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Impact of Belimumab on Organ Damage in Systemic Lupus Erythematosus.

Authors :
Urowitz, Murray B.
Aranow, Cynthia
Asukai, Yumi
Bass, Damon L.
Bruce, Ian N.
Chauhan, Deven
Dall'Era, Maria
Furie, Richard
Fox, Norma Lynn
Gilbride, Jennifer A.
Hammer, Anne
Ginzler, Ellen M.
Gonzalez‐Rivera, Tania
Levy, Roger A.
Merrill, Joan T.
Quasny, Holly
Roth, David A.
Stohl, William
van Vollenhoven, Ronald
Wallace, Daniel J.
Source :
Arthritis Care & Research; Nov2022, Vol. 74 Issue 11, p1822-1828, 7p
Publication Year :
2022

Abstract

Organ damage is a key determinant of poor long‐term prognosis and early death in patients with systemic lupus erythematosus (SLE). Prevention of damage is a key treatment goal of the 2019 update of the European Alliance of Associations for Rheumatology (EULAR) recommendations for SLE management. Belimumab is a monoclonal antibody that inhibits B lymphocyte stimulator (BLyS) and is the only therapy approved for both SLE and lupus nephritis. Here, we review the clinical trial and real‐world data on the effects of belimumab on organ damage in adult patients with SLE. Across 4 phase III studies, belimumab in combination with background SLE therapy demonstrated consistent reductions in key drivers of organ damage including disease activity, risk of new severe flares, and glucocorticoid exposure compared to background therapy alone. Long‐term belimumab use in SLE also reduced organ damage progression measured by the Systemic Lupus International Collaborating Clinics/American College of Rheumatology Damage Index, as reported in open‐label extension studies, and propensity score–matched comparative analyses to background therapy alone. Results from a clinical trial showed that in patients with active lupus nephritis, belimumab treatment improved renal response, reduced the risk of renal‐related events, and impacted features related to kidney damage progression compared to background therapy alone. The decrease of organ damage accumulation observed with belimumab treatment in SLE, including lupus nephritis, suggest a disease‐modifying effect. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
2151464X
Volume :
74
Issue :
11
Database :
Complementary Index
Journal :
Arthritis Care & Research
Publication Type :
Academic Journal
Accession number :
159814489
Full Text :
https://doi.org/10.1002/acr.24901