Safety analyses of the phase 3 VISION trial of [(177)Lu]Lu-PSMA-617 in patients with metastatic castration-resistant prostate cancer Journal Article


Authors: Chi, K. N.; Armstrong, A. J.; Krause, B. J.; Herrmann, K.; Rahbar, K.; de Bono, J. S.; Adra, N.; Garje, R.; Michalski, J. M.; Kempel, M. M.; Fizazi, K.; Morris, M. J.; Sartor, O.; Brackman, M.; DeSilvio, M.; Wilke, C.; Holder, G.; Tagawa, S. T.
Article Title: Safety analyses of the phase 3 VISION trial of [(177)Lu]Lu-PSMA-617 in patients with metastatic castration-resistant prostate cancer
Abstract: Background and objective: [177Lu]Lu-PSMA-617 (177Lu-PSMA-617) plus the standard of care (SoC) significantly improved overall survival and radiographic progression-free survival versus SoC alone in patients with prostate-specific membrane antigen (PSMA)-positive metastatic castration-resistant prostate cancer in the VISION trial. We evaluated the safety of additional cycles of 177Lu-PSMA-617 and the impact of longer observation time for patients receiving 177Lu-PSMA-617 plus SoC. Methods: VISION was an international, open-label study. Patients were randomised 2:1 to receive 177Lu-PSMA-617 plus SoC or SoC alone. The incidence of treatment-emergent adverse events (TEAEs) was assessed in prespecified subgroups of patients who received ≤4 cycles versus 5–6 cycles of treatment and during each cycle of treatment. The TEAE incidence was also adjusted for treatment exposure to calculate the incidence per 100 patient-treatment years of observation. This analysis was performed for the first occurrence of TEAEs. Key findings and limitations: The any-grade TEAE incidence was similar in cycles 1–4 and cycles 5–6. TEAE frequency was similar across all cycles of 177Lu-PSMA-617 treatment. No additional safety concerns were reported for patients who received >4 cycles. The exposure-adjusted safety analysis revealed that the overall TEAE incidence was similar between arms, but distinct trends for different TEAE types were noted and the incidence of events associated with 177Lu-PSMA-617 remained higher in the 177Lu-PSMA-617 arm. Conclusions and clinical implications: Longer exposure to 177Lu-PSMA-617 plus SoC was not associated with a higher toxicity risk, and the extended time for safety observation could account for the higher TEAE incidence in comparison to SoC alone. The findings support a favourable benefit-risk profile for 6 cycles of 177Lu-PSMA-617 in this setting and the use of up to 6 cycles of 177Lu-PSMA-617 in patients who are clinically benefiting from and tolerating this therapy. Patient summary: For patients with metastatic prostate cancer no longer responding to hormone therapy, an increase in the number of cycles of treatment with a radioactive compound called 177Lu-PSMA-617 from four to six had no additional adverse side effects. © 2024 The Authors
Keywords: adult; controlled study; treatment outcome; major clinical study; overall survival; clinical trial; fatigue; neutropenia; treatment duration; radiopharmaceuticals; prostate specific antigen; progression free survival; multiple cycle treatment; anemia; leukopenia; randomized controlled trial; thrombocytopenia; incidence; risk assessment; lymphocytopenia; prostate-specific antigen; health care quality; prostate specific membrane antigen; multicenter study; radiopharmaceutical agent; xerostomia; phase 3 clinical trial; informed consent; disease exacerbation; treatment withdrawal; chronic kidney failure; bone marrow toxicity; castration resistant prostate cancer; dipeptides; urosepsis; urinary tract obstruction; single heterocyclic rings; heterocyclic compounds, 1-ring; lutetium; lutetium 177; dipeptide; metastatic prostate cancer; metastatic castration-resistant prostate cancer; humans; human; male; article; prostatic neoplasms, castration-resistant; metastatic castration resistant prostate cancer; treatment exposure; radioligand therapy; vipivotide tetraxetan; psma-617; vipivotide tetraxetan lutetium lu 177; <sup>177</sup>lu-psma-617; treatment-emergent adverse events
Journal Title: European Urology
Volume: 85
Issue: 4
ISSN: 0302-2838
Publisher: Elsevier Science, Inc.  
Date Published: 2024-04-01
Start Page: 382
End Page: 391
Language: English
DOI: 10.1016/j.eururo.2023.12.004
PUBMED: 38185538
PROVIDER: scopus
PMCID: PMC11859717
DOI/URL:
Notes: Article -- Source: Scopus
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  1. Michael Morris
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