Zhao Yin, Qi Fumin, Bai Jinyu, Zhang Na, Yang Tong, Sun Wenwen, Li Xin, Wei Wei
Department of Nephrology and Rheumatology, The Affiliated Hospital of Yunnan University (The Second People's Hospital of Yunnan Province), Kunming, Yunnan, China.
Department of Rheumatology and Immunology, Tianjin Medical University General Hospital, Tianjin, China.
Rheumatology (Oxford). 2025 Jan 1;64(1):108-116. doi: 10.1093/rheumatology/kead629.
The objective of this study was to explore the efficacy and safety of belimumab among Chinese patients with SLE in a real-world setting.
A prospective cohort study was performed, and SLE patients taking belimumab on a background of standard-of-care (SoC) treatment were consecutively enrolled from July 2021 to December 2022. Based on baseline characteristics, the patients were divided into three groups: the newly diagnosed group, the relapsed group and the refractory group. Patients in the newly diagnosed group were newly diagnosed with SLE within 4 weeks of starting belimumab. Patients in the relapse group had experienced a severe flare. Refractory patients were patients with unsatisfactory GC taper and/or disease activity control. Clinical data were collected, and disease assessments were conducted regularly. Newly diagnosed patients with SoC alone and healthy controls (HCs) were also enrolled.
A total of 123 SLE patients were included in the analysis, with a median follow-up period of 12 months (range 3-18 months). Thirty-three out of 123 patients were newly diagnosed, 32 had relapsed disease, and 58 had refractory disease. The SLE Responder Index 4 (SRI-4) response was achieved with good tolerance by 55.77% of patients at 3 months, 56.63% at 6 months, 63.24% at 9 months, 63.64% at 12 months and 57.14% at 18 months. Serological parameters (anti-dsDNA and C3/C4), SLEDAI-2K and daily prednisone intake were improved overall and in each group. Of the three groups, the newly diagnosed group had the highest SRI-4 rate as well as the greatest improvement in serological parameters and SLEDAI-2K. Compared with newly diagnosed patients with SoC alone, the cumulative prednisone intake of newly diagnosed patients taking belimumab was significantly decreased.
Our data supported the efficacy of belimumab in Chinese SLE patients in a real-life setting. Our study also provided new evidence indicating remarkable achievement of the SRI-4 response during belimumab therapy in newly diagnosed SLE patients.
本研究旨在探讨贝利尤单抗在中国系统性红斑狼疮(SLE)患者真实世界中的疗效和安全性。
进行了一项前瞻性队列研究,2021年7月至2022年12月连续纳入在标准治疗(SoC)基础上接受贝利尤单抗治疗的SLE患者。根据基线特征,将患者分为三组:新诊断组、复发组和难治组。新诊断组患者在开始使用贝利尤单抗后4周内新诊断为SLE。复发组患者经历了严重的病情复发。难治性患者是指糖皮质激素减量和/或疾病活动控制不理想的患者。收集临床数据并定期进行疾病评估。还纳入了仅接受SoC治疗的新诊断患者和健康对照(HCs)。
共123例SLE患者纳入分析,中位随访期为12个月(范围3 - 18个月)。123例患者中,33例为新诊断患者,32例为病情复发患者,58例为难治性患者。3个月时55.77%的患者、6个月时56.63%的患者、9个月时63.24%的患者、12个月时63.64%的患者以及18个月时57.14%的患者达到SLE缓解指数4(SRI - 4)反应且耐受性良好。血清学参数(抗双链DNA和C3/C4)、SLE疾病活动指数2000(SLEDAI - 2K)和每日泼尼松摄入量在总体及各亚组中均有所改善。三组中,新诊断组的SRI - 4率最高,血清学参数和SLEDAI - 2K改善也最为显著。与仅接受SoC治疗的新诊断患者相比,接受贝利尤单抗治疗的新诊断患者的累积泼尼松摄入量显著降低。
我们的数据支持贝利尤单抗在中国SLE患者现实生活中的疗效。我们的研究还提供了新的证据,表明新诊断的SLE患者在贝利尤单抗治疗期间显著实现了SRI - 4反应。