Efficacy of Voclosporin in Proliferative Lupus Nephritis with High Levels of Proteinuria

被引:1
|
作者
Menn-Josephy, Hanni [1 ]
Hodge, Lucy S. [2 ]
Birardi, Vanessa [2 ]
Leher, Henry [2 ]
机构
[1] Boston Univ, Sch Med, Boston, MA USA
[2] Aurinia Pharmaceut Inc, 140 14315-118 Ave, Edmonton, AB T5L 4S6, Canada
关键词
lupus nephritis; renal failure; renal function; renal function decline; systemic lupus erythematosus; KIDNEY-FUNCTION; RISK; OUTCOMES; DISEASE; INJURY; COHORT;
D O I
10.2215/CJN.0000000000000297
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background In a phase 3 study of adults with active lupus nephritis, addition of voclosporin to mycophenolate mofetil (MMF) and low-dose glucocorticoids led to significant improvements in the proportion of participants achieving complete and partial renal response as well as sustained reduction in proteinuria. This analysis examined the efficacy and safety of voclosporin in a subgroup of the phase 3 study with proliferative lupus nephritis and high levels of proteinuria.Methods Participants were randomized to oral voclosporin (23.7 mg twice daily) or placebo for 12 months; all participants received MMF and low-dose glucocorticoids. This analysis includes participants with class III or IV (+/- class V) lupus nephritis and baseline urine protein-creatinine ratio (UPCR) >= 3 g/g. Efficacy end points included complete renal response (UPCR <= 0.5 g/g with stable eGFR, low-dose glucocorticoids, and no rescue medication), partial renal response >= 50% reduction from baseline UPCR), and UPCR over time. Safety outcomes were also assessed.Results A total of 148 participants were in the voclosporin (n=76) and control (n=72) arms. At 12 months, 34% and 11% of participants in the voclosporin and control arms, respectively, achieved a complete renal response (odds ratio, 4.43; 95% confidence interval [CI], 1.78 to >9.99; P = 0.001). A partial renal response was achieved by 65% of the voclosporin arm and 51% of the control arm at 12 months (odds ratio, 1.60; 95% CI, 0.8 to 3.20; P = 0.18). More voclosporin- than control-treated participants achieved UPCR <= 0.5 g/g (51% versus 26%), and voclosporin-treated participants met this end point significantly earlier (hazard ratio, 2.07; 95% CI, 1.19 to 3.60; P = 0.01). The incidence of adverse events was similar between the arms; mean eGFR values remained stable and within normal range in both arms.Conclusions Addition of voclosporin to MMF and low-dose glucocorticoids resulted in a significantly higher proportion of participants with proliferative lupus nephritis achieving complete and partial renal responses as well as earlier reductions in proteinuria, with no evidence of worsening kidney function.
引用
收藏
页码:309 / 318
页数:10
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