Disease-modifying effect and long-term safety of belimumab in patients with systemic lupus erythematosus: A single-center retrospective study

Author:

Nakai Takehiro1ORCID,Fukui Sho1234ORCID,Sawada Haruki15,Ikada Yukihiko1,Tamaki Hiromichi1,Kishimoto Mitsumasa16,Okada Masato1

Affiliation:

1. Immuno-Rheumatology Center, St Luke’s International Hospital, Tokyo, Japan

2. Center for Clinical Epidemiology, St Luke’s International University, Tokyo, Japan

3. Department of Emergency and General Medicine, Kyorin University School of Medicine, Tokyo, Japan

4. Division of Rheumatology, Inflammation, and Immunity, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, MA, USA

5. Department of Medicine, John A. Burns School of Medicine, University of Hawaii, Honolulu, HI, USA

6. Department of Nephrology and Rheumatology, Kyorin University School of Medicine, Tokyo, Japan

Abstract

Background Disease modification in systemic lupus erythematosus (SLE) is important for minimizing disease activity while limiting treatment-associated toxicities. Belimumab can be used as a remission-induction/maintenance systemic lupus erythematosus therapy; however, its disease-modifying effects are unclear. We aimed to determine these effects in patients with systemic lupus erythematosus. Methods This single-center retrospective cohort study included 92 patients with systemic lupus erythematosus treated with belimumab. We analyzed the changes in flare free rate/lupus low disease activity state (LLDAS) attainment rate/glucocorticoid dosage/Systemic Lupus International Collaborating Clinics and American College of Rheumatology damage index (SDI) score/drug retention rate after treatment initiation. Results Fifty-two weeks after initiating belimumab, the flare rate decreased from 82.6% to 14.1% ( p < .01). Until week 52 and 1000 days after initiating belimumab treatment, > 70% and ∼90% of the patients attained lupus low disease activity state, respectively. Belimumab treatment significantly reduced glucocorticoid demand (initiation day, 8.88 (6.00–15.00) mg/d; week 52, 5.00 (2.00–7.00) mg/d; final day of the study period, 3.00 (0.46–6.06) mg/d, initiation day vs. week 52: p < .01, initiation day vs. final day: p < .01); at the end of the study period, 68.5% of patients required ≤5 mg/d prednisolone, and 22.8% discontinued glucocorticoids. Most patients were SDI progression-free (week 52, ∼95%; day 1000, ∼90%), and belimumab showed a high drug retention rate (week 52, 90%; day 1000 > 80%). Conclusion Most patients experienced lupus low disease activity state, reduced flare rate and glucocorticoid demand, and a stable SDI trend after belimumab treatment initiation. Given its efficacy and retention rate, belimumab treatment may serve as a fundamental strategy in disease modification.

Publisher

SAGE Publications

Subject

Rheumatology

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