Ridruejo Ezequiel
Ezequiel Ridruejo, Hepatology Section, Departament of Medicine, Centro de Educación Médica e Investigaciones Clínicas Norberto Quirno "CEMIC", Ciudad Autónoma de Buenos Aires, C1425ASG Buenos Aires, Argentina.
World J Gastroenterol. 2014 Jun 21;20(23):7169-80. doi: 10.3748/wjg.v20.i23.7169.
Results from phase III clinical trials clearly demonstrate the efficacy and safety of entecavir and tenofovir in the controlled environment of randomized clinical studies. There are several studies with both drugs performed in clinical practice (also called "real life studies"). Despite the pros and cons, studies performed in real life conditions represent everyday practice and add important information about long term treatment effectiveness and safety in this clinical setting. This review shows that patients treated with first line nucleos(t)ide analogs at referral centres, with good clinical follow-up and adherence to international guidelines, can achieve high treatment response rates with a very low rate of adverse events.
III期临床试验结果清楚地证明了恩替卡韦和替诺福韦在随机临床研究的可控环境中的疗效和安全性。有多项针对这两种药物在临床实践中开展的研究(也称为“真实生活研究”)。尽管有其利弊,但在真实生活条件下开展的研究代表了日常实践,并为这种临床环境下的长期治疗有效性和安全性增添了重要信息。本综述表明,在转诊中心接受一线核苷(酸)类似物治疗、有良好临床随访且遵循国际指南的患者,能够实现高治疗反应率,且不良事件发生率极低。