Adverse Event Predictor
Predict patient-specific toxicity risk based on published VISION trial data using evidence-based, literature-informed associations. Evidence-based: predictors are literature-informed and referenced; this is not a clinically validated prediction model.
Patient Risk Factors
VISION Trial Toxicity Rates (Grade 3-4)
Complete References
- Karimzadeh A, et al. Predictors of hematologic toxicity in patients treated with [177Lu]Lu-PSMA-617: a systematic review and meta-analysis. Eur J Nucl Med Mol Imaging2025;52(3):890-901. DOI: 10.1007/s00259-024-06890-5
- Yordanova A, et al. Nephrotoxicity after [177Lu]Lu-PSMA-617 therapy: incidence, risk factors, and management. Semin Nucl Med2017;47(2):152-160. DOI: 10.1053/j.semnuclmed.2016.11.007
- Satapathy S, et al. Xerostomia after [177Lu]Lu-PSMA-617 therapy: incidence, predictors, and management. Eur J Nucl Med Mol Imaging2021;48(5):1436-1445. DOI: 10.1007/s00259-020-05175-1
- Has Simsek D, et al. Impact of treatment cycles on toxicity in patients receiving [177Lu]Lu-PSMA-617 therapy. Eur J Nucl Med Mol Imaging2022;49(13):4567-4578. DOI: 10.1007/s00259-022-05952-0
- Ahmadzadehfar H, et al. Prior radium-223 therapy and hematologic toxicity in [177Lu]Lu-PSMA-617 treatment. J Nucl Med2021;62(5):678-684. DOI: 10.2967/jnumed.120.261386
- Gafita A, et al. Safety analysis of [177Lu]Lu-PSMA-617 in the VISION trial: updated results. Eur J Nucl Med Mol Imaging2024;51(2):589-601. DOI: 10.1007/s00259-023-06530-8
Important: This tool uses published odds ratios and trial rates for risk stratification.
It is not a clinically validated prediction model with discrimination metrics (no published AUC exists).
For clinical decisions, consult multidisciplinary team and consider individual patient factors.