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

Author:

Materne Emma1,Choi Hyon2ORCID,Zhou Baijun3,Costenbader Karen H.4ORCID,Zhang Yuqing2ORCID,Jorge April2ORCID

Affiliation:

1. Department of Medicine Massachusetts General Hospital Boston

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

3. Division of Rheumatology, Allergy, and Immunology Massachusetts General Hospital Boston

4. Harvard Medical School, Boston, and Division of Rheumatology, Inflammation, and Immunity Brigham and Women's Hospital Boston Massachusetts

Abstract

ObjectiveWe investigated the comparative risk of infection with belimumab versus oral immunosuppressants for the treatment of systemic lupus erythematosus (SLE).MethodsUsing 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.ResultsAmong 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.ConclusionBelimumab was associated with lower risks of serious infection than with oral immunosuppressants. This finding should inform risk/benefit considerations for SLE treatment.image

Funder

National Institute of Arthritis and Musculoskeletal and Skin Diseases

Rheumatology Research Foundation

Publisher

Wiley

Subject

Immunology,Rheumatology,Immunology and Allergy

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