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静脉注射贝利尤单抗治疗成年系统性红斑狼疮患者的真实世界有效性:俄罗斯联邦观察性OBSErve研究结果

Real-world effectiveness of intravenous belimumab in adults with systemic lupus erythematosus: results of the observational OBSErve study in the Russian Federation.

作者信息

Lila Alexander Mikhailovich, Aseeva Elena Aleksandrovna, Zagrebneva Alyona Igorevna, Vinogradova Irina Borisovna, Samigullina Ruzana Ramilovna, Khamashta Munther, Elfishawy Tamer, Teichman Lindsey, Dos Santos Debora, Queiroz Juliana, Kniazeva Larisa Alexandrovna, Noibi Saeed

机构信息

Institute of Rheumatology by V.A. Nasonova, Russian Academy of Science, Moscow, Russian Federation.

Moscow City Clinical Hospital №52, Ministry of Health of Moscow, Moscow, Russian Federation.

出版信息

BMC Rheumatol. 2025 Jan 8;9(1):4. doi: 10.1186/s41927-024-00452-0.

Abstract

BACKGROUND

The real-world effectiveness of intravenous (IV) belimumab in treating systemic lupus erythematosus (SLE) has been demonstrated in various countries through the OBSErve (evaluation Of use of Belimumab in clinical practice SEttings) program. Here we describe the clinical effectiveness of IV belimumab for treating SLE in real-world clinical practice in the Russian Federation.

METHODS

In the retrospective, observational OBSErve Russia study (GSK Study 215349), eligible physicians enrolled adults with SLE receiving IV belimumab as part of their standard care. De-identified data were collected from patient medical records from September 2021 to March 2022. The primary outcome was the physician-assessed overall clinical response at 6 months post-index versus index (belimumab initiation) among patients receiving belimumab for ≥6 months. Other endpoints included change in Safety of Estrogens in Lupus Erythematosus National Assessment - SLE Disease Activity Index (SELENA-SLEDAI) score and glucocorticoid use.

RESULTS

Overall, 59 patients initiated IV belimumab, mainly due to the previous regimen not being effective and to decrease glucocorticoid use (76.3% each); 15.3% of patients started belimumab within the first year of SLE diagnosis. Only 13.6% of patients discontinued belimumab within the first 6 months, mainly due to loss to follow-up and loss of insurance/reimbursement. At 6 months post-index, among patients who completed ≥6 months of belimumab therapy (full analysis set, n = 53), 90.6% and 60.4% had an overall clinical improvement of ≥20% and ≥50%, respectively. Mean (standard deviation, SD) change in SELENA-SLEDAI score from index to 6 months post-index was -5.9 (4.3). Mean (SD) glucocorticoid dose decreased from 12.2 (7.3) mg/day at index to 8.6 (5.1) mg/day at 6 months post-index (n = 50).

CONCLUSIONS

Patients with SLE receiving IV belimumab for 6 months in real-world settings in the Russian Federation experienced overall clinical improvements and reductions in glucocorticoid use, which is an important long-term strategy of SLE treatment.

摘要

背景

通过观察(在临床实践环境中评估贝利尤单抗的使用)项目,已在多个国家证明静脉注射贝利尤单抗治疗系统性红斑狼疮(SLE)的真实世界有效性。在此,我们描述静脉注射贝利尤单抗在俄罗斯联邦真实世界临床实践中治疗SLE的临床有效性。

方法

在回顾性观察性俄罗斯观察研究(葛兰素史克研究215349)中,符合条件的医生纳入接受静脉注射贝利尤单抗作为标准治疗一部分的成年SLE患者。从2021年9月至2022年3月的患者病历中收集去识别化数据。主要结局是在接受贝利尤单抗治疗≥6个月的患者中,与基线(贝利尤单抗起始)相比,基线后6个月时医生评估的总体临床反应。其他终点包括狼疮性红斑全国评估 - SLE疾病活动指数(SELENA - SLEDAI)评分变化和糖皮质激素使用情况。

结果

总体而言,59例患者开始静脉注射贝利尤单抗,主要原因是先前治疗方案无效以及减少糖皮质激素使用(各占76.3%);15.3%的患者在SLE诊断的第一年内开始使用贝利尤单抗。仅13.6%的患者在最初6个月内停用贝利尤单抗,主要原因是失访以及失去保险/报销资格。在基线后6个月时,在完成≥6个月贝利尤单抗治疗的患者(全分析集,n = 53)中,分别有90.6%和60.4%的患者总体临床改善≥20%和≥50%。从基线到基线后6个月,SELENA - SLEDAI评分的平均(标准差,SD)变化为 -5.9(4.3)。糖皮质激素平均(SD)剂量从基线时的12.2(7.3)mg/天降至基线后6个月时的8.6(5.1)mg/天(n = 50)。

结论

在俄罗斯联邦的真实世界环境中,接受静脉注射贝利尤单抗治疗6个月的SLE患者总体临床状况得到改善,糖皮质激素使用减少,这是SLE治疗的一项重要长期策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a9b/11708191/7b4f759d6851/41927_2024_452_Fig1_HTML.jpg

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