Bogner Katja, Engelhard Karl, Wuest Wolfgang, Hamel Sajad
Institute of Radiology, Martha-Maria Hospital, Stadenstrasse 58, 90491, Nuremberg, Germany.
Abdom Radiol (NY). 2022 Jun;47(6):2187-2196. doi: 10.1007/s00261-022-03444-1. Epub 2022 Mar 21.
To evaluate the validity of PI-RADS categories 1 and 2 version 2.1 (V2.1) as predictors of the absence of carcinoma and to reevaluate lesions that were analysed as suspicious prior to PI-RADS or according to PI-RADS versions 1 and 2 and classified as PI-RADS 1 or 2 in V2.1.
Retrospective evaluation of 1170 multiparametric MRIs performed at one academic teaching hospital (2012-2019). Study cohort comprised 188 men that achieved PI-RADS scores 1 or 2 (V2.1) and underwent systematic and targeted biopsy, split into one group with suspect findings in the original reports that were created prior to PI-RADS or with version 1 and 2, and another group with unremarkable reports. Differences in presence of prostate cancer and PSA density were assessed by Chi-square and Fisher's exact test, and the negative predictive value (NPV) for both groups was conducted.
The NPV for clinically significant carcinoma (csCa) was 89.1% for 55 men with suspect findings in the original report and 93.2% for 133 men with negative MRI. There was no difference between the groups regarding the detection of csCa (p = 0.103). PSA density was significantly higher in the group with suspect original reports (p = 0.015).
A PI-RADS score 1 or 2 appears less likely to miss existing prostate cancer, although a small amount of csCa can be overlooked. In case of clinical suspicion or elevated PSA density and PI-RADS score 1 or 2, an individual decision has to be taken if biopsy is necessary or if monitoring is sufficient.
评估前列腺影像报告和数据系统(PI-RADS)第2.1版(V2.1)中1类和2类作为无癌预测指标的有效性,并重新评估在PI-RADS之前或根据PI-RADS第1版和第2版分析为可疑且在V2.1中分类为PI-RADS 1类或2类的病变。
对一家学术教学医院(2012 - 2019年)进行的1170例多参数磁共振成像(MRI)进行回顾性评估。研究队列包括188名获得PI-RADS评分1或2(V2.1)并接受系统和靶向活检的男性,分为一组,其原始报告(在PI-RADS之前或第1版和第2版时创建)中有可疑发现,另一组报告无异常。通过卡方检验和Fisher精确检验评估前列腺癌存在情况和前列腺特异抗原(PSA)密度的差异,并计算两组的阴性预测值(NPV)。
原始报告中有可疑发现的55名男性中,临床显著癌(csCa)的NPV为89.1%,MRI阴性的133名男性中为93.2%。两组在csCa检测方面无差异(p = 0.103)。原始报告有可疑发现的组中PSA密度显著更高(p = 0.015)。
PI-RADS评分1或2似乎不太可能漏诊现有的前列腺癌,尽管少量的csCa可能会被忽略。在临床怀疑或PSA密度升高且PI-RADS评分1或2的情况下,必须就是否需要活检或监测是否足够做出个体化决策。