Diagnostic potential of PET/CT using a <sup>68</sup>Ga-labelled prostate-specific membrane antigen ligand in whole-body staging of renal cell carcinoma: initial experience.

Sawicki, Lino M; Buchbender, Christian; Boos, Johannes; Giessing, Markus; Ermert, Johannes; Antke, Christina; Antoch, Gerald; Hautzel, Hubertus · Eur J Nucl Med Mol Imaging · 2017

case_series · Level IV

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Abstract

To evaluate the diagnostic potential of whole-body PET/CT using a <sup>68</sup>Ga-labelled PSMA ligand in renal cell carcinoma (RCC). Six patients with histopathologically proven RCC underwent <sup>68</sup>Ga-PSMA PET/CT. Each PET/CT scan was evaluated in relation to lesion count, location and dignity. SUVmax was measured in primary tumours and PET-positive metastases. Tumour-to-background SUVmax ratios (TBR<sub>SUVmax</sub>) were calculated for primary RCCs in relation to the surrounding normal renal parenchyma. Metastasis-to-background SUVmax ratios (MBR<sub>SUVmax</sub>) were calculated for PET-positive metastases in relation to gluteal muscle. Five primary RCCs and 16 metastases were evaluated. The mean SUVmax of the primary RCCs was 9.9 ± 9.2 (range 1.7 - 27.2). Due to high uptake in the surrounding renal parenchyma, the mean TBR<sub>SUVmax</sub> of the primary RCCs was only 0.2 ± 0.3 (range 0.02 - 0.7). Eight metastases showed focal <sup>68</sup>Ga-PSMA uptake (SUVmax 9.9 ± 8.3, range 3.4 - 25.6). The mean MBR<sub>SUVmax</sub> of these PET-positive metastases was 11.7 ± 0.2 (range 4.4 - 28.1). All PET-negative metastases were subcentimetre lung metastases. <sup>68</sup>Ga-PSMA PET/CT appears to be a promising method for detecting RCC metastases. However, no additional diagnostic value in assessing the primary tumour was found.

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