Beer Arno, Mayer Gert, Kronbichler Andreas
Department of Internal Medicine IV (Nephrology and Hypertension), Medical University of Innsbruck, Anichstraße 35, 6020 Innsbruck, Austria.
Biomed Res Int. 2016;2016:4192578. doi: 10.1155/2016/4192578. Epub 2016 Apr 7.
Adult primary focal segmental glomerulosclerosis (FSGS) remains a therapeutic challenge for the treating physician. With the advent of novel immunosuppressive measures, our arsenal of therapeutic options increased considerably. The aim of this review was to summarize reports published over the last two decades which reported on treatment outcome. Most reports included patients with a steroid-resistant (SR) disease course, yet the cohort with the highest unmet need, since persistent nephrotic range proteinuria is associated with a poor renal prognosis and portends a high risk of developing end-stage renal disease. While in first-line treatment, steroid treatment remains the recommended standard with an overall remission rate of 50% and higher, optimal treatment strategies for steroid-dependent/multirelapsing (SD/MR) and SR patients have to be defined. In both entities, calcineurin inhibitors showed good efficacy, while mycophenolate mofetil was less effective in SR cases compared to those with SD/MR. The same was true for rituximab, a monoclonal antibody targeting B-cells. In resistant cases, addition of extracorporeal treatment options or treatment with alkylating agents may be considered. To shape the future for treatment of FSGS, international collaborations to conduct larger clinical trials are needed to identify potential novel efficacious immunosuppressive or immunomodulatory therapies.
成人原发性局灶节段性肾小球硬化(FSGS)对治疗医生来说仍然是一个治疗挑战。随着新型免疫抑制措施的出现,我们的治疗选择手段大幅增加。本综述的目的是总结过去二十年发表的关于治疗结果的报告。大多数报告纳入了具有激素抵抗(SR)病程的患者,然而这是未满足需求最高的队列,因为持续性肾病范围蛋白尿与不良肾脏预后相关,并预示着发展为终末期肾病的高风险。在一线治疗中,激素治疗仍然是推荐的标准治疗方法,总体缓解率达50%及以上,但必须确定针对激素依赖/多次复发(SD/MR)和SR患者的最佳治疗策略。在这两种情况下,钙调神经磷酸酶抑制剂均显示出良好疗效,而与SD/MR患者相比,霉酚酸酯在SR病例中的效果较差。靶向B细胞的单克隆抗体利妥昔单抗也是如此。在耐药病例中,可考虑增加体外治疗选择或使用烷化剂进行治疗。为了塑造FSGS治疗领域的未来,需要开展国际合作以进行更大规模的临床试验,从而确定潜在的新型有效免疫抑制或免疫调节疗法。