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使用磁共振成像-超声融合技术实现靶向前列腺活检。

Use of MRI-ultrasound Fusion to Achieve Targeted Prostate Biopsy.

作者信息

Jayadevan Rajiv, Zhou Steve, Priester Alan M, Delfin Merdie, Marks Leonard S

机构信息

Department of Urology, University of California Los Angeles;

Department of Urology, University of California Los Angeles.

出版信息

J Vis Exp. 2019 Apr 9(146). doi: 10.3791/59231.

DOI:10.3791/59231
PMID:31033955
Abstract

Here, we present a protocol to perform targeted prostate biopsy using a magnetic resonance imaging-ultrasound (MRI/US) fusion system. Prostate cancer has traditionally been diagnosed via transrectal ultrasound (TRUS) biopsy. Though considered the gold standard, TRUS is unable to visualize most prostate cancer lesions and therefore requires sampling of the entire prostate. This biopsy method often undergrades prostate cancer and fails to detect up to 35% of cancers on initial biopsy. Prostate MRI has been shown to have excellent sensitivity in the detection of cancerous lesions, and advancements in MRI technology during the last decade have led to the development of targeted biopsy. In targeted biopsy, a software platform overlays MRI data onto live TRUS images to create a fused MRI/US three-dimensional model of the prostate. Regions suspicious for malignancy on MRI are contoured by a radiologist, uploaded into the fusion system, and then displayed within the live MRI/US fused model. The urologist is then able to directly biopsy these targets. When compared to conventional TRUS biopsy, MRI/US fusion technology has been demonstrated to improve the detection of clinically significant cancer while reducing insignificant cancer detection. This technology, therefore, has the potential to diagnose prostate cancer primarily in men who would benefit from treatment.

摘要

在此,我们介绍一种使用磁共振成像 - 超声(MRI/US)融合系统进行靶向前列腺活检的方案。传统上,前列腺癌是通过经直肠超声(TRUS)活检来诊断的。尽管TRUS被视为金标准,但它无法可视化大多数前列腺癌病灶,因此需要对整个前列腺进行采样。这种活检方法常常会低估前列腺癌,并且在初次活检时高达35%的癌症无法被检测到。前列腺MRI已被证明在检测癌性病灶方面具有出色的敏感性,过去十年间MRI技术的进步促使了靶向活检的发展。在靶向活检中,一个软件平台将MRI数据叠加到实时TRUS图像上,以创建前列腺的融合MRI/US三维模型。放射科医生勾勒出MRI上可疑的恶性区域,上传到融合系统中,然后显示在实时MRI/US融合模型内。随后,泌尿科医生能够直接对这些靶点进行活检。与传统的TRUS活检相比,MRI/US融合技术已被证明可以提高对具有临床意义的癌症的检测率,同时减少对无意义癌症的检测。因此,这项技术有可能主要在那些将从治疗中受益的男性中诊断前列腺癌。

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Use of MRI-ultrasound Fusion to Achieve Targeted Prostate Biopsy.使用磁共振成像-超声融合技术实现靶向前列腺活检。
J Vis Exp. 2019 Apr 9(146). doi: 10.3791/59231.
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An initial negative round of targeted biopsies in men with highly suspicious multiparametric magnetic resonance findings does not exclude clinically significant prostate cancer-Preliminary experience.多参数磁共振检查结果高度可疑的男性患者首轮靶向活检结果为阴性,并不排除存在具有临床意义的前列腺癌——初步经验
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In patients with a previous negative prostate biopsy and a suspicious lesion on magnetic resonance imaging, is a 12-core biopsy still necessary in addition to a targeted biopsy?对于既往前列腺活检结果为阴性但磁共振成像显示有可疑病变的患者,除了靶向活检外,是否仍需要进行12针活检?
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Targeted MRI-guided prostate biopsies for the detection of prostate cancer: initial clinical experience with real-time 3-dimensional transrectal ultrasound guidance and magnetic resonance/transrectal ultrasound image fusion.靶向 MRI 引导下的前列腺活检在前列腺癌检测中的应用:实时 3 维经直肠超声引导与磁共振/经直肠超声图像融合技术的初步临床经验。
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[Real-time MRI/US fusion-guided biopsy in biopsy-naïve and pre-biopsied patients with suspicion for prostate cancer].[实时MRI/超声融合引导下对初诊及活检前疑似前列腺癌患者进行活检]
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Magnetic resonance imaging-targeted biopsy may enhance the diagnostic accuracy of significant prostate cancer detection compared to standard transrectal ultrasound-guided biopsy: a systematic review and meta-analysis.磁共振成像靶向活检可能比标准经直肠超声引导活检更能提高显著前列腺癌检测的诊断准确性:系统评价和荟萃分析。
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Front Oncol. 2021 Mar 5;11:612157. doi: 10.3389/fonc.2021.612157. eCollection 2021.
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A Quality Control System for Automated Prostate Segmentation on T2-Weighted MRI.一种用于T2加权磁共振成像上前列腺自动分割的质量控制系统。
Diagnostics (Basel). 2020 Sep 18;10(9):714. doi: 10.3390/diagnostics10090714.
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Prostate Cancer Detection Rate of Freehand versus 3-Dimensional Template Mapping Biopsy Using a Magnetic Resonance Imaging-Ultrasound Fusion Device in Biopsy Naïve Men.
磁共振超声融合引导下徒手与三维模板定位靶向穿刺活检在初次活检前列腺癌患者中的应用比较
J Urol. 2020 Apr;203(4):699-705. doi: 10.1097/JU.0000000000000587. Epub 2019 Oct 9.