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

贝里穆马布 医学 硫唑嘌呤 内科学 危险系数 狼疮性肾炎 倾向得分匹配 免疫学 疾病 置信区间 抗体 B细胞 B细胞激活因子
作者
Emma Materne,Hyon K. Choi,Baijun Zhou,Karen H. Costenbader,Yuqing Zhang,April Jorge
出处
期刊:Arthritis & rheumatology [Wiley]
卷期号:75 (11): 1994-2002 被引量:7
标识
DOI:10.1002/art.42620
摘要

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. image

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