Context: Phosphaturic mesenchymal tumors (PMTs) are small, typically difficult to localize, and express somatostatin receptors. Recent work suggests imaging studies using Gallium (Ga)-conjugated somatostatin peptide analogues, such as 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid (DOTA)TATE, which enables somatostatin receptor imaging with positron emission tomography (PET), may be useful at identifying these tumors.
Objective: Our objective was to evaluate the use of Ga-DOTATATE PET/computed tomography (CT) for tumor localization in tumor-induced osteomalacia (TIO).
Design: This was a single-center prospective study of patients with TIO.
Setting: The study was conducted at the National Institutes of Health Clinical Center between February 2014 and February 2015.
Subjects: Eleven subjects (six females, five males) with TIO were included.
Intervention: Subjects underwent Ga-DOTATATE PET/CT in addition to In-pentetreotide single-photon emission CT (Octreoscan- SPECT/CT) and fluorodeoxyglucose-PET/CT (F FDG-PET/CT) scan.
Main Outcome Measures: Localization of PMTs on the previously described imaging modalities were determined.
Results: The tumor was successfully localized in 6/11 (54.5%) subjects (one was metastatic). The tumor was identified by Ga-DOTATATE in all six cases. Both Octreoscan-SPECT/CT and F FDG-PET each identified the tumor in 4/6. In no cases was Ga-DOTATATE the only imaging study to identify the tumor.
Conclusions: In this first prospective study comparing Ga-DOTATATE PET/CT to Octreoscan-SPECT/CT and F FDG-PET in TIO localization, Ga-DOTATATE PET/CT demonstrated the greatest sensitivity and specificity, suggesting that it may be the best single study for localization of PMTs in TIO.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5052344 | PMC |
http://dx.doi.org/10.1210/jc.2016-2052 | DOI Listing |
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