Multiparametric transrectal ultrasound for the diagnosis of peripheral zone prostate cancer and clinically significant prostate cancer: novel scoring systems

被引:5
作者
Chen, Tong [1 ]
Wang, Fei [1 ]
Chen, Hanbing [1 ]
Wang, Meng [1 ]
Liu, Peiqing [1 ]
Liu, Songtao [1 ]
Zhou, Yibin [2 ]
Ma, Qi [1 ]
机构
[1] Soochow Univ, Affiliated Hosp 2, Dept Ultrasound, Suzhou, Jiangsu, Peoples R China
[2] Soochow Univ, Affiliated Hosp 2, Dept Urol, Suzhou, Jiangsu, Peoples R China
关键词
Transrectal ultrasound; Scoring system; Logistic regression model; Prostate cancer; PI-RADS; Decision curve analysis; CONTRAST-ENHANCED SONOGRAPHY; BIOPSIES; CARCINOMA;
D O I
10.1186/s12894-022-01013-8
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background To evaluate the diagnostic performance of multiparametric transrectal ultrasound (TRUS) and to design diagnostic scoring systems based on four modes of TRUS to predict peripheral zone prostate cancer (PCa) and clinically significant prostate cancer (csPCa). Methods A development cohort involved 124 nodules from 116 patients, and a validation cohort involved 72 nodules from 67 patients. Predictors for PCa and csPCa were extracted to construct PCa and csPCa models based on regression analysis of the development cohort. An external validation was performed to assess the performance of models using area under the curve (AUC). Then, PCa and csPCa diagnostic scoring systems were established to predict PCa and csPCa. The diagnostic accuracy was compared between PCa and csPCa scores and PI-RADS V2, using receiver operating characteristics (ROC) and decision curve analysis (DCA). Results Regression models were established as follows: PCa = - 8.284 + 4.674 x Margin + 1.707 x Adler grade + 3.072 x Enhancement patterns + 2.544 x SR; csPCa = - 7.201 + 2.680 x Margin + 2.583 x Enhancement patterns + 2.194 x SR. The PCa score ranged from 0 to 6 points, and the csPCa score ranged from 0 to 3 points. A PCa score of 5 or higher and a csPCa score of 3 had the greatest diagnostic performance. In the validation cohort, the AUC for the PCa score and PI-RADS V2 in diagnosing PCa were 0.879 (95% confidence interval [CI] 0.790-0.967) and 0.873 (95%CI 0.778-0.969). For the diagnosis of csPCa, the AUC for the csPCa score and PI-RADS V2 were 0.806 (95%CI 0.700-0.912) and 0.829 (95%CI 0.727-0.931). Conclusions The multiparametric TRUS diagnostic scoring systems permitted better identifications of peripheral zone PCa and csPCa, and their performances were comparable to that of PI-RADS V2.
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页数:12
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