37 research outputs found

    Accuracy of [<sup>18</sup>F]FDG PET/MRI for the Detection of Liver Metastases

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    <div><p>Background</p><p>The aim of this study was to compare the diagnostic accuracy of [<sup>18</sup>F]FDG-PET/MRI with PET/CT for the detection of liver metastases.</p><p>Methods</p><p>32 patients with solid malignancies underwent [<sup>18</sup>F]FDG-PET/CT and subsequent PET/MRI of the liver. Two readers assessed both datasets regarding lesion characterization (benign, indeterminate, malignant), conspicuity and diagnostic confidence. An imaging follow-up (mean interval: 185±92 days) and/-or histopathological specimen served as standards of reference. Sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV) were calculated for both modalities. Accuracy was determined by calculating the area under the receiver operating characteristic (ROC) curve. Values of conspicuity and diagnostic confidence were compared using Wilcoxon-signed-rank test.</p><p>Results</p><p>The standard of reference revealed 113 liver lesions in 26 patients (malignant: n = 45; benign: n = 68). For PET/MRI a higher accuracy (PET/CT: 82.4%; PET/MRI: 96.1%; p<0.001) as well as sensitivity (67.8% vs. 92.2%, p<0.01) and NPV (82.0% vs. 95.1%, p<0.05) were observed. PET/MRI offered higher lesion conspicuity (PET/CT: 2.0±1.1 [median: 2; range 0–3]; PET/MRI: 2.8±0.5 [median: 3; range 0–3]; p<0.001) and diagnostic confidence (PET/CT: 2.0±0.8 [median: 2; range: 1–3]; PET/MRI 2.6±0.6 [median: 3; range: 1–3]; p<0.001). Furthermore, PET/MRI enabled the detection of additional PET-negative metastases (reader 1: 10; reader 2: 12).</p><p>Conclusions</p><p>PET/MRI offers higher diagnostic accuracy compared to PET/CT for the detection of liver metastases.</p></div

    Acquisition parameters for the applied MR-sequences (A-F).

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    <p>A) A coronal T1w in and opposed phase Volumetric Interpolated Breath-hold Examination (VIBE) for calculation of the Dixon-based fat-/water-images as well as the μ-map.</p><p>B) An axial, pre-contrast T1w Fast Low Angle Shot (FLASH).</p><p>C) An axial T2w 2D half Fourier acquisition single shot turbo spin echo (HASTE).</p><p>D) An axial diffusion weighted echo planar sequence (EPI DWI) with B values of 0, 500 and 1000 s/mm<sup>2</sup>.</p><p>E) An axial T2w fat saturated turbo spin echo (TSE) sequence in breath-hold.</p><p>F) A dynamic axial T1w VIBE. Four repetitive scans were performed (pre-contrast, arterial phase [20s delay], portal venous phase [60 sec delay], venous phase [100 sec delay]) after i.v.-injection of 0.1 ml/kg body weight Gadobutrol (Gadovist®, Bayer Healthcare, Berlin, Germany).</p><p>G) An axial post-contrast T1w FLASH.</p><p>Acquisition parameters for the applied MR-sequences (A-F).</p

    Patient without liver metastases.

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    <p>PET/CT with a false positive result showing a hypodense pseudolesion with a diameter 9 mm in the CT dataset without correlate in PET. In the later acquired PET/MRI (C-E) no correlate in PET nor in the morphological datasets (D: T1w VIBE portal-venous phase; E: T2w TSE fs).</p

    Patient with breast cancer.

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    <p>Both PET/CT (A,B) as well as PET/MRI (C; D; VIBE, portal venous phase) show a lesion with elevated FDG-uptake and ill-defined lesion borders as well as central contrast enhancement as signs of malignancy. Based on these findings the lesion was correctly identified as metastasis in both modalities.</p
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