The impact of integrating PRIMARY score or SUVmax with MRI-based risk models for the detection of clinically significant prostate cancer

被引:1
作者
Guo, Shikuan [1 ,2 ]
Ren, Jing [3 ]
Meng, Qingze [2 ]
Zhang, Boyuan [1 ]
Jiao, Jianhua [1 ]
Han, Donghui [1 ]
Wu, Peng [1 ]
Ma, Shuaijun [1 ]
Zhang, Jing [4 ]
Xing, Nianzeng [5 ]
Qin, Weijun [1 ]
Kang, Fei [6 ]
Zhang, Jingliang [1 ]
机构
[1] Fourth Mil Med Univ, Xijing Hosp, Dept Urol, 127 Changle West Rd, Xian 710032, Shaanxi, Peoples R China
[2] 988 Hosp Joint Logist Support Force, Dept Urol, Zhengzhou 450042, Henan, Peoples R China
[3] Fourth Mil Med Univ, Xijing Hosp, Dept Radiol, Xian 710032, Shaanxi, Peoples R China
[4] Fourth Mil Med Univ, Xijing Hosp, Dept Pathol, Xian 710032, Peoples R China
[5] Chinese Acad Med Sci & Peking Union Med Coll, Natl Clin Res Ctr Canc, Natl Canc Ctr, Dept Urol,Canc Hosp, Beijing 100021, Peoples R China
[6] Fourth Mil Med Univ, Xijing Hosp, Dept Nucl Med, Xian 710032, Shaanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Prostate cancer; PRIMARY score; PSMA PET/CT; SUVmax; Magnetic resonance imaging; Risk calculator; MULTIPARAMETRIC MRI; PI-RADS; DIAGNOSIS; ADENOCARCINOMA; VERSION; PET/CT;
D O I
10.1007/s00259-024-06916-2
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Purpose An MRI-based risk calculator (RC) has been recommended for diagnosing clinically significant prostate cancer (csPCa). PSMA PET/CT can detect lesions that are not visible on MRI, and the addition of PSMA PET/CT to MRI may improve diagnostic performance. The aim of this study was to incorporate the PRIMARY score or SUVmax derived from [Ga-68]Ga-PSMA-11 PET/CT into the RC and compare these models with MRI-based RC to assess whether this can further reduce unnecessary biopsies. Methods A total of 683 consecutive biopsy-na & iuml;ve men who underwent both [Ga-68]Ga-PSMA-11 PET/CT and MRI before biopsy were temporally divided into a development cohort (n = 552) and a temporal validation cohort (n = 131). Three logistic regression RCs were developed and compared: MRI-RC, MRI-SUVmax-RC and MRI-PRIMARY-RC. Discrimination, calibration, and clinical utility were evaluated. The primary outcome was the clinical utility of the risk calculators for detecting csPCa and reducing the number of negative biopsies. Results The prevalence of csPCa was 47.5% (262/552) in the development cohort and 41.9% (55/131) in the temporal validation cohort. In the development cohort, the AUC of MRI-PRIMARY-RC was significantly higher than that of MRI-RC (0.924 vs. 0.868, p < 0.001) and MRI-SUVmax-RC (0.924 vs. 0.904, p = 0.002). In the temporal validation cohort, MRI-PRIMARY-RC also showed the best discriminative ability with an AUC of 0.921 (95% CI: 0.873-0.969). Bootstrapped calibration curves revealed that the model fit was acceptable. MRI-PRIMARY-RC exhibited near-perfect calibration within the range of 0-40%. DCA showed that MRI-PRIMARY-RC had the greatest net benefit for detecting csPCa compared with MRI-RC and MRI-SUVmax-RC at a risk threshold of 5-40% for csPCa in both the development and validation cohorts. Conclusion The addition of the PRIMARY score to MRI-based multivariable model improved the accuracy of risk stratification prior to biopsy. Our novel MRI-PRIMARY prediction model is a promising approach for reducing unnecessary biopsies and improving the early detection of csPCa.
引用
收藏
页码:756 / 765
页数:10
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