Departments of Radiology, Pathology, and Urology, Pellegrin Hospital, Place Amélie Raba Léon, 33076 Bordeaux, France.
Radiology. 2013 Oct;269(1):159-66. doi: 10.1148/radiol.13122393. Epub 2013 May 8.
To retrospectively evaluate diagnostic accuracy of real-time contrast material-enhanced (CE) ultrasonography (US) transrectal US-guided biopsies in patients with persistently elevated prostate-specific antigen (PSA) levels, previous negative systematic transrectal US-guided biopsy results, and positive prostate multiparametric magnetic resonance (MR) findings.
Institutional review board approval was obtained for this retrospective study. Informed consent was waived. From 2007 to 2011, 178 patients with increased PSA levels (mean, 10.7 ng/mL [10.7 μg/L]), previous negative findings of random biopsies, and targets depicted at multiparametric MR imaging underwent transrectal US-guided prostate biopsies after injection of sulfur hexafluoride microbubbles. CE US-targeted biopsies were performed systematically in cancer-suggestive regions, followed by random acquisition of 12 nontargeted cores in all other regions. Diagnostic accuracy of CE US-targeted biopsies was measured with sensitivity, specificity, and positive and negative predictive values. Fisher exact and Mann-Whitney U tests were used to compare subgroups of patients. Potential predictive variables were examined with a logistic regression model.
CE US findings were positive in a first group of 158 patients and negative in a second group of 20 patients. Prostate carcinoma (PCa) was detected in 75 patients in the first group (47.5%) and in eight of the second group (40.0%). Overall cancer detection rate was 46.6% (83 of 178). In the first group, PCa was detected with targeted biopsies alone in 18 patients (24%), with nontargeted biopsies alone in 23 (30.7%), and with both in 34 (45.3%). Mean number of CE US-targeted cores per cancer-suggestive region was 2.2. CE US-targeted biopsies had a positive overall detection rate of 30.9%, while it was 6.9% for 12-core nontargeted biopsies (P < .001). PSA level and Gleason score were associated with positivity of CE US-targeted biopsies (P = .031 and P = .015, respectively).
Real-time CE US-targeted transrectal US biopsy offers excellent sensitivity for PCa detection in men with previous negative biopsy results and positive findings at multiparametric MR imaging. It may be combined with conventional random biopsies to increase specificity.
回顾性评估实时对比增强(CE)超声(US)经直肠 US 引导活检在前列腺特异性抗原(PSA)水平持续升高、先前系统经直肠 US 引导活检结果阴性和前列腺多参数磁共振(MR)检查阳性的患者中的诊断准确性。
本回顾性研究获得了机构审查委员会的批准。豁免了知情同意。2007 年至 2011 年,178 例 PSA 水平升高(平均 10.7ng/mL[10.7μg/L])、先前随机活检结果阴性和多参数 MR 成像显示目标的患者接受了注射六氟化硫微泡后的经直肠 US 引导前列腺活检。CE US 靶向活检在可疑癌症区域系统进行,然后在所有其他区域随机采集 12 个非靶向核心。CE US 靶向活检的诊断准确性通过敏感性、特异性、阳性和阴性预测值进行测量。使用 Fisher 精确检验和 Mann-Whitney U 检验比较患者亚组。使用逻辑回归模型检查潜在的预测变量。
在第一组 158 例患者中,CE US 结果为阳性,在第二组 20 例患者中为阴性。在第一组中,75 例患者(47.5%)发现前列腺癌(PCa),第二组中有 8 例(40.0%)。178 例患者中总癌症检出率为 46.6%(83 例)。在第一组中,18 例(24%)仅通过靶向活检、23 例(30.7%)仅通过非靶向活检、34 例(45.3%)同时通过这两种方法检测到 PCa。每个可疑癌症区域的 CE US 靶向活检的平均活检核心数为 2.2 个。CE US 靶向活检的总体阳性检出率为 30.9%,而 12 针非靶向活检的阳性检出率为 6.9%(P<.001)。PSA 水平和 Gleason 评分与 CE US 靶向活检的阳性结果相关(P=.031 和 P=.015)。
在先前活检结果阴性且多参数 MR 成像阳性的患者中,实时 CE US 靶向经直肠 US 活检对前列腺癌具有极好的敏感性。它可以与常规的随机活检相结合,以提高特异性。