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Chinese study develops nomogram for prostate cancer prediction in men with PSA 4-20 ng/mL

Chinese study develops nomogram for prostate cancer prediction in men with PSA 4-20 ng/mL
Photo by Kelly Chiang / Unsplash
Key Takeaway
Consider this prostate cancer prediction nomogram as preliminary evidence requiring prospective validation.

A retrospective cohort study at tertiary medical centers in China analyzed 314 patients undergoing prostate biopsy with prostate-specific antigen values of 4–20 ng/mL. Researchers developed and validated a clinical nomogram for predicting prostate cancer, using a training cohort of 219 patients and a validation cohort of 95 patients. The study did not report specific intervention or comparator details.

Multivariate analysis identified triglycerides, PI-RADS score, albumin, and prostate health index as independent predictors of prostate cancer, though specific effect sizes and p-values were not reported. In the training cohort, the nomogram demonstrated an area under the receiver operating characteristic curve of 0.75 for discriminatory performance. Calibration curves and the Hosmer–Lemeshow test indicated good agreement between predicted and observed outcomes. The validation cohort showed consistent performance, though specific metrics were not provided.

Safety and tolerability data were not reported. Key limitations include the retrospective design and single-country setting at Chinese tertiary centers. The study suggests integrating clinical parameters into a PHI-based model may enhance prostate cancer risk stratification, potentially reducing unnecessary biopsies. However, this requires external validation and cannot infer causality due to the observational nature of the evidence.

Study Details

Study typeCohort
EvidenceLevel 3
PublishedMar 2026
View Original Abstract ↓
BackgroundGiven the established diagnostic utility of the prostate health index (PHI) in prostate cancer (PCa), this study sought to incorporate PHI into a clinically applicable prediction model alongside conventional parameters, with the goal of refining biopsy selection in men presenting with PSA values of 4–20 ng/mL.MethodsWe retrospectively collected clinical data from patients undergoing prostate biopsy at tertiary medical centers in China. Candidate variables were screened using least absolute shrinkage and selection operator (LASSO) regression, and the selected predictors were incorporated into a multivariable logistic regression model, which was subsequently presented as a nomogram. Model performance was evaluated in both the training and validation cohorts in terms of discrimination, calibration, and clinical utility.ResultsA total of 314 patients were included, with 219 assigned to the training cohort and 95 to the validation cohort. LASSO regression identified prostate volume, blood glucose, low-density lipoprotein, triglycerides, urinary leukocyte count, hypertension, Prostate Imaging–Reporting and Data System score, platelet-to-lymphocyte ratio, albumin, the fPSA/tPSA ratio, and PHI as candidate variables. Multivariate analysis demonstrated that triglycerides, PI-RADS score, ALB, and PHI were independent predictors of PCa. The nomogram achieved good discriminatory performance, with an area under the receiver operating characteristic curve of 0.75 in the training cohort. Calibration curves and the Hosmer–Lemeshow test indicated good agreement between predicted and observed outcomes. Consistent performance was observed in the validation cohort.ConclusionsOur findings suggest that integrating clinical parameters into a PHI-based model can enhance the stratification of prostate cancer risk, potentially reducing unnecessary biopsies and improving patient outcomes.
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