Overall, 16,049 patients with low- or intermediate risk PCa treated with RP were identified. Misclassification was defined as non-organ confined or grade group ≥3 disease at RP. The coefficients of a logistic regression model predicting classification were used to develop a risk score. Furthermore, a systematic analysis of different cut-offs to discriminate between patients with or without unfavorable disease was performed and was compared to available AS criteria.
Overall, 5,289 (33.0%) patients had unfavorable disease. At multivariable analyses all the following were associated with the risk of unfavorable disease (all P<0.001):
- PSA (Odds ratio [OR]: 1.12; 95% confidence interval [CI]: 1.11-1.13)
- Clinical stage T2 (OR: 2.27; 95%CI: 2.10-2.46)
- Biopsy grade group 2 (OR: 2.66; 95%CI: 2.46-2.87)
- Biopsy grade group 3 (OR: 7.21; 95%CI: 6.5-7.9)
- The number of positive cores (OR: 1.10; 95%CI: 1.09-1.11)
- PSA density (OR: 1.20; 95%CI: 1.15-1.25)
Approximately 13% of patients potentially eligible for AS according to the PRIAS protocol, who will undergo RP, will ultimately harbor unfavorable disease characteristics at final pathology. The use of a novel risk score for the selection of men who should be included in AS protocols would result in a 50% increase in the number of patients potentially eligible for this approach. This occurs without increasing the risk of adverse pathological outcomes.
Presented by: Gandaglia G, San Raffaele Hospital, Dept. of Urology, Milan, Italy
Written by: Hanan Goldberg, MD, Urologic Oncology Fellow (SUO), University of Toronto, Princess Margaret Cancer Centre, twitter: @GoldbergHanan at the 2018 European Association of Urology Meeting EAU18, 16-20 March, 2018 Copenhagen, Denmark