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Early Diagnosis of Therapy-associated Cardiotoxicity Basing on PET/CT in Lymphoma

Early Diagnosis of Therapy-associated Cardiotoxicity Basing on PET/CT in Lymphoma

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05411250
Enrollment
40
Registered
2022-06-09
Start date
2022-06-01
Completion date
2023-07-31
Last updated
2022-06-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Positron-Emission Tomography

Keywords

cardiotoxicity, early

Brief summary

To explore the value of 18F-fluorodeoxyglucose (FDG) PET/CT imaging in early diagnosis of treatment-related cardiotoxicity (TACT) of lymphoma using visual method and semi-quantitative method.

Detailed description

First of all, the cardiac 18F-FDG uptake in patients with lymphoma will be observed by visual method: according to the uptake site, it will be divided into left ventricular uptake and biventricular uptake, and according to the degree of uptake, it will be divided into equal uptake (myocardial uptake is lower than cardiac blood pool uptake), moderate uptake (myocardial uptake is between cardiac blood pool uptake and liver uptake) and high uptake (myocardial uptake is higher than liver uptake). According to the uptake pattern, it can be divided into diffuse and segmental uptake.Then,using the region of interest method to mesure the value of myocardial uptake of 18F-FDG.The difference value of heart's SUVmax (Δ SUVmax- heart) and% Δ SUVmax- heart before and after chemotherapy or immunotherapy will be calculated. And SUVmax- heart / SUVmax- mediastinum ratio, SUVmax- heart / SUVmax- liver ratio and SUVmax- heart / SUVmax- background ratio (left gluteal muscle) after treatment. Taking the abnormality of ECG (early TACT) as the end point.

Interventions

None listed

Sponsors

Peking University Cancer Hospital & Institute
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

1. No previous history of heart disease. 2. normal echocardiography, ECG and laboratory tests (creatine kinase, myoglobin, troponin, brain natriuretic peptide) before treatment. 3.18F-FDG PET/CT examination before and after treatment \-

Exclusion criteria

1.receiving radiotherapy and chemotherapy at the same time. 2.previous chest radiotherapy. 3. with severe hepatic or renal dysfunction. \-

Design outcomes

Primary

MeasureTime frameDescription
SUVmax150 daysthe standardized uptake value

Secondary

MeasureTime frameDescription
SUVR150 daysthe ratio of the standardized uptake value for the heart to the normal tissue such as hepatic blood poor and gluteus

Contacts

Primary ContactXuejuan Wang, MD
xuejuan_wang@hotmail.com8601088196363

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026