Ticagrelor plus aspirin versus cilostazol plus aspirin in the acute-phase treatment of large-vessel minor stroke or TIA: A randomized controlled multi-center trial, the TACTIS trial.

IF 6.9 2区 医学 Q1 CLINICAL NEUROLOGY
International Journal of Stroke Pub Date : 2026-08-01 Epub Date: 2025-12-02 DOI:10.1177/17474930251406865
Mohamed Ismaiel, Sherihan Rezk Ahmed, Mohamed Fouad Elsayed Khalil, Ahmad Galal Elmesallami, Ahmed Ahmed Mohamed Kamal Ebied, Ahmed Zaki Omar Akl, Youssry Salah Shafiq Kerolos, Mohamed Elshafei, Enji Hamdy Elsawy Khalil, Ahmed Mohamed Ali Daabis, Romany Adly Yousef, Dalia Maher Samy, Hamada Zehry, Ashraf Ali Soliman, Ghada Abd Elwahab Khalil Ibrahim, Mohamed G Zeinhom
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引用次数: 0

Abstract

Introduction: More intensive antiplatelet agents may reduce recurrent stroke risk in minor stroke and TIA, particularly those with non-cardioembolic stroke. The SOCRATES trial showed that ticagrelor was not superior to aspirin in decreasing the risk of stroke, heart attack, or death at 90 days in patients with minor ischemic stroke or TIA. Cilostazol has been shown to have similar effects on platelet reactivity and aggregation to those produced by ticlopidine and aspirin, but may be associated with fewer hemorrhagic side effects. It is also cheaper than ticagrelor; for example, it is approximately half that of ticagrelor, making it a potentially cost-effective antiplatelet agent, especially in low and middle-income countries.

Aim: To evaluate the benefits or hazards of adding cilostazol or ticagrelor to aspirin in patients with minor ischemic stroke or TIA.

Methods: We randomized 900 first-ever, large-vessel occlusion minor ischemic stroke or TIA patients in a one-to-one ratio to receive either a 200 mg loading dose of cilostazol within 24 h after acute stroke symptoms, then 100 mg twice daily until day 90 post-stroke, or a 180 mg loading dose of ticagrelor during the first 24 h, followed by 90 mg twice daily from day 2 to day 90. Both groups received an open-label 300 mg loading dose of aspirin during the first 24 h, then 75 mg once daily. We followed up with our patients for 3 months.

Results: 857 patients completed the 3-month follow-up study 34 (7.6%) patients in the cilostazol group and 29 (6.4%) patients in the ticagrelor group experienced a new stroke (either hemorrhagic or ischemic) (HR 1.37; 95% CI, 0.84-2.26; p-value = 0.21), and 44 (9.8%) patients in the cilostazol group and 40 (8.9%) patients in the ticagrelor group experienced a composite of a new stroke, myocardial infarction (MI), or death due to vascular insults (HR 1.11; 95% CI, 0.64-1.93; p-value = 0.30). Fifteen (3.3%) patients in the cilostazol arm and 30 (6.7%) patients in the ticagrelor arm experienced drug-related hemorrhagic complications (HR 0.32; 95% CI, 0.19-0.68; p-value = 0.01).

Conclusion: Combining cilostazol with aspirin in large-vessel occlusion minor ischemic stroke or TIA was as effective as ticagrelor and aspirin in preventing recurrent stroke, MI, and death due to vascular events, but resulted in significantly lower rates of hemorrhagic complications.

替格瑞洛加阿司匹林与西洛他唑加阿司匹林在急性期治疗大血管轻微卒中或TIA:一项随机对照多中心试验,即tips试验。
大血管闭塞(LVO)卒中约占缺血性卒中的三分之一;此外,有症状性颅内或颅外动脉狭窄的患者卒中发生和早期卒中复发的风险增加。几项试验评估了替格瑞洛在缺血性卒中中的潜在作用,SOCRATES试验显示,替格瑞洛在降低轻度缺血性卒中或TIA患者90天卒中、心脏病发作或死亡风险方面并不优于阿司匹林。当西洛他唑与阿司匹林和噻氯匹定比较时,它显示出与噻氯匹定和阿司匹林相当的抑制血小板反应性和聚集的能力。此外,西洛他唑与较少的出血性副作用相关。在埃及,西洛沙唑100 mg Bid的月费用约为替格瑞洛90 mg Bid的一半,使其成为具有潜在成本效益的抗血小板药物,特别是在经历经济危机的国家。据我们所知,没有这样的研究比较西洛他唑和替格瑞洛在非洲轻度卒中或TIA患者中的应用,因此我们的目的是评估在轻度缺血性卒中或TIA患者中加入西洛他唑或替格瑞洛的益处或危害,以支持量身定制使用西洛他唑,这是一种更便宜的抗血小板药物,出血并发症的风险更低。方法随机招募900例非心源性小卒中或TIA患者,按1比1比例给予西洛他唑加阿司匹林或替格瑞洛加阿司匹林负荷和维持剂量,随访3个月。结果900例患者按1比1的比例被分配到西洛他唑和阿司匹林组或替格瑞洛和阿司匹林组;857名患者完成了为期三个月的随访研究西洛他唑组(7.6%)患者和替卡格雷洛组29例(6.4%)患者发生了新的卒中(出血性或缺血性)(HR 1.37; 95% CI, 0.84-2.26; p值= 0.21),西洛他唑组44例(9.8%)患者和替卡格雷洛组40例(8.9%)患者由于血管损伤合并发生了新的卒中、心肌梗死或死亡(HR 1.11; 95% CI, 0.64-1.93; p值= 0.30)。西洛他唑组15例(3.3%)患者和替格瑞洛组30例(6.7%)患者出现药物相关出血并发症(HR 0.32; 95% CI 0.19-0.68; p值= 0.01)。西洛他唑组15例(3.3%)患者和替格瑞洛组28例(6.2%)患者由于无法忍受的出血性和非出血性不良反应而过早停药(HR 0.28; 95% CI, 0.16-0.57; p值= 0.02)。结论:西洛他唑联合阿司匹林治疗埃及非心源性轻微缺血性卒中或TIA患者,可降低卒中复发、心肌梗死和血管事件所致死亡的发生率,与替格瑞洛联合阿司匹林的发生率相当;此外,西洛他唑和阿司匹林的出血性并发症发生率明显低于替格瑞洛和阿司匹林。注册:临床试验,NCT06591377, 09-08-2024。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
International Journal of Stroke
International Journal of Stroke 医学-外周血管病
CiteScore
13.90
自引率
6.00%
发文量
132
审稿时长
6-12 weeks
期刊介绍: The International Journal of Stroke is a welcome addition to the international stroke journal landscape in that it concentrates on the clinical aspects of stroke with basic science contributions in areas of clinical interest. Reviews of current topics are broadly based to encompass not only recent advances of global interest but also those which may be more important in certain regions and the journal regularly features items of news interest from all parts of the world. To facilitate the international nature of the journal, our Associate Editors from Europe, Asia, North America and South America coordinate segments of the journal.
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