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FAPI PET/CT Imaging in Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) (FAPI-ARVC)) (FAPI-ARVC)

2026년 4월 30일 업데이트: Şükrü Arslan, Istanbul University - Cerrahpasa

Incremental Diagnostic and Prognostic Value of 68Ga-DOTA-SA-FAPI PET/CT Imaging in Patients With Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC)

Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited heart muscle disease associated with fibrofatty myocardial replacement, ventricular arrhythmias, and an increased risk of sudden cardiac death. Although current diagnostic approaches, including the 2010 Task Force Criteria and the Padua criteria, improve recognition of the disease, early diagnosis remains challenging, particularly when structural abnormalities are subtle or absent on conventional imaging. Echocardiography and cardiac magnetic resonance imaging are central to evaluation, but their sensitivity for early or active fibrotic remodeling may be limited. This limitation may be particularly relevant in patients who are unable to undergo cardiac magnetic resonance imaging, in whom 68Ga-DOTA-SA-FAPI PET/CT may provide complementary diagnostic information.

This prospective single-group diagnostic imaging study aims to investigate the incremental value of protocol-specified 68Ga-DOTA-SA-FAPI PET/CT imaging in patients with ARVC. FAPI PET/CT is a novel molecular imaging method that targets activated fibroblasts and may allow non-invasive detection of active myocardial fibrosis.Fifteen adult patients with an established diagnosis of ARVC will undergo protocol-specified 68Ga-DOTA-SA-FAPI PET/CT imaging in addition to clinical evaluation, electrocardiography, echocardiography, and review of previously obtained cardiac magnetic resonance imaging findings. FAPI PET/CT findings will be compared with conventional diagnostic criteria and other clinical and imaging parameters, including previously available cardiac magnetic resonance imaging findings. Participants will also be followed clinically for 6 months after imaging to explore possible associations between FAPI uptake and short-term clinical outcomes, including arrhythmic events, ventricular function, and laboratory markers.

The study is expected to provide preliminary evidence on whether 68Ga-DOTA-SA-FAPI PET/CT may improve the detection of myocardial fibrosis and contribute to diagnostic assessment and risk stratification in ARVC. It may also help clarify the potential role of FAPI PET/CT in patients who are unable to undergo cardiac magnetic resonance imaging. The findings may support future larger prospective studies in this field.

연구 개요

상세 설명

Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited myocardial disease characterized by progressive fibro-fatty replacement of the ventricular myocardium, predominantly involving the right ventricle, although left ventricular and biventricular forms are increasingly recognized. The disease is associated with ventricular arrhythmias, progressive ventricular dysfunction, heart failure, and sudden cardiac death. Because phenotypic expression is variable and may evolve over time, early diagnosis remains challenging, particularly in patients with subtle structural abnormalities or incomplete expression of conventional diagnostic criteria.

Current diagnostic evaluation relies on a multiparametric approach integrating electrocardiographic, arrhythmic, structural, functional, histopathological, and genetic findings. The revised 2010 Task Force Criteria improved standardization of diagnosis, and the Padua criteria further expanded the disease concept by incorporating left ventricular involvement. However, despite these advances, important limitations remain, especially in the early stages of disease, when conventional imaging may not adequately detect active myocardial remodeling.

Echocardiography and cardiac magnetic resonance imaging are central imaging modalities in ARVC. Echocardiography allows assessment of chamber dimensions, ventricular systolic function, and regional wall motion abnormalities, whereas cardiac magnetic resonance imaging provides more detailed characterization of ventricular volumes, function, and tissue abnormalities. Nevertheless, both techniques primarily reflect structural and functional consequences of disease and may be less sensitive for detecting early or biologically active fibrotic remodeling. This limitation is particularly relevant in a disease in which myocardial fibrosis is a major pathological substrate for electrical instability and arrhythmogenesis. It may also be especially important in patients who are unable to undergo cardiac magnetic resonance imaging because of contraindications or technical limitations. In such cases, 68Ga-DOTA-SA-FAPI PET/CT may provide complementary diagnostic information by enabling non-invasive assessment of active myocardial fibrotic remodeling.

Molecular imaging with fibroblast activation protein inhibitor positron emission tomography/computed tomography (FAPI PET/CT) has emerged as a promising non-invasive technique for visualizing activated fibroblasts in vivo. Fibroblast activation protein is overexpressed in activated fibroblasts involved in tissue remodeling and fibrogenesis. In cardiovascular disease, FAPI-based imaging has attracted growing interest as a potential marker of active fibrosis. In ARVC, where fibro-fatty myocardial replacement is a defining pathological feature, 68Ga-DOTA-SA-FAPI PET/CT may offer additional biological information beyond conventional imaging by identifying active fibroblast-related remodeling.

