Evaluation of 18F-TFB PET/CT Scan in Patients With Differentiated Thyroid Cancer

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorMayo Clinic

About this trial

This phase II study evaluates F-18 tetrafluoroborate (18F-TFB) PET/CT scan in patients with differentiated thyroid cancer. Diagnostic imaging is necessary for planning treatment, monitoring therapy response, and identifying sites of recurrent or metastatic disease in differentiated thyroid cancer. 18F-TFB PET/CT may accurately detect recurrent and metastatic thyroid cancer lesions, with the potential to provide information for patient management that is better than the current standard of care imaging practices.

Eligibility criteria

Qualifiers

Subject has biopsy-proven papillary or follicular thyroid cancer

Subject is clinically indicated for 123I-SPECT/CT total body iodine (TBI) scan

Subject agrees to undergo 18F-TFB PET/CT scan following TBI scan

Karnofsky performance status of >= 50 (or Eastern Cooperative Oncology Group [ECOG]/World Health Organization [WHO] equivalent)

Disqualifiers

Contrast-enhanced CT within 4 last weeks

Amiodarone within last 4 months

Ingested iodine, kelp tablets, Lugols iodine, or potassium iodide (SSKI) within 2 weeks

Unable to lie flat, still or tolerate a PET scan

Trial design

Treatments tested in this trial

  • Computed Tomography
  • Fluorine F 18 Tetrafluoroborate
  • Positron Emission Tomography
  • Survey Administration

Treatment groups

24 Participants
are divided into 1 treatment group

Sponsors and collaborators