Long-Term Safety, Clinical and Immunological Outcomes in Primary Membranous Nephropathy with Severe Renal Impairment Treated with Cyclophosphamide and Steroid-Based Regimen.

Omar Ragy, Patrick Hamilton, Anjali Pathi, Adil Abdalla Mohamed Ahmed, Sandip Mitra, Durga A K Kanigicherla
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Abstract

Introduction and aims: Therapy of primary membranous nephropathy (PMN) with progressive advanced kidney dysfunction is challenging with limited literature and no clear therapeutic strategies. This is due to the scant evidence of effectiveness and uncertainty around the risk-benefit profile of immunosuppression (ImS) when eGFR is less than 30 mL/min. We aimed to determine long-term clinical outcomes in patients with PMN and severe renal impairment treated with combined cyclophosphamide and steroids.

Methods: The study is a single-center retrospective longitudinal cohort study. All patients (between 2004 and 2019) with biopsy confirmed PMN who initiated combination therapy with steroids and cyclophosphamide and had an eGFR of ≤30 mL/min/1.73 m2 at the time of initiation of therapy were included for analysis. Clinical and laboratory parameters including anti-PLA2R-Ab were monitored as per standard clinical guidance. Primary outcome was achievement of partial remission. Secondary outcomes included immunological remission, need for renal replacement therapy, and adverse effects.

Results: Eighteen patients with median age of 68 (IQR 58-73) years and 5:1 M:F ratio received the combination therapy when eGFR was ≤30 mL/min/1.73 m2 (CKD-EPI). At time of ImS, median eGFR and uPCR were 23 (IQR 18-27) mL/min/1.73 m2 and 8.4 (IQR 6.9-10.7) g/g, respectively. Median follow-up was for 67 (IQR 27-80) months. 16 patients (89%) achieved partial remission and 7 (39%) achieved complete remission. eGFR increased by 7 mL/min/1.73 m2 (27%) after 1 year of starting ImS treatment and 12 mL/min/1.73 m2 at end of follow-up. Two patients (11%) developed end-stage renal disease needing renal replacement therapy. 67% achieved both immunological and clinical remission. At the end of the follow-up period, 2 (11%) patients required hospitalization secondary to infections, 4 (22%) patients developed cancer and 4 patients died (22%).

Conclusion: Combination therapy with cyclophosphamide and steroids is effective in achieving partial remission and improving renal function in PMN with advanced renal dysfunction. Prospective controlled studies are required to provide further evidence to rationalize treatment and improve outcomes in such patients.

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环磷酰胺和类固醇治疗原发性膜性肾病伴严重肾损害的长期安全性、临床和免疫学结果
简介和目的:原发性膜性肾病(PMN)伴进行性晚期肾功能障碍的治疗具有挑战性,文献有限,没有明确的治疗策略。这是因为当eGFR低于30 mL/min时,免疫抑制(ImS)的有效性证据不足,风险-收益谱不确定。我们的目的是确定联合环磷酰胺和类固醇治疗PMN和严重肾损害患者的长期临床结果。方法:本研究为单中心回顾性纵向队列研究。所有活检证实PMN的患者(2004年至2019年),开始类固醇和环磷酰胺联合治疗,开始治疗时eGFR≤30 mL/min/1.73 m2,均被纳入分析。按照标准临床指南监测抗pla2r - ab等临床和实验室参数。主要结局是部分缓解的实现。次要结局包括免疫缓解,需要肾脏替代治疗和不良反应。结果:18例患者在eGFR≤30 mL/min/1.73 m2 (CKD-EPI)时接受联合治疗,中位年龄68 (IQR 58-73)岁,M:F比为5:1。在ImS时,中位eGFR和uPCR分别为23 (IQR 18-27) mL/min/1.73 m2和8.4 (IQR 6.9-10.7) g/g。中位随访时间为67个月(IQR 27-80)。16例(89%)患者获得部分缓解,7例(39%)患者获得完全缓解。开始ImS治疗1年后,eGFR增加了7 mL/min/1.73 m2(27%),随访结束时增加了12 mL/min/1.73 m2。2名患者(11%)发展为终末期肾病,需要肾脏替代治疗。67%达到免疫和临床缓解。随访结束时,2例(11%)患者因感染需要住院治疗,4例(22%)患者发生癌症,4例(22%)患者死亡。结论:环磷酰胺联合类固醇治疗PMN伴晚期肾功能不全患者可获得部分缓解和改善肾功能。需要前瞻性对照研究来提供进一步的证据来合理化治疗并改善此类患者的预后。
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