Daniel Eleni, Newell-Price John D C
Department of Human MetabolismAcademic Unit of EndocrinologyDepartment of Endocrinology, University of Sheffield, Beech Hill Road, Sheffield S10 2RX, UK.
Department of Human MetabolismAcademic Unit of EndocrinologyDepartment of Endocrinology, University of Sheffield, Beech Hill Road, Sheffield S10 2RX, UK
Eur J Endocrinol. 2015 Jun;172(6):R263-80. doi: 10.1530/EJE-14-1014. Epub 2015 Jan 30.
Steroidogenesis enzyme inhibitors are the mainstay of medical therapy in Cushing's syndrome (CS). Ketoconazole (KTZ) and metyrapone are the most commonly used agents. Although there is considerable experience of their use in individual specialist centres, these drugs have not been rigorously tested in prospective clinical trials. Clinicians face uncertainties and concerns with respect to the safety profile of these agents, and best means to monitor effect. We review steroidogenesis inhibitors in the management of CS, including older agents (KTZ, metyrapone, etomidate and mitotane) and those currently under development (LCI699, non-racemic KTZ), and offer a practical approach for their use in clinical practice.
类固醇生成酶抑制剂是库欣综合征(CS)医学治疗的主要手段。酮康唑(KTZ)和甲吡酮是最常用的药物。尽管在个别专科中心有大量使用这些药物的经验,但这些药物尚未在前瞻性临床试验中得到严格测试。临床医生在这些药物的安全性以及监测疗效的最佳方法方面面临不确定性和担忧。我们综述了类固醇生成抑制剂在CS治疗中的应用,包括较老的药物(KTZ、甲吡酮、依托咪酯和米托坦)以及目前正在研发的药物(LCI699、非消旋KTZ),并提供了在临床实践中使用这些药物的实用方法。