Bailout intracranial angioplasty or stenting following thrombectomy for acute large vessel occlusion in China (ANGEL-REBOOT): a multicentre, open-label, blinded-endpoint, randomised controlled trial.

IF 46.5 1区 医学 Q1 CLINICAL NEUROLOGY
Lancet Neurology Pub Date : 2024-08-01 Epub Date: 2024-06-21 DOI:10.1016/S1474-4422(24)00186-8
Feng Gao, Xu Tong, Baixue Jia, Ming Wei, Yuesong Pan, Ming Yang, Dapeng Sun, Thanh N Nguyen, Zeguang Ren, Francis Demiraj, Xiaoxi Yao, Chenghua Xu, Guangxiong Yuan, Yue Wan, Jianjun Tang, Jing Wang, Yuanfei Jiang, Chaobin Wang, Xiang Luo, Haihua Yang, Ruile Shen, Zhilin Wu, Zhengzhou Yuan, Dongjun Wan, Wei Hu, Yan Liu, Ping Jing, Liping Wei, Tuanyuan Zheng, Yingchun Wu, Xinguang Yang, Yaxuan Sun, Changming Wen, Mingze Chang, Bo Yin, Di Li, Jixin Duan, Dianjing Sun, Zaiyu Guo, Guodong Xu, Guoqing Wang, Liyu Wang, Yang Wang, Weihua Jia, Gaoting Ma, Xiaochuan Huo, Dapeng Mo, Ning Ma, Liping Liu, Xingquan Zhao, Yilong Wang, Jens Fiehler, Yongjun Wang, Zhongrong Miao
{"title":"Bailout intracranial angioplasty or stenting following thrombectomy for acute large vessel occlusion in China (ANGEL-REBOOT): a multicentre, open-label, blinded-endpoint, randomised controlled trial.","authors":"Feng Gao, Xu Tong, Baixue Jia, Ming Wei, Yuesong Pan, Ming Yang, Dapeng Sun, Thanh N Nguyen, Zeguang Ren, Francis Demiraj, Xiaoxi Yao, Chenghua Xu, Guangxiong Yuan, Yue Wan, Jianjun Tang, Jing Wang, Yuanfei Jiang, Chaobin Wang, Xiang Luo, Haihua Yang, Ruile Shen, Zhilin Wu, Zhengzhou Yuan, Dongjun Wan, Wei Hu, Yan Liu, Ping Jing, Liping Wei, Tuanyuan Zheng, Yingchun Wu, Xinguang Yang, Yaxuan Sun, Changming Wen, Mingze Chang, Bo Yin, Di Li, Jixin Duan, Dianjing Sun, Zaiyu Guo, Guodong Xu, Guoqing Wang, Liyu Wang, Yang Wang, Weihua Jia, Gaoting Ma, Xiaochuan Huo, Dapeng Mo, Ning Ma, Liping Liu, Xingquan Zhao, Yilong Wang, Jens Fiehler, Yongjun Wang, Zhongrong Miao","doi":"10.1016/S1474-4422(24)00186-8","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Unsuccessful recanalisation or reocclusion after thrombectomy is associated with poor outcomes in patients with large vessel occlusion (LVO) acute ischaemic stroke (LVO-AIS). Bailout angioplasty or stenting (BAOS) could represent a promising treatment for these patients. We conducted a randomised controlled trial with the aim to investigate the safety and efficacy of BAOS following thrombectomy in patients with LVO.</p><p><strong>Methods: </strong>ANGEL-REBOOT was an investigator-initiated, multicentre, prospective, randomised, controlled, open-label, blinded-endpoint clinical trial conducted at 36 tertiary hospitals in 19 provinces in China. Participants with LVO-AIS 24 h after symptom onset were eligible if they had unsuccessful recanalisation (expanded Thrombolysis In Cerebral Infarction score of 0-2a) or risk of reocclusion (residual stenosis >70%) after thrombectomy. Eligible patients were randomly assigned by the minimisation method in a 1:1 ratio to undergo BAOS as the intervention treatment, or to receive standard therapy (continue or terminate the thrombectomy procedure) as a control group, both open-label. In both treatment groups, tirofiban could be recommended for use during and after the procedure. The primary outcome was the change in modified Rankin Scale score at 90 days, assessed in the intention-to-treat population. Safety outcomes were compared between groups. This trial was completed and registered at ClinicalTrials.gov (NCT05122286).</p><p><strong>Findings: </strong>From Dec 19, 2021, to March 17, 2023, 706 patients were screened, and 348 were enrolled, with 176 assigned to the intervention group and 172 to the control group. No patients withdrew from the trial or were lost to follow-up for the primary outcome. The median age of patients was 63 years (IQR 55-69), 258 patients (74%) were male, and 90 patients (26%) were female; all participants were Chinese. After random allocation, tirofiban was administered either intra-arterially, intravenously, or both in 334 [96%] of 348 participants. No between-group differences were observed in the primary outcome (common odds ratio 0·86 [95% CI 0·59-1·24], p=0·41). Mortality was similar between the two groups (19 [11%] of 176 vs 17 [10%] of 172), but the intervention group showed a higher risk of symptomatic intracranial haemorrhage (eight [5%] of 175 vs one [1%] of 169), parenchymal haemorrhage type 2 (six [3%] of 175 vs none in the control group), and procedure-related arterial dissection (24 [14%] of 176 vs five [3%] of 172).</p><p><strong>Interpretation: </strong>Among Chinese patients with unsuccessful recanalisation or who are at risk of reocclusion after thrombectomy, BAOS did not improve clinical outcome at 90 days, and incurred more complications compared with standard therapy. The off-label use of tirofiban might have affected our results and their generalisability, but our findings do not support the addition of BAOS for such patients with LVO-AIS.</p><p><strong>Funding: </strong>Beijing Natural Science Foundation, National Natural Science Foundation of China, National Key R&D Program Beijing Municipal Administration of Hospitals Incubating Program, Shanghai HeartCare Medical Technology, HeMo (China) Bioengineering, Sino Medical Sciences Technology.</p>","PeriodicalId":17989,"journal":{"name":"Lancet Neurology","volume":" ","pages":"797-806"},"PeriodicalIF":46.5000,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Lancet Neurology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/S1474-4422(24)00186-8","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/6/21 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Unsuccessful recanalisation or reocclusion after thrombectomy is associated with poor outcomes in patients with large vessel occlusion (LVO) acute ischaemic stroke (LVO-AIS). Bailout angioplasty or stenting (BAOS) could represent a promising treatment for these patients. We conducted a randomised controlled trial with the aim to investigate the safety and efficacy of BAOS following thrombectomy in patients with LVO.

