Boschheidgen M, Schimmöller L, Radtke J P, Kastl R, Jannusch K, Lakes J, Drewes L R, Radke K L, Esposito I, Albers P, Antoch G, Ullrich T, Al-Monajjed R
Department of Diagnostic and Interventional Radiology, University Dusseldorf, Medical Faculty, D-40225, Dusseldorf, Germany.
Department of Diagnostic, Interventional Radiology and Nuclear Medicine, Marien Hospital Herne, University Hospital of the Ruhr-University Bochum, Herne, Germany.
Eur Radiol. 2025 Apr;35(4):2170-2179. doi: 10.1007/s00330-024-11062-2. Epub 2024 Sep 13.
This study aims to analyse multiparametric MRI (mpMRI) characteristics of patients diagnosed with ISUP grade group (GG) 1 prostate cancer (PC) on initial target plus systematic MRI/TRUS fusion-guided biopsy and investigate histopathological progression during follow-up.
A retrospective single-centre cohort analysis was conducted on consecutive patients with mpMRI visible lesions (PI-RADS ≥ 3) and detection of ISUP-1-PC at the time of initial biopsy. The study assessed clinical, mpMRI, and histopathological parameters. Subcohorts were analysed with (1) patients who had confirmed ISUP-1-PC and (2) patients who experienced histopathological upgrading to ISUP ≥ 2 PC during follow-up either at re-biopsy or radical prostatectomy (RP).
A total of 156 patients (median age 65 years) between March 2014 and August 2021 were included. Histopathological upgrading to ISUP ≥ 2 was detected in 55% of patients during a median follow-up of 9.5 months (IQR 2.2-16.4). When comparing subgroups with an ISUP upgrade and sustained ISUP 1 PC, they differed significantly in contact length of the index lesion to the pseudocapsule, ADC value, PI-RADS category, and the MRI grading group (mGG) (p < 0.05). In the ISUP GG ≥ 2 subgroup, 91% of men had PI-RADS category 4 or 5 and 82% exhibited the highest mGG (mGG3). In multivariate analysis, mGG was the only independent parameter for predicting ISUP ≥ 2-PC in these patients.
MRI reveals important information about PC aggressiveness and should be incorporated into clinical decision-making when ISUP-1-PC is diagnosed. In cases of specific MRI characteristics adverse to the histopathology, early re-biopsy might be considered.
In cases with clear MRI characteristics for clinically significant prostate cancer (e.g., mGG 3 and/or PI-RADS 5, cT3, or clear focal PI-RADS 4 lesions on MRI) and ISUP GG 1 PC diagnosed on initial prostate biopsy, MRI findings should be incorporated into clinical decision-making and early re-biopsy (e.g., within 6 months) might be considered.
MRI reveals important information about prostate cancer (PC) aggressiveness. MRI should be incorporated into clinical decision-making when ISUP GG 1 PC is diagnosed on initial prostate biopsy. In cases of specific MRI characteristics adverse to the histopathology, early re-biopsy might be considered.
本研究旨在分析在初始靶向加系统性MRI/TRUS融合引导活检中被诊断为国际泌尿病理学会(ISUP)分级组(GG)1级前列腺癌(PC)患者的多参数MRI(mpMRI)特征,并调查随访期间的组织病理学进展情况。
对连续的mpMRI可见病变(前列腺影像报告和数据系统 [PI-RADS]≥3)且在初始活检时检测到ISUP-1-PC的患者进行回顾性单中心队列分析。该研究评估了临床、mpMRI和组织病理学参数。对亚组进行分析,其中包括(1)确诊为ISUP-1-PC的患者,以及(2)在再次活检或根治性前列腺切除术(RP)随访期间组织病理学升级为ISUP≥2级PC的患者。
纳入了2014年3月至2021年8月期间的156例患者(中位年龄65岁)。在中位随访9.5个月(四分位间距2.2 - 16.4)期间,55%的患者检测到组织病理学升级为ISUP≥2级。在比较有ISUP升级和持续ISUP 1级PC的亚组时,它们在索引病变与假包膜的接触长度、表观扩散系数(ADC)值、PI-RADS类别和MRI分级组(mGG)方面存在显著差异(p<0.05)。在ISUP GG≥2亚组中,91%的男性PI-RADS类别为4或5,82%表现为最高的mGG(mGG3)。在多变量分析中,mGG是预测这些患者中ISUP≥2级PC的唯一独立参数。
MRI揭示了有关PC侵袭性的重要信息,当诊断为ISUP-1-PC时应纳入临床决策。在MRI特征对组织病理学不利的情况下,可考虑早期再次活检。
对于临床上有意义的前列腺癌具有明确MRI特征的病例(例如,mGG 3和/或PI-RADS 5、cT3或MRI上明确的局灶性PI-RADS 4病变),且在初始前列腺活检时诊断为ISUP GG 1级PC,MRI结果应纳入临床决策,可考虑早期再次活检(例如,在6个月内)。
MRI揭示了有关前列腺癌(PC)侵袭性的重要信息。当在初始前列腺活检中诊断为ISUP GG 1级PC时,MRI应纳入临床决策。在MRI特征对组织病理学不利的情况下,可考虑早期再次活检。