Rituximab in Steroid-Dependent Podocytopathies.

Glomerular diseases Pub Date : 2024-07-01 eCollection Date: 2024-01-01 DOI:10.1159/000539922
Cláudia Costa, Amélia Antunes, João Oliveira, Marta Pereira, Iolanda Godinho, Paulo Fernandes, Sofia Jorge, José António Lopes, Joana Gameiro
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Abstract

Introduction: Rituximab (RTX) has been reported as an effective treatment alternative in primary forms of minimal change disease (MCD) and focal segmental glomerulosclerosis (FSGS) associated with steroid dependence and frequent relapses. However, the optimal RTX regimen and the outcomes of further doses of RTX remain unclear. This study aimed to evaluate the use of induction and maintenance RTX therapy for adults with primary podocytopathies.

Methods: We performed a retrospective case series on adult patients with steroid-dependent podocytopathies who received an induction RTX therapy. Maintenance therapy was performed at physician's discretion. Remission and relapse rates, concomitant corticosteroids and immunosuppressants use, B-cell depletion and adverse events were analyzed.

Results: Fourteen patients (mean age at start of RTX 29.1 ± 21.9 years) with MCD (n = 7) or FSGS (n = 7) were treated with 2 doses of 1,000 mg 2 weeks apart (n = 13) or four doses of 375 mg/m2 (n = 1) of RTX. At last follow-up (mean 47.3 ± 101.7 months), 10 patients were in complete remission and two remained in partial remission. A reduction in the number of relapses, number of patients under corticosteroids and immunosuppressants, and dose of prednisolone was observed when compared to baseline (14 [100%] vs. 5 [35.7%]; 8/14 [57.1%] vs. 4/12 [33.3%]; 13/14 [92.9%] vs. 7/12 [58.3%]; 20 mg/day vs. 5.25 mg/day, respectively). Maintenance RTX therapy was used in 6 patients, with sustained complete remission. Infusion reactions were observed in 4 patients (one required treatment withdrawal).

Conclusions: Our findings support the use of RTX for a steroid-free remission in podocytopathies and suggest that maintenance RTX is well-tolerated and associated with prolonged remission. Further studies are needed to confirm its efficacy and safety and establish the optimal induction and maintenance RTX regimen in steroid-dependent podocytopathies.

类固醇依赖性荚膜细胞病中的利妥昔单抗
简介:据报道,对于伴有类固醇依赖和频繁复发的原发性微小病变(MCD)和局灶节段性肾小球硬化症(FSGS),利妥昔单抗(RTX)是一种有效的替代治疗方法。然而,最佳的RTX治疗方案和进一步加大RTX剂量的结果仍不清楚。本研究旨在评估成人原发性荚膜细胞病诱导和维持 RTX 治疗的使用情况:我们对接受 RTX 诱导治疗的类固醇依赖性荚膜细胞病成人患者进行了回顾性病例系列研究。维持治疗由医生决定。对缓解率和复发率、皮质类固醇和免疫抑制剂的同时使用、B细胞耗竭和不良反应进行了分析:14名MCD(7人)或FSGS(7人)患者(开始接受RTX治疗时的平均年龄为29.1 ± 21.9岁)接受了2次剂量为1000毫克、间隔2周的RTX治疗(13人)或4次剂量为375毫克/平方米的RTX治疗(1人)。在最后一次随访中(平均 47.3 ± 101.7 个月),10 名患者病情完全缓解,2 名患者病情仍部分缓解。与基线相比,复发次数、使用皮质类固醇和免疫抑制剂的患者人数以及泼尼松龙的剂量均有所减少(分别为 14 [100%] 对 5 [35.7%];8/14 [57.1%] 对 4/12 [33.3%];13/14 [92.9%] 对 7/12 [58.3%];20 毫克/天对 5.25 毫克/天)。6名患者接受了RTX维持治疗,病情持续完全缓解。4例患者出现输液反应(其中1例需要停药):我们的研究结果支持在荚膜细胞病中使用 RTX 实现无类固醇缓解,并表明 RTX 的耐受性良好,且可延长缓解期。还需要进一步的研究来确认其疗效和安全性,并确定类固醇依赖性荚膜细胞病的最佳诱导和维持 RTX 方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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