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贝丽珠单抗治疗系统性红斑狼疮患者的疗效:一项单中心、真实世界的回顾性研究。

Use of belimumab in treating patients with systemic lupus erythematosus: a single-center, real-world retrospective study.

机构信息

Department of Rheumatology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.

出版信息

Arthritis Res Ther. 2024 Sep 18;26(1):163. doi: 10.1186/s13075-024-03389-4.

Abstract

OBJECTIVE

To investigate the efficacy and safety of belimumab in the treatment of systemic lupus erythematosus (SLE) in a real-world setting and provide a valuable reference for clinical treatment.

METHODS

In this retrospective study, 101 patients with SLE who came to our hospital from March 2020 to September 2022, 56 of whom with lupus nephritis (LN), were selected. All patients received belimumab in combination with standard of care(SoC)therapy regimen for more than 52 weeks and their clinical/laboratory data, assessment of disease activity, glucocorticoids dosage and occurrence of adverse events were recorded. Lupus Low Disease Activity State (LLDAS) and DORIS remission as a primary goal in the treatment of SLE. The groups were classified according to the Systemic Lupus Erythematosus Disease Activity Index 2000 (SLEDAI-2 K): SLEDAI-2 K < 6 was categorized as the mild group (mild activity) and SLEDAI-2 K ≥ 6 was categorized as the active group (moderate-severe activity). The disease of the two groups mentioned above were assessed using the SELENA-SLEDAI Flare Index (SFI) and the SLE Responder Index-4 (SRI-4), respectively. Furthermore, we used complete remission (CR) and partial remission (PR) in the kidney as the standard for efficacy evaluation for LN patients.

RESULTS

After 52 weeks of treatment with belimumab, patients' complement levels increased significantly (p < 0.05); Other indicators such as 24-hour urine protein quantification and daily glucocorticoids dose decreased compared to pretreatment (p < 0.05). At 52 weeks, (i) after evaluation, the whole group of patients showed significant improvement in their condition; (ii) 55.4% of patients achieved LLDAS and 23.8% achieved DORIS remission; (iii) 73.2% of patients with LN achieved CR, 16.1% achieved PR. Adverse reactions were observed in 15 patients (14.9%), all of which normalized after symptomatic treatment.

CONCLUSIONS

In general, during treatment with belimumab, immunological and biochemical indices improved in SLE patients, urinary protein levels were reduced in LN patients, and the rate of renal function remission was effectively increased; At the same time, the use of belimumab is associated with a low frequency of side effects, good overall tolerability and a favorable safety profile.

摘要

目的

在真实环境中研究贝利尤单抗治疗系统性红斑狼疮(SLE)的疗效和安全性,并为临床治疗提供有价值的参考。

方法

本回顾性研究纳入 2020 年 3 月至 2022 年 9 月期间来我院就诊的 101 例 SLE 患者,其中 56 例狼疮肾炎(LN)患者。所有患者均接受贝利尤单抗联合标准治疗(SoC)方案治疗超过 52 周,并记录其临床/实验室数据、疾病活动评估、糖皮质激素剂量和不良事件发生情况。以狼疮低疾病活动状态(LLDAS)和 DORIS 缓解作为 SLE 治疗的主要目标。根据系统性红斑狼疮疾病活动指数 2000(SLEDAI-2K)将患者分为两组:SLEDAI-2K<6 为轻度组(轻度活动),SLEDAI-2K≥6 为活动组(中重度活动)。分别使用 SELENA-SLEDAI flares index(SFI)和 SLE responder index-4(SRI-4)评估两组患者的疾病活动度。此外,我们将 LN 患者的肾脏完全缓解(CR)和部分缓解(PR)作为疗效评估的标准。

结果

在贝利尤单抗治疗 52 周后,患者的补体水平显著升高(p<0.05);与治疗前相比,其他指标(如 24 小时尿蛋白定量和每日糖皮质激素剂量)均降低(p<0.05)。在 52 周时:(i)经过评估,整组患者的病情均有显著改善;(ii)55.4%的患者达到 LLDAS,23.8%的患者达到 DORIS 缓解;(iii)73.2%的 LN 患者达到 CR,16.1%的患者达到 PR。15 例(14.9%)患者出现不良反应,均经对症治疗后恢复正常。

结论

总的来说,在使用贝利尤单抗治疗期间,SLE 患者的免疫和生化指标改善,LN 患者的尿蛋白水平降低,肾功能缓解率有效提高;同时,贝利尤单抗的使用与不良反应发生率低、总体耐受性好、安全性良好相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c38b/11409747/793af6d312fb/13075_2024_3389_Figa_HTML.jpg

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