Department of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
Diagnostic and Interventional Neuroradiology Department, University Hospital of Tours, Tours, France.
JAMA Neurol. 2023 Aug 1;80(8):824-832. doi: 10.1001/jamaneurol.2023.2094.
It is unknown whether intravenous thrombolysis using tenecteplase is noninferior or preferable compared with alteplase for patients with acute ischemic stroke.
To examine the safety and efficacy of tenecteplase compared to alteplase among patients with large vessel occlusion (LVO) stroke.
DESIGN, SETTING, AND PARTICIPANTS: This was a prespecified analysis of the Intravenous Tenecteplase Compared With Alteplase for Acute Ischaemic Stroke in Canada (ACT) randomized clinical trial that enrolled patients from 22 primary and comprehensive stroke centers across Canada between December 10, 2019, and January 25, 2022. Patients 18 years and older with a disabling ischemic stroke within 4.5 hours of symptom onset were randomly assigned (1:1) to either intravenous tenecteplase or alteplase and were monitored for up to 120 days. Patients with baseline intracranial internal carotid artery (ICA), M1-middle cerebral artery (MCA), M2-MCA, and basilar occlusions were included in this analysis. A total of 1600 patients were enrolled, and 23 withdrew consent.
Intravenous tenecteplase (0.25 mg/kg) vs intravenous alteplase (0.9 mg/kg).
The primary outcome was the proportion of modified Rankin scale (mRS) score 0-1 at 90 days. Secondary outcomes were an mRS score from 0 to 2, mortality, and symptomatic intracerebral hemorrhage. Angiographic outcomes were successful reperfusion (extended Thrombolysis in Cerebral Infarction scale score 2b-3) on first and final angiographic acquisitions. Multivariable analyses (adjusting for age, sex, National Institute of Health Stroke Scale score, onset-to-needle time, and occlusion location) were carried out.
Among 1577 patients, 520 (33.0%) had LVO (median [IQR] age, 74 [64-83] years; 283 [54.4%] women): 135 (26.0%) with ICA occlusion, 237 (45.6%) with M1-MCA, 117 (22.5%) with M2-MCA, and 31 (6.0%) with basilar occlusions. The primary outcome (mRS score 0-1) was achieved in 86 participants (32.7%) in the tenecteplase group vs 76 (29.6%) in the alteplase group. Rates of mRS 0-2 (129 [49.0%] vs 131 [51.0%]), symptomatic intracerebral hemorrhage (16 [6.1%] vs 11 [4.3%]), and mortality (19.9% vs 18.1%) were similar in the tenecteplase and alteplase groups, respectively. No difference was noted in successful reperfusion rates in the first (19 [9.2%] vs 21 [10.5%]) and final angiogram (174 [84.5%] vs 177 [88.9%]) among 405 patients who underwent thrombectomy.
The findings in this study indicate that intravenous tenecteplase conferred similar reperfusion, safety, and functional outcomes compared to alteplase among patients with LVO.
尚不清楚对于急性缺血性脑卒中患者,使用替奈普酶静脉溶栓是否不劣于或优于阿替普酶。
评估替奈普酶与阿替普酶治疗大血管闭塞(LVO)卒中患者的安全性和有效性。
设计、地点和参与者:这是加拿大急性缺血性卒中静脉内替奈普酶与阿替普酶比较(ACT)随机临床试验的预先指定分析,该试验于 2019 年 12 月 10 日至 2022 年 1 月 25 日期间在加拿大 22 个初级和综合卒中中心招募了患者。症状发作后 4.5 小时内出现致残性缺血性卒中的 18 岁及以上患者被随机分配(1:1)接受替奈普酶或阿替普酶静脉溶栓,并在 120 天内进行监测。本分析纳入了基线颅内颈内动脉(ICA)、M1 大脑中动脉(MCA)、M2-MCA 和基底动脉闭塞的患者。共纳入 1600 例患者,23 例患者退出了研究。
替奈普酶(0.25mg/kg)与阿替普酶(0.9mg/kg)。
主要结局是 90 天时改良 Rankin 量表(mRS)评分 0-1 的比例。次要结局为 mRS 评分 0-2、死亡率和症状性颅内出血。血管造影结局为首次和最终血管造影采集时达到扩展的血栓溶解治疗脑梗死量表评分 2b-3 的成功再灌注。多变量分析(调整年龄、性别、国立卫生研究院卒中量表评分、发病至溶栓时间和闭塞位置)。
在 1577 例患者中,520 例(33.0%)有 LVO(中位数[IQR]年龄,74[64-83]岁;283[54.4%]为女性):ICA 闭塞 135 例(26.0%),M1-MCA 闭塞 237 例(45.6%),M2-MCA 闭塞 117 例(22.5%),基底动脉闭塞 31 例(6.0%)。替奈普酶组有 86 例(32.7%)达到主要结局(mRS 评分 0-1),阿替普酶组有 76 例(29.6%)。mRS 0-2 评分(129[49.0%]vs.131[51.0%])、症状性颅内出血(16[6.1%]vs.11[4.3%])和死亡率(19.9%vs.18.1%)在替奈普酶和阿替普酶组中相似。在 405 例接受血栓切除术的患者中,首次(19[9.2%]vs.21[10.5%])和最终血管造影(174[84.5%]vs.177[88.9%])成功再灌注率无差异。
这项研究的结果表明,与阿替普酶相比,替奈普酶静脉溶栓在 LVO 患者中具有相似的再灌注、安全性和功能结局。