Cypryk Katarzyna, Małecki Piotr
Endokrynol Pol. 2018;69(4). doi: 10.5603/EP.2018.0053.
Type 2 diabetes is a complex metabolic disorder associated with a high risk of cardiovascular complications. In December 2008, due to concerns about the cardiac safety of antihyperglycaemic therapies, the Food and Drug Administration (FDA) published a new guidance on special requirements for the demonstration of cardiovascular safety for these medications. In 2012, similar recommendations were made for antidiabetic drug manufacturers by the European Medicines Agency (EMA). Since then, both FDA and EMA recommendations have been applied in cardiovascular outcome trials (CVOTs) for several new antihyperglycaemic drugs. Unlike conventional trials, CVOTs are usually placebo controlled, non-inferiority trials that examine the cardiovascular safety of a drug compared to standard of care in large cohorts of patients with high cardiovascular risk or established cardiovascular disease. Patients in CVOTs are also monitored for a longer observation period than in typical randomised controlled trials to provide data on long-term cardiovascular risk. To date, nine CVOTs involving patients with type 2 diabetes have been completed, and at least 13 are still ongoing. These studies focus on a variety of antihyper-glycaemic drugs, including incretin-based agents, sodium-glucose cotransporter 2 inhibitor (SGLT-2) inhibitors, and insulin formulations. This article takes a critical look at these CVOTs and summarises the results of the completed trials.
2型糖尿病是一种复杂的代谢紊乱疾病,伴有心血管并发症的高风险。2008年12月,由于对抗高血糖治疗的心脏安全性的担忧,美国食品药品监督管理局(FDA)发布了一项关于这些药物心血管安全性证明特殊要求的新指南。2012年,欧洲药品管理局(EMA)对抗糖尿病药物制造商提出了类似建议。从那时起,FDA和EMA的建议都已应用于几种新型抗高血糖药物的心血管结局试验(CVOTs)中。与传统试验不同,CVOTs通常是安慰剂对照的非劣效性试验,在大量心血管风险高或已确诊心血管疾病的患者队列中,将药物的心血管安全性与标准治疗进行比较。与典型的随机对照试验相比,CVOTs中的患者也会接受更长时间的观察,以提供长期心血管风险的数据。迄今为止,已经完成了9项涉及2型糖尿病患者的CVOTs,至少还有13项仍在进行中。这些研究聚焦于多种抗高血糖药物,包括肠促胰岛素类药物、钠-葡萄糖协同转运蛋白2抑制剂(SGLT-2)和胰岛素制剂。本文批判性地审视了这些CVOTs,并总结了已完成试验的结果。