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RECRUITINGINTERVENTIONAL

F-18 Tetrafluoroborate PET/CT in Differentiated Thyroid Cancer

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

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.

Who May Be Eligible (Plain English)

Who May Qualify: - 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 willing to sign a consent form Who Should NOT Join This Trial: - Age under 18 years - Pregnancy or breastfeeding - Failure to provide written willing to sign a consent form Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: * 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 Exclusion Criteria: * Age under 18 years * Pregnancy or breastfeeding * Failure to provide written informed consent

Treatments Being Tested

DIAGNOSTIC_TEST

F-18-Tetrafluoroborate PET/CT

F-18-Tetrafluoroborate whole body PET/CT

Locations (2)

Ankara University Medical School Nuclear Medicine Department
Ankara, Ankara, Turkey (Türkiye)
Hacettepe University Medical School Nuclear Medicine Department
Ankara, Ankara, Turkey (Türkiye)