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.
Arthritis Rheumatol. 2023 Nov;75(11):1994-2002. doi: 10.1002/art.42620. Epub 2023 Oct 8.
We investigated the comparative risk of infection with belimumab versus oral immunosuppressants for the treatment of systemic lupus erythematosus (SLE).
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.
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.
Belimumab was associated with lower risks of serious infection than with oral immunosuppressants. This finding should inform risk/benefit considerations for SLE treatment.
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。
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。
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。
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。