Real-world efficacy of belimumab in achieving remission or low-disease activity in systemic lupus erythematosus: A retrospective study

医学 内科学 倾向得分匹配 贝里穆马布 危险系数 关节炎 回顾性队列研究 糖皮质激素 疾病 痹症科 比例危险模型 红斑狼疮 免疫学 胃肠病学 置信区间 抗体 B细胞 B细胞激活因子
作者
Yasuhiro Hasegawa,Yoshiyuki Arinuma,Hirotomo Asakura,Risa Shindo,Kazuma Ino,Yoshiro Kanayama,Tomoki Tanaka,Yu Matsueda,Tatsuhiko Wada,Kenji Oku,Kunihiro Yamaoka
出处
期刊:Modern Rheumatology [Oxford University Press]
卷期号:34 (4): 732-740 被引量:1
标识
DOI:10.1093/mr/road078
摘要

ABSTRACT Objectives We investigated the effect of belimumab (BEL) on achieving low disease activity (LDA) and remission as an additive molecular-targeting agent to standard of care (SoC) in patients with systemic lupus erythematosus (SLE). Methods Clinical information was retrospectively collected from patients with SLE who received BEL additive to SoC (BEL + SoC), and from patients treated with SoC alone as a control arm. Disease activity was measured by SLE-disease activity score (SLE-DAS). The proportion of patients in LDA and remission at 12 months was compared after propensity score matching. The factors contributing to LDA and remission achievement were identified by Cox proportional hazard model. Results BEL + SoC significantly reduced SLE-DAS at 6 months, with a significantly higher proportion of patients achieving LDA and remission at 12 months compared to SoC alone. The presence of arthritis at baseline was significantly associated with achieving LDA and remission. Additionally, both treatment groups experienced a significant reduction in daily glucocorticoid dose. Conclusions Adding BEL to SoC was beneficial for patients with arthritis, leading to higher proportion of achieving LDA and remission, while also reducing their glucocorticoid dose. Our results indicate the utility of BEL in a treat-to-target approach for SLE patients in a real-world setting.
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