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奥妥珠单抗对利妥昔单抗难治性磷脂酶A2受体相关膜性肾病的治疗有效。

Obinutuzumab is effective for the treatment of rituximab-refractory PLA2R-associated membranous nephropathy.

作者信息

Su Wenyan, Li Jianyi, Men Jinzhao, Zhong Shuo, Wang Yunzhao, Zhang Yao, Xu Liang, Gao Jie, Liu Dan, Wang Rong, Sun Jing, Wang Haiping

机构信息

Department of Nephrology, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, China.

Department of Nephrology, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, China.

出版信息

Clin Kidney J. 2025 May 1;18(5):sfaf026. doi: 10.1093/ckj/sfaf026. eCollection 2025 May.

Abstract

BACKGROUND

Clinical experience with obinutuzumab in patients with rituximab-refractory phospholipase A2 receptor (PLA2R)-associated membranous nephropathy remains limited. This study aimed to evaluate the efficacy and safety of obinutuzumab in treating patients with rituximab-refractory PLA2R-associated membranous nephropathy.

METHODS

A single-center retrospective study was conducted on 20 patients with rituximab-refractory PLA2R-associated membranous nephropathy who received two doses of 1 g obinutuzumab, administered 2 weeks apart. At 6 months, patients with urinary protein levels exceeding 3.5 g/d received an additional dose of 1-2 g obinutuzumab. The primary clinical outcome was a composite measure of complete or partial remission during follow-up. Continuous secondary outcomes included 24-hour urinary protein, serum albumin, serum creatinine, serum anti-PLA2R levels, and CD19 B-cell counts at the time of obinutuzumab infusion, at 3 months, and at the last visit.

RESULTS

A total of 20 patients with clinical manifestations of nephrotic syndrome were included in this study, with a median follow-up period of 9 months. The mean age of the patients was 46.25 ± 13.05 years. At a median follow-up of 4.50 months (3.00-8.25 months) after obinutuzumab therapy, remission was achieved in 16 patients. Two patients (10%) achieved complete remission, while 14 (70%) attained partial remission. At baseline, 16 out of 20 patients tested positive for serum anti-PLA2R antibodies, and immunological remission was observed in 11 of these 16 patients during follow-up. All patients experienced B-lymphocyte depletion within 1 month after receiving obinutuzumab infusion and maintained this depletion at 3 months. B-lymphocyte reconstitution was noted in 4 out of 20 patients (20%) at 6 months. No patients experienced fatal adverse events.

CONCLUSION

Obinutuzumab mainly induces short-term partial remissions in patients with rituximab-refractory primary membranous nephropathy, which may be related to the short follow-up period. However, this study demonstrates that obinutuzumab is an effective and safe treatment for rituximab-refractory PLA2R-associated membranous nephropathy.

摘要

背景

奥妥珠单抗用于治疗对利妥昔单抗耐药的磷脂酶A2受体(PLA2R)相关膜性肾病患者的临床经验仍然有限。本研究旨在评估奥妥珠单抗治疗对利妥昔单抗耐药的PLA2R相关膜性肾病患者的疗效和安全性。

方法

对20例对利妥昔单抗耐药的PLA2R相关膜性肾病患者进行了一项单中心回顾性研究,这些患者接受了两剂1g奥妥珠单抗治疗,间隔2周给药。在6个月时,尿蛋白水平超过3.5g/d的患者额外接受1-2g奥妥珠单抗治疗。主要临床结局是随访期间完全或部分缓解的综合指标。连续性次要结局包括奥妥珠单抗输注时、3个月时和最后一次就诊时的24小时尿蛋白、血清白蛋白、血清肌酐、血清抗PLA2R水平以及CD19 B细胞计数。

结果

本研究共纳入20例有肾病综合征临床表现的患者,中位随访期为9个月。患者的平均年龄为46.25±13.05岁。在奥妥珠单抗治疗后的中位随访4.50个月(3.00-8.25个月)时,16例患者实现缓解。2例患者(10%)实现完全缓解,14例(70%)达到部分缓解。基线时,20例患者中有16例血清抗PLA2R抗体检测呈阳性,随访期间这16例患者中有11例出现免疫缓解。所有患者在接受奥妥珠单抗输注后1个月内均出现B淋巴细胞耗竭,并在3个月时维持这种耗竭状态。6个月时,20例患者中有4例(20%)出现B淋巴细胞重建。无患者发生致命不良事件。

结论

奥妥珠单抗主要诱导对利妥昔单抗耐药的原发性膜性肾病患者短期部分缓解,这可能与随访期短有关。然而,本研究表明奥妥珠单抗是治疗对利妥昔单抗耐药的PLA2R相关膜性肾病的一种有效且安全的疗法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52d7/12056547/024c07820925/sfaf026fig1.jpg

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