OncoMatch

OncoMatch/Clinical Trials/NCT06914999

Comparing an Investigational Scan (F-18 NaF PET/CT) to Standard of Care Imaging (F-18 FDG PET/CT) for Evaluating Vascular Complications in Patients Receiving Radiation Therapy for Head and Neck Cancer

Is NCT06914999 recruiting? Yes, currently enrolling (May 2026). This Early Phase 1 trial studies Sodium Fluoride F-18 for clinical stage i hpv-mediated (p16-positive) oropharyngeal carcinoma ajcc v8.

Early Phase 1RecruitingEmory UniversityNCT06914999Data as of May 2026

Treatment: Sodium Fluoride F-18This early phase I trial compares sodium fluoride F-18 (F-18 NaF) positron emission tomography (PET)/computed tomography (CT) to the standard of care imaging scan (and fludeoxyglucose F-18 \[F-18 FDG\] PET/CT) for assessing the effects radiation therapy has on the blood vessels in the neck in patients with head and neck cancers. For people with cancers in the head and neck, doctors often use radiation to target both the tumor and nearby glands. Radiation therapy to this region can affect the blood vessels in the neck that supply blood to the brain. F-18 NaF and F-18 FDG are contrast agents that can be used together with PET/CT imaging to visualize areas inside the body. A PET scan is a procedure in which a small amount of radioactive glucose (sugar) is injected into a vein, and a scanner is used to make detailed, computerized pictures of areas inside the body where the glucose is taken up. A CT scan is a procedure that uses a computer linked to an x-ray machine to make a series of detailed pictures of areas inside the body. The pictures are taken from different angles and are used to create 3-dimensional views of tissues and organs. Combining a PET scan with a CT scan can help make the image easier to interpret. PET/CT scans are hybrid scanners that combine both modalities into a single scan during the same examination. Imaging with F-18 NaF PET/CT may be as effective or more effective than the standard F-18 FDG PET/CT for assessing the effects radiation therapy has on blood vessels in the neck in patients with head and neck cancers.

Check if I qualify

Extracted eligibility criteria

Cancer type

Head and Neck Squamous Cell Carcinoma

Biomarker criteria

Required: CDKN2A p16-negative (negative)

Required: CDKN2A p16-positive (positive)

Disease stage

Required: Stage III, IVB, I, II (AJCC 8th edition)

clinical stage III-IVb (American Joint Committee on Cancer [AJCC] 8th edition) ... or clinical stage I-III (AJCC 8th edition) HPV-associated squamous cell carcinoma of the oropharynx

Prior therapy

No prior treatment (treatment-naive required)
Max 0 prior lines

Cannot have received: chemotherapy

Patients who have had chemotherapy ... within 4 weeks prior to entering the study

Cannot have received: radiotherapy

Patients who have had ... radiotherapy within 4 weeks prior to entering the study

Cannot have received: immunotherapy

Patients planned to receive any immunotherapy agent during their radiotherapy or in the interval between radiotherapy and post-RT PET/CT imaging

Cannot have received: investigational agent

Patients who are receiving any other investigational agents or an investigational device within 21 days before administration of the F-18 NaF for the pre-RT PET/CT imaging

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • Emory University Hospital Midtown · Atlanta, Georgia

Showing up to 5 US sites. See all sites on ClinicalTrials.gov →

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

Check if I qualify