Cortazar Frank B, Leaf David E, Owens Charles T, Laliberte Karen, Pendergraft William F, Niles John L
Vasculitis and Glomerulonephritis Center, Division of Nephrology, Massachusetts General Hospital, 101 Merrimac St, Boston, 02114, MA, USA.
Division of Renal Medicine, Brigham and Women's Hospital, Boston, MA, USA.
BMC Nephrol. 2017 Feb 1;18(1):44. doi: 10.1186/s12882-017-0459-z.
Membranous nephropathy is a common cause of the nephrotic syndrome. Treatment with standard regimens fails to induce complete remission in most patients. We evaluated the efficacy of combination therapy with rituximab, low-dose, oral cyclophosphamide, and an accelerated prednisone taper (RCP) for the treatment of idiopathic membranous nephropathy.
We analyzed 15 consecutive patients with idiopathic membranous nephropathy treated with RCP at Massachusetts General Hospital. Seven patients (47%) received RCP as initial therapy, and the other eight patients (53%) received RCP for relapsing or refractory disease. All patients had at least 1 year of follow-up. The co-primary outcomes were attainment of partial and complete remission. Partial remission was defined as a urinary protein to creatinine ratio (UPCR) < 3 g/g and a 50% reduction from baseline. Complete remission was defined as a UPCR < 0.3 g/g. Secondary outcomes were serious adverse events and the change in proteinuria, serum creatinine, serum albumin, cholesterol, triglycerides, and immunoglobulin G levels after 1 year of treatment.
Over a median follow-up time of 37 (IQR, 34-44) months, 100% of patients achieved partial remission and 93% of patients achieved complete remission at a median time of 2 and 13 months, respectively. After 1 year of treatment, median (IQR) UPCR declined from 8.2 (6.6-11.1) to 0.3 (0.2-0.7) g/g (P < 0.001). Three serious adverse events occurred over 51 patient years. No patients died or progressed to ESKD.
Treatment of idiopathic membranous nephropathy with RCP resulted in high rates of complete remission. Larger studies evaluating this regimen are warranted.
膜性肾病是肾病综合征的常见病因。大多数患者采用标准方案治疗无法诱导完全缓解。我们评估了利妥昔单抗、低剂量口服环磷酰胺和加速泼尼松减量联合治疗(RCP)对特发性膜性肾病的疗效。
我们分析了在马萨诸塞州总医院接受RCP治疗的15例连续的特发性膜性肾病患者。7例患者(47%)接受RCP作为初始治疗,另外8例患者(53%)接受RCP治疗复发或难治性疾病。所有患者至少随访1年。共同主要结局是达到部分缓解和完全缓解。部分缓解定义为尿蛋白与肌酐比值(UPCR)<3 g/g且较基线降低50%。完全缓解定义为UPCR<0.3 g/g。次要结局是严重不良事件以及治疗1年后蛋白尿、血清肌酐、血清白蛋白、胆固醇、甘油三酯和免疫球蛋白G水平的变化。
在中位随访时间37(四分位间距,34 - 44)个月时,100%的患者达到部分缓解,93%的患者分别在中位时间2个月和13个月时达到完全缓解。治疗1年后,中位(四分位间距)UPCR从8.2(6.6 - 11.1)降至0.3(0.2 - 0.7)g/g(P<0.001)。在51患者年中发生了3起严重不良事件。没有患者死亡或进展为终末期肾病。
用RCP治疗特发性膜性肾病可导致高完全缓解率。有必要进行更大规模的研究来评估该方案。