Icosapent Ethyl for High-Risk Coronary Plaques Assessed by 18F-NaF PET/CT (IPE-NaF)
A Randomized Controlled Trial Evaluating the Effect of Icosapent Ethyl on High-Risk Coronary Plaques Using 18F-Sodium Fluoride PET/CT
This randomized controlled study will evaluate whether icosapent ethyl (IPE) can improve and stabilize high-risk coronary plaques in patients receiving stable low-density lipoprotein cholesterol (LDL-C)-lowering therapy. Potential participants will have coronary plaques identified by coronary computed tomography angiography (CCTA), with 30% to 70% narrowing in at least one major coronary artery and at least one high-risk plaque feature.
After baseline imaging with fluorine-18 sodium fluoride positron emission tomography/computed tomography (18F-NaF PET/CT), eligible participants will be randomly assigned in a 1:1 ratio to receive either IPE 2 g twice daily plus standard LDL-C-lowering therapy or standard LDL-C-lowering therapy alone for 12 months. At the end of treatment, participants will undergo repeat CCTA and 18F-NaF PET/CT. Blood biomarkers and major adverse cardiovascular events will also be assessed during follow-up.
研究概览
地位
详细说明
This study consists of three main stages. First, a screening cohort will be established using CCTA. Individuals with 30% to 70% diameter narrowing in at least one major coronary artery-the left anterior descending, left circumflex, or right coronary artery-and at least one high-risk plaque feature will be considered for further screening. High-risk plaque features assessed by experienced imaging specialists include increased pericoronary fat attenuation, low-attenuation plaque, positive remodeling, spotty calcification, and the napkin-ring sign. This screening process is intended to identify appropriate and reliably characterized candidates for the randomized study.
Eligible participants will undergo baseline 18F-NaF PET/CT imaging and then be randomly assigned in a 1:1 ratio using a centralized block randomization system. Participants in the intervention group will receive IPE 2 g twice daily for 12 months in addition to stable LDL-C-lowering therapy. Participants in the control group will continue stable LDL-C-lowering therapy without IPE. The LDL-C-lowering regimen should be stable for more than 4 weeks before randomization.
After 12 months, participants in both groups will undergo follow-up CCTA and 18F-NaF PET/CT to evaluate changes in coronary plaque characteristics and disease activity. Follow-up will also include measurements of relevant plasma biomarkers and monitoring for major adverse cardiovascular events. Imaging data will be acquired using standardized procedures and interpreted by experienced imaging specialists.
研究类型
注册 (估计的)
阶段
- 第四阶段
联系人和位置
学习联系方式
- 姓名:Naqiong Wu, Doctor
- 电话号码:+86 13501139869
- 邮箱:fuwainaqiongwu@163.com
研究联系人备份
- 姓名:Zheng Yin, Master
- 电话号码:+8615359270767
- 邮箱:yinzheng@fuwai.com
学习地点
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Beijing Municipality
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Beijing、Beijing Municipality、中国、100037
- Fuwai Hospital
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接触:
- Jianing Zhang, Master
- 电话号码:+86 (010) 88398662
- 邮箱:Zhangjianing@fuwai.com
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首席研究员:
- Naqiong Wu, Doctor
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参与标准
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
描述
Inclusion Criteria:
- Male or female participants aged 18 to 75 years.
- Ability to understand the study and provide written informed consent before enrollment.
- Receiving a stable lipid-lowering regimen before enrollment, with the type and dose of statin therapy remaining unchanged for at least 4 weeks.
- Fasting triglyceride level below 5.6 mmol/L.
- Presence of at least one of the following high-risk plaque features on coronary computed tomography angiography (CCTA):Pericoronary fat attenuation index greater than -70.1 Hounsfield units;
- Low-attenuation plaque below 30 Hounsfield units;
- Positive remodeling index greater than 1.1;
- Spotty calcification;
- or Napkin-ring sign, defined as a low-attenuation plaque core surrounded by a rim of higher attenuation.
Exclusion Criteria:
- Current participation in another investigational drug, device, or procedure study, or receipt of an investigational drug or device within 4 weeks before enrollment.
- Treatment with icosapent ethyl within 12 months before enrollment.
- Known intolerance or hypersensitivity to icosapent ethyl or fish oil.
- A previous diagnosis of homozygous familial hypercholesterolemia or hyperlipidemia requiring hemodialysis.
- Myocardial infarction, unstable angina, percutaneous coronary intervention, coronary artery bypass grafting, or stroke within 3 months before enrollment;
- Planned cardiac surgery, percutaneous coronary intervention, or carotid artery stenting, or planned major noncardiac surgery during the study.
- A known contraindication or limitation to PET/CT, including exceeding scanner weight limits or having a device, carotid or aortic stent, or vascular graft that may cause imaging artifacts.
- Autoimmune disease, vasculitis, or active inflammatory disease.
- Serious infection within 1 month before enrollment or a current infection requiring intravenous antibiotic treatment.
