Rovin Brad H, Furie Richard A, Ross Terres Jorge A, Giang Sophia, Schindler Thomas, Turchetta Armando, Garg Jay P, Pendergraft William F, Malvar Ana
The Ohio State University Wexner Medical Center, Columbus.
Northwell Health, Great Neck, New York.
Arthritis Rheumatol. 2024 Feb;76(2):247-254. doi: 10.1002/art.42734. Epub 2023 Nov 10.
To determine whether adding obinutuzumab to standard-of-care lupus nephritis (LN) therapy could improve the likelihood of long-term preservation of kidney function and do so with less glucocorticoids.
Post hoc analyses of the phase II NOBILITY trial were performed. Time to unfavorable kidney outcome (a composite of treatment failure, doubling of serum creatinine, or death), LN flare, first 30% and 40% declines in estimated glomerular filtration rate (eGFR) from baseline, and chronic eGFR slope during the trial were compared between patients with active LN who were randomized to take obinutuzumab (n = 63) or placebo (n = 62) in combination with mycophenolate mofetil and glucocorticoids. The number of patients who achieved complete renal response (CRR) on 7.5 mg or less per day of prednisone was also determined.
Obinutuzumab reduced the risk of developing the composite kidney outcome by 60%, LN flare by 57%, and first eGFR decline of 30% or 40% by 80% and 91%, respectively. Patients receiving obinutuzumab had a significantly slower decline in eGFR than patients receiving placebo, with an annualized eGFR slope advantage of 4.1 ml/min/1.73 m /year (95% confidence interval 0.14-8.08). Overall, 38% of patients receiving obinutuzumab compared with 16% of patients receiving placebo achieved CRR at week 76 while receiving 7.5 mg or less per day of prednisone (P < 0.01); at week 104, the difference did not achieve significance (38% vs 22%; P = 0.06).
Post hoc analyses of NOBILITY demonstrated that compared with standard-of-care therapy, obinutuzumab treatment resulted in superior preservation of kidney function and prevention of LN flares. More patients achieved CRR at week 76 with less glucocorticoid use in the obinutuzumab group.
确定在狼疮性肾炎(LN)标准治疗方案中添加奥妥珠单抗是否能提高长期肾功能保留的可能性,并减少糖皮质激素的使用量。
对II期NOBILITY试验进行事后分析。比较了随机接受奥妥珠单抗(n = 63)或安慰剂(n = 62)联合霉酚酸酯和糖皮质激素治疗的活动性LN患者发生不良肾脏结局(治疗失败、血清肌酐翻倍或死亡的复合结局)的时间、LN复发、估计肾小球滤过率(eGFR)从基线水平首次下降30%和40%的时间,以及试验期间慢性eGFR斜率。还确定了每天服用泼尼松7.5 mg或更少剂量时达到完全肾脏缓解(CRR)的患者数量。
奥妥珠单抗使复合肾脏结局的发生风险降低了60%,LN复发风险降低了57%,eGFR首次下降30%或40%的风险分别降低了80%和91%。接受奥妥珠单抗治疗的患者eGFR下降速度明显慢于接受安慰剂治疗的患者,年化eGFR斜率优势为4.1 ml/min/1.73 m²/年(95%置信区间0.14 - 8.08)。总体而言,在第76周时,接受奥妥珠单抗治疗的患者中有38%达到CRR,而接受安慰剂治疗的患者中这一比例为16%,此时患者每天服用泼尼松7.5 mg或更少剂量(P < 0.01);在第104周时,差异无统计学意义(38%对22%;P = 0.06)。
NOBILITY试验的事后分析表明,与标准治疗方案相比,奥妥珠单抗治疗在肾功能保留和预防LN复发方面表现更优。在第76周时,奥妥珠单抗组更多患者实现了CRR,且糖皮质激素使用量更少。