稳定性冠心病患者低剂量秋水仙碱的疗效:LoDoCo2 试验的原理、设计和基线特征。

The effect of low-dose colchicine in patients with stable coronary artery disease: The LoDoCo2 trial rationale, design, and baseline characteristics.

机构信息

GenesisCare Western Australia, Perth, Australia; Heart Research Institute of Western Australia, Perth, Australia.

Dutch Network for Cardiovascular Research (WCN), Utrecht, The Netherlands; The Netherlands Heart Institute, Utrecht, The Netherlands; Department of Cardiology, University Medical Center Utrecht, Utrecht, The Netherlands.

出版信息

Am Heart J. 2019 Dec;218:46-56. doi: 10.1016/j.ahj.2019.09.011. Epub 2019 Oct 20.

Abstract

Because patients with stable coronary artery disease are at continued risk of major atherosclerotic events despite effective secondary prevention strategies, there is a need to continue to develop additional safe, effective and well-tolerated therapies for secondary prevention of cardiovascular disease. RATIONALE AND DESIGN: The LoDoCo (Low Dose Colchicine) pilot trial showed that the anti-inflammatory drug colchicine 0.5 mg once daily appears safe and effective for secondary prevention of cardiovascular disease. Colchicine's low cost and long-term safety suggest that if its efficacy can be confirmed in a rigorous trial, repurposing it for secondary prevention of cardiovascular disease would have the potential to impact the global burden of cardiovascular disease. LoDoCo2 is an investigator-initiated, international, multicentre, double-blind, event driven trial in which 5522 patients with stable coronary artery disease tolerant to colchicine during a 30-day run-in phase have been randomized to colchicine 0.5 mg daily or matching placebo on a background of optimal medical therapy. The study will have 90% power to detect a 30% reduction in the composite primary endpoint: cardiovascular death, myocardial infarction, ischemic stroke and ischemia-driven coronary revascularization. Adverse events potentially related to the use of colchicine will also be collected, including late gastrointestinal intolerance, neuropathy, myopathy, myositis, and neutropenia. CONCLUSION: The LoDoCo2 Trial will provide information on the efficacy and safety of low-dose colchicine for secondary prevention in patients with stable coronary artery disease.

摘要

由于稳定型冠状动脉疾病患者尽管采取了有效的二级预防策略,但仍有发生主要动脉粥样硬化事件的持续风险,因此需要继续开发其他安全、有效且耐受良好的二级预防心血管疾病治疗方法。

背景和目的

低剂量秋水仙碱(LoDoCo)先导试验表明,抗炎药秋水仙碱 0.5mg 每日一次用于二级预防心血管疾病似乎是安全有效的。秋水仙碱的低成本和长期安全性表明,如果其疗效能够在严格的试验中得到证实,将其重新用于二级预防心血管疾病有可能对全球心血管疾病负担产生影响。LoDoCo2 是一项由研究者发起的、国际性的、多中心、双盲、事件驱动的试验,在 30 天的导入期内,对 5522 例稳定型冠状动脉疾病患者进行了耐受性评估,这些患者在最佳药物治疗的基础上,随机分为每日服用秋水仙碱 0.5mg 或匹配安慰剂组。该研究将有 90%的把握度检测到复合主要终点(心血管死亡、心肌梗死、缺血性卒中和缺血驱动的冠状动脉血运重建)降低 30%。还将收集与秋水仙碱使用相关的不良事件,包括迟发性胃肠道不耐受、神经病、肌病、肌炎和中性粒细胞减少症。

结论

LoDoCo2 试验将提供关于稳定型冠状动脉疾病患者使用低剂量秋水仙碱进行二级预防的疗效和安全性信息。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索