Methods: ANGEL-REBOOT was an investigator-initiated, multicentre, prospective, randomised, controlled, open-label, blinded-endpoint clinical trial conducted at 36 tertiary hospitals in 19 provinces in China. Participants with LVO-AIS 24 h after symptom onset were eligible if they had unsuccessful recanalisation (expanded Thrombolysis In Cerebral Infarction score of 0-2a) or risk of reocclusion (residual stenosis >70%) after thrombectomy. Eligible patients were randomly assigned by the minimisation method in a 1:1 ratio to undergo BAOS as the intervention treatment, or to receive standard therapy (continue or terminate the thrombectomy procedure) as a control group, both open-label. In both treatment groups, tirofiban could be recommended for use during and after the procedure. The primary outcome was the change in modified Rankin Scale score at 90 days, assessed in the intention-to-treat population. Safety outcomes were compared between groups. This trial was completed and registered at ClinicalTrials.gov (NCT05122286).

Findings: From Dec 19, 2021, to March 17, 2023, 706 patients were screened, and 348 were enrolled, with 176 assigned to the intervention group and 172 to the control group. No patients withdrew from the trial or were lost to follow-up for the primary outcome. The median age of patients was 63 years (IQR 55-69), 258 patients (74%) were male, and 90 patients (26%) were female; all participants were Chinese. After random allocation, tirofiban was administered either intra-arterially, intravenously, or both in 334 [96%] of 348 participants. No between-group differences were observed in the primary outcome (common odds ratio 0·86 [95% CI 0·59-1·24], p=0·41). Mortality was similar between the two groups (19 [11%] of 176 vs 17 [10%] of 172), but the intervention group showed a higher risk of symptomatic intracranial haemorrhage (eight [5%] of 175 vs one [1%] of 169), parenchymal haemorrhage type 2 (six [3%] of 175 vs none in the control group), and procedure-related arterial dissection (24 [14%] of 176 vs five [3%] of 172).

Interpretation: Among Chinese patients with unsuccessful recanalisation or who are at risk of reocclusion after thrombectomy, BAOS did not improve clinical outcome at 90 days, and incurred more complications compared with standard therapy. The off-label use of tirofiban might have affected our results and their generalisability, but our findings do not support the addition of BAOS for such patients with LVO-AIS.

