Evaluation of belimumab in treatment of Chinese childhood-onset systemic lupus erythematosus: a prospective analysis from a multicentre study

医学 贝里穆马布 内科学 强的松 泊松回归 前瞻性队列研究 系统性红斑狼疮 物理疗法 入射(几何) 儿科 疾病 免疫学 人口 B细胞激活因子 抗体 物理 B细胞 环境卫生 光学
作者
Li Wang,Xiaohua Liang,Zhilang Cao,Dahai Wang,Ying Luo,Yuan Feng,Chong Luo,Shufeng Zhi,Yiling Huang,Zhidan Fan,Chaoying Wang,Haimei Liu,Jinxiang Liu,Tianyu Zhang,Qiuting Cheng,Xue Xie,Lanjun Shuai,Zanhua Rong,Ping Zeng,Haiguo Yu
出处
期刊:Rheumatology [Oxford University Press]
卷期号:63 (5): 1437-1446 被引量:6
标识
DOI:10.1093/rheumatology/kead406
摘要

Abstract Objective The aim of this study is to identify whether low lupus disease activity status (LLDAS) and clinical remission (CR) of belimumab plus standard of care (SoC) therapy are achievable goals in childhood-onset SLE (cSLE). Methods This multicentre, one arm pre-post intervention study was conducted at 15 centres in China. The primary end point was to describe the proportion of patients who achieved LLDAS and CR after 3, 6 and 12 months after treatment with belimumab plus SoC therapy. A multiple regression model was used to impute missing data. A Poisson regression model was used to calculate the effect of belimumab treatment on the reduced risk of serious diseases and the incidence of new damage. Result A total of 193 (92.2% female) with active cSLE from 15 centres were included. At 3, 6 and 12 months, the proportion of LLDAS (CR) was 12.4% (1.0%), 25.6% (4.5%) and 70.3% (29.7%), respectively. The mean SELENA-SLEDAI score decreased from 11.0 at baseline to 3.7, 2.9 and 1.7 at 3, 6 and 12 months. At baseline, all patients received steroids at a mean (s.d.) prednisone equivalent dose of 31.0 (18.2) mg/day, which decreased to 19.4 (10.8) mg/day at month 3, 12.6 (7.2) mg/day at month 6 and 6.7 (5.3) mg/day at month 12. The symptoms and immunological indicators were also significantly improved. Conclusion This is the first and largest sample size prospective clinical intervention study of cSLE patients treated with belimumab in China. LLDAS and CR were attainable treat-to-target of belimumab plus SoC therapy in cSLE.
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