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Efficacy and safety of a modified- ‘modified Ponticelli’ regimen for treatment of primary membranous nephropathy

机译:经改良的“改良庞蒂切利”方案治疗原发性膜性肾病的疗效和安全性

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Background : Modified Ponticelli regimen (mPR), consisting of cyclical steroids and cyclophosphamide, is the most established therapy for primary membranous nephropathy (MN). Yet, the potential toxicity of this treatment regimen poses a significant concern. Objectives : The aim of this study was to assess the efficacy and safety of a modified version of the conventional mPR for primary MN using lower-than-standard dose pulse steroids. Patients and Methods : This was a retrospective single-center analysis of patients admitted between January 2008 to December 2017. All treatment-naive patients with biopsy-proven primary MN treated with a lower-than-standard dose pulse steroid-based modification of the conventional mPR (intravenous pulse of 500 mg methyl-prednisolone, instead of 1000 mg) were included. We report the remission rates at the end of 6 months (both complete and partial), relapses and adverse effects of treatment at the end of follow-up. Results : A total of 41 individuals were included. Of 31 individuals who completed six months of treatment (six were lost to follow-up, while four discontinued immunosuppression due to infections), 71% (n=22) responded to treatment [complete remission in 25.8% (n=8), partial remission in 45.2% (n=14)]. Most common complications detected throughout the treatment were steroid induced diabetes mellitus in 40% (n=14/35), infections in 25.7% (of which immunosuppression was discontinued for four participants), and leucopenia in 8.5% (n=3/35). Relapses were seen in 29% (n=9) during follow-up (mean follow-up period: 36 months). Conclusions : The modified- ‘modified Ponticelli’ regimen with lower-than-standard dose intravenous steroids and cyclophosphamide was efficient in attaining remission in primary MN.
机译:背景:由周期性类固醇和环磷酰胺组成的改良庞帝塞利疗法(mPR)是最有效的原发性膜性肾病(MN)治疗方法。然而,这种治疗方案的潜在毒性引起了极大的关注。目的:本研究的目的是评估使用低于标准剂量脉冲类固醇的常规mPR改良版对原发性MN的疗效和安全性。患者和方法:这是对2008年1月至2017年12月期间入院患者的回顾性单中心分析。所有未经活检证实为原发性MN的未接受过治疗的初治患者均接受了低于标准剂量脉冲类固醇的常规治疗包括mPR(500 mg甲基强的松龙的静脉脉冲,而不是1000 mg)。我们在随访结束时报告6个月末的缓解率(完全缓解和部分缓解),复发和治疗的不良反应。结果:总共包括41个人。在完成六个月治疗的31位患者中(六位失去随访,而四位由于感染而停止免疫抑制),有71%(n = 22)对治疗有反应[完全缓解25.8%(n = 8),部分缓解缓解率为45.2%(n = 14)]。在整个治疗过程中发现的最常见并发症是类固醇诱导的糖尿病(40%(n = 14/35)),感染(25.7%)(其中四名参与者已停止免疫抑制)和白细胞减少症(8.5%(n = 3/35)) 。随访期间复发率为29%(n = 9)(平均随访期:36个月)。结论:改良的“改良庞蒂塞利”方案采用低于标准剂量的静脉类固醇和环磷酰胺,可有效缓解原发性MN。

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