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ADPKD 的现行治疗方法和正在进行的试验。

ADPKD current management and ongoing trials.

机构信息

UOC Divisione di Nefrologia Dialisi e Trapianto, AOU Policlinico di Modena, Modena, Italy.

Dipartimento Chirurgico Medico Odontoiatrico e di Scienze Morfologiche con Interesse Trapiantologico, Oncologico e di Medicina Rigenerativa, Università di Modena e Reggio Emilia, Modena, Italy.

出版信息

J Nephrol. 2020 Apr;33(2):223-237. doi: 10.1007/s40620-019-00679-y. Epub 2019 Dec 18.

Abstract

Among the diseases that require renal replacement therapy (RRT), ADPKD is the fourth for incidence and prevalence. In Italy, there are at least 32,000 patients affected by ADPKD, of which about 2900 in dialysis. The pure costs of dialysis treatment for the Italian National Health Service can be conservatively estimated at 87 million euros per year. Even a modest slowdown in the evolution of the disease would obtain an important result in terms of reduction of health expenditure. In recent years, many new or repurposed drugs have been evaluated in clinical trials for ADPKD. In this review we will mainly focus on advanced stage clinical trials (phase 2 and 3). We have grouped these studies according to the molecular pathway addressed by the experimental drug or the therapeutic strategy. More than 10 years after the start of the first Phase III clinical trials in ADPKD, the first drug active in slowing disease progression is finally available. It cannot be considered a goal but only the beginning of a journey because of the significant side effects and the high cost of Tolvaptan. An exuberant basic research activity in the field, together with the large number of ongoing protocols, keep the nephrologists and their patients positive with regard to the discovery of new and better therapies in a not-too-distant future.

摘要

在需要肾脏替代治疗 (RRT) 的疾病中,ADPKD 的发病率和患病率位居第四。在意大利,至少有 32000 名 ADPKD 患者,其中约 2900 名患者接受透析治疗。意大利国家卫生服务机构对透析治疗的纯费用估计每年至少为 8700 万欧元。即使疾病的发展稍微减缓,也将在减少卫生支出方面取得重要成果。近年来,许多新的或重新定位的药物已在 ADPKD 的临床试验中进行了评估。在这篇综述中,我们将主要关注晚期临床试验(第 2 阶段和第 3 阶段)。我们根据实验药物或治疗策略针对的分子途径对这些研究进行了分组。在 ADPKD 的第一个 III 期临床试验开始 10 多年后,终于有了第一种可有效减缓疾病进展的药物。托伐普坦虽然不能被视为目标,但由于其副作用明显且成本高昂,它只是旅程的开始。该领域丰富的基础研究活动以及正在进行的大量方案,使肾病学家及其患者对未来不久发现新的、更好的疗法持乐观态度。

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