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Value of F-FDG Hybrid PET/MR in Differentiated Thyroid Cancer Patients with Negative I Whole-Body Scan and Elevated Thyroglobulin Levels. | LitMetric

Value of F-FDG Hybrid PET/MR in Differentiated Thyroid Cancer Patients with Negative I Whole-Body Scan and Elevated Thyroglobulin Levels.

Cancer Manag Res

Department of Nuclear Medicine, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, People's Republic of China.

Published: March 2021

Purpose: To evaluate the diagnostic performance of F-FDG PET/MR in detecting recurrent or metastatic disease in patients with differentiated thyroid cancer (DTC) who have increased thyroglobulin (Tg) levels but a negative I whole-body scan (WBS). The relationship between F-FDG PET/MR and serum Tg levels was explored. We also evaluated the therapeutic impact of PET/MR on patient clinical management.

Patients And Methods: Twenty-nine DTC patients with a negative I-WBS of the last post-therapeutic and increased Tg levels under thyroid-stimulating hormone suppression treatment who underwent F-FDG PET/MR examination were retrospectively analyzed.

Results: Of those 29 patients, F-FDG PET/MR findings were true positive, true negative, false positive, and false negative in 18, 7, 2, and 2 patients, respectively. The overall sensitivity, specificity, and accuracy were 90.0%, 77.8%, and 86.2%, respectively. We noticed significant differences in serum Tg levels between the PET/MR-positive and PET/MR-negative patient groups (=0.049). Receiver operating characteristic curve analysis showed that a Tg level of 2.4 ng/mL was the optimal cut-off value for predicting PET/MR results. The sensitivity, specificity, and accuracy of PET/MR were higher in patients with Tg levels greater than 2.4 ng/mL than in patients with lower levels. By detecting recurrent or metastatic disease, F-FDG PET/MR altered the clinical management in 7 patients (24.1%) of the overall population.

Conclusion: F-FDG PET/MR has high diagnostic accuracy for detecting recurrent or metastatic diseases in DTC patients and is useful for clinical management.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8018385PMC
http://dx.doi.org/10.2147/CMAR.S293005DOI Listing

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