Funding: Beijing Natural Science Foundation, National Natural Science Foundation of China, National Key R&D Program Beijing Municipal Administration of Hospitals Incubating Program, Shanghai HeartCare Medical Technology, HeMo (China) Bioengineering, Sino Medical Sciences Technology.

中国急性大血管闭塞血栓切除术后的颅内血管成形术或支架植入术(ANGEL-REBOOT):一项多中心、开放标签、盲终点、随机对照试验。
背景:对于大血管闭塞(LVO)急性缺血性卒中(LVO-AIS)患者来说,血栓切除术后未成功再通畅或再闭塞与不良预后有关。保外血管成形术或支架植入术(BAOS)可能是治疗这些患者的一种很有前景的方法。我们进行了一项随机对照试验,旨在研究 LVO 患者血栓切除术后 BAOS 的安全性和有效性:ANGEL-REBOOT 是一项由研究者发起的多中心、前瞻性、随机对照、开放标签、盲终点临床试验,在中国 19 个省的 36 家三级医院进行。在症状出现 24 小时后出现 LVO-AIS 的患者,如果再通不成功(脑梗塞溶栓治疗扩展评分为 0-2a)或血栓切除术后有再闭塞风险(残余狭窄 >70%),则符合条件。符合条件的患者通过最小化方法以1:1的比例随机分配接受BAOS作为干预治疗,或接受标准治疗(继续或终止血栓切除术)作为对照组,两组均为开放标签。在两组治疗中,均可推荐在术中和术后使用替罗非班。主要研究结果是90天时改良Rankin量表评分的变化,在意向治疗人群中进行评估。安全性结果在各组之间进行比较。该试验已完成并在ClinicalTrials.gov(NCT05122286)上注册:从2021年12月19日到2023年3月17日,共筛选出706名患者,348名患者入组,其中176名患者被分配到干预组,172名患者被分配到对照组。在主要结果方面,没有患者退出试验或失去随访。患者的中位年龄为63岁(IQR 55-69),258名患者(74%)为男性,90名患者(26%)为女性;所有参与者均为中国人。随机分配后,348名参与者中有334人(96%)接受了动脉内注射、静脉注射或两者兼用的替罗非班治疗。在主要结果方面未观察到组间差异(常见几率比 0-86 [95% CI 0-59-1-24],P=0-41)。两组死亡率相似(176 人中有 19 人[11%] 对 172 人中有 17 人[10%]),但干预组发生症状性颅内出血(175 人中有 8 人[5%] 对 169 人中有 1 人[1%])、2 型实质出血(175 人中有 6 人[3%] 对对照组无)和手术相关动脉夹层(176 人中有 24 人[14%] 对 172 人中有 5 人[3%])的风险更高:解读:在血栓切除术后未成功再通或有再闭塞风险的中国患者中,BAOS并不能改善90天后的临床预后,而且与标准疗法相比会产生更多并发症。在标签外使用替罗非班可能会影响我们的结果及其普遍性,但我们的研究结果并不支持对这类LVO-AIS患者加用BAOS:基金:北京市自然科学基金、国家自然科学基金、国家重点研发计划北京市属医院孵化项目、上海心康医疗科技有限公司、和睦家(中国)生物工程有限公司、信和医疗科技有限公司。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Lancet Neurology
Lancet Neurology 医学-临床神经学
CiteScore
58.70
自引率
1.00%
发文量
572
审稿时长
6-12 weeks
期刊介绍: The Lancet Neurology is the world-leading clinical neurology journal. It publishes original research that advocates for change in, or sheds light on, neurological clinical practice. The topics covered include cerebrovascular disease, Alzheimer's disease and other dementias, epilepsy, migraine, neurological infections, movement disorders, multiple sclerosis, neuromuscular disorders, peripheral nerve disorders, pediatric neurology, sleep disorders, and traumatic brain injury. The journal publishes a range of article types, including Articles (including randomized clinical trials and meta-analyses), Review, Rapid Review, Comment, Correspondence, and Personal View. It also publishes Series and Commissions that aim to shape and drive positive change in clinical practice and health policy in areas of need in neurology. The Lancet Neurology is an internationally trusted source of clinical, public health, and global health knowledge. It has an Impact Factor of 48.0, making it the top-ranked clinical neurology journal out of 212 journals worldwide.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信