Suppr超能文献

比较非肾脏系统性红斑狼疮患者使用贝利尤单抗与口服免疫抑制剂的感染风险。

Comparative Risks of Infection With Belimumab Versus Oral Immunosuppressants in Patients With Nonrenal Systemic Lupus Erythematosus.

机构信息

Department of Medicine, Massachusetts General Hospital, Boston.

Department of Medicine, Massachusetts General Hospital, Boston, Division of Rheumatology, Allergy, and Immunology, Massachusetts General Hospital, Boston, and Harvard Medical School, Boston, Massachusetts.

出版信息

Arthritis Rheumatol. 2023 Nov;75(11):1994-2002. doi: 10.1002/art.42620. Epub 2023 Oct 8.

Abstract

OBJECTIVE

We investigated the comparative risk of infection with belimumab versus oral immunosuppressants for the treatment of systemic lupus erythematosus (SLE).

METHODS

Using observational data from a US multicenter electronic health record database, we identified patients with SLE but without lupus nephritis who initiated belimumab, azathioprine, methotrexate, or mycophenolate between 2011 and 2021. We designed and emulated hypothetical target trials to estimate the cumulative incidence and hazard ratios (HRs) of serious infection and hospitalization for serious infection comparing belimumab versus each oral immunosuppressant. We used propensity score overlap weighting to balance baseline covariates and adjusted for adherence to treatment group using inverse probability of treatment weighting. We also assessed the control outcome of traumatic injury.

RESULTS

Among 21,481 patients, we compared 2841 and 6343 initiators of belimumab and azathioprine, 2642 and 8242 initiators of belimumab and methotrexate, and 2813 and 8407 initiators of belimumab and mycophenolate, respectively. After propensity score overlap weighting, all covariates were balanced in each comparison. The mean age of the cohort was 45 years, and 94% were women. Compared with azathioprine and mycophenolate, belimumab was associated with lower risks of both serious infection (HR 0.82; 95% confidence interval [CI] 0.72-0.92 and HR 0.69; 95% CI 0.61-0.78) and hospitalization for infection (HR 0.73; 95% CI 0.57-0.94 and HR 0.56 95% CI 0.43-0.71). The risk of infection was also lower for belimumab compared with methotrexate (HR 0.86; 95% CI 0.76-0.97). There were no differences in traumatic injury risks across treatment groups.

CONCLUSION

Belimumab was associated with lower risks of serious infection than with oral immunosuppressants. This finding should inform risk/benefit considerations for SLE treatment.

摘要

目的

我们研究了治疗系统性红斑狼疮(SLE)时,贝鲁单抗与口服免疫抑制剂相比的感染风险。

方法

我们使用来自美国多中心电子病历数据库的观察性数据,确定了 2011 年至 2021 年间开始接受贝鲁单抗、硫唑嘌呤、甲氨蝶呤或霉酚酸酯治疗但无狼疮肾炎的 SLE 患者。我们设计并模拟了假设性目标试验,以估计贝鲁单抗与每种口服免疫抑制剂相比严重感染的累积发生率和风险比(HR)以及严重感染住院的 HR。我们使用倾向评分重叠加权来平衡基线协变量,并使用治疗组的逆概率治疗加权来调整对治疗的依从性。我们还评估了创伤性损伤的对照结局。

结果

在 21481 名患者中,我们比较了 2841 名和 6343 名贝鲁单抗与硫唑嘌呤的起始者、2642 名和 8242 名贝鲁单抗与甲氨蝶呤的起始者、2813 名和 8407 名贝鲁单抗与霉酚酸酯的起始者。在倾向评分重叠加权后,每个比较中所有协变量均得到平衡。队列的平均年龄为 45 岁,94%为女性。与硫唑嘌呤和霉酚酸酯相比,贝鲁单抗与严重感染(HR 0.82;95%置信区间 [CI] 0.72-0.92 和 HR 0.69;95%CI 0.61-0.78)和感染住院(HR 0.73;95%CI 0.57-0.94 和 HR 0.56;95%CI 0.43-0.71)的风险降低相关。贝鲁单抗与甲氨蝶呤相比,感染风险也较低(HR 0.86;95%CI 0.76-0.97)。治疗组之间的创伤性损伤风险没有差异。

