Why the study?
161Tb offers physical advantages over 177Lu by emitting low-energy Auger and conversion electrons that result in higher locally absorbed doses, but initial clinical experience across settings following initial PSMA RLT was needed.
Does [161Tb]Tb-PSMA-617 RLT improve outcomes in patients with mCRPC after initial PSMA RLT?
Does [161Tb]Tb-PSMA-617 RLT improve outcomes in patients with mCRPC after initial PSMA RLT?
[161Tb]Tb-PSMA-617 RLT shows promising efficacy and safety in patients with advanced mCRPC who previously received standard PSMA RLT.
May inform salvage strategies in mCRPC; leaves open randomized trials versus 177Lu-PSMA.
Rationale:The radionuclide 161 Tb is an increasingly discussed potential candidate for radioligand therapy (RLT).Through the considerable emitted amount of low-energy Auger and conversion electrons, 161 Tb offers physical advantages over the commonly used 177 Lu, resulting in higher locally absorbed doses.In this study, we present initial experience with [ 161 Tb]Tb-PSMA-617 RLT across different clinical settings following initial PSMA RLT.Methods: The study involved n=18 patients with metastasized castration-resistant prostate cancer (mCRPC) participating in a prospective registry (NCT04833517) and receiving [ 161 Tb]Tb-PSMA-617 after initial PSMA RLT with established radionuclides ( 177 Lu, 225 Ac).In total 47 cycles of [ 161 Tb]Tb-PSMA-617 RLT were administered with a median of 3 cycles (1 -4 cycles) per patient.The mean administered activity of 161 Tb per cycle was 6.2 0.8 GBq, the mean cumulative activity was 16.1 4.9 GBq.Outcome was evaluated by biochemical and molecular imaging response, progression-free survival (PFS), and overall survival (OS).Adverse events were assessed by 'Common Terminology Criteria for Adverse Events' (CTCAE v.5.0) grading system.Results: In the heterogeneous cohort of patients previously experiencing insufficient response or progression post RLT with [ 177 Lu]Lu-PSMA-617, or even after 225 Ac augmentation, biochemical and molecular imaging response rates were 38.9% and 44.4%, median PFS and OS 3.5 and 11.3 months, respectively.The best response and outcome were observed in patients who initially responded to [ 177 Lu]Lu-PSMA-617 RLT.The majority of all post therapeutically recorded adverse events were mild or moderate (CTCAE 1 or 2); higher grades (CTCAE 3 or 4) were rarely observed (2 cases of thrombocytopenia, 4 cases of anemia and 4 cases of renal impairment).No treatment discontinuation due to therapy related adverse events was recorded.Conclusion: These pilot results confirm 161 Tb as a promising radionuclide for PSMA RLT and suggest [ 161 Tb]Tb-PSMA-617 as a potential effective and safe treatment option even in the advanced mCRPC setting after multi-line systemic therapies including standard PSMA RLT.Larger studies are warranted to confirm and extend this initial experience and clinical trials even in earlier CRPC settings appear promising based on our initial impression of this radionuclide-based novelty in PSMA RLT.
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Rosar et al. (2025) studied this question.
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