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利妥昔单抗治疗对传统疗法耐药的狼疮性肾炎:单中心经验

Rituximab Treatment in Lupus Nephritis Resistant to Conventional Therapy: A Single-Centre Experience.

作者信息

Senturk Esra F, Ogun Hande, Durucan Ibrahim, Yurttas Berna, Ugurlu Serdal

机构信息

Division of Rheumatology, Department of Internal Medicine, Cerrahpasa Medical Faculty, Istanbul University-Cerrahpasa, Istanbul, Turkey.

Division of Rheumatology, Department of Internal Medicine, Tekirdag Ismail Fehmi Cumalioglu City Hospital, Tekirdag, Turkey.

出版信息

Mediterr J Rheumatol. 2025 Jan 23;36(2):229-235. doi: 10.31138/mjr.250124.rtl. eCollection 2025 Jun.

Abstract

BACKGROUND

Treatment-resistant lupus nephritis (LN) is a challenging condition, often causing significant morbidity. While midterm outcomes of anti-CD20 therapies are well-studied, their long-term effects remain unclear.

OBJECTIVE

To assess Rituximab's long-term efficacy and safety in patients with refractory LN.

METHODS

The study, conducted retrospectively at a single centre between 2010-2022, included lupus nephritis patients who met the American College of Rheumatology's criteria for SLE. We evaluated 24-hour proteinuria, creatinine clearance, serum creatinine, and SLEDAI-2K, before and after rituximab treatment. The primary endpoints as a response to treatment were defined as the attainment of a prednisolone dose of 5mg and 24-hour proteinuria of 500mg. Additionally, we investigated any adverse effects of Rituximab.

RESULTS

Patients (34 females, 13 males; mean age 42.3 years; mean disease duration 10.4 years) received a median 3 of rituximab courses. Before treatment, median amount of proteinuria was 3050mg/day. Following the final course of rituximab, the median amount of proteinuria significantly decreased to 747mg/day (p<0.001). SLEDAI-2K score also reduced significantly, from 16.3±6.2 to 7.2±4.8 (p<0.001). The mean steroid dose in the final rituximab course was 7.5±5.8 mg/day (p<0.001), compared to the initial dose of 24.13±18.47mg/day. At primary endpoint, 53.1% of patients achieved a prednisolone dose of 5mg, 36.1% had a 24-hour proteinuria level of 500mg, and 25.5% met both criteria.

CONCLUSION

Rituximab significantly improved disease activity in lupus nephritis patients, reducing proteinuria, SLEDAI-2K scores, and allowing for steroid dose reduction. Given its efficacy and safety, rituximab may be a promising option for patients resistant to conventional therapy.

摘要

背景

难治性狼疮性肾炎(LN)是一种具有挑战性的疾病,常导致严重的发病率。虽然抗CD20疗法的中期疗效已得到充分研究,但其长期效果仍不明确。

目的

评估利妥昔单抗对难治性LN患者的长期疗效和安全性。

方法

该研究于2010年至2022年在单一中心进行回顾性研究,纳入符合美国风湿病学会SLE标准的狼疮性肾炎患者。我们评估了利妥昔单抗治疗前后的24小时蛋白尿、肌酐清除率、血清肌酐和SLEDAI-2K。作为治疗反应的主要终点定义为泼尼松龙剂量达到5mg且24小时蛋白尿为500mg。此外,我们调查了利妥昔单抗的任何不良反应。

结果

患者(34名女性,13名男性;平均年龄42.3岁;平均病程10.4年)接受了中位数为3个疗程的利妥昔单抗治疗。治疗前,蛋白尿中位数为3050mg/天。在最后一个利妥昔单抗疗程后,蛋白尿中位数显著降至747mg/天(p<0.001)。SLEDAI-2K评分也显著降低,从16.3±6.2降至7.2±4.8(p<0.001)。最后一个利妥昔单抗疗程的平均类固醇剂量为7.5±5.8mg/天(p<0.001),而初始剂量为24.13±18.47mg/天。在主要终点,53.1%的患者泼尼松龙剂量达到5mg,36.1%的患者24小时蛋白尿水平为500mg,25.5%的患者符合这两个标准。

结论

利妥昔单抗显著改善了狼疮性肾炎患者的疾病活动度,减少了蛋白尿、SLEDAI-2K评分,并允许减少类固醇剂量。鉴于其疗效和安全性,利妥昔单抗可能是对传统治疗耐药患者的一个有前景的选择。

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Clinical efficacy and safety of rituximab in lupus nephritis.利妥昔单抗治疗狼疮性肾炎的临床疗效与安全性。
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Immunosuppressive treatment for proliferative lupus nephritis.增殖性狼疮性肾炎的免疫抑制治疗
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