The present study is a prospective single-group diagnostic imaging study designed to evaluate the incremental value of protocol-specified 68Ga-DOTA-SA-FAPI PET/CT imaging in adult patients with ARVC. The central hypothesis is that FAPI PET/CT may improve the non-invasive assessment of myocardial fibrotic activity and provide complementary information to conventional multimodality evaluation.In particular, the study seeks to explore whether myocardial FAPI uptake is detectable in patients with ARVC and whether uptake patterns correlate with established clinical, electrocardiographic, echocardiographic, and previously obtained cardiac magnetic resonance findings. The study will also explore the potential usefulness of FAPI PET/CT in patients in whom cardiac magnetic resonance imaging is unavailable or cannot be performed.

The study will be conducted through collaboration between the Istanbul University-Cerrahpaşa Institute of Cardiology, Department of Cardiology, and the Istanbul Training and Research Hospital, Department of Nuclear Medicine. Fifteen adult patients with established ARVC who are under clinical follow-up will be enrolled prospectively. Following informed consent, participants will undergo comprehensive clinical evaluation together with electrocardiography, transthoracic echocardiography, review of previously obtained cardiac magnetic resonance imaging findings, and protocol-specified 68Ga-DOTA-SA-FAPI PET/CT imaging. No new cardiac magnetic resonance imaging will be performed as part of the study protocol.

The PET/CT imaging protocol includes intravenous administration of approximately 150-200 MBq of 68Ga-DOTA-SA-FAPI. No fasting or specific dietary preparation is required. After tracer injection, participants will rest during an uptake period of approximately 40-60 minutes. Imaging will then be performed using a hybrid PET/CT scanner. A low-dose CT acquisition will be obtained for attenuation correction and anatomical localization, followed by three-dimensional PET acquisition focused on the thoracic region for cardiac assessment. Images will be reconstructed according to standard institutional protocols using attenuation, scatter, and decay correction methods.

Image analysis will focus on the presence, localization, and pattern of myocardial FAPI uptake. Particular attention will be paid to uptake involving the right ventricular free wall, right ventricular outflow tract, interventricular septum, left ventricular myocardium, or biventricular distribution. Where technically feasible, semi-quantitative parameters such as standardized uptake values may also be recorded. These findings will be interpreted in relation to conventional imaging, including previously available cardiac magnetic resonance imaging, and clinical phenotype in order to assess the potential complementary role of FAPI PET/CT in ARVC characterization.

Participants will also undergo clinical follow-up for 6 months after PET/CT imaging. Follow-up data will include interval symptoms, arrhythmic events, clinical status, routine electrocardiographic findings, echocardiographic reassessment where available, and selected laboratory parameters obtained during standard care. This follow-up is intended to provide preliminary exploratory information regarding possible associations between baseline myocardial FAPI uptake and short-term clinical course.

As an exploratory pilot study, this project is primarily intended to generate early clinical evidence regarding the feasibility and potential usefulness of FAPI PET/CT in ARVC. The study is expected to clarify whether imaging of fibroblast activation may complement current structural and functional assessment, especially in cases where conventional modalities provide limited or equivocal information. It may also provide preliminary evidence regarding the potential role of FAPI PET/CT in the diagnostic evaluation of patients with ARVC who are unable to undergo cardiac magnetic resonance imaging, while also allowing comparison with previously obtained cardiac magnetic resonance data in patients with established ARVC. If myocardial uptake patterns appear biologically and clinically meaningful, the results may support the development of larger prospective studies investigating the diagnostic and prognostic role of FAPI PET/CT in arrhythmogenic cardiomyopathy.

Data will be collected and managed by the study investigators in accordance with institutional ethical standards. Study data will be coded and de-identified before analysis to protect participant confidentiality. Because this is an investigator-initiated academic study, analyses and interpretation will be performed independently by the research team. The results are expected to provide pilot data relevant to future multicentre research and to the broader investigation of molecular imaging biomarkers in inherited cardiomyopathies.

연구 유형

중재적

등록 (추정된)

15

단계

  • 해당 없음

연락처 및 위치

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연구 연락처

연구 연락처 백업

연구 장소

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

  • 성인
  • 고령자

건강한 자원 봉사자를 받아들입니다

아니

설명

Inclusion Criteria:

  • Adults aged 18 years or older
  • Established diagnosis of arrhythmogenic right ventricular cardiomyopathy according to the 2010 Revised Task Force Criteria and/or the Padua criteria
  • Under active follow-up at the study center
  • Ability to understand the study procedures and provide written informed consent

Exclusion Criteria:

  • History of malignancy
  • Severe renal impairment
  • Severe hepatic impairment
  • Pregnancy or breastfeeding
  • Prior 68Ga-DOTA-SA-FAPI PET/CT imaging
  • Inability or unwillingness to provide written informed consent
  • Any medical, clinical, or logistical condition that, in the opinion of the investigators, could interfere with study participation, image interpretation, or completion of follow-up

