Developing a diagnostic model for predicting prostate cancer: a retrospective study based on Chinese multicenter clinical data

被引:3
作者
Wang, Chang-Ming [1 ]
Yuan, Lei [2 ]
Liu, Xue-Han [3 ]
Chen, Shu-Qiu [4 ]
Wang, Hai-Feng [5 ,6 ]
Dong, Qi-Fei [7 ]
Zhang, Bin [7 ]
Huang, Ming-Shuo [1 ]
Zhang, Zhi-Yong [1 ]
Xiao, Jun [1 ]
Tao, Tao [1 ]
机构
[1] Univ Sci & Technol China, Affiliated Hosp USTC 1, Dept Urol, Div Life Sci & Med, Hefei 230001, Peoples R China
[2] Univ Sci & Technol China, Affiliated Hosp USTC 1, Dept Radiol, Div Life Sci & Med, Hefei 230001, Peoples R China
[3] Univ Sci & Technol China, Affiliated Hosp USTC 1, Core Facil Ctr Med Sci, Div Life Sci & Med, Hefei 230001, Peoples R China
[4] Southeast Univ, Affiliated Zhongda Hosp, Dept Urol, Nanjing 210009, Peoples R China
[5] Tongji Univ, Shanghai East Hosp, Sch Med, Dept Urol, Shanghai 200120, Peoples R China
[6] Second Mil Med Univ, Shanghai Changhai Hosp, Dept Urol, Shanghai 200000, Peoples R China
[7] Anhui Med Univ, Affiliated Anhui Prov Hosp, Dept Urol, Hefei 230001, Peoples R China
来源
ASIAN JOURNAL OF ANDROLOGY | 2024年 / 26卷 / 01期
关键词
nomogram; prostate biopsy; prostate cancer; Prostate Imaging-Reporting and Data System; prostate-specific antigen density; PREVENTION TRIAL; RISK CALCULATORS; MEN; SURVEILLANCE; VALIDATION; ANTIGEN; PART; PSA;
D O I
10.4103/aja202342
中图分类号
R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
摘要
The overdiagnosis of prostate cancer (PCa) caused by nonspecific elevation serum prostate-specific antigen (PSA) and the overtreatment of indolent PCa have become a global problem that needs to be solved urgently. We aimed to construct a prediction model and provide a risk stratification system to reduce unnecessary biopsies. In this retrospective study, clinical data of 1807 patients from three Chinese hospitals were used. The final model was built using stepwise logistic regression analysis. The apparent performance of the model was assessed by receiver operating characteristic curves, calibration plots, and decision curve analysis. Finally, a risk stratification system of clinically significant prostate cancer (csPCa) was created, and diagnosis-free survival analyses were performed. Following multivariable screening and evaluation of the diagnostic performances, a final diagnostic model comprised of the PSA density and Prostate Imaging-Reporting and Data System (PI-RADS) score was established. Model validation in the development cohort and two external cohorts showed excellent discrimination and calibration. Finally, we created a risk stratification system using risk thresholds of 0.05 and 0.60 as the cut-off values. The follow-up results indicated that the diagnosis-free survival rate for csPCa at 12 months and 24 months postoperatively was 99.7% and 99.4%, respectively, for patients with a risk threshold below 0.05 after the initial negative prostate biopsy, which was significantly better than patients with higher risk. Our diagnostic model and risk stratification system can achieve a personalized risk calculation of csPCa. It provides a standardized tool for Chinese patients and physicians when considering the necessity of prostate biopsy.
引用
收藏
页码:34 / 40
页数:10
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