Liam Widjaja, Johannes Hornfeck, Sophie C. Siegmund, F.J. Gildehaus, Nina-Sophie Schmidt-Hegemann, Vera Wenter, Gabriel T. Sheikh, Konrad Klimek, Jozefina Casuscelli, Christian G. Stief, Mathias J. Zacherl, Rudolf A. Werner
Abstract Purpose This study aimed to evaluate the efficacy and safety of Lutetium-177/Actinium-225 prostate-specific membrane antigen tandem radioligand therapy ([ 177 Lu]Lu/[ 225 Ac]Ac-PSMA tandem RLT) and to explore clinical and imaging-based predictors of treatment response to support individualized patient selection. Methods This retrospective, single-center study included 23 patients with mCRPC who underwent Fluor-18 ([ 18 F]F)-PSMA-1007 positron emission tomography/computed tomography (PET/CT) and subsequent tandem RLT. Whole-body tumor segmentation on PET/CT and standard laboratory values were acquired before treatment initiation. Primary endpoint was partial response (PR), defined as either a decline in prostate specific antigen of ≥ 50% (according to prostate cancer clinical trial working group) or PET-based response according to Response Evaluation Criteria on PSMA PET/CT. Safety assessment included renal and hematological side effects following common terminology criteria of adverse events version 5. Results Following two cycles of tandem RLT, 11 patients (48%) achieved a PR. The treatment was generally tolerated well. Grade 3 events included renal impairment in two (9%) and grade 3 anemia in five (22%) patients, while no Grade 4/5 events occurred. Patients with increased PSMA expression on pretherapeutic PET (defined by the average mean standardized uptake value of all tumor lesions [SUV mean ]) had a higher response rate (86%; 6 out of 7) compared to those with decreased SUV mean (31%; 5 out of 16). In Cox regression analysis, SUV mean was significantly associated with PR with a hazard ratio of 1.34 (95% CI, 1.01–1.77; P = 0.042). PSMA-tumor volume ( P = 0.036) and total lesion-PSMA ( P = 0.041) were also significant predictors, whereas none of the clinical parameters showed predictive value. Kaplan-Meier analysis further confirmed SUV mean as the strongest PR ( P = 0.003). Conclusion [ 177 Lu]Lu/[ 225 Ac]Ac-PSMA tandem RLT may offer a safe, effective treatment option. Assessment of PSMA expression on pretherapeutic PET predicts response, supporting its use in guiding personalized treatment.