直肠检查
前列腺癌
前列腺特异性抗原
医学
前列腺癌筛查
前列腺
人工智能
肿瘤科
机器学习
内科学
算法
癌症
妇科
计算机科学
作者
Nicolas Martelin,Brian De Witt,Bowen Chen,Pascal Eschwège
出处
期刊:The Prostate
[Wiley]
日期:2024-04-04
卷期号:84 (9): 842-849
被引量:1
摘要
Abstract Purpose Prostate specific antigen (PSA) testing is a low‐cost screening method for prostate cancer (PCa). However, its accuracy is limited. While progress is being made using medical imaging for PCa screening, PSA testing can still be improved as an easily accessible first step in the screening process. We aimed to develop and validate a new model by further personalizing the analysis of PSA with demographic, medical history, lifestyle parameters, and digital rectal examination (DRE) results. Methods Using data from 34,224 patients in the screening arm of the PLCO trial (22,188 for the training set and 12,036 for the validation set), we applied a gradient‐boosting model whose features (Model 1) were one PSA value and the personal variables available in the PLCO trial except those that signaled an ex‐ante assumption of PCa. A second algorithm (Model 2) included a DRE result. The primary outcome was the occurrence of PCa, while the aggressiveness of PCa was a secondary outcome. ROC analyses were used to compare both models to other initial screening tests. Results The areas under the curve (AUC) for Model 2 was 0.894 overall and 0.908 for patients with a suspicious DRE, compared to 0.808 for PSA for patients with a suspicious DRE. The AUC for Model 1 was 0.814 compared to 0.821 for PSA. Model 2 predicted 58% more high‐risk PCa than PSA ≥4 combined with an abnormal DRE and had a positive predictive value of 74.7% (vs. 50.6%). Conclusion Personalizing the interpretation of PSA values and DRE results with a gradient‐boosting model showed promising results as a potential novel, low‐cost method for the initial screening of PCa. The importance of DRE, when included in such a model, was also highlighted.
科研通智能强力驱动
Strongly Powered by AbleSci AI