PET/MR Pre- and Post Radiotherapy for Cardiopulmonary Dysfunction Evaluation
Recruiting now NCT04901884
Run by University Health Network, Toronto · for 18 and older · All sexes
What this study is about
Radiotherapy (RT) is a well-known and established therapy or adjuvant therapy for the treatment of thoracic cancer It uses a high energy radiation from x-rays, gamma rays and other charged particles that assist in damaging the cancer DNA. PET/MR as imaging biomarkers for cardiopulmonary dysfunction with a focus on Pulmonary hypertension (PH). Despite the measures taken to reduce the total radiation dose and to limit the radiation to normal tissues, there is evidence of transient or permanent radiotherapy induced myocardial and pulmonary dysfunction leading to PH in patients who receive radiotherapy above a certain threshold of received dose. To be able to Demonstrate correlation of combined PET/MR and plasma metabolomics markers in patients at risk of developing cardiopulmonary disfunction after RT.
Who can join (things the study team will check)
✅ You may be able to join if…
- Age ≥18 years
- Biopsy or otherwise clinically proven thoracic malignant mass which is intended to be treated with radio(chemo)therapy
- Intention to treat with radio(chemo)therapy with incidental cardiac irradiation of at least 25Gy.
- A negative urine or serum pregnancy test within the two week interval immediately prior to imaging, in women of child-bearing age.
- Ability to provide written informed consent to participate in the study (for all components of the trial: imaging with cardiac PET/MR, blood sampling for plasma metabolomics and circulating DNA).
🚫 You may not be able to join if…
- Contraindication for MR as per current institutional guidelines.
- Contraindication for Gadolinium injection as per current institutional guidelines.
- Inability to lie supine for at least 45 minutes.
- Any patient who is pregnant or breastfeeding.
- Any patient with known hypersensitivity to 18F-FDG.
Where this trial is running
- University Health Network, Toronto, Ontario, Canada
Who to contact
Patrick Veit-Haibach, MD · 416-340-4800 · Patrick.Veit-Haibach@uhn.ca
It's completely normal to call and ask questions before deciding anything. Mention the study ID: NCT04901884.
Verify everything on the official ClinicalTrials.gov record. Page updated July 2026.