Schoots Ivo G
Department of Radiology & Nuclear Medicine, Erasmus MC University Medical Center, Rotterdam, The Netherlands.
Transl Androl Urol. 2018 Feb;7(1):70-82. doi: 10.21037/tau.2017.12.31.
This review focuses on indeterminate lesions on prostate magnetic resonance imaging (MRI), assigned as PI-RADS category 3. The prevalence of PI-RADS 3 index lesion in the diagnostic work-up is significant, varying between one in three (32%) to one in five (22%) men, depending on patient cohort of first biopsies, previously negative biopsies, and active surveillance biopsies. A management strategy must be developed for this group of men with an indeterminate suspicion of having clinically significant prostate cancer (csPCa). Currently available data show that the actual prevalence of csPCa after targeted biopsy in PI-RADS 3 lesions vary between patients groups from one in five (21%) to one in six (16%), depending on previous biopsy status. Although this prevalence is lower in comparison to PI-RADS 4 and PI-RADS 5 lesions, still a considerable proportion of men harbor significant disease. Men with such a PI-RADS 3 lesion should therefore be adequately managed. In general, the clinical approach of using a threshold of PI-RADS ≥4 instead of PI-RADS ≥3 to select MRI for targeted biopsies is not supported by data from our explorative literature search using current definitions of csPCa. A possible adaptation to the threshold of PI-RADS ≥4 in combination with other clinical markers could be considered within an active surveillance protocol, where the balance between the individual risk of missing csPCa and the constant process of repeating prostate biopsies is crucial. In the future, improvements in MR imaging and interpretation, combined with molecular biomarkers and multivariate risk models will all be employed in prostate cancer detection and monitoring. These combinations will aid decision-making in challenging circumstances, such as unclear and diagnostic equivocal results for csPCa at early detection.
本综述聚焦于前列腺磁共振成像(MRI)上的不确定病变,即PI-RADS分类为3类的病变。在诊断检查中,PI-RADS 3类索引病变的患病率相当高,根据首次活检、既往阴性活检和主动监测活检的患者队列不同,每三到五名男性中就有一名(分别为32%和22%)存在此类病变。对于这组疑似患有临床显著前列腺癌(csPCa)的男性,必须制定一种管理策略。目前可得的数据表明,根据既往活检状态,PI-RADS 3类病变经靶向活检后csPCa的实际患病率在不同患者群体中有所不同,从五分之一(21%)到六分之一(16%)不等。尽管与PI-RADS 4类和PI-RADS 5类病变相比,该患病率较低,但仍有相当比例的男性患有严重疾病。因此,对于患有此类PI-RADS 3类病变的男性应进行妥善管理。一般来说,我们使用当前csPCa定义进行的探索性文献检索数据并不支持采用PI-RADS≥4而非PI-RADS≥3的阈值来选择MRI进行靶向活检的临床方法。在主动监测方案中,可以考虑将PI-RADS≥4的阈值与其他临床标志物相结合,在这种情况下,错过csPCa的个体风险与重复前列腺活检的持续过程之间的平衡至关重要。未来,磁共振成像及解读的改进,结合分子生物标志物和多变量风险模型,都将应用于前列腺癌的检测和监测。这些组合将有助于在具有挑战性的情况下做出决策,例如在早期检测中csPCa的结果不明确且诊断存在疑问的情况。