雷西纳德治疗痛风患者高尿酸血症的疗效和安全性。

Efficacy and safety of lesinurad for the treatment of hyperuricemia in gout.

作者信息

Pérez-Ruiz Fernando, Jansen Tim, Tausche Anne-Katrin, Juárez-Campo Mónica, Gurunath Ravichandra Karra, Richette Pascal

机构信息

Rheumatology Division, Hospital de Cruces, Vizcaya, Spain.

Department of Rheumatology, VieCuri Medisch Centrum, Venlo, The Netherlands.

出版信息

Drugs Context. 2019 May 29;8:212581. doi: 10.7573/dic.212581. eCollection 2019.

Abstract

The aim of this review is to present current evidence about the efficacy and safety of lesinurad in combination with xanthine oxidase inhibitors (XOIs) in the treatment of hyperuricemia in patients with gout. Gout is the most common inflammatory form of arthritis. It is caused by an elevated concentration of serum uric acid (UA) that leads to the formation of monosodium urate crystals in joints and different tissues. The goal of therapy is to maintain serum UA levels at <6 mg/dL (0.36 mmol/L), to prevent the formation and deposition of monosodium urate crystals, and to dissolve existing crystals. Lesinurad, a new uricosuric, increases renal urate excretion by selectively inhibiting the renal uric acid transporter 1 (URAT1). Lesinurad is indicated in adults, in combination with a XOI, for the adjunctive treatment of hyperuricemia in patients with gout (with or without tophi) who have not achieved target serum UA levels with an adequate dose of a XOI alone. With the combination strategy, serum UA targets could be reached with the consequence of inhibiting formation of new crystals and promoting dissolution of existing crystals and, therefore, inducing improvement of outcomes such as flares and tophi. The approval of lesinurad was based on data from three pivotal phase III studies (CLEAR 1, CLEAR 2, and CRYSTAL). These clinical studies assessed lesinurad 200 and 400 mg doses. As only lesinurad 200 mg/day dose was finally approved and commercialized, it will be the focus of this paper. In the pivotal clinical trials, the target serum UA level was achieved by significantly more patients in lesinurad 200 mg plus allopurinol group (CLEAR 1 and CLEAR 2 trials) or lesinurad 200 mg plus febuxostat group (CRYSTAL study) compared with patients who received either XOI alone. In these trials, the safety profile of lesinurad 200 mg plus a XOI was comparable to allopurinol or febuxostat alone. Lesinurad, in combination with a XOI, is an effective and safe treatment that covers unmet needs in adults with gout who have not achieved target serum UA levels with a XOI alone.

摘要

本综述的目的是展示关于雷西纳德与黄嘌呤氧化酶抑制剂(XOIs)联合用于治疗痛风患者高尿酸血症的疗效和安全性的现有证据。痛风是最常见的炎性关节炎形式。它由血清尿酸(UA)浓度升高引起,导致关节和不同组织中尿酸钠晶体的形成。治疗的目标是将血清UA水平维持在<6mg/dL(0.36mmol/L),防止尿酸钠晶体的形成和沉积,并溶解现有的晶体。雷西纳德是一种新型促尿酸排泄药,通过选择性抑制肾尿酸转运蛋白1(URAT1)增加肾脏尿酸排泄。雷西纳德适用于成人,与XOIs联合,用于辅助治疗单用足量XOIs未达到目标血清UA水平的痛风患者(有或无痛风石)。采用联合治疗策略,可达到血清UA目标,从而抑制新晶体的形成并促进现有晶体的溶解,进而改善如痛风发作和痛风石等结局。雷西纳德的获批基于三项关键的III期研究(CLEAR 1、CLEAR 2和CRYSTAL)的数据。这些临床研究评估了雷西纳德200mg和400mg的剂量。由于最终仅200mg/天剂量的雷西纳德获批并上市,它将成为本文的重点。在关键临床试验中,与单用XOIs的患者相比,雷西纳德200mg加别嘌醇组(CLEAR 1和CLEAR 2试验)或雷西纳德200mg加非布司他组(CRYSTAL研究)中有更多患者达到了目标血清UA水平。在这些试验中,雷西纳德200mg加XOIs的安全性与单用别嘌醇或非布司他相当。雷西纳德与XOIs联合是一种有效且安全的治疗方法,满足了单用XOIs未达到目标血清UA水平的痛风成人患者的未满足需求。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c572/6544139/d7c6cc291aae/dic-8-212581-g001.jpg

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