- Use within 6 weeks before enrollment or current use of medications that may significantly affect plaque inflammation, including oral, rectal, or injectable corticosteroids or immunosuppressive agents, such as cyclosporine, methotrexate, tacrolimus, azathioprine, antithymocyte globulin, sirolimus, anti-tumor necrosis factor agents such as infliximab, anti-interleukin-6 therapy such as tocilizumab, or anti-interleukin-1 therapy.
- Use within 6 weeks before enrollment or current use of aspirin at a dose greater than 325 mg/day or nonsteroidal anti-inflammatory drugs at a dose greater than 1,000 mg/day.
- Treatment within 12 months before enrollment with a cholesteryl ester transfer protein inhibitor, including anacetrapib, dalcetrapib, or evacetrapib, or with mipomersen or lomitapide.
- Known clinically significant systemic disease, including hepatic, renal, hematologic, or malignant disease, or any other clinically significant comorbidity that may interfere with study participation or study assessments.
- History of malignancy within the previous 5 years, except nonmelanoma skin cancer, cervical carcinoma in situ, ductal carcinoma in situ of the breast, or stage I prostate cancer.
- Inability or anticipated inability to complete all protocol-required visits or procedures, or any condition that may make the participant unreliable for study participation, including alcohol or other substance abuse within the previous year or a psychiatric disorder.
- Pregnancy or breastfeeding, or plans to become pregnant or breastfeed during study treatment or within 15 weeks after the last dose of study treatment.
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:单身的
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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实验性的:Icosapent Ethyl Plus Standard LDL-C-Lowering Therapy
Participants will receive oral icosapent ethyl 2 g twice daily for 12 months in addition to their stable LDL-C-lowering therapy.
CCTA and 18F-NaF PET/CT will be performed at baseline and after 12 months, together with biomarker and clinical event follow-up.
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Icosapent ethyl will be administered orally at a dose of 2 g twice daily (total daily dose of 4 g) for 12 months, in addition to stable LDL-C-lowering therapy.
其他名称:
Participants will continue an individualized, stable LDL-C-lowering regimen throughout the 12-month study period.
The LDL-C-lowering regimen must have remained stable for more than 4 weeks before randomization.
This background therapy will be administered in both study arms.
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有源比较器:Standard LDL-C-Lowering Therapy Alone
Participants will continue their stable LDL-C-lowering therapy for 12 months without receiving icosapent ethyl.
CCTA and 18F-NaF PET/CT will be performed at baseline and after 12 months, together with biomarker and clinical event follow-up.
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Participants will continue an individualized, stable LDL-C-lowering regimen throughout the 12-month study period.
The LDL-C-lowering regimen must have remained stable for more than 4 weeks before randomization.
This background therapy will be administered in both study arms.
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研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Absolute Change From Baseline in Maximum Target-to-Background Ratio of the Target Coronary Lesion
大体时间:Baseline and Month 12
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The target lesion is defined as the coronary lesion with the highest maximum target-to-background ratio (TBRmax) at baseline.
TBRmax is calculated as the maximum standardized uptake value (SUVmax) of the target lesion divided by the mean standardized uptake value (SUVmean) of the blood-pool background measured in the right atrium, superior vena cava, or inferior vena cava.
Absolute change is calculated as the Month 12 TBRmax minus the baseline TBRmax.
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Baseline and Month 12
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Percentage Change From Baseline in TBRmax of the Target Coronary Lesion
大体时间:Baseline and Month 12
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The target lesion is the coronary lesion with the highest TBRmax at baseline.
Percentage change is calculated as [(Month 12 TBRmax - baseline TBRmax) / baseline TBRmax] × 100%.
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Baseline and Month 12
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Change From Baseline in SUVmax of the Target Coronary Lesion
大体时间:Baseline and Month 12
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Change in the maximum standardized uptake value of the prespecified target coronary lesion, calculated as the Month 12 value minus the baseline value.
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Baseline and Month 12
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Change From Baseline in Total Volume of 18F-NaF-Positive Coronary Plaque
大体时间:Baseline and Month 12
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Total volume of coronary plaque demonstrating positive 18F-NaF uptake, defined as TBRmax greater than 1.25.
Change is calculated as the Month 12 volume minus the baseline volume.
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Baseline and Month 12
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Change From Baseline in the Number of 18F-NaF-Positive Coronary Segments
大体时间:Baseline and Month 12
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Number of coronary artery segments with positive 18F-NaF uptake, defined as TBRmax greater than 1.25.
Change is calculated as the Month 12 count minus the baseline count.
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Baseline and Month 12
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Change From Baseline in Pericoronary Fat Attenuation Index at the Target Plaque
大体时间:Baseline and Month 12
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Pericoronary fat attenuation index (FAI), measured in Hounsfield units using CCTA at the location of the target plaque.
Change is calculated as the Month 12 value minus the baseline value.
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Baseline and Month 12
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Change From Baseline in Percent Atheroma Volume at the Target Plaque
大体时间:Baseline and Month 12
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Percent atheroma volume (PAV) will be measured using CCTA.
Change is calculated as the Month 12 value minus the baseline value.