结论

贝鲁单抗与严重感染的风险低于口服免疫抑制剂。这一发现应该为 SLE 治疗的风险/获益考虑提供信息。

相似文献

1
Comparative Risks of Infection With Belimumab Versus Oral Immunosuppressants in Patients With Nonrenal Systemic Lupus Erythematosus.
Arthritis Rheumatol. 2023 Nov;75(11):1994-2002. doi: 10.1002/art.42620. Epub 2023 Oct 8.
3
Belimumab for systemic lupus erythematosus.
Cochrane Database Syst Rev. 2021 Feb 25;2(2):CD010668. doi: 10.1002/14651858.CD010668.pub2.
5
New onset of lupus nephritis in two patients with SLE shortly after initiation of treatment with belimumab.
Semin Arthritis Rheum. 2017 Jun;46(6):788-790. doi: 10.1016/j.semarthrit.2016.09.006. Epub 2016 Sep 28.

引用本文的文献

2
New Mechanisms and Therapeutic Targets in Systemic Lupus Erythematosus.
MedComm (2020). 2025 Jun 9;6(6):e70246. doi: 10.1002/mco2.70246. eCollection 2025 Jun.
4
Comparative effectiveness of disease-modifying antirheumatic drugs for patients with cardiac sarcoidosis.
Rheumatology (Oxford). 2025 Jun 1;64(6):3303-3308. doi: 10.1093/rheumatology/keae692.
5
Association of CD19-targeted chimeric antigen receptor (CAR) T-cell therapy with hypogammaglobulinemia, infection, and mortality.
J Allergy Clin Immunol. 2025 Feb;155(2):605-615. doi: 10.1016/j.jaci.2024.10.021. Epub 2024 Nov 4.
6
Advances in Systemic Lupus Erythematosus Treatment With Monoclonal Antibodies: A Mini-Review.
Cureus. 2024 Jul 8;16(7):e64090. doi: 10.7759/cureus.64090. eCollection 2024 Jul.
7
Disease-modifying therapies in systemic lupus erythematosus for extrarenal manifestations.
Lupus Sci Med. 2024 May 22;11(1):e001124. doi: 10.1136/lupus-2023-001124.
8
Reply.
Arthritis Rheumatol. 2024 Feb;76(2):316-317. doi: 10.1002/art.42692. Epub 2023 Oct 15.

本文引用的文献

1
Predictors of infection requiring hospitalization in patients with systemic lupus erythematosus: a time-to-event analysis.
Semin Arthritis Rheum. 2022 Dec;57:152099. doi: 10.1016/j.semarthrit.2022.152099. Epub 2022 Sep 19.
2
Infection hospitalisation in systemic lupus in Sweden.
Lupus Sci Med. 2021 Sep;8(1). doi: 10.1136/lupus-2021-000510.
3
Validity of ICD-10-CM diagnoses to identify hospitalizations for serious infections among patients treated with biologic therapies.
Pharmacoepidemiol Drug Saf. 2021 Jul;30(7):899-909. doi: 10.1002/pds.5253. Epub 2021 May 3.
4
Belimumab for systemic lupus erythematosus.
Cochrane Database Syst Rev. 2021 Feb 25;2(2):CD010668. doi: 10.1002/14651858.CD010668.pub2.
6
Emulating a target trial in case-control designs: an application to statins and colorectal cancer.
Int J Epidemiol. 2020 Oct 1;49(5):1637-1646. doi: 10.1093/ije/dyaa144.
7
Comparison of an administrative algorithm for SLE disease severity to clinical SLE Disease Activity Index scores.
Rheumatol Int. 2020 Feb;40(2):257-261. doi: 10.1007/s00296-019-04477-4. Epub 2019 Nov 29.
8
2019 update of the EULAR recommendations for the management of systemic lupus erythematosus.
Ann Rheum Dis. 2019 Jun;78(6):736-745. doi: 10.1136/annrheumdis-2019-215089. Epub 2019 Mar 29.
9
Per-Protocol Analyses of Pragmatic Trials.
N Engl J Med. 2017 Oct 5;377(14):1391-1398. doi: 10.1056/NEJMsm1605385.
10
Examining Bias in Studies of Statin Treatment and Survival in Patients With Cancer.
JAMA Oncol. 2018 Jan 1;4(1):63-70. doi: 10.1001/jamaoncol.2017.2752.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验