Comparations of efficacy and safety of rituximab, calcineurin inhibitors and cyclophosphamide in primary membranous nephropathy: a single-center retrospective analysis

Author:

Lu Luying1,Zhu Huayan2,Cai Shasha3,Liu Guangjun1,Wang Yaomin1,Ren Pingping1,Lan Lan1,Shen Xiaoqi1,Chen Liangliang1,Xu Ying1,Cheng Jun1,Li Xiayu1,Chen Jianghua1,Han Fei1

Affiliation:

1. Zhejiang University, Zhejiang University, National Key Clinical Department of Kidney Diseases, Zhejiang Clinical Research Center of Kidney and Urinary System Disease

2. Huzhou First People's Hospital

3. Wenling First People's Hospital

Abstract

Abstract Background Rituximab (RTX), calcineurin inhibitor (CNI) and cyclophosphamide (CTX) plus glucocorticoids are first-line therapeutic options for primary membranous nephropathy (PMN). Methods Totally 478 biopsy-proven PMN patients in single center were retrospectively included. After 1:1 propensity score matching (PSM), 258 patients were included in RTX, CNI or CTX group (86 patients in each group). Results After PSM, there were no differences on serum creatinine, eGFR, serum albumin, urine protein, anti-PLA2R antibody among groups. The follow-up duration was 12 (10.5, 18) months in CNI group, 12 (12, 18) months in CTX group and 12 (12, 18) months in RTX group. Throughout entire follow-up period, 39 patients (45.3%) in CNI group, 47 patients (54.7%) in CTX group, and 59 patients (68.6%) in RTX group achieved composite response (complete remission and partial remission). The survival curve showed a higher composite response in RTX group than CNI group (p=0.018). A relapse occurred in 15 of 39 (38.5%) patients in CNI group, significantly higher than CTX group (4.3%, p<0.001) and RTX group (3.4%, p<0.001). In CNI group, 36% patients had a ≥25% decline in eGFR, and 15.1% of patients had a ≥50% decline in eGFR. Conclusions RTX may be more effective than CNI in inducing remission in PMN and showed similar efficacy to CTX. CNI may have a high risk of proteinuria relapse and eGFR decline.

Publisher

Research Square Platform LLC

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