[225Ac]Ac-PSMA for the treatment of metastatic castration-resistant prostate cancer: A systematic review and meta-analysis.

Abstract

Background: Approximately 10%-20% of prostate cancers progress to metastatic and castration-resistant forms (mCRPC). Radioligand (RLT) therapy with [¹⁷⁷Lu]Lu-prostate-specific membrane antigen (PSMA) is an approved treatment for metastasized mCRPC. Moreover, Actinium-225 (²²⁵Ac), an alpha-emitter isotope, has also been used to label PSMA and, recently, to treat mCRPC patients with encouraging results. However, robust clinical data on [²²⁵Ac]Ac-PSMA therapy and its comparison with [¹⁷⁷Lu]Lu-PSMA are still limited. Our aim was to evaluate the role of [²²⁵Ac]Ac-PSMA in treating mCRPC and compare it with conventional [¹⁷⁷Lu]Lu-PSMA therapy.

Methods: A systematic search was performed in PubMed, Web of Science, Scopus and the Cochrane Register of Controlled Trials from June 2023 to January 2024. This work was conducted in accordance with PRISMA guidelines.

Results: After screening and study selection according to PRISMA guidelines, 11 studies were included, 9 of which focused on [²²⁵Ac]Ac-PSMA only and two on tandem therapy ([²²⁵Ac]Ac-PSMA/[¹⁷⁷Lu]Lu-PSMA). Overall, the pooled proportion of PSA decline in patients was .85 (95% CI: .79-.91, p < .001); patients pretreated with [¹⁷⁷Lu]Lu-PSMA achieved a pooled proportion of PSA decline of .90 (95% CI: .82-.97, p < .001). In patients treated with tandem therapy, PSA decline was observed in approximately 90% of them, while PSA response rates above 50% ranged from 53.3% to 65%. Xerostomia was the most frequently reported side effect, along with anaemia, thrombocytopenia and nephrotoxicity.

Conclusions: Overall, the main results of our study showed that [²²⁵Ac]Ac-PSMA-617 had a significant therapeutic effect on mCRPC with an acceptable toxicity level. The latter, however, appears greater than with [¹⁷⁷Lu]Lu-PSMA-617. In future studies, an adequate analysis of the incidence of side effects associated with [²²⁵Ac]Ac-PSMA should be performed to evaluate the role of cumulative toxicity of earlier treatments and the higher frailty of heavily pretreated patients.