Interventional Neuroradiology, Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
China National Clinical Research Center for Neurological Diseases, Beijing.
JAMA. 2024 Oct 1;332(13):1059-1069. doi: 10.1001/jama.2024.12829.
Previous randomized clinical trials did not demonstrate the superiority of endovascular stenting over aggressive medical management for patients with symptomatic intracranial atherosclerotic stenosis (sICAS). However, balloon angioplasty has not been investigated in a randomized clinical trial.
To determine whether balloon angioplasty plus aggressive medical management is superior to aggressive medical management alone for patients with sICAS.
DESIGN, SETTING, AND PARTICIPANTS: A randomized, open-label, blinded end point clinical trial at 31 centers across China. Eligible patients aged 35 to 80 years with sICAS defined as recent transient ischemic attack (<90 days) or ischemic stroke (14-90 days) before enrollment attributed to a 70% to 99% atherosclerotic stenosis of a major intracranial artery receiving treatment with at least 1 antithrombotic drug and/or standard risk factor management were recruited between November 8, 2018, and April 2, 2022 (final follow-up: April 3, 2023).
Submaximal balloon angioplasty plus aggressive medical management (n = 249) or aggressive medical management alone (n = 252). Aggressive medical management included dual antiplatelet therapy for the first 90 days and risk factor control.
The primary outcome was a composite of any stroke or death within 30 days after enrollment or after balloon angioplasty of the qualifying lesion or any ischemic stroke in the qualifying artery territory or revascularization of the qualifying artery after 30 days through 12 months after enrollment.
Among 512 randomized patients, 501 were confirmed eligible (mean age, 58.0 years; 158 [31.5%] women) and completed the trial. The incidence of the primary outcome was lower in the balloon angioplasty group than the medical management group (4.4% vs 13.5%; hazard ratio, 0.32 [95% CI, 0.16-0.63]; P < .001). The respective rates of any stroke or all-cause death within 30 days were 3.2% and 1.6%. Beyond 30 days through 1 year after enrollment, the rates of any ischemic stroke in the qualifying artery territory were 0.4% and 7.5%, respectively, and revascularization of the qualifying artery occurred in 1.2% and 8.3%, respectively. The rate of symptomatic intracranial hemorrhage in the balloon angioplasty and medical management groups was 1.2% and 0.4%, respectively. In the balloon angioplasty group, procedural complications occurred in 17.4% of patients and arterial dissection occurred in 14.5% of patients.
In patients with sICAS, balloon angioplasty plus aggressive medical management, compared with aggressive medical management alone, statistically significantly lowered the risk of a composite outcome of any stroke or death within 30 days or an ischemic stroke or revascularization of the qualifying artery after 30 days through 12 months. The findings suggest that balloon angioplasty plus aggressive medical management may be an effective treatment for sICAS, although the risk of stroke or death within 30 days of balloon angioplasty should be considered in clinical practice.
ClinicalTrials.gov Identifier: NCT03703635.
先前的随机临床试验并未证明症状性颅内动脉粥样硬化狭窄(sICAS)患者血管内支架置入术优于积极的药物治疗。然而,球囊血管成形术尚未在随机临床试验中进行研究。
确定球囊血管成形术加积极药物治疗是否优于单纯积极药物治疗sICAS 患者。
设计、地点和参与者:这是一项在中国 31 个中心进行的随机、开放标签、盲法终点临床试验。符合条件的患者年龄在 35 岁至 80 岁之间,在入组前最近有短暂性脑缺血发作(<90 天)或缺血性卒(14-90 天),归因于主要颅内动脉的 70%-99%的粥样硬化狭窄,正在接受至少 1 种抗血栓药物和/或标准危险因素管理治疗。这些患者于 2018 年 11 月 8 日至 2022 年 4 月 2 日(最终随访:2023 年 4 月 3 日)期间被招募。
次最大球囊血管成形术加积极药物治疗(n=249)或单纯积极药物治疗(n=252)。积极的药物治疗包括前 90 天使用双联抗血小板治疗和危险因素控制。
主要结局是在入组后 30 天内或在符合条件的病变球囊血管成形术后 30 天至 12 个月内发生任何卒中和死亡、符合条件的动脉区域内任何缺血性卒中和符合条件的动脉再通的复合结局。
在 512 名随机患者中,501 名患者符合条件(平均年龄 58.0 岁,158[31.5%]名女性)并完成了试验。球囊血管成形术组的主要结局发生率低于药物治疗组(4.4%比 13.5%;风险比,0.32[95%CI,0.16-0.63];P<0.001)。30 天内任何卒中和全因死亡的发生率分别为 3.2%和 1.6%。入组后 30 天至 1 年,符合条件的动脉区域内任何缺血性卒的发生率分别为 0.4%和 7.5%,符合条件的动脉再通发生率分别为 1.2%和 8.3%。球囊血管成形术组和药物治疗组症状性颅内出血的发生率分别为 1.2%和 0.4%。在球囊血管成形术组,17.4%的患者发生了手术并发症,14.5%的患者发生了动脉夹层。
在 sICAS 患者中,与单纯积极药物治疗相比,球囊血管成形术加积极药物治疗可显著降低 30 天内任何卒中和死亡的复合结局风险,或 30 天至 12 个月内符合条件的动脉发生缺血性卒或再通的风险。研究结果表明,球囊血管成形术加积极药物治疗可能是 sICAS 的有效治疗方法,尽管应在临床实践中考虑球囊血管成形术后 30 天内发生卒或死亡的风险。
ClinicalTrials.gov 标识符:NCT03703635。