FAPI PET/CT for Ovarian Cancer
(FAST HOC Trial)
What You Need to Know Before You Apply
What is the purpose of 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.
Are You a Good Fit for This Trial?
This trial is for people with suspected or confirmed high-grade serous ovarian cancer (HGSOC) at stage III or IV, who are being considered for surgery or chemotherapy. Participants must have had a recent contrast CT scan of the abdomen and pelvis within the last 6 weeks.Inclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Initial PET/CT Scan
Participants undergo an initial PET/CT scan to assess disease extent
Follow-up PET/CT Scan
Participants undergo a follow-up PET/CT scan within six weeks of the initial scan
Follow-up
Participants are monitored for safety and effectiveness after scans
What Are the Treatments Tested in This Trial?
Interventions
- 68Ga-PNT6555 (FAPI) PET-CT
Trial Overview
The study is testing whether a new imaging method called FAPI PET-CT can better show how far ovarian cancer has spread compared to standard CT scans. All participants will receive this special PET-CT scan.
How Is the Trial Designed?
1
Treatment groups
Experimental Treatment
individuals who have been diagnosed or are suspected to have high-grade serous ovarian cancers (HGSOC). They must have had a CT scan of their abdomen and pelvis within 6 weeks before enrolling in the study and be at clinical stage III or IV.
Find a Clinic Near You
Who Is Running the Clinical Trial?
University Health Network, Toronto
Lead Sponsor
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