Targeted radionuclide therapy (TRT) has become a standard of care for patients with metastatic castration-resistant prostate cancer (mCRPC). Lutetium-177 labeled PSMA radioligand therapy ([¹⁷⁷Lu]Lu-PSMA) is an established and effective treatment option, while [²²⁵Ac]Ac-PSMA shows promise in refractory cases. The tandem use of [225Ac] Ac and [177Lu] Lu-labeled PSMA ligands is currently being explored to harness the complementary advantages of both isotopes. This meta-analysis investigates the efficacy and safety of [²²⁵Ac]Ac -/[¹⁷⁷Lu]Lu-PSMA radioligand therapy (RLT) in patients with mCRPC.
This systematic review is reported in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA). A comprehensive literature search was performed in PubMed, EMBASE, Web of Science (WOS), and Scopus databases, covering all records from inception through March 2025. The primary endpoints focused on therapeutic efficacy, assessed through PSA-based biochemical responses. These included any PSA decline, a PSA decline of more than 50% from baseline, stable disease (defined as a PSA increase of < 25% PSA increase or a decrease of < 50%), and progressive disease (defined as an increase of ≥ 25% PSA) following tandem 225Ac-/177Lu-PSMA tandem RLT. Secondary endpoints included overall survival (OS) and treatment-related adverse events. A random-effects model was used to generate pooled proportions through meta-analysis.
Eight studies, including a total of 323 patients treated with [²²⁵Ac]-/[¹⁷⁷Lu]-PSMA combination therapy, were analyzed. The pooled response rates showed that 47% (95% CI: 37%-56%) experienced a PSA decline greater than 50%, while 78% (95% CI: 70%-86%) had any measurable PSA decline. The estimated median OS was 11.8 months (95% CI: 9.0-14.6 months). Severe toxicities were infrequent; the most common severe grade ≥ 3 adverse events were anemia (10%) and thrombocytopenia (6%). No cases of grade ≥ 3 xerostomia were reported.
[²²⁵Ac]Ac-/[¹⁷⁷Lu]Lu-PSMA RLT shows encouraging activity and manageable safety in patients with advanced mCRPC. Given the retrospective nature of the available evidence and limited data, these findings should be further evaluated in prospective trials to determine long-term efficacy and survival outcomes.
European journal of nuclear medicine and molecular imaging. 2025 Nov 18 [Epub ahead of print]
Zineddine Belabaci, Giulio Brignoli, Thomas Zilli, Miloš Grujić, Issa Mohamad, Akram Al-Ibraheem, Mohamed Shelan, Ali Afshar-Oromieh
Faculty of Medicine, Djillali Liabes University, Sidi Bel Abbes, Algeria., Department of Radiation Oncology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland., Radiation Oncology, Oncology Institute of Southern Switzerland (IOSI), EOC, Bellinzona, Switzerland., Center for Radiation Oncology, University Clinical Centar Kragujevac, Kragujevac, 34000, Serbia., Department of Radiation Oncology, King Hussein Cancer Center, Amman, Jordan., Department of Nuclear Medicine, King Hussein Cancer Center, Amman, Jordan., Department of Radiation Oncology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland. ., Department of Nuclear Medicine, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.