Refining the clinical utility of [<sup>177</sup>Lu]Lu/[<sup>225</sup>Ac]Ac-PSMA tandem RLT in patients with metastatic castration resistant prostate cancer.
retrospective_cohort · Level III
Where this comes from
- Record sourced from PubMed, PMID 41174098.
- Also identified by DOI 10.1007/s00259-025-07632-1 and PMC identifier 12920758.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
This study aimed to evaluate the efficacy and safety of Lutetium-177/Actinium-225 prostate-specific membrane antigen tandem radioligand therapy ([<sup>177</sup>Lu]Lu/[<sup>225</sup>Ac]Ac-PSMA tandem RLT) and to explore clinical and imaging-based predictors of treatment response to support individualized patient selection. This retrospective, single-center study included 23 patients with mCRPC who underwent Fluor-18 ([<sup>18</sup>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. 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<sub>mean</sub>]) had a higher response rate (86%; 6 out of 7) compared to those with decreased SUV<sub>mean</sub> (31%; 5 out of 16). In Cox regression analysis, SUV<sub>mean</sub> 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<sub>mean</sub> as the strongest PR (P = 0.003). [<sup>177</sup>Lu]Lu/[<sup>225</sup>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.
Medical subject headings
- Prostatic Neoplasms, Castration-Resistant
- Lutetium
- Actinium