Sporadic Primary Pheochromocytoma: A Prospective Intraindividual Comparison of Six Imaging Tests (CT, MRI, and PET/CT Using <sup>68</sup>Ga-DOTATATE, FDG, <sup>18</sup>F-FDOPA, and <sup>18</sup>F-FDA).
prospective_cohort · Level II
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- Record sourced from PubMed, PMID 34431366.
- Also identified by DOI 10.2214/AJR.21.26071 and PMC identifier 10389669.
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Abstract
<b>BACKGROUND</b>. Recent professional society guidelines for radionuclide imaging of sporadic pheochromocytoma (PHEO) recommend <sup>18</sup>F-fluorodihydroxyphenylala-nine (<sup>18</sup>F-FDOPA) as the radiotracer of choice, deeming <sup>68</sup>Ga-DOTATATE and FDG to be second- and third-line agents, respectively. An additional agent, <sup>18</sup>F-fluorodopamine (<sup>18</sup>F-FDA), remains experimental for PHEO detection. A paucity of research has performed head-to-head comparison among these agents. <b>OBJECTIVE</b>. The purpose of this study was to perform an intraindividual comparison of <sup>68</sup>Ga-DOTATATE PET/CT, FDG PET/CT, <sup>18</sup>F-FDOPA PET/CT, <sup>18</sup>F-FDA PET/CT, CT, and MRI in visualization of sporadic primary PHEO. <b>METHODS</b>. This prospective study enrolled patients referred with clinical suspicion for sporadic PHEO. Patients were scheduled for <sup>68</sup>Ga-DOTATATE PET/CT, FDG PET/CT, <sup>18</sup>F-FDOPA PET/CT, <sup>18</sup>F-FDA PET/CT, whole-body staging CT (portal venous phase), and MRI within a 3-month period. PET/CT examinations were reviewed by two nuclear medicine physicians, and CT and MRI were reviewed by two radiologists; differences were resolved by consensus. Readers scored lesions in terms of confidence in diagnosis of PHEO (1-5 scale; 4-5 considered positive for PHEO). Lesion-to-liver SUV<sub>max</sub> was computed using both readers' measurements. Interreader agreement was assessed using intraclass correlation coefficients (ICCs) for SUV<sub>max</sub>. Analysis included only patients with histologically confirmed PHEO on resection. <b>RESULTS</b>. The analysis included 14 patients (eight women, six men; mean age, 52.4 ± 16.8 [SD] years) with PHEO. Both <sup>68</sup>Ga-DOTATATE PET/CT and FDG PET/CT were completed in all 14 patients, <sup>18</sup>F-FDOPA PET/CT in 11, <sup>18</sup>F-FDA PET/CT in 7, CT in 12, and MRI in 12. Mean conspicuity score for PHEO was 5.0 ± 0.0 for <sup>18</sup>F-FDOPA PET/CT, 4.7 ± 0.5 for MRI, 4.6 ± 0.8 for <sup>18</sup>F-FDA PET/CT, 4.4 ± 1.0 for <sup>68</sup>Ga-DOTATATE PET/CT, 4.3 ± 1.0 for CT, and 4.1 ± 1.5 for FDG PET/CT. The positivity rate for PHEO was 100.0% (11/11) for <sup>18</sup>F-FDOPA PET/CT, 100.0% (12/12) for MRI, 85.7% (6/7) for <sup>18</sup>F-FDA PET/CT, 78.6% (11/14) for FDG PET/CT, 78.6% (11/14) for <sup>68</sup>Ga-DOTATATE PET/CT, and 66.7% (8/12) for CT. Lesion-to-liver SUV<sub>max</sub> was 10.5 for <sup>18</sup>F-FDOPA versus 3.0-4.2 for the other tracers. Interreader agreement across modalities ranged from 85.7% to 100.0% for lesion positivity with ICCs of 0.55-1.00 for SUV<sub>max</sub> measurements. <b>CONCLUSION</b>. Findings from this small intraindividual comparative study support <sup>18</sup>F-FDOPA PET/CT as a preferred first-line imaging modality in evaluation of sporadic PHEO. <b>CLINICAL IMPACT</b>. This study provides data supporting current guidelines for imaging evaluation of suspected PHEO. <b>TRIAL REGISTRATION</b>. ClinicalTrials.gov NCT00004847.
Medical subject headings
- Adrenal Gland Neoplasms
- Fluorodeoxyglucose F18
- Gallium Radioisotopes
- Magnetic Resonance Imaging
- Pheochromocytoma
- Positron Emission Tomography Computed Tomography
- Radiopharmaceuticals