Development and External Validation of a Machine Learning-Derived Risk Stratification Score for Metastatic Castration-Resistant Prostate Cancer.

Published in JCO clinical cancer informatics. Abstract: Metastatic castration-resistant prostate cancer (mCRPC) shows marked clinical heterogeneity and poor long-term survival, highlighting the need for simple and reliable risk stratification tools beyond the limited usability of existing complex prognostic models. In this study, we developed and validated PROGRESS (Prostate Cancer Global Risk Evaluation and Stratification Score), a simplified prognostic score derived through machine learning‑guided feature selection distilled into a simple laboratory-based tool. Baseline data from 2,035 patients with mCRPC (training set) were embedded into synthetic representations, reduced with UMAP, and clustered with DBSCAN to discover outcome-related subpopulations. Feature contribution analysis informed a multivariable model that yielded three independent predictors (prostate specific antigen [PSA], alkaline phosphatase [ALP], and AST) composing PROGRESS. External validation used two independent data sets (n = 1,239) across different therapeutic settings. Overall survival (OS) was analyzed with Kaplan-Meier and Cox regression; discrimination was assessed by ROC-AUC, AUC(t), and Harrel C-index. Unsupervised modeling identified two patient risk subpopulations with significantly different OS rates (median 27.4 v 17.7 months; hazard ratio [HR], 2.20 [95% CI, 1.91 to 2.54]; P < .00001). The three retained predictors (PSA, ALP, and AST) were combined into a composite score (PROGRESS) that showed strong discrimination in the training cohort (ROC-AU...

5 Key Takeaways

1. PROGRESS, a three-predictor score using PSA, ALP, and AST, demonstrated strong discrimination in the training cohort with a ROC-AUC of 0.89.
2. External validation across two independent datasets confirmed consistent prognostic performance.
3. Patients classified as increased risk by PROGRESS had significantly shorter median survival than low-risk patients.

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