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. 2025 May 29;6(6):e70026.
doi: 10.1002/bco2.70026. eCollection 2025 Jun.

First validation of the Prostatype® P-score in an Asian cohort: Improving risk stratification for prostate cancer

Affiliations

First validation of the Prostatype® P-score in an Asian cohort: Improving risk stratification for prostate cancer

See-Tong Pang et al. BJUI Compass. .

Abstract

Objectives: To evaluate the prognostic performance of the Prostatype® score (P-score) in the Asian prostate cancer (PCa) cohort and to assess its ability to refine risk stratification compared to the National Comprehensive Cancer Network (NCCN) guidelines. This study aimed to determine whether the P-score, previously validated in European populations, maintains its predictive accuracy in a genetically and clinically distinct high-risk Asian cohort, where late-stage diagnosis is more common.

Patients and methods: This retrospective study included 148 PCa patients diagnosed at Taiwan Chang Gung Memorial Hospital between 2012 and 2017. Of these, 56 had primary metastases at diagnosis. The P-score was calculated based on gene expression in core needle biopsies and clinical data collected from patients' medical records. The primary endpoint was PCa-specific mortality (PCSM). The secondary endpoints were adverse pathology (AP) and biochemical failure.

Results: The P-score significantly outperformed NCCN in predicting PCSM, achieving a higher C-index (0.90 vs. 0.73, P < 0.005), which reflects superior prognostic accuracy. Notably, 19.6% of patients were reclassified into different risk categories compared to NCCN, improving risk stratification and potentially altering treatment decisions for nearly one in five patients. The P-score was also an independent predictor of adverse pathology (P = 0.003, AUC: 0.81) and biochemical failure (P = 0.03, AUC: 0.89).

Conclusions: This study validated the P-score for the first time in a non-European population, confirming its predictive power in an Asian high-risk setting. The reclassification of 19.6% of patients suggests that the P-score refines risk stratification beyond NCCN, offering a more precise distinction between favourable and unfavourable outcomes, enabling more informed treatment decisions. These findings highlight the global applicability of the P-score and its potential to improve risk assessment and personalized treatment for PCa patients worldwide.

Keywords: biomarkers; mortality; prostate cancer; risk stratification; therapy.

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Conflict of interest statement

EB is employed by Prostatype Genomics AB. LDX was employed by Prostatype Genomics AB. The authors report no other conflicts of interest in this work.

Figures

FIGURE 1
FIGURE 1
Cohort selection in the study.
FIGURE 2
FIGURE 2
A: reclassification of NCCN favourable intermediate‐risk, unfavourable intermediate‐risk, and high‐risk prostate cancer patients with the P‐score in the subgroup of patients without metastases at diagnosis (n = 92). B: prediction accuracy of prostate cancer‐specific mortality in a C‐index analysis comparing the P‐score, NCCN score and clinicopathological parameters. C: predictive accuracy of 9‐year prostate cancer‐specific mortality for the P‐score, P‐score clinical, and the NCCN score.
FIGURE 3
FIGURE 3
Prostate cancer‐specific survival by P‐score risk group (low‐ and intermediate‐ risk vs. high‐risk) (n = 148).
FIGURE 4
FIGURE 4
P‐score association with adverse pathology (AP) in the subgroup of patients who underwent radical prostatectomy (RP). Area under the curve (AUC) assessed by receiver operating characteristic (ROC) analysis.
FIGURE 5
FIGURE 5
A: distribution of the P‐score across treatment groups. B: treatment and survival status of P‐score low‐risk patients. C: treatment and survival status of P‐score intermediate‐risk patients. D‐F: treatment and survival status of P‐score high‐risk patients.

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