Lutetium-177–PSMA-617 for Metastatic Castration-Resistant Prostate Cancer

Oliver Sartor(Tulane University), Johann S. de Bono(Cornell University), Kim N.(BC Cancer Agency), Karim Fizazi(Cornell University), Ken Herrmann(Cornell University), Kambiz Rahbar(Cornell University), Scott T. Tagawa(Cornell University), Luke T. Nordquist(Cornell University), Nitin Vaishampayan(Wayne State University), Ghassan El‐Haddad(Cornell University), Chandler H. Park(Norton Healthcare), Tomasz M. Beer(Oregon Health & Science University), Alison Armour(Cornell University), Wendy J. Pérez-Contreras(Cornell University), Michelle DeSilvio(Cornell University), Euloge Kpamegan(Cornell University), Germo Gericke(Novartis (Switzerland)), Richard A. Messmann(Cornell University), Michael J. Morris(Memorial Sloan Kettering Cancer Center), Bernd J. Krause(Cornell University)
New England Journal of Medicine
June 23, 2021
Cited by 2,526Open Access
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Abstract

BACKGROUND: Lu)-PSMA-617 is a radioligand therapy that delivers beta-particle radiation to PSMA-expressing cells and the surrounding microenvironment. METHODS: Ra), and investigational drugs. The alternate primary end points were imaging-based progression-free survival and overall survival, which were powered for hazard ratios of 0.67 and 0.73, respectively. Key secondary end points were objective response, disease control, and time to symptomatic skeletal events. Adverse events during treatment were those occurring no more than 30 days after the last dose and before subsequent anticancer treatment. RESULTS: Lu-PSMA-617 than without (52.7% vs. 38.0%), but quality of life was not adversely affected. CONCLUSIONS: Lu-PSMA-617 prolonged imaging-based progression-free survival and overall survival when added to standard care in patients with advanced PSMA-positive metastatic castration-resistant prostate cancer. (Funded by Endocyte, a Novartis company; VISION ClinicalTrials.gov number, NCT03511664.).


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