首页> 外文期刊>BMC Urology >The prostate cancer detection rates of CEUS-targeted versus MRI-targeted versus systematic TRUS-guided biopsies in biopsy-na?ve men: a prospective, comparative clinical trial using the same patients
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The prostate cancer detection rates of CEUS-targeted versus MRI-targeted versus systematic TRUS-guided biopsies in biopsy-na?ve men: a prospective, comparative clinical trial using the same patients

机译:初次活检男性中以CEUS为靶标,以MRI为靶标,以系统TRUS指导的活检的前列腺癌检出率:一项使用相同患者的前瞻性比较临床试验

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Background The current standard for Prostate Cancer (PCa) detection in biopsy-na?ve men consists of 10–12 systematic biopsies under ultrasound guidance. This approach leads to underdiagnosis and undergrading of significant PCa while insignificant PCa may be overdiagnosed. The recent developments in MRI and Contrast Enhanced Ultrasound (CEUS) imaging have sparked an increasing interest in PCa imaging with the ultimate goal of replacing these “blind” systematic biopsies with reliable imaging-based targeted biopsies. Methods/design In this trial, we evaluate and compare the PCa detection rates of multiparametric (mp)MRI-targeted biopsies, CEUS-targeted biopsies and systematic biopsies under ultrasound guidance in the same patients. After informed consent, 299 biopsy-na?ve men will undergo mpMRI scanning and CEUS imaging 1?week prior to the prostate biopsy procedure. During the biopsy procedure, a systematic transrectal 12-core biopsy will be performed by one operator blinded for the imaging results and targeted biopsy procedure. Subsequently a maximum of 4 CEUS-targeted biopsies and/or 4 mpMRI-targeted biopsies of predefined locations determined by an expert CEUS reader using quantification techniques and an expert radiologist, respectively, will be taken by a second operator using an MRI-US fusion device. The primary outcome is the detection rate of PCa (all grades) and clinically significant PCa (defined as Gleason score ≥7) compared between the three biopsy protocols. Discussion This trial compares the detection rate of (clinically significant) PCa, between both traditional systematic biopsies and targeted biopsies based on predefined regions of interest identified by two promising imaging technologies. It follows published recommendations on study design for the evaluation of imaging guided prostate biopsy techniques, minimizing bias and allowing data pooling. It is the first trial to combine mpMRI imaging and advanced CEUS imaging with quantification. Trial registration The Dutch Central Committee on Research Involving Human Subjects registration number NL52851.018.15, registered on 3 Nov 2015. Clinicaltrials.gov database registration number NCT02831920 , retrospectively registered on 5 July 2016.
机译:背景技术目前,在未进行过活检的男性中,前列腺癌(PCa)检测的标准包括在超声引导下进行的10至12次系统活检。这种方法会导致对重要PCa的诊断不足和降级,而对无关紧要的PCa可能会进行过度诊断。 MRI和对比度增强超声(CEUS)成像技术的最新发展引起了人们对PCa成像技术的越来越浓厚的兴趣,其最终目标是用可靠的基于成像的靶向活检技术代替这些“盲”系统活检技术。方法/设计在该试验中,我们评估和比较了超声引导下多参数(mp)MRI活检,CEUS活检和系统活检的PCa检测率。在获得知情同意后,将对299名未进行活检的男性进行前列腺活检之前1周进行mpMRI扫描和CEUS成像。在活检过程中,将由一名对影像学结果和靶向活检过程不知情的操作者进行系统的经直肠12核活检。随后,第二名操作员将使用MRI-US融合设备分别分别由专家CEUS读取器使用定量技术和专家放射线医师分别确定的预定位置的最多4个以CEUS为目标的活检和/或以mpMRI为目标的预定义位置的活检。主要结果是三种活检方案之间的PCa(所有级别)和临床上显着的PCa(定义为Gleason评分≥7)的检出率。讨论该试验基于两种有前途的成像技术确定的预定目标区域,比较了传统的系统活检和目标活检之间的(临床意义上的)PCa的检测率。它遵循已发表的有关研究设计的建议,以评估成像引导的前列腺活检技术,最小化偏倚并允许数据合并。这是将mpMRI成像和高级CEUS成像与定量相结合的第一项试验。试用注册荷兰涉及人类受试者的研究中央委员会注册号为NL52851.018.15,于2015年11月3日注册。Clinicaltrials.gov数据库注册号为NCT02831920,其追溯注册于2016年7月5日。

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