗开始后血清肌酐升高≥50%)是最常见的不良反应,20例(11.0%)患者观察到,其次是血糖升高和感染,但后两者主要发生在他克莫司联合皮质类固醇治疗期间。结论:他克莫司治疗MN有效,但复发率高。需要更大样本量的临床研究来进一步探讨他克莫司在膜性肾病治疗中的应用。
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来源期刊
Therapeutics and Clinical Risk Management
Therapeutics and Clinical Risk Management HEALTH CARE SCIENCES & SERVICES-
CiteScore
4.80
自引率
3.60%
发文量
139
审稿时长
16 weeks
期刊介绍: Therapeutics and Clinical Risk Management is an international, peer-reviewed journal of clinical therapeutics and risk management, focusing on concise rapid reporting of clinical studies in all therapeutic areas, outcomes, safety, and programs for the effective, safe, and sustained use of medicines, therapeutic and surgical interventions in all clinical areas. The journal welcomes submissions covering original research, clinical and epidemiological studies, reviews, guidelines, expert opinion and commentary. The journal will consider case reports but only if they make a valuable and original contribution to the literature. As of 18th March 2019, Therapeutics and Clinical Risk Management will no longer consider meta-analyses for publication. The journal does not accept study protocols, animal-based or cell line-based studies.
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