Germain Dominique P, Elliott Perry M, Falissard Bruno, Fomin Victor V, Hilz Max J, Jovanovic Ana, Kantola Ilkka, Linhart Aleš, Mignani Renzo, Namdar Mehdi, Nowak Albina, Oliveira João-Paulo, Pieroni Maurizio, Viana-Baptista Miguel, Wanner Christoph, Spada Marco
French Referral Center for Fabry disease, Division of Medical Genetics and INSERM U1179, University of Versailles, Paris-Saclay University, Montigny, France.
University College London and Barts Heart Centre, London, United Kingdom.
Mol Genet Metab Rep. 2019 Feb 6;19:100454. doi: 10.1016/j.ymgmr.2019.100454. eCollection 2019 Jun.
Enzyme replacement therapy (ERT) with recombinant human α-galactosidase has been available for the treatment of Fabry disease since 2001 in Europe and 2003 in the USA. Treatment outcomes with ERT are dependent on baseline patient characteristics, and published data are derived from heterogeneous study populations.
We conducted a comprehensive systematic literature review of all original articles on ERT in the treatment of Fabry disease published up until January 2017. This article presents the findings in adult male patients.
Clinical evidence for the efficacy of ERT in adult male patients was available from 166 publications including 36 clinical trial publications. ERT significantly decreases globotriaosylceramide levels in plasma, urine, and in different kidney, heart, and skin cell types, slows the decline in estimated glomerular filtration rate, and reduces/stabilizes left ventricular mass and cardiac wall thickness. ERT also improves nervous system, gastrointestinal, pain, and quality of life outcomes.
ERT is a disease-specific treatment for patients with Fabry disease that may provide clinical benefits on several outcomes and organ systems. Better outcomes may be observed when treatment is started at an early age prior to the development of organ damage such as chronic kidney disease or cardiac fibrosis. Consolidated evidence suggests a dose effect. Data described in male patients, together with female and paediatric data, informs clinical practice and therapeutic goals for individualized treatment.
自2001年起在欧洲以及2003年起在美国,重组人α-半乳糖苷酶的酶替代疗法(ERT)已可用于治疗法布里病。ERT的治疗效果取决于患者的基线特征,且已发表的数据来自异质性研究人群。
我们对截至2017年1月发表的关于ERT治疗法布里病的所有原创文章进行了全面的系统文献综述。本文呈现了成年男性患者的研究结果。
来自166篇出版物(包括36篇临床试验出版物)的临床证据表明ERT对成年男性患者有效。ERT可显著降低血浆、尿液以及不同肾脏、心脏和皮肤细胞类型中的球三糖基神经酰胺水平,减缓估计肾小球滤过率的下降,并减少/稳定左心室质量和心脏壁厚度。ERT还可改善神经系统、胃肠道、疼痛和生活质量方面的结果。
ERT是针对法布里病患者的一种疾病特异性治疗方法,可能在多个结果和器官系统方面带来临床益处。在器官损伤(如慢性肾病或心脏纤维化)发生之前的早年开始治疗,可能会观察到更好的结果。综合证据表明存在剂量效应。男性患者的数据,连同女性和儿科数据,为个体化治疗的临床实践和治疗目标提供了依据。