New York University Grossman School of Medicine, 550 First Avenue, MSB 593D, New York, NY, 10016, USA.
Albert Einstein College of Medicine, Bronx, New York, NY, USA.
Arthritis Res Ther. 2024 Feb 20;26(1):54. doi: 10.1186/s13075-024-03275-z.
Leveraging the Accelerating Medicines Partnership (AMP) Lupus Nephritis (LN) dataset, we evaluated longitudinal patterns, rates, and predictors of response to standard-of-care therapy in patients with lupus nephritis.
Patients from US academic medical centers with class III, IV, and/or V LN and a baseline urine protein/creatinine (UPCR) ratio ≥ 1.0 (n = 180) were eligible for this analysis. Complete response (CR) required the following: (1) UPCR < 0.5; (2) normal serum creatinine (≤ 1.3 mg/dL) or, if abnormal, ≤ 125% of baseline; and (3) prednisone ≤ 10 mg/day. Partial response (PR) required the following: (1) > 50% reduction in UPCR; (2) normal serum creatinine or, if abnormal, ≤ 125% of baseline; and (3) prednisone dose ≤ 15 mg/day.
Response rates to the standard of care at week 52 were CR = 22.2%; PR = 21.7%; non-responder (NR) = 41.7%, and not determined (ND) = 14.4%. Only 8/180 (4.4%) patients had a week 12 CR sustained through week 52. Eighteen (10%) patients attained a week 12 PR or CR and sustained their responses through week 52 and 47 (26.1%) patients achieved sustained PR or CR at weeks 26 and 52. Week 52 CR or PR attainment was associated with baseline UPCR > 3 (OR = 3.71 [95%CI = 1.34-10.24]; p = 0.012), > 25% decrease in UPCR from baseline to week 12 (OR = 2.61 [95%CI = 1.07-6.41]; p = 0.036), lower chronicity index (OR 1.33 per unit decrease [95%CI = 1.10-1.62]; p = 0.003), and positive anti-dsDNA antibody (OR = 2.61 [95%CI = 0.93-7.33]; p = 0.069).
CR and PR rates at week 52 were consistent with the standard-of-care response rates observed in prospective registrational LN trials. Low sustained response rates underscore the need for more efficacious therapies and highlight how critically important it is to understand the molecular pathways associated with response and non-response.
利用加速药物研发合作组织(AMP)狼疮肾炎(LN)数据集,我们评估了狼疮肾炎患者接受标准治疗后反应的纵向模式、发生率和预测因素。
符合该分析条件的患者来自美国学术医疗中心,患有 III、IV 和/或 V 型 LN,且基线尿蛋白/肌酐(UPCR)比值≥1.0(n=180)。完全缓解(CR)需要满足以下条件:(1)UPCR<0.5;(2)血清肌酐正常(≤1.3mg/dL)或异常时,≤基线的 125%;和(3)泼尼松剂量≤10mg/天。部分缓解(PR)需要满足以下条件:(1)UPCR降低>50%;(2)血清肌酐正常或异常时,≤基线的 125%;和(3)泼尼松剂量≤15mg/天。
第 52 周时,标准治疗的缓解率为 CR=22.2%;PR=21.7%;无反应(NR)=41.7%,未确定(ND)=14.4%。只有 8/180(4.4%)例患者在第 12 周时的 CR 持续至第 52 周。第 12 周时,有 18 例(10%)患者达到 PR 或 CR,并在第 52 周时维持其反应,47 例(26.1%)患者在第 26 周和第 52 周时达到持续 PR 或 CR。第 52 周时达到 CR 或 PR 与基线 UPCR>3(比值比[OR]=3.71[95%置信区间[CI]:1.34-10.24];p=0.012)、从基线到第 12 周 UPCR 降低>25%(OR=2.61[95%CI:1.07-6.41];p=0.036)、慢性指数较低(每单位降低 OR 为 1.33[95%CI:1.10-1.62];p=0.003)和抗 dsDNA 抗体阳性(OR=2.61[95%CI:0.93-7.33];p=0.069)相关。
第 52 周时的 CR 和 PR 率与前瞻性注册 LN 试验中观察到的标准治疗反应率一致。持续缓解率较低突出表明需要更有效的治疗方法,并强调了解与反应和无反应相关的分子途径是多么重要。