Thyroid Cancer Clinical Trials

Find Thyroid Cancer Clinical Trials Near You

F-18 Tetrafluoroborate PET/CT in Differentiated Thyroid Cancer

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Diagnostic test
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

In patients who have undergone surgery for differentiated thyroid cancer and who demonstrate elevated serum Tg and/or ATg levels during follow-up after radioactive iodine therapy, lesion detection is performed using neck ultrasonography, thorax CT, and F-18 FDG PET/CT. Diagnostic whole-body scanning with low-dose I-131 is not routinely recommended in follow-up due to its low sensitivity and specificity. F-18 TFB is a highly specific imaging agent for differentiated thyroid cancer, entering thyroid follicular epithelial cells via the sodium-iodide symporter (NIS), which is expressed on the cell surface and functions through a mechanism similar to that of I-131. As a PET radiotracer, F-18 TFB has been shown to be superior to I-131 in previous studies. The primary aim of this study is to comparatively evaluate the role of F-18 TFB PET/CT versus the standard imaging modality F-18 Fluorodeoxyglucose (FDG) PET/CT in lesion detection in patients with differentiated thyroid cancer who demonstrate elevated serum Tg and/or ATg levels during follow-up after radioactive iodine therapy. The secondary aims are to investigate the factors predicting F-18 TFB PET/CT positivity and to assess the relationship between the semi-quantitative and quantitative parameters derived from F-18 TFB PET/CT and serum thyroglobulin (Tg) and anti-thyroglobulin (ATg) levels.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Having undergone surgery for differentiated thyroid cancer and received radioactive iodine therapy

• Being evaluated for lesion detection due to elevated serum Tg and/or ATg levels during post-treatment follow-up

• Negative or equivocal I-131 whole-body scan findings

• Karnofsky Performance Status ≥ 50 (or equivalent Eastern Cooperative Oncology Group \[ECOG\]/World Health Organization \[WHO\] performance status)

• Giving written informed consent

Locations
Other Locations
Turkey
Ankara University Medical School Nuclear Medicine Department
RECRUITING
Ankara
Hacettepe University Medical School Nuclear Medicine Department
RECRUITING
Ankara
Contact Information
Primary
Mine Araz, Assoc.Prof.Dr.
minesoylu@yahoo.com
+905326667313
Time Frame
Start Date: 2025-11-01
Estimated Completion Date: 2026-10-01
Participants
Target number of participants: 50
Treatments
Experimental: F-18-TFB PET/CT arm
DTC patients who underwent F-18-TFB PET/CT
Related Therapeutic Areas
Sponsors
Leads: Ankara University

This content was sourced from clinicaltrials.gov

Similar Clinical Trials