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PET/CT Imaging of Differentiated and Medullary Thyroid Carcinoma Using the Novel SSTR-targeting Peptide [F]SiTATE - First Clinical Experiences

Abstract

Purpose: The novel F-labeled somatostatin receptor (SSTR)-directed radiotracer [F]SiTATE demonstrated promising results for the imaging of various SSTR-expressing tumor types. Although thyroid carcinomas (TC) express SSTR, data on [F]SiTATE PET/CT imaging in TC are lacking. This study explores the use of [F]SiTATE PET/CT in a patient cohort with histologically proven TC.

Methods: As part of a prospective observational study at a single tertiary cancer center, 21 patients with TC (10 medullary (MTC) and 11 differentiated (DTC)) who underwent at least one [F]SiTATE PET/CT were included (37 scans in total). Mean SUV and SUV of tumoral lesions, mean total-tumor-volume (TTV), and whole-body (WB)-SUV and WB-SUV on PET with their standard deviations (SDs) were determined. PET parameters were correlated to clinical parameters including tumor marker levels (thyroglobulin for DTC, calcitonin for MTC).

Results: 89 lesions were included in the analysis. Metastases were localized in the bone, lymph nodes, lung, soft tissue, and thyroid bed. Osseous (31 lesions; SUV 8.6 ± 8.0; SUV 5.8 ± 5.4) and nodal (37 lesions; SUV 8.7 ± 7.8; SUV 5.7 ± 5.4) metastases showed the highest uptake. The MTC disease burden on PET significantly correlated with the calcitonin tumor marker level (e.g., TTV: r = 0.771, r = 0.594, p = 0.002). For DTC, no such correlation was present.

Conclusion: Our data demonstrate high feasibility of [F]SiTATE PET/CT in a small cohort of patients with MTC and DTC. The use of [F]SiTATE may overcome logistical disadvantages of Ga-based tracers and facilitate SSTR-targeted PET/CT imaging of thyroid carcinoma.

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