Prospective study of the effect of rituximab on kidney function in membranous nephropathy.

IF 3.9 2区 医学 Q1 UROLOGY & NEPHROLOGY Clinical Kidney Journal Pub Date : 2024-06-18 eCollection Date: 2024-08-01 DOI:10.1093/ckj/sfae179
Durga A K Kanigicherla, Angie A Kehagia, Babak Jamshidi, Lina Manounah, Anna Barnes, Hannah Patrick, Helen Powell, Catrin Austin, Stephen Norton, Lisa Willcocks, Megan Griffith, Fiona Braddon, Retha Steenkamp, William S McKane, Arif Khwaja
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Abstract

Background: Patients with membranous nephropathy (MN) and poor kidney function or active disease despite previous immunosuppression are underrepresented in clinical trials. It is unknown how effective rituximab is in this population.

Methods: This prospective, multi-centre, single-arm, real-world study of patients with active MN [urine protein-creatinine ratio (uPCR) >350 mg/mmol and serum albumin <30 g/L, or a fall in estimated glomerular filtration rate (eGFR) of at least 20% or more over at least 3 months] evaluated rituximab in those with contraindications to calcineurin inhibitors and cytotoxic therapy. The primary outcome was change in rate of eGFR decline before and after rituximab. Complete or partial remission were defined as uPCR <30 mg/mmol or uPCR <350 mg/mmol with a ≥50% fall from baseline, respectively.

Results: A total of 180 patients [median age 59 years, interquartile range (IQR) 48-68] received rituximab and were followed up for a median duration of 17 months. Seventy-seven percent had prior immunosuppression. Median eGFR and uPCR at baseline were 49.2 mL/min/1.73 m2 (IQR 34.4-80.6) and 766 mg/mmol (IQR 487-1057), respectively. The annual rate of decline of eGFR fell from 13.9 to 1.7 mL/min/1.73 m2/year following rituximab (Z score = 2.48, < .0066). At 18 months 12% and 42% of patients were in complete or partial remission, respectively. Rituximab was well tolerated; patient survival was 95.6% at 2 years and in patients in whom eGFR was available, kidney survival was 93% at 2 years.

Conclusion: Rituximab significantly reduced the rate of eGFR decline in active MN including those who had received prior immunosuppression or with poor baseline kidney function.

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利妥昔单抗对膜性肾病患者肾功能影响的前瞻性研究。
背景:在临床试验中,膜性肾病(MN)患者和肾功能不良或既往免疫抑制后仍有活动性疾病的患者所占比例较低。目前尚不清楚利妥昔单抗对这类患者的疗效如何:这项前瞻性、多中心、单臂、真实世界研究的对象是活动性 MN 患者[尿蛋白-肌酐比值(uPCR)>350 毫克/毫摩尔,血清白蛋白] :共有 180 名患者[中位年龄 59 岁,四分位数间距 (IQR) 48-68]接受了利妥昔单抗治疗,随访时间中位数为 17 个月。77%的患者曾接受过免疫抑制治疗。基线中位 eGFR 和 uPCR 分别为 49.2 mL/min/1.73 m2 (IQR 34.4-80.6) 和 766 mg/mmol(IQR 487-1057)。利妥昔单抗治疗后,eGFR的年下降率从13.9毫升/分钟/1.73平方米/年降至1.7毫升/分钟/1.73平方米/年(Z评分=2.48,P 结论:利妥昔单抗可显著降低患者eGFR的年下降率:利妥昔单抗可明显降低活动性 MN(包括既往接受过免疫抑制或基线肾功能较差的患者)的 eGFR 下降率。
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来源期刊
Clinical Kidney Journal
Clinical Kidney Journal Medicine-Transplantation
CiteScore
6.70
自引率
10.90%
发文量
242
审稿时长
8 weeks
期刊介绍: About the Journal Clinical Kidney Journal: Clinical and Translational Nephrology (ckj), an official journal of the ERA-EDTA (European Renal Association-European Dialysis and Transplant Association), is a fully open access, online only journal publishing bimonthly. The journal is an essential educational and training resource integrating clinical, translational and educational research into clinical practice. ckj aims to contribute to a translational research culture among nephrologists and kidney pathologists that helps close the gap between basic researchers and practicing clinicians and promote sorely needed innovation in the Nephrology field. All research articles in this journal have undergone peer review.
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