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三维声辐射力脉冲(ARFI)成像用于靶向前列腺活检引导的临床可行性

Clinical Feasibility of 3-D Acoustic Radiation Force Impulse (ARFI) Imaging for Targeted Prostate Biopsy Guidance.

作者信息

Chan Derek Y, Moavenzadeh Spencer R, Wightman Wren E, Palmeri Mark L, Polascik Thomas J, Nightingale Kathryn R

机构信息

Department of Biomedical Engineering, Duke University, Durham, NC, USA.

Departments of Urology and Radiology, Duke University Medical Center, Durham, NC, USA.

出版信息

Ultrason Imaging. 2025 Mar;47(2):79-92. doi: 10.1177/01617346241311901. Epub 2025 Jan 6.

Abstract

We have developed a 3-D acoustic radiation force impulse (ARFI) prostate imaging system to identify regions suspicious for cancer and guide a targeted prostate biopsy in a single visit. The system uses a side-fire transrectal probe and an automated rotation stage to acquire ARFI and B-mode image volumes, combined with 3-D visualization and targeting software to enable biopsy target identification and guide a transperineal (TP) biopsy. The system was tested in the first clinical trial of its kind, with subjects serially undergoing ARFI-guided targeted TP biopsy, multiparametric magnetic resonance imaging (mpMRI)-ultrasound fusion TP biopsy, and systematic sampling TP biopsy. The findings indicate that the ARFI system is feasible for guiding a targeted biopsy. For lower-grade cancer (grade groups [GG] 1-2), ARFI underperformed mpMRI and systematic sampling, detecting cancer in 54% of GG 2 subjects. However, ARFI performance improved with increasing cancer grade; for higher-grade cancer (GG 3-5), ARFI performed comparably to the other biopsy approaches, and detected cancer in all GG 4 and 5 subjects. The findings also suggest the benefit of using 2-D ARFI imaging to confirm target location during live B-mode imaging, which could improve existing ultrasonic fusion biopsy workflows. This study is registered with ClinicalTrials.gov as NCT04607135.

摘要

我们开发了一种三维声辐射力脉冲(ARFI)前列腺成像系统,以识别可疑的癌症区域,并在一次就诊中指导靶向前列腺活检。该系统使用侧射经直肠探头和自动旋转平台来获取ARFI和B模式图像容积,并结合三维可视化和靶向软件,以实现活检靶点识别并指导经会阴(TP)活检。该系统在同类首次临床试验中进行了测试,受试者依次接受ARFI引导的靶向TP活检、多参数磁共振成像(mpMRI)-超声融合TP活检和系统采样TP活检。研究结果表明,ARFI系统在指导靶向活检方面是可行的。对于低级别癌症(分级组[GG]1-2),ARFI的表现不如mpMRI和系统采样,在GG 2受试者中检测到癌症的比例为54%。然而,随着癌症分级的增加,ARFI的性能有所改善;对于高级别癌症(GG 3-5),ARFI的表现与其他活检方法相当,在所有GG 4和5受试者中均检测到癌症。研究结果还表明,在实时B模式成像期间使用二维ARFI成像来确认靶点位置具有益处,这可能会改善现有的超声融合活检工作流程。本研究已在ClinicalTrials.gov上注册,注册号为NCT04607135。

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