The First Department of Internal Medicine, University of Occupational and Environmental Health, Japan, Kitakyushu, Japan.
Department of Rheumatology and Infectious Diseases, Kitasato University School of Medicine, Kanagawa, Japan.
Mod Rheumatol. 2023 Jan 3;33(1):145-153. doi: 10.1093/mr/roac007.
Although recommended in established international guidelines for lupus nephritis (LN), rituximab is not officially approved for LN treatment, making all such use off-label. The Japan College of Rheumatology (JCR) conducted a retrospective observational study on real-world efficacy and safety of rituximab treatment for LN in Japan.
Clinical data were collected from 47 hospitals for LN patients treated with rituximab to retrospectively investigate dosing schedule, efficacy, and safety.
This retrospective analysis included 115 patients: 84 (73%) received 375 mg/m2 weekly up to four doses, and 31 (27%) received 1000 mg/body in one or two doses 2 weeks apart. Rituximab significantly improved findings for urinalysis, systemic lupus erythematosus serology, and systemic lupus erythematosus disease activity and was assessed as 'extremely effective' in 24.8% of patients and 'effective' in 60.2%. The renal response by the JCR-I criteria was 52.5% for overall response rate (ORR) (complete renal response rate 20.8% and partial renal response rate 31.7%) and that by the JCR-II criteria was 49.5% (21.8% and 27.7%, respectively). Corticosteroid dose was significantly reduced. Rituximab was well tolerated, with frequent but manageable adverse events of infusion reaction and infection.
Rituximab is effective for the treatment of Japanese patients with LN refractory to conventional therapy.
尽管利妥昔单抗在已确立的狼疮肾炎(LN)国际指南中被推荐,但尚未获得 LN 治疗的官方批准,因此所有此类用途均为超适应证用药。日本风湿病学会(JCR)对日本真实世界中利妥昔单抗治疗 LN 的疗效和安全性进行了回顾性观察性研究。
从接受利妥昔单抗治疗的 LN 患者的 47 家医院收集临床数据,回顾性调查其剂量方案、疗效和安全性。
本回顾性分析纳入了 115 例患者:84 例(73%)接受每周 375mg/m2 至 4 个剂量,31 例(27%)接受 2 周间隔的 1000mg/体 1 或 2 个剂量。利妥昔单抗显著改善了尿液分析、系统性红斑狼疮血清学和系统性红斑狼疮疾病活动度的结果,24.8%的患者评估为“非常有效”,60.2%的患者评估为“有效”。根据 JCR-I 标准,整体反应率(ORR)的肾脏反应为 52.5%(完全肾脏反应率 20.8%,部分肾脏反应率 31.7%),根据 JCR-II 标准为 49.5%(完全肾脏反应率 21.8%,部分肾脏反应率 27.7%)。皮质类固醇剂量显著减少。利妥昔单抗具有良好的耐受性,输注反应和感染等常见但可管理的不良反应。
利妥昔单抗对治疗对常规治疗无效的日本 LN 患者有效。