Baruah Sasanka Kumar, Das Nabajeet, Baruah Saumar Jyoti, Rajeev T P, Bagchi Puskal Kumar, Sharma Debanga, Phukan Mandeep
Department of Urology, Gauhati Medical College and Hospital, Guwahati, India.
World J Oncol. 2019 Dec;10(6):218-225. doi: 10.14740/wjon1230. Epub 2019 Dec 16.
Any non-invasive test that can predict the absence of prostate cancer (PCa) or absence of clinically significant PCa (CSPCa) is necessary, as it can reduce the number of unnecessary biopsies in patients with gray zone prostate-specific antigen (PSA, 4 - 10 ng/mL). This study evaluated the diagnostic performance of free PSA% and PSA density (PSAD), and Prostate Imaging Reporting and Data System (PIRADS) score (version 2.0) alone and combined in predicting CSPCa in patients with PSA between 4 and 10 ng/mL.
This prospective study included a total of 104 consecutive patients with lower urinary tract symptoms (LUTS) and serum PSA between 4 and 10 ng/mL, with or without abnormal digital rectal examination (DRE) findings or any hypoechoic lesion on ultrasound sonography of prostate and without prior transrectal ultrasound (TRUS) biopsy of prostate. PIRADS score was calculated using multi-parametric magnetic resonance imaging (mp-MRI) before TRUS biopsy of prostate. Relationships among PIRADS score, PSAD, free PSA% and presence of CSPCa in TRUS biopsy were statistically analyzed.
In patients with CSPCa, significantly higher median age (P = 0.001), PSA level (P < 0.001), PSAD (P < 0.001) and significantly lower prostate volume (P < 0.001) and free PSA% were observed as compared to patients with non-CSPCa. Significantly higher proportion of patients with CSPCa showed PIRADS positive test compared to those with non-CSPCa (86.4% vs. 53.3%, P < 0.001). Cut-off values for PSAD and free PSA% were 0.12 ng/mL and 25%, respectively. Age, PSAD and free PSA% were significant predictors of PCa, while age and PSAD were significant predictors of CSPCa. Criteria 2, 3 and 4 demonstrated higher specificity and positive predictive value (PPV) in predicting CSPCa as compared to criterion 1. The overall accuracies of criterion 1, 2, 3 and 4 were 64.42%, 85.58%, 80.77% and 79.81%, respectively. The area under the curve (AUC) values of criterion 2, 3 and 4 were higher (0.827, 0.732 and 0.792) than criterion 1 (0.665).
Using PIRADS score for predicting CSPCa as a screening test, criteria 2, 3 and 4 have much higher diagnostic performance and present accuracy of mp-MRI to predict CSPCa can be increased with addition of PSAD and free PSA%.
任何能够预测前列腺癌(PCa)不存在或临床意义重大的前列腺癌(CSPCa)不存在的非侵入性检测都是必要的,因为它可以减少前列腺特异性抗原(PSA)处于灰色区域(4 - 10 ng/mL)的患者进行不必要活检的数量。本研究评估了游离PSA%、PSA密度(PSAD)和前列腺影像报告和数据系统(PIRADS)评分(版本2.0)单独及联合应用在预测PSA为4至10 ng/mL的患者中CSPCa的诊断性能。
这项前瞻性研究共纳入了104例连续的下尿路症状(LUTS)患者,其血清PSA在4至10 ng/mL之间,无论直肠指检(DRE)结果是否异常或前列腺超声检查是否有低回声病变,且之前未进行过经直肠超声(TRUS)引导的前列腺活检。在进行TRUS引导的前列腺活检前,使用多参数磁共振成像(mp-MRI)计算PIRADS评分。对PIRADS评分、PSAD、游离PSA%与TRUS活检中CSPCa的存在情况之间的关系进行了统计学分析。
与非CSPCa患者相比,CSPCa患者的中位年龄(P = 0.001)、PSA水平(P < 0.001)、PSAD(P < 0.001)显著更高,而前列腺体积(P < 刚0.001)和游离PSA%显著更低。与非CSPCa患者相比,CSPCa患者中PIRADS检测呈阳性的比例显著更高(86.4%对53.3%,P < 0.001)。PSAD和游离PSA%的临界值分别为0.12 ng/mL和25%。年龄、PSAD和游离PSA%是PCa的显著预测因素,而年龄和PSAD是CSPCa的显著预测因素。与标准1相比,标准2、3和4在预测CSPCa方面表现出更高的特异性和阳性预测值(PPV)。标准1、2、3和4的总体准确率分别为64.42%、85.58%、80.77%和79.81%。标准2、3和4的曲线下面积(AUC)值(0.827、0.732和0.792)高于标准1(0.665)。
将PIRADS评分用于预测CSPCa作为一种筛查检测,标准2、3和4具有更高的诊断性能,并且通过添加PSAD和游离PSA%可以提高mp-MRI预测CSPCa的准确性。