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Two-Year, Randomized, Controlled Trial of Belimumab in Lupus Nephritis.

Authors :
UCL - SSS/IREC/RUMA - Pôle de Pathologies rhumatismales
UCL - (SLuc) Service de rhumatologie
Furie, Richard
Rovin, Brad H
Houssiau, Frédéric
Malvar, Ana
Teng, Y K Onno
Contreras, Gabriel
Amoura, Zahir
Yu, Xueqing
Mok, Chi-Chiu
Santiago, Mittermayer B
Saxena, Amit
Green, Yulia
Ji, Beulah
Kleoudis, Christi
Burriss, Susan W
Barnett, Carly
Roth, David A
UCL - SSS/IREC/RUMA - Pôle de Pathologies rhumatismales
UCL - (SLuc) Service de rhumatologie
Furie, Richard
Rovin, Brad H
Houssiau, Frédéric
Malvar, Ana
Teng, Y K Onno
Contreras, Gabriel
Amoura, Zahir
Yu, Xueqing
Mok, Chi-Chiu
Santiago, Mittermayer B
Saxena, Amit
Green, Yulia
Ji, Beulah
Kleoudis, Christi
Burriss, Susan W
Barnett, Carly
Roth, David A
Source :
The New England journal of medicine, Vol. 383, no.12, p. 1117-1128 (2020)
Publication Year :
2020

Abstract

BACKGROUND: In adults with active lupus nephritis, the efficacy and safety of intravenous belimumab as compared with placebo, when added to standard therapy (mycophenolate mofetil or cyclophosphamide-azathioprine), are unknown. METHODS: In a phase 3, multinational, multicenter, randomized, double-blind, placebo-controlled, 104-week trial conducted at 107 sites in 21 countries, we assigned adults with biopsy-proven, active lupus nephritis in a 1:1 ratio to receive intravenous belimumab (at a dose of 10 mg per kilogram of body weight) or matching placebo, in addition to standard therapy. The primary end point at week 104 was a primary efficacy renal response (a ratio of urinary protein to creatinine of ≤0.7, an estimated glomerular filtration rate [eGFR] that was no worse than 20% below the value before the renal flare (pre-flare value) or ≥60 ml per minute per 1.73 m2 of body-surface area, and no use of rescue therapy), and the major secondary end point was a complete renal response (a ratio of urinary protein to creatinine of <0.5, an eGFR that was no worse than 10% below the pre-flare value or ≥90 ml per minute per 1.73 m2, and no use of rescue therapy). The time to a renal-related event or death was assessed. RESULTS: A total of 448 patients underwent randomization (224 to the belimumab group and 224 to the placebo group). At week 104, significantly more patients in the belimumab group than in the placebo group had a primary efficacy renal response (43% vs. 32%; odds ratio, 1.6; 95% confidence interval [CI], 1.0 to 2.3; P = 0.03) and a complete renal response (30% vs. 20%; odds ratio, 1.7; 95% CI, 1.1 to 2.7; P = 0.02). The risk of a renal-related event or death was lower among patients who received belimumab than among those who received placebo (hazard ratio, 0.51; 95% CI, 0.34 to 0.77; P = 0.001). The safety profile of belimumab was consistent with that in previous trials. CONCLUSIONS: In this trial involving patients with active lupus nephritis, more patients

Details

Database :
OAIster
Journal :
The New England journal of medicine, Vol. 383, no.12, p. 1117-1128 (2020)
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1288278394
Document Type :
Electronic Resource