본문으로 건너뛰기
← 뒤로

Improving the Potential for Predicting Prostate Cancer Progression in Patients on Active Surveillance Using Explainable Artificial Intelligence.

Cancers 2025 Vol.17(22)

Vershinina O, Sushentsev N, Zaikin A, Blyuss O, Barrett T, Ivanchenko M

📝 환자 설명용 한 줄

: Approximately half of prostate cancer (PCa) patients present with low- or intermediate-risk disease eligible for active surveillance (AS).

이 논문을 인용하기

BibTeX ↓ RIS ↓
APA Vershinina O, Sushentsev N, et al. (2025). Improving the Potential for Predicting Prostate Cancer Progression in Patients on Active Surveillance Using Explainable Artificial Intelligence.. Cancers, 17(22). https://doi.org/10.3390/cancers17223598
MLA Vershinina O, et al.. "Improving the Potential for Predicting Prostate Cancer Progression in Patients on Active Surveillance Using Explainable Artificial Intelligence.." Cancers, vol. 17, no. 22, 2025.
PMID 41300965

Abstract

: Approximately half of prostate cancer (PCa) patients present with low- or intermediate-risk disease eligible for active surveillance (AS). However, a substantial proportion of individuals experience pathological progression during follow-up. In this study, we developed predictive models for histopathological PCa progression in patients on AS. : The dataset comprised patients with biopsy-confirmed PCa and a minimum follow-up of two years. All patients underwent regular surveillance, including prostate-specific antigen (PSA) measurements and MRI examinations. Each patient had three to six consecutive MRI scans available for analysis. Histopathological progression was defined as an upgrade to a higher grade group on repeat targeted biopsy. Predictive modeling integrated radiomic and clinical variables using machine learning (ML). SHapley Additive exPlanations (SHAP) was used for feature interpretation. : Three models were obtained: (1) a baseline model utilizing radiomic features from initial MRI scans combined with baseline PSA density (PSAd) (AUC = 0.793, sensitivity = 0.690, specificity = 0.830); (2) a delta model incorporating feature changes between latest and baseline available MRI scans with final PSAd (AUC = 0.913, sensitivity = 0.793, specificity = 0.936); and (3) a time series model analyzing the complete series of radiomic features and PSAd (AUC = 0.917, sensitivity = 0.828, specificity = 0.894). : Our predictive models demonstrated strong performance in distinguishing progressors from non-progressors, suggesting that radiomic analysis combined with ML has significant potential to enhance PCa management. This approach could enable more personalized treatment strategies and improve clinical decision-making for patients undergoing AS.