About this trial
The investigator will use a technology called PET-CT that combines a Positron Emission Tomography (PET) scan with a computed tomography (CT) scan. This combined imaging test, where PET and CT data are gathered at one time, will be performed on an integrated PET-CT scanner located at Princess Margaret Cancer Centre.
The purpose of this study is to find out if the use of 68Ga-PNT6555 (FAPI) PET-CT will improve the assessment of disease extent as compared to routine CT scans.
Eligibility criteria
Qualifiers
Age ≥18 years.
Cytological or histological diagnosis of HGSOC, or clinical suspicion of HGSOC based on symptoms, physical exam, tumour markers, and imaging findings.
Clinical stage III or IV, being considered for PCS or NACT.
Contrast-enhanced CT abdomen and pelvis within 6 weeks of PET (prior to enrolment).
Disqualifiers
Inability to provide informed consent.
Contraindications for PET examination as per institutional safety guidelines, including but not limited to pregnancy, or inability to lie still for PET examination.
Evidence of the following epithelial ovarian cancer histological subtypes: Mucinous, low-grade serous, low-grade endometrioid, and low-malignant potential tumours.
Non-ovarian advanced gynecological malignancy
Trial design
Treatments tested in this trial
- FAPI PET CT