A phase I dose-escalation/expansion study of fractionated-dose and multiple cycle anti-PSMA-targeted alpha emitter 225Ac-J591 in patients with prostate cancer.

To test safety of two regimens at differing levels of radioactivity of PSMA-targeted alpha radionuclide 225Ac-J591.

Patients with progressive, metastatic androgen pathway modulator resistant prostate cancer were enrolled in two parallel dose-escalation cohorts: (1) fractionated-dose regimen (single cycle of 45 - 65 KBq/kg of 225Ac-J591 on day 1 and day 15; main cohort agnostic to prior receipt of 177Lu-PSMA, additional cohort post 177Lu-PSMA) and (2) multiple cycles of 225Ac-J591 (45 - 65 KBq/kg administered every 6 weeks for up to 4 cycles). PSMA PET not utilized for eligibility. Primary end point was determination of dose-limiting toxicity (DLT) and recommended phase 2 dose (RP2D); the fractionated cohort was expanded.

42 patients were enrolled in fractionated (23 dose-escalation, 11 expansion, 8 post 177Lu-PSMA), 18 multiple dose. All received > 1 prior AR pathway inhibitor, 72% chemotherapy, 18% 177Lu-PSMA. Three patients had DLT in fractionated regimen with RP2D of 60 KBq/kg x2. Seven had DLT in multiple cycle regimen; this regimen is not recommended for further development. Amongst adverse events of special interest, temporary hematologic toxicity was most common [93% thrombocytopenia (32% grade >3), 65% neutropenia (13% grade >3), 63% anemia (20% grade >3)]; dry mouth occurred in 62% (2% grade 2). Across fractionated cohorts with or without prior 177Lu-PSMA, 60% with >50% PSA decline as best response; 28% with >50% PSA decline in multiple cycle.

Fractionated dosing of 225Ac-J591 appears promising. Further investigation is underway.

Clinical cancer research : an official journal of the American Association for Cancer Research. 2026 Jul 22 [Epub ahead of print]

Scott T Tagawa, Charlene Thomas, Abdul Baseet Arham, Aaron Holmes, Valentina Marulanda Corzo, Tobechukwu Okobi, Shankar Vallabhajosula, Vasilios Avlonitis, Sandra Huicochea Castellanos, Jones T Nauseef, Elisabeth O'Dwyer, Maham Fatima, Peter Gregos, Sarah Yuan, Cora N Sternberg, Ana Molina, David M Nanus, Neil H Bander, Joseph Osborne

Weill Cornell Medicine New York, NY United States., Weill Cornell Medicine New York United States., NewYork-Presbyterian Brooklyn Methodist Hospital New York, NY United States.