Division of Angiology, Medical University of Graz, Graz, Austria.
Department of Angiology, Hanusch Hospital, Vienna, Austria.
Vascular. 2024 Aug;32(4):850-857. doi: 10.1177/17085381231162128. Epub 2023 Mar 15.
The TOBA (Tack Optimized Balloon Angioplasty) II trial is a prospective, single-arm, multicenter study that investigated Tack treatment for patients with dissection after angioplasty in the superficial femoral artery and/or proximal popliteal artery. The Tack device is a nitinol-based, short (6 mm), stent-like implant with low outward force that can be deployed in a targeted fashion to treat vascular dissection. TOBA II primary results through 12 months have been published previously. This report provides follow-up safety and efficacy results through 24 months (RC).
The TOBA II trial enrolled 213 patients with Rutherford classification 2 to 4 and a de novo or non-stented restenotic lesion in the superficial femoral artery and/or proximal popliteal artery who developed a dissection of any grade after treatment with plain balloon or drug-coated balloon (DCB) angioplasty. Participants were followed for 30 days, 6 months, 12 months, 24 months, and 36 months following the procedure. Evaluations included clinically driven target lesion revascularization (CD-TLR), ankle-brachial index, Rutherford classification, peripheral artery questionnaire, quality of life assessed by the EQ-5D-3L, and the Walking Impairment Questionnaire.
At enrollment, mean age was 68.2 ± 9.1 years, 70.9% were male, and 95.8% of patients were categorized as RC 2 or 3. The distribution of balloon types in the study were standard balloons: 42.3%; and drug-coated balloons: 57.7%. At 24-month follow-up, 167 patients (78.4%) had available data. The overall survival rate at 24 months was 95.4% and there were no major amputations during this time. After 24 months of follow-up, the Kaplan-Meier freedom from CD-TLR was 77.7%. Rutherford classification, ankle-brachial index, and quality of life were significantly improved compared with baseline through 24 months.
The TOBA II 24-month data demonstrate durable intermediate-term outcomes with the use of the Tack Endovascular System. Tack deployment was a safe and effective therapeutic option for dissection repair following angioplasty.
TOBA(Tack 优化球囊血管成形术)II 试验是一项前瞻性、单臂、多中心研究,旨在研究 Tack 治疗股浅动脉和/或腘动脉段球囊血管成形术后夹层的疗效。Tack 装置是一种基于镍钛诺的、短(6 毫米)、支架样植入物,具有低向外力,可以以靶向方式部署,以治疗血管夹层。TOBA II 的主要结果在 12 个月前已经发表。本报告提供了通过 24 个月(RC)的随访安全性和疗效结果。
TOBA II 试验纳入了 213 例 Rutherford 分级 2 至 4 级的患者,这些患者在接受普通球囊或药物涂层球囊(DCB)血管成形术后,股浅动脉和/或腘动脉段发生了任何分级的夹层,且存在新发或未支架的再狭窄病变。参与者在术后 30 天、6 个月、12 个月、24 个月和 36 个月进行随访。评估包括临床驱动的靶病变血运重建(CD-TLR)、踝肱指数、Rutherford 分级、外周动脉问卷、EQ-5D-3L 评估的生活质量和步行障碍问卷。
在入组时,平均年龄为 68.2 ± 9.1 岁,70.9%为男性,95.8%的患者为 RC 2 或 3 级。研究中球囊类型的分布为:标准球囊:42.3%;药物涂层球囊:57.7%。在 24 个月的随访中,167 例患者(78.4%)有可用数据。24 个月时的总生存率为 95.4%,在此期间没有发生主要截肢。经过 24 个月的随访,Kaplan-Meier 无 CD-TLR 生存率为 77.7%。与基线相比,Rutherford 分级、踝肱指数和生活质量在 24 个月时均显著改善。
TOBA II 24 个月的数据显示,使用 Tack 血管内系统具有持久的中期疗效。在血管成形术后,Tack 部署是一种安全有效的夹层修复治疗选择。