Ball Mark W, Ross Ashley E, Ghabili Kamyar, Kim Chunwoo, Jun Changhan, Petrisor Doru, Pan Li, Epstein Jonathan I, Macura Katarzyna J, Stoianovici Dan S, Allaf Mohamad E
The James Buchanan Brady Urological Institute and Department of Urology, The Johns Hopkins University School of Medicine, Baltimore, MD.
Siemens Healthcare, Baltimore, MD.
Urology. 2017 Nov;109:216-221. doi: 10.1016/j.urology.2017.07.010. Epub 2017 Jul 19.
To evaluate safety and feasibility in a first-in-human trial of a direct magnetic resonance imaging (MRI)-guided prostate biopsy using a novel robotic device.
MrBot is an MRI-safe robotic device constructed entirely with nonconductive, nonmetallic, and nonmagnetic materials and developed by our group. A safety and feasibility clinical trial was designed to assess the safety and feasibility of a direct MRI-guided biopsy with MrBot and to determine its targeting accuracy. Men with elevated prostate-specific antigen levels, prior negative prostate biopsies, and cancer-suspicious regions (CSRs) on MRI were enrolled in the study. Biopsies targeting CSRs, in addition to sextant locations, were performed.
Five men underwent biopsy with MrBot. Two men required Foley catheter insertion after the procedure, with no other complications or adverse events. Even though this was not a study designed to detect prostate cancer, biopsies confirmed the presence of a clinically significant cancer in 2 patients. On a total of 30 biopsy sites, the robot achieved an MRI-based targeting accuracy of 2.55 mm and a precision of 1.59 mm normal to the needle, with no trajectory corrections and no unsuccessful attempts to target a site.
Robot-assisted MRI-guided prostate biopsy appears safe and feasible. This study confirms that a clinically significant prostate cancer (≥5-mm radius, 0.5 cm) depicted in MRI may be accurately targeted. Direct confirmation of needle placement in the CSR may present an advantage over fusion-based technology and gives more confidence in a negative biopsy result. Additional study is warranted to evaluate the efficacy of this approach.
在一项首次人体试验中,使用一种新型机器人设备评估直接磁共振成像(MRI)引导下前列腺活检的安全性和可行性。
MrBot是一种MRI安全的机器人设备,完全由非导电、非金属和非磁性材料构建,由我们团队研发。设计了一项安全性和可行性临床试验,以评估使用MrBot进行直接MRI引导活检的安全性和可行性,并确定其靶向准确性。纳入前列腺特异性抗原水平升高、既往前列腺活检阴性且MRI上有癌症可疑区域(CSR)的男性。除了前列腺六分区活检外,还针对CSR进行活检。
5名男性接受了MrBot活检。两名男性术后需要插入Foley导管,无其他并发症或不良事件。尽管这不是一项旨在检测前列腺癌的研究,但活检证实2例患者存在临床意义上的癌症。在总共30个活检部位,机器人基于MRI的靶向准确性为2.55毫米,垂直于针的精度为1.59毫米,无需轨迹校正,也没有未成功靶向位点的情况。
机器人辅助MRI引导下的前列腺活检似乎是安全可行的。这项研究证实,MRI中显示的临床意义上的前列腺癌(半径≥5毫米,0.5厘米)可以被准确靶向。与基于融合的技术相比,直接确认针在CSR中的位置可能具有优势,并能让人们对阴性活检结果更有信心。需要进一步研究来评估这种方法的疗效。