Angiogenic Gene Therapy for Refractory Angina: Results of the EXACT Phase 2 Trial.

IF 6.1 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Kenta Nakamura, Timothy D Henry, Jay H Traverse, David A Latter, Nahush A Mokadam, Geoffrey A Answini, Adam R Williams, Benjamin C Sun, Christopher R Burke, Faisal G Bakaeen, Marcelo F DiCarli, Bernard R Chaitman, Mark W Peterson, Dawn G Byrnes, E Magnus Ohman, Carl J Pepine, Ronald G Crystal, Todd K Rosengart, Elaine Kowalewski, Gary G Koch, Howard C Dittrich, Thomas J Povsic
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引用次数: 0

Abstract

Background: XC001 is a novel adenoviral-5 vector designed to express multiple isoforms of VEGF (vascular endothelial growth factor) and more safely and potently induce angiogenesis. The EXACT trial (Epicardial Delivery of XC001 Gene Therapy for Refractory Angina Coronary Treatment) assessed the safety and preliminary efficacy of XC001 in patients with no option refractory angina.

Methods: In this single-arm, multicenter, open-label trial, 32 patients with no option refractory angina received a single treatment of XC001 (1×1011 viral particles) via transepicardial delivery.

Results: There were no severe adverse events attributed to the study drug. Twenty expected severe adverse events in 13 patients were related to the surgical procedure. Total exercise duration increased from a mean±SD of 359.9±105.55 seconds at baseline to 448.2±168.45 (3 months), 449.2±175.9 (6 months), and 477.6±174.7 (12 months; +88.3 [95% CI, 37.1-139.5], +84.5 [95% CI, 34.1-134.9], and +115.5 [95% CI, 59.1-171.9]). Total myocardial perfusion deficit on positron emission tomography imaging decreased by 10.2% (95% CI, -3.1% to 23.5%), 14.3% (95% CI, 2.8%-25.7%), and 10.2% (95% CI, -0.8% to -21.2%). Angina frequency decreased from a mean±SD 12.2±12.5 episodes to 5.2±7.2 (3 months), 5.1±7.8 (6 months), and 2.7±4.8 (12 months), with an average decrease of 7.7 (95% CI, 4.1-11.3), 6.6 (95% CI, 3.5-9.7), and 8.8 (4.6-13.0) episodes at 3, 6, and 12 months. Angina class improved in 81% of participants at 6 months.

Conclusions: XC001 administered via transepicardial delivery is safe and generally well tolerated. Exploratory improvements in total exercise duration, ischemic burden, and subjective measures support a biologic effect sustained to 12 months, warranting further investigation.

Registration: URL: https://www.clinicaltrials.gov; Unique identifier: NCT04125732.

治疗难治性心绞痛的血管生成基因疗法:EXACT 2 期试验结果。
背景:XC001是一种新型腺病毒-5载体,旨在表达血管内皮生长因子(VEGF)的多种异构体,更安全、更有效地诱导血管生成。EXACT 试验(用于难治性心绞痛冠状动脉治疗的 XC001 基因疗法心外膜给药试验)评估了 XC001 在无选择难治性心绞痛患者中的安全性和初步疗效:在这项单臂、多中心、开放标签试验中,32名无选择性难治性心绞痛患者通过经心皮给药接受了XC001(1×1011病毒颗粒)的单次治疗:研究药物未导致严重不良事件。13例患者中的20例预期严重不良事件与手术过程有关。总运动时间从基线时的平均值(±SD)359.9±105.55 秒增加到 448.2±168.45(3 个月)、449.2±175.9(6 个月)和 477.6±174.7(12 个月;+88.3 [95% CI, 37.1-139.5]、+84.5 [95% CI, 34.1-134.9]和+115.5 [95% CI, 59.1-171.9])。正电子发射断层扫描成像的总心肌灌注缺损分别减少了10.2%(95% CI,-3.1%至23.5%)、14.3%(95% CI,2.8%至25.7%)和10.2%(95% CI,-0.8%至-21.2%)。心绞痛发作频率从平均值±SD 12.2±12.5次降至5.2±7.2次(3个月)、5.1±7.8次(6个月)和2.7±4.8次(12个月),3个月、6个月和12个月的平均发作次数分别为7.7次(95% CI,4.1-11.3)、6.6次(95% CI,3.5-9.7)和8.8次(4.6-13.0)。81%的参与者在6个月时心绞痛等级有所改善:XC001经心包给药安全且耐受性良好。总运动时间、缺血负担和主观测量的探索性改善支持生物效应持续到 12 个月,值得进一步研究:URL:https://www.clinicaltrials.gov;唯一标识符:NCT04125732。
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来源期刊
Circulation: Cardiovascular Interventions
Circulation: Cardiovascular Interventions CARDIAC & CARDIOVASCULAR SYSTEMS-
CiteScore
10.30
自引率
1.80%
发文量
221
审稿时长
6-12 weeks
期刊介绍: Circulation: Cardiovascular Interventions, an American Heart Association journal, focuses on interventional techniques pertaining to coronary artery disease, structural heart disease, and vascular disease, with priority placed on original research and on randomized trials and large registry studies. In addition, pharmacological, diagnostic, and pathophysiological aspects of interventional cardiology are given special attention in this online-only journal.
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