
The clinical efficacy of targeted radioligand therapy with (177Lu) vipivotide tetraxetan (177Lu-PSMA-617) was seen in patients with advanced prostate-specific membrane antigen (PSMA) PET-positive metastatic castration-resistant prostate cancer (mCRPC) regardless of prior treatment or standard of care chosen, according to a post-hoc analysis of data from the VISION trial (Abstract 5001).
According to Nitin Vaishampayan, MD, of Wayne State University School of Medicine and colleagues, who will present the analysis at the 2022 ASCO Annual Meeting, these findings suggest that “disease biology rather than prior and concomitant treatment context drives outcomes.”
In the VISION trial, patients with disease previously treated with at least one androgen receptor pathway inhibitor (ARPI) and one to two taxane regimens were randomly assigned to 177Lu-PSMA-617 plus standard of care or standard of care alone. 177Lu-PSMA-617 significantly prolonged radiographic progression-free survival and overall survival compared with standard of care in patients with advanced PSMA PET-positive mCRPC. The therapy was granted Food and Drug Administration approval based on these results.