Early Diagnosis of Therapy-associated Cardiotoxicity Basing on Multi-tracer Multimodality PET/MRI

NCT ID: NCT04555642

Last Updated: 2021-02-26

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

120 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-09-15

Study Completion Date

2022-02-28

Brief Summary

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Using Multi-tracer to early diagnosis of therapy-associated cardiotoxicity using multimodality PET/MRI.

Detailed Description

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In this study investigators evaluated cardiac uptake by different molecular probe such as FDG, FAPI-04 using multimodality PET/MRI. Previous studies have shown that increased cardiac uptake of FDG on PET may be an indicator of myocardial injury after chemotherapy. Cardiac magnetic resonance (CMR) allows for multiparametric evaluation of cardiac morphology, ventricular function, myocardial perfusion, and viability. The combination of PET with MR (PET/MR) is therefore an alternative attractive pairing for diagnostic imaging. The aim of this study is to find noninvasive and effective method for early diagnosis of cardiotoxicity after chemotherapy or immunotherapy

Conditions

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Positron-Emission Tomography Magnetic Resonance Imaging

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Study Groups

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therapy group

lymphoma patients planned chemotherapy or immunotherapy scheme

No interventions assigned to this group

healthy control group

Inclusion criteria for the controls were no known diseases or syndromes, within the age range from 18 to 35 years.

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* availability of a clinical pre- and post-therapy clinical evaluation encompassing electrocardiogram (ECG) ;
* normal findings at pre-therapy clinical evaluation;
* cancer planned chemotherapy or immunotherapy scheme ;
* available staging FDG-PET/CT scan (PET0);

Exclusion Criteria

* cannot lie supine for half an hour;
* refuse to join the clinical researcher;
* without metal implants.
Minimum Eligible Age

18 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Peking University Cancer Hospital & Institute

OTHER

Sponsor Role lead

Responsible Party

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Xuejuan Wang,MD

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Zhi Yang, PhD

Role: STUDY_DIRECTOR

Peking University Cancer Hospital & Institute

Locations

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Peking University Cancer Hospital

Beijing, Beijing Municipality, China

Site Status RECRUITING

Countries

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China

Central Contacts

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Xuejuan Wang, MD

Role: CONTACT

86 010 88196363

Facility Contacts

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Xuejuan Wang, MD

Role: primary

86 10-88196363

Other Identifiers

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XW-Heart-001

Identifier Type: -

Identifier Source: org_study_id

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