<sup>68</sup>Ga-PSMA PET/CT for Response Evaluation of <sup>223</sup>Ra Treatment in Metastatic Prostate Cancer.

de Jong, Anouk C; Segbers, Marcel; Ling, Sui Wai; Graven, Laura H; Mehra, Niven; Hamberg, Paul; Brabander, Tessa; de Wit, Ronald et al. · J Nucl Med · 2023

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Abstract

CT and bone scintigraphy are not useful for response evaluation of bone metastases to <sup>223</sup>Ra treatment in metastatic castration-resistant prostate cancer (mCRPC). PET using <sup>68</sup>Ga prostate-specific membrane antigen 11 (<sup>68</sup>Ga-PSMA) is a promising tool for response evaluation of mCRPC. The aim of this study was to determine the utility of <sup>68</sup>Ga-PSMA PET/CT for response evaluation of <sup>223</sup>Ra treatment in patients with mCRPC. <b>Methods:</b> Within this prospective, multicenter, imaging discovery study, 28 patients with mCRPC, eligible for <sup>223</sup>Ra treatment, were included between 2019 and 2022. Patients received <sup>223</sup>Ra according to the standard of care. Study procedures included CT, bone scintigraphy, and <sup>68</sup>Ga-PSMA PET/CT at baseline, after 3 and 6 cycles of <sup>223</sup>Ra treatment, and on treatment failure. Response to <sup>223</sup>Ra treatment was visually assessed on all 3 imaging modalities. Total tumor volume within bone (TTV<sub>bone</sub>) was determined on <sup>68</sup>Ga-PSMA PET/CT. Intrapatient heterogeneity in response was studied using a newly developed image-registration tool for sequential images of PET/CT. Results were compared with failure-free survival (good responders vs. poor responders; cutoff, 24 wk) and alkaline phosphatase (ALP) response after 3 cycles. <b>Results:</b> Visual response assessment criteria could not distinguish good responders from poor responders on <sup>68</sup>Ga-PSMA PET/CT and bone scintigraphy. For <sup>68</sup>Ga-PSMA PET/CT, TTV<sub>bone</sub> at baseline was lower in good responders than in poor responders, whereas TTV<sub>bone</sub> increased in both groups during treatment. TTV<sub>bone</sub> was higher in patients with new extraosseous metastases during <sup>223</sup>Ra treatment. Although TTV<sub>bone</sub> and ALP correlated at baseline, changes in TTV<sub>bone</sub> and ALP on treatment did not. <sup>68</sup>Ga-PSMA response of TTV<sub>bone</sub> showed intrapatient heterogeneity in most patients. <b>Conclusion:</b> mCRPC patients with lower TTV<sub>bone</sub> on <sup>68</sup>Ga-PSMA PET/CT have the best clinical outcome after <sup>223</sup>Ra treatment. Response is highly heterogeneous in most patients. A decrease in ALP, which occurred in most patients, was not correlated with a decrease in TTV<sub>bone</sub>, which might make one question the value of ALP for disease monitoring during <sup>223</sup>Ra treatment in clinical practice.

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