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Baseline and Month 12
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Change From Baseline in CCTA-Derived Coronary Plaque Component Volumes
大体时间:Baseline and Month 12
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CCTA will be used to measure changes in total plaque, noncalcified plaque, calcified plaque, and low-attenuation noncalcified plaque volumes.
For each component, change is calculated as the Month 12 volume minus the baseline volume.
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Baseline and Month 12
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其他结果措施
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Change in Plasma triglycerides Levels From Baseline to Month 12
大体时间:Baseline and Month 12
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Plasma levels of triglycerides (TG) will be measured.
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Baseline and Month 12
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Percentage Change From Baseline in Plasma High-Sensitivity C-Reactive Protein Level
大体时间:Baseline and Month 12
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Percentage change will be calculated as [(Month 12 hs-CRP - baseline hs-CRP) / baseline hs-CRP] × 100%.
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Baseline and Month 12
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Change in Plasma Eicosapentaenoic Acid Level From Baseline to Month 12
大体时间:Baseline and Month 12
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Plasma eicosapentaenoic acid (EPA) concentration will be measured and reported in its applicable concentration unit (e.g., μg/mL or % of total fatty acids, according to the laboratory assay).
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Baseline and Month 12
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Exploratory Incidence of Three-Point Major Adverse Cardiovascular Events
大体时间:From randomization through Month 12
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Number and percentage of participants experiencing a three-point major adverse cardiovascular event (3P-MACE), defined as the composite of all-cause death, nonfatal myocardial infarction, or nonfatal stroke.
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From randomization through Month 12
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Exploratory Incidence of Four-Point Major Adverse Cardiovascular Events
大体时间:From randomization through Month 12
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Number and percentage of participants experiencing a four-point major adverse cardiovascular event (4P-MACE), defined as 3P-MACE plus ischemia-driven coronary revascularization.
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From randomization through Month 12
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合作者和调查者
出版物和有用的链接
一般刊物
- Budoff MJ, Bhatt DL, Kinninger A, Lakshmanan S, Muhlestein JB, Le VT, May HT, Shaikh K, Shekar C, Roy SK, Tayek J, Nelson JR. Effect of icosapent ethyl on progression of coronary atherosclerosis in patients with elevated triglycerides on statin therapy: final results of the EVAPORATE trial. Eur Heart J. 2020 Oct 21;41(40):3925-3932. doi: 10.1093/eurheartj/ehaa652.
- Moss A, Daghem M, Tzolos E, Meah MN, Wang KL, Bularga A, Adamson PD, Kwiecinski J, Fletcher A, Dawson D, Arumugam P, Sabharwal N, Greenwood JP, Townend JN, Calvert PA, Rudd JHF, Berman D, Verjans J, Slomka P, Dey D, Forsyth L, Murdoch L, Lee RJ, Lewis S, Mills NL, van Beek EJR, Williams MC, Dweck MR, Newby DE; PREFFIR Investigators. Coronary Atherosclerotic Plaque Activity and Future Coronary Events. JAMA Cardiol. 2023 Aug 1;8(8):755-764. doi: 10.1001/jamacardio.2023.1729.
- Sayah N, Bhatt DL, Miller M, Brinton EA, Jacobson TA, Ketchum SB, Jiao L, Pineda AL, Doyle RT Jr, Tardif JC, Ballantyne CM, Steg PG. Icosapent ethyl following acute coronary syndrome: the REDUCE-IT trial. Eur Heart J. 2024 Apr 1;45(13):1173-1176. doi: 10.1093/eurheartj/ehad889. No abstract available.
- Yang S, Hoshino M, Koo BK, Yonetsu T, Zhang J, Hwang D, Shin ES, Doh JH, Nam CW, Wang J, Chen S, Tanaka N, Matsuo H, Kubo T, Chang HJ, Kakuta T, Narula J. Relationship of Plaque Features at Coronary CT to Coronary Hemodynamics and Cardiovascular Events. Radiology. 2022 Dec;305(3):578-587. doi: 10.1148/radiol.213271. Epub 2022 Aug 16.
- Gallone G, Bellettini M, Gatti M, Tore D, Bruno F, Scudeler L, Cusenza V, Lanfranchi A, Angelini A, de Filippo O, Iannaccone M, Baldetti L, Audisio K, Demetres M, Risi G, Rizzello G, Porto I, Fonio P, Prati F, Williams MC, Koo BK, Pontone G, Depaoli A, Libby P, Stone GW, Narula J, de Ferrari GM, d'Ascenzo F. Coronary Plaque Characteristics Associated With Major Adverse Cardiovascular Events in Atherosclerotic Patients and Lesions: A Systematic Review and Meta-Analysis. JACC Cardiovasc Imaging. 2023 Dec;16(12):1584-1604. doi: 10.1016/j.jcmg.2023.08.006. Epub 2023 Oct 4.
研究记录日期
研究主要日期
学习开始 (估计的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
关键字
其他相关的 MeSH 术语
其他研究编号
- 2026-3220
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
IPD 计划说明
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
在美国制造并从美国出口的产品
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