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| Natura: | Artículo Open Access |
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Wiley
2025
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| Accesso online: | https://bjui-journals.onlinelibrary.wiley.com/doi/10.1002/bco2.70026 |
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| author | See‐Tong Pang Po‐Hung Lin Emelie Berglund Lidi Xu I‐Hung Shao Kai‐Jie Yu Chin‐Hsuan Hsieh Tzu‐Hsuan Chang Yu Chen Wen‐Hui Weng Cheng‐Keng Chuang |
| author_facet | See‐Tong Pang Po‐Hung Lin Emelie Berglund Lidi Xu I‐Hung Shao Kai‐Jie Yu Chin‐Hsuan Hsieh Tzu‐Hsuan Chang Yu Chen Wen‐Hui Weng Cheng‐Keng Chuang See‐Tong Pang Po‐Hung Lin Emelie Berglund Lidi Xu I‐Hung Shao Kai‐Jie Yu Chin‐Hsuan Hsieh Tzu‐Hsuan Chang Yu Chen Wen‐Hui Weng Cheng‐Keng Chuang |
| collection | Wiley Open Access |
| contents | First validation of the Prostatype® P‐score in an Asian cohort: Improving risk stratification for prostate cancer See‐Tong Pang Po‐Hung Lin Emelie Berglund Lidi Xu I‐Hung Shao Kai‐Jie Yu Chin‐Hsuan Hsieh Tzu‐Hsuan Chang Yu Chen Wen‐Hui Weng Cheng‐Keng Chuang BJUI Compass AbstractObjectivesTo 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 methodsThis 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.ResultsThe 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).ConclusionsThis 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. 10.1002/bco2.70026 http://creativecommons.org/licenses/by/4.0/ |
| doi_str_mv | 10.1002/bco2.70026 |
| format | Artículo Open Access |
| id | wiley_oa_10_1002_bco2_70026 |
| institution | Wiley Open Access |
| license_str_mv | http://creativecommons.org/licenses/by/4.0/ |
| publishDate | 2025 |
| publisher | Wiley |
| record_format | wiley_oa |
| spellingShingle | First validation of the Prostatype® P‐score in an Asian cohort: Improving risk stratification for prostate cancer See‐Tong Pang Po‐Hung Lin Emelie Berglund Lidi Xu I‐Hung Shao Kai‐Jie Yu Chin‐Hsuan Hsieh Tzu‐Hsuan Chang Yu Chen Wen‐Hui Weng Cheng‐Keng Chuang BJUI Compass First validation of the Prostatype® P‐score in an Asian cohort: Improving risk stratification for prostate cancer See‐Tong Pang Po‐Hung Lin Emelie Berglund Lidi Xu I‐Hung Shao Kai‐Jie Yu Chin‐Hsuan Hsieh Tzu‐Hsuan Chang Yu Chen Wen‐Hui Weng Cheng‐Keng Chuang BJUI Compass AbstractObjectivesTo 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 methodsThis 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.ResultsThe 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).ConclusionsThis 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. 10.1002/bco2.70026 http://creativecommons.org/licenses/by/4.0/ |
| title | First validation of the Prostatype® P‐score in an Asian cohort: Improving risk stratification for prostate cancer |
| topic | BJUI Compass |
| url | https://bjui-journals.onlinelibrary.wiley.com/doi/10.1002/bco2.70026 |