O'Shaughnessy Michelle M, Troost Jonathan P, Bomback Andrew S, Hladunewich Michelle A, Ashoor Isa F, Gibson Keisha L, Matar Raed Bou, Selewski David T, Srivastava Tarak, Rheault Michelle N, Al-Uzri Amira, Kogon Amy J, Khalid Myda, Vento Suzanne, Sanghani Neil S, Gillespie Brenda W, Gipson Debbie S, Wang Chia-Shi, Parsa Afshin, Guay-Woodford Lisa, Laurin Louis-Philippe
Division of Nephrology, Stanford University School of Medicine, Palo Alto, California, USA.
Division of Nephrology, Department of Pediatrics, University of Michigan, Ann Arbor, Michigan, USA.
Kidney Int Rep. 2019 Sep 16;4(12):1725-1734. doi: 10.1016/j.ekir.2019.09.005. eCollection 2019 Dec.
The 2012 Kidney Disease: Improving Global Outcomes (KDIGO) Clinical Practice Guidelines for Glomerulonephritis recommend that patients with membranous nephropathy (MN) at risk for progression receive immunosuppressive therapy (IST), usually after 6 months of observation. A cyclophosphamide (CYC) or calcineurin inhibitor (CNI)-based regimen is recommended as first-line IST. However, the extent to which KDIGO recommendations are adopted in practice remains largely unknown.
We evaluated prescribing practice among patients with primary MN (diagnosed 2010-2018) enrolled in the Cure Glomerulonephropathy Network (CureGN) cohort study. We also evaluated the availability of testing for phospholipase A2 receptor (PLA2R) in the contemporary era.
Among 361 patients (324 adults and 37 children) with MN who were IST-naïve at biopsy and had at least 6 months of follow-up, 55% of adults and 58% of children initiated IST <6 months after biopsy. Of these, 1 in 5 had no indication for (i.e., urine protein-to-creatinine ratio [uPCR] <4 g/g) or an apparent contraindication to (i.e., an estimated glomerular filtration rate [eGFR] <30 ml/min per 1.73 m) IST. As first-line IST, half of treated patients received either CYC (16% of adults; 0% of children) or a CNI (40% and 46%, respectively), whereas 1 in 5 received corticosteroid monotherapy (20% and 27%, respectively) and 1 in 6 rituximab (15% and 15%, respectively). More than 80% of surveyed centers had access to PLA2R testing.
These findings suggest that providers are not aware of, or lack confidence in, current KDIGO guidelines for MN. Treatment patterns observed in this cohort might critically inform the drafting of planned updates to KDIGO guidelines.
2012年改善全球肾脏病预后组织(KDIGO)肾小球肾炎临床实践指南建议,有疾病进展风险的膜性肾病(MN)患者通常在观察6个月后接受免疫抑制治疗(IST)。推荐以环磷酰胺(CYC)或钙调神经磷酸酶抑制剂(CNI)为基础的方案作为一线IST。然而,KDIGO建议在实际应用中的采纳程度很大程度上仍不明确。
我们评估了参与肾小球肾炎治愈网络(CureGN)队列研究的原发性MN患者(2010 - 2018年确诊)的处方实践。我们还评估了当代磷脂酶A2受体(PLA2R)检测的可及性。
在361例MN患者(324例成人和37例儿童)中,活检时未接受过IST且至少随访6个月,55%的成人和58%的儿童在活检后<6个月开始接受IST。其中,五分之一的患者没有IST指征(即尿蛋白与肌酐比值[uPCR]<4 g/g)或明显的IST禁忌证(即估计肾小球滤过率[eGFR]<30 ml/min/1.73 m²)。作为一线IST,一半的接受治疗患者接受了CYC(成人中的16%;儿童中的0%)或CNI(分别为40%和46%),而五分之一的患者接受了糖皮质激素单药治疗(分别为20%和27%),六分之一的患者接受了利妥昔单抗治疗(分别为15%和15%)。超过80%的接受调查中心可以进行PLA2R检测。
这些发现表明,医疗服务提供者不了解或对当前KDIGO的MN指南缺乏信心。在该队列中观察到的治疗模式可能会为KDIGO指南计划更新的起草提供关键信息。