<sup>68</sup>Ga-FAPI as a Diagnostic Tool in Sarcoma: Data from the <sup>68</sup>Ga-FAPI PET Prospective Observational Trial.

Kessler, Lukas; Ferdinandus, Justin; Hirmas, Nader; Bauer, Sebastian; Dirksen, Uta; Zarrad, Fadi; Nader, Michael; Chodyla, Michal et al. · J Nucl Med · 2022

prospective_cohort · Level II

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Abstract

Bone and soft-tissue sarcomas express fibroblast activation protein (FAP) on tumor cells and associated fibroblasts. Therefore, FAP is a promising therapeutic and diagnostic target. Novel radiolabeled FAP inhibitors (e.g., <sup>68</sup>Ga-FAPI-46) have shown high tumor uptake on PET in sarcoma patients. Here, we report the endpoints of the <sup>68</sup>Ga-FAPI PET prospective observational trial. <b>Methods:</b> Forty-seven patients with bone or soft-tissue sarcomas undergoing clinical <sup>68</sup>Ga-FAPI PET were eligible for enrollment into the <sup>68</sup>Ga-FAPI PET observational trial. Of these patients, 43 also underwent <sup>18</sup>F-FDG PET. The primary study endpoint was the association between <sup>68</sup>Ga-FAPI PET uptake intensity and histopathologic FAP expression analyzed with Spearman <i>r</i> correlation. Secondary endpoints were detection rate, positive predictive value (PPV), interreader reproducibility, and change in management. Datasets were interpreted by 2 masked readers. <b>Results:</b> The primary endpoint was met, and the association between <sup>68</sup>Ga-FAPI PET uptake intensity and histopathologic FAP expression was significant (Spearman <i>r</i> = 0.43; <i>P</i> = 0.03). By histopathologic validation, PPV was 1.00 (95% CI, 0.87-1.00) on a per-patient and 0.97 (95% CI, 0.84-1.00) on a per-region basis. In cases with histopathologic validation, 27 of 28 (96%) confirmed patients and 32 of 34 (94%) confirmed regions were PET-positive, resulting in an SE of 0.96 (95% CI, 0.82-1.00) on a per-patient and 0.94 (95% CI, 0.80-0.99) on a per-region basis. The detection rate on a per-patient basis in <sup>68</sup>Ga-FAPI and <sup>18</sup>F-FDG PET was 76.6% and 81.4%, respectively. In 8 (18.6%) patients, <sup>68</sup>Ga-FAPI PET resulted in an upstaging compared with <sup>18</sup>F-FDG PET. <sup>68</sup>Ga-FAPI PET readers showed substantial to almost perfect agreement for the defined regions (Fleiss κ: primary κ = 0.78, local nodal κ = 0.54, distant nodal κ = 0.91, lung κ = 0.86, bone κ = 0.69, and other κ = 0.65). Clinical management changed in 13 (30%) patients after <sup>68</sup>Ga-FAPI PET. <b>Conclusion:</b> We confirm an association between tumoral <sup>68</sup>Ga-FAPI PET uptake intensity and histopathologic FAP expression in sarcoma patients. Further, with masked readings and independent histopathologic validation, <sup>68</sup>Ga-FAPI PET had a high PPV and sensitivity for sarcoma staging.

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