Sivaraman Arjun, Sanchez-Salas Rafael, Barret Eric, Macek Petr, Validire Pierre, Galiano Marc, Rozet Francois, Cathelineau Xavier
Department of Urology, Institute Mutualiste Monsouris, 42, Bd Jourdan, 75674, Paris Cedex 14, France.
Department of Pathology, Institute Mutualiste Monsouris, Paris, France.
World J Urol. 2015 Oct;33(10):1475-9. doi: 10.1007/s00345-014-1434-y. Epub 2014 Dec 12.
To evaluate the feasibility of prostate histoscanning true targeting (PHS-TT) guided transrectal ultrasound (TRUS) biopsy.
This is a prospective, single center, pilot study performed during February 2013-September 2013. All consecutive patients planned for prostate biopsy were included in the study, and all the procedure was performed by a single surgeon aided by the specialized true targeting software. Initially, the patients underwent PHS to map the abnormal areas within the prostate that were ≥0.2 cm(3). TRUS guided biopsies were performed targeting the abnormal areas with a specialized software. Additionally, routine bisextant biopsies were also taken. The final histopathology of the target cores was compared with the bisextant cores.
A total of 43 patients underwent combined 'targeted PHS guided' and 'standard 12 core systematic' biopsies. The mean volume of abnormal area detected by PHS is 4.3 cm(3). The overall cancer detection rate was 46.5 % (20/43) with systemic cores and target cores detecting cancer in 44 % (19/43) and 26 % (11/43), respectively. The mean % cancer/core length of the PHS-TT cores were significantly higher than the systematic cores (55.4 vs. 37.5 %. p < 0.05). In biopsy naïve patients, the cancer detection rate (43.7 % vs. 14.8 %. p = 0.06) and the cancer positivity of the cores (30.1 vs. 6.8 %. p < 0.01) of target cores were higher than those patients with prior biopsies.
PHS-TT is feasible and can be an effective tool for real-time guidance of prostate biopsies.
评估前列腺组织扫描真靶向(PHS-TT)引导下经直肠超声(TRUS)活检的可行性。
这是一项于2013年2月至2013年9月进行的前瞻性、单中心试点研究。所有计划进行前列腺活检的连续患者均纳入本研究,所有操作均由一名外科医生在专门的真靶向软件辅助下完成。最初,患者接受PHS以绘制前列腺内≥0.2 cm³的异常区域。使用专门软件针对异常区域进行TRUS引导下活检。此外,还进行常规的双侧活检。将靶向活检组织的最终组织病理学结果与双侧活检组织进行比较。
共有43例患者接受了“靶向PHS引导”和“标准12针系统”联合活检。PHS检测到的异常区域平均体积为4.3 cm³。系统活检组织和靶向活检组织的总体癌症检出率分别为46.5%(20/43)、44%(19/43)和26%(11/43)。PHS-TT活检组织的平均癌症/针长度百分比显著高于系统活检组织(55.4%对37.5%,p<0.05)。在初次活检患者中,靶向活检组织的癌症检出率(43.7%对14.8%,p = 0.06)和活检组织的癌症阳性率(30.1%对6.8%,p<0.01)高于既往有活检史的患者。
PHS-TT是可行的,可成为前列腺活检实时引导的有效工具。