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 특수 증상
  • 할당: 해당 없음
  • 중재 모델: 단일 그룹 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: Adults With ARVC
Participants in this single-arm diagnostic imaging study will undergo protocol-specified 68Ga-DOTA-SA-FAPI PET/CT for assessment of myocardial fibroblast-related remodeling in arrhythmogenic right ventricular cardiomyopathy. All participants will also undergo clinical evaluation, 12-lead electrocardiography, transthoracic echocardiography, and review of previously obtained cardiac magnetic resonance imaging findings, followed by 6 months of protocol-defined clinical follow-up.
Protocol-specified 68Ga-DOTA-SA-FAPI positron emission tomography/computed tomography performed for assessment of myocardial fibroblast-related remodeling in patients with arrhythmogenic right ventricular cardiomyopathy. The imaging protocol includes intravenous administration of approximately 150-200 MBq of 68Ga-DOTA-SA-FAPI, an uptake period of 40-60 minutes, low-dose CT for attenuation correction and anatomical localization, and thoracic PET acquisition for cardiac assessment.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Myocardial 68Ga-DOTA-SA-FAPI Uptake on PET/CT
기간: At baseline (time of PET/CT imaging)
Presence and distribution of myocardial 68Ga-DOTA-SA-FAPI uptake on PET/CT, assessed qualitatively and, where feasible, semi-quantitatively by maximum standardized uptake value (SUVmax).
At baseline (time of PET/CT imaging)

2차 결과 측정

결과 측정
측정값 설명
기간
Correlation Between Myocardial FAPI PET/CT Uptake and Fibrosis-Related Findings on Previously Obtained Cardiac Magnetic Resonance Imaging
기간: At baseline
Correlation between myocardial 68Ga-DOTA-SA-FAPI uptake on PET/CT and fibrosis-related abnormalities identified on previously obtained cardiac magnetic resonance imaging.
At baseline
Correlation Between Myocardial FAPI PET/CT Uptake and Right Ventricular Fractional Area Change on Transthoracic Echocardiography
기간: At baseline
Correlation between myocardial 68Ga-DOTA-SA-FAPI uptake on PET/CT and right ventricular fractional area change measured by transthoracic echocardiography.
At baseline
Incidence of Arrhythmic Events During 6-Month Follow-Up
기간: Within 6 months after PET/CT imaging
Incidence of documented arrhythmic events during the 6 months following baseline 68Ga-DOTA-SA-FAPI PET/CT imaging.
Within 6 months after PET/CT imaging
Diagnostic Concordance Rate Between FAPI PET/CT and Previously Obtained Cardiac Magnetic Resonance Imaging
기간: At baseline
Concordance rate between myocardial abnormalities detected by 68Ga-DOTA-SA-FAPI PET/CT and fibrosis-related abnormalities identified on previously obtained cardiac magnetic resonance imaging.
At baseline
Diagnostic Concordance Between FAPI PET/CT and Established ARVC Evaluation
기간: At baseline
Exploratory comparison of myocardial 68Ga-DOTA-SA-FAPI PET/CT findings with established diagnostic evaluation based on clinical assessment and conventional multimodality imaging in ARVC.
At baseline
Correlation Between Myocardial FAPI PET/CT Uptake and Electrocardiographic Abnormalities on 12-Lead Electrocardiography
기간: At baseline
Correlation between myocardial 68Ga-DOTA-SA-FAPI uptake on PET/CT and predefined electrocardiographic abnormalities of ARVC on baseline 12-lead electrocardiography, including T-wave inversion, epsilon wave, and QRS prolongation.
At baseline

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여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

간행물 및 유용한 링크

연구에 대한 정보 입력을 담당하는 사람이 자발적으로 이러한 간행물을 제공합니다. 이것은 연구와 관련된 모든 것에 관한 것일 수 있습니다.

일반 간행물

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (실제)

2025년 4월 16일

기본 완료 (추정된)

2026년 8월 25일

연구 완료 (추정된)

2026년 10월 26일

연구 등록 날짜

최초 제출

2026년 4월 22일

QC 기준을 충족하는 최초 제출

2026년 4월 30일

처음 게시됨 (실제)

2026년 5월 4일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 5월 4일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 4월 30일

마지막으로 확인됨

2026년 4월 1일

추가 정보

이 연구와 관련된 용어

개별 참가자 데이터(IPD) 계획

개별 참가자 데이터(IPD)를 공유할 계획입니까?

미정

IPD 계획 설명

Individual participant data sharing has not yet been determined. Any future data sharing will be considered in accordance with institutional policies, ethics committee approval, participant confidentiality, and applicable data protection regulations.

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

아니

미국 FDA 규제 기기 제품 연구

아니

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

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