Department of Urology, University Hospital Heidelberg, Heidelberg, Germany; Department of Radiology, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Department of Urology, University Hospital Heidelberg, Heidelberg, Germany.
Eur Urol Focus. 2021 Jan;7(1):102-110. doi: 10.1016/j.euf.2019.03.001. Epub 2019 Mar 13.
Contemporary selection criteria for men with prostate cancer (PC) suitable for active surveillance (AS) are unsatisfactory, leading to high disqualification rates based on tumor misclassification. Conventional biopsy protocols are based on standard 12-core transrectal ultrasound (TRUS) biopsy.
To assess the value of magnetic resonance imaging (MRI)/TRUS fusion biopsy over 4-yr follow-up in men on AS for low-risk PC.
DESIGN, SETTING, AND PARTICIPANTS: Between 2010 and 2018, a total of 273 men were included. Of them, 157 men with initial 12-core TRUS biopsy and 116 with initial MRI/TRUS fusion biopsy were followed by systematic and targeted transperineal MRI/TRUS fusion biopsies based on Prostate Cancer Research International Active Surveillance criteria. MRI from follow-up MRI/TRUS fusion biopsy was assessed using the Prostate Cancer Radiological Estimation of Change in Sequential Evaluation (PRECISE) scoring system.
AS-disqualification rates for patients on AS initially diagnosed by either 12-core TRUS biopsy or by MRI/TRUS fusion biopsy were compared using Kaplan-Meier estimates, log-rank tests, and regression analyses. We also analyzed the influence of negative primary MRI and PRECISE scoring to predict AS disqualification using Kaplan-Meier estimates, log-rank tests, and receiver operating characteristic (ROC) curve analysis.
Of men diagnosed by 12-core TRUS biopsy, 59% were disqualified from AS based on the results of subsequent MRI/TRUS fusion biopsy. In the initial MRI fusion biopsy cohort, upgrading occurred significantly less frequently (19%, p<0.001). ROC curve analyses demonstrated good discrimination for the PRECISE score with an area under the curve of 0.83. No men with a PRECISE score of 1 or 2 (demonstrating absence or downgrading of lesions in follow-up MRI) were disqualified from AS. In our cohort, a negative baseline MRI scan was not a predictor of nondisqualification from AS. Limitations include transperineal approach and extended systematic biopsies used with MRI/TRUS fusion biopsy, which may not be representative of other centers.
MRI/TRUS fusion biopsies allow a reliable risk classification for patients who are candidates for AS. The application of the PRECISE scoring system demonstrated good discrimination.
In this study, we investigated the value of multiparametric magnetic resonance imaging (MRI) and MRI/transrectal ultrasound (TRUS) fusion biopsies for the assessment of active surveillance (AS) reliability using the Prostate Cancer Radiological Estimation of Change in Sequential Evaluation criteria. Standard TRUS biopsies lead to significant underestimation of prostate cancer. In contrast, MRI/TRUS fusion biopsies allowed for a more reliable risk classification. For appropriate inclusion into AS, men should receive either an initial or a confirmatory MRI/TRUS fusion biopsy.
目前适用于前列腺癌(PC)主动监测(AS)的男性选择标准并不令人满意,这导致基于肿瘤错误分类而出现较高的淘汰率。传统的活检方案基于标准的 12 针经直肠超声(TRUS)活检。
评估在接受低危 PC 主动监测的男性中,4 年随访期间 MRI/TRUS 融合活检的价值。
设计、地点和参与者:2010 年至 2018 年期间,共纳入 273 名男性。其中,157 名男性接受了初始的 12 针 TRUS 活检,116 名男性接受了初始的 MRI/TRUS 融合活检,根据前列腺癌研究国际主动监测标准,对他们进行了系统和靶向经会阴 MRI/TRUS 融合活检。根据前列腺癌放射学连续评估变化估计(PRECISE)评分系统评估随访 MRI/TRUS 融合活检的 MRI。
使用 Kaplan-Meier 估计、对数秩检验和回归分析比较了最初通过 12 针 TRUS 活检或 MRI/TRUS 融合活检诊断的患者在 AS 中的淘汰率。我们还使用 Kaplan-Meier 估计、对数秩检验和受试者工作特征(ROC)曲线分析,分析了阴性原发性 MRI 和 PRECISE 评分对预测 AS 淘汰的影响。
在接受 12 针 TRUS 活检诊断的男性中,59%的男性因随后的 MRI/TRUS 融合活检结果而被淘汰出 AS。在初始 MRI 融合活检队列中,升级的发生率显著降低(19%,p<0.001)。ROC 曲线分析表明,PRECISE 评分具有良好的区分度,曲线下面积为 0.83。在 PRECISE 评分中为 1 或 2 的男性(在随访 MRI 中显示病变缺失或降级)均未被淘汰出 AS。在我们的队列中,基线 MRI 扫描阴性并不是 AS 淘汰的预测因素。局限性包括经会阴入路和 MRI/TRUS 融合活检中使用的扩展系统活检,这可能与其他中心不具有代表性。
MRI/TRUS 融合活检可对适合 AS 的患者进行可靠的风险分类。PRECISE 评分系统的应用具有良好的判别力。
在这项研究中,我们使用前列腺癌放射学连续评估变化估计标准,研究了多参数磁共振成像(MRI)和 MRI/TRUS 融合活检在评估主动监测(AS)可靠性方面的价值。标准的 TRUS 活检导致前列腺癌的严重低估。相比之下,MRI/TRUS 融合活检可以进行更可靠的风险分类。为了适当纳入 AS,男性应接受初始或确认性的 MRI/TRUS 融合活检。