Majchrzak Natalia, Cieśliński Piotr, Milecki Tomasz, Twardosz Krzysztof, Głyda Maciej, Karmelita-Katulska Katarzyna
Transplantology, General Surgery and Urology Department, Poznań District Hospital, Poznań, Poland.
Department and Clinic of Urology and Oncological Urology, Poznań University of Medical Sciences, Poznań, Poland.
Cent European J Urol. 2021;74(3):321-326. doi: 10.5173/ceju.2021.3.R2.0111. Epub 2021 Jul 7.
The study aimed to assess the suitability of multiparametric magnetic resonance prostate imaging (mpMRI) in combination with clinical parameters [prostate-specific antigen (PSA), digital rectal examination (DRE)] in the identification of men at risk of the presence of prostate cancer (PCa) and clinically significant prostate cancer (csPCa, Gleason Score ≥3+4) in the cognitive fusion with systematic prostate biopsy.
We retrospectively evaluated a population of 215 biopsy - naive patients with a clinical suspicion of prostate cancer. The results of mpMRI, DRE, PSA and biopsy were analyzed. MpMRI of the prostate according to the Prostate Imaging Reporting and Data System (PI-RADS) v.2.0 scheme preceded cognitive fusion and systematic transrectal prostate biopsy. Uni- and multivariable logistic regression analysis (MVA) was used to identify the variables determining the risk of detecting PCa overall and csPCa.
In MVA, it was established that the combination of variables such as PSA level [odds ratio (OR) 1.195; p = 0.002], PI-RADS ≥3 (OR 7.7; p = 0.002), prostate volume (OR 0.98; p = 0.017) significantly determines the probability of PCa detection in biopsy, while for csPCa it is PSA level (OR 1.14; p = 0.004), DRE (+) (OR 5.75; p <0.001), PI-RADS ≥4 (OR 6.5; p <0.001). Analysis of mpMRI diagnostic value for PI-RADS ≥4 revealed better sensitivity (88.9% vs 82.6%) and better negative predictive value (NPV) (94.5% vs 82.4%) for detection of csPCa than for PCa overall.
MpMRI results combining with DRE and PSA parameters help to identify men at high - or low risk of csPCa detection in the first - time biopsy.
本研究旨在评估多参数磁共振前列腺成像(mpMRI)联合临床参数[前列腺特异性抗原(PSA)、直肠指检(DRE)]在认知融合系统性前列腺活检中识别有前列腺癌(PCa)风险及临床显著前列腺癌(csPCa,Gleason评分≥3+4)男性的适用性。
我们回顾性评估了215例临床怀疑患有前列腺癌且未进行过活检的患者群体。分析了mpMRI、DRE、PSA及活检结果。根据前列腺影像报告和数据系统(PI-RADS)v.2.0方案对前列腺进行mpMRI检查,随后进行认知融合和系统性经直肠前列腺活检。采用单变量和多变量逻辑回归分析(MVA)来确定决定总体检测PCa和csPCa风险的变量。
在MVA中,确定了诸如PSA水平[比值比(OR)1.195;p = 0.002]、PI-RADS≥3(OR 7.7;p = 0.002)、前列腺体积(OR 0.98;p = 0.017)等变量的组合显著决定了活检中检测到PCa的概率,而对于csPCa而言,是PSA水平(OR 1.14;p = 0.004)、DRE(阳性)(OR 5.75;p <0.001)、PI-RADS≥4(OR 6.5;p <0.001)。对PI-RADS≥4的mpMRI诊断价值分析显示,与总体PCa检测相比,检测csPCa具有更高的敏感性(88.9%对82.6%)和更好的阴性预测值(NPV)(94.5%对82.4%)。
mpMRI结果与DRE和PSA参数相结合有助于在首次活检中识别有高或低csPCa检测风险的男性。