1 Department of Medical Imaging, The Ottawa Hospital, The University of Ottawa, Ottawa, Ottawa Hospital, 1551 Riverside Dr, Ste 1104, Ottawa, ON K1G 4B5, Canada.
2 Department of Anatomical Pathology, The Ottawa Hospital, The University of Ottawa, Ottawa, ON, Canada.
AJR Am J Roentgenol. 2018 Sep;211(3):W158-W165. doi: 10.2214/AJR.17.18958. Epub 2018 Jul 11.
The purpose of this study was to evaluate quantitative apparent diffusion coefficient (ADC) metrics for the downgrading of Gleason score (GS) 9 or 10 prostate cancer (PCa) diagnosed by means of nontargeted transrectal ultrasound-guided biopsy.
Between 2012 and 2015, 30 men with a diagnosis of GS 9 or 10 PCa at nontargeted transrectal ultrasound-guided biopsy underwent 3-T multiparametric MRI before radical prostatectomy (RP). Two radiologists blinded to the histopathologic results independently assessed multiparametric MR images using Prostate Imaging Reporting and Data System (PI-RADS) version 2. Whole-lesion ADC mean, centile, and texture features were extracted from coregistered ADC and RP maps by a third blinded radiologist. Comparisons were performed by chi-square, multivariable logistic regression, and ROC analysis.
Tumors were downgraded to intermediate risk (GS 4 + 3 [n = 7] and GS 3 + 4 [n = 2]) PCa in 30.0% (9/30) of men after RP. There were no statistically significant differences between groups with respect to age (p = 0.028), prostate-specific antigen level (p = 0.018), or clinical stage (p = 0.021). PI-RADS version 2 scores did not differ between groups (p = 0.035, p = 0.091) with moderate agreement (κ = 0.48). There were no differences in mean or centile ADC (p = 0.269-0.634) between the two groups. ADC entropy was significantly lower in downgraded tumors (5.542 ± 0.721 [SD] vs 8.089 ± 1.237, p < 0.001) with no difference in kurtosis or skewness (p = 0.133, p = 0.296). The ROC AUC for the diagnosis of downgrading was 0.93 (95% CI, 0.84-1.00) with sensitivity of 85.7% and specificity of 88.9% when entropy was less than 6.31.
ADC entropy was significantly lower in GS 9 and 10 tumors diagnosed by means of nontargeted transrectal ultrasound-guided biopsy that were eventually downgraded to intermediate risk (GS 7) after RP. ADC texture analysis may be useful for further risk stratification of PCa diagnosed at biopsy.
本研究旨在评估通过非靶向经直肠超声引导活检诊断的 GS 9 或 10 级前列腺癌(PCa)的 ADC 值定量指标是否可降级。
2012 年至 2015 年,30 名经非靶向经直肠超声引导活检诊断为 GS 9 或 10 级 PCa 的男性患者在根治性前列腺切除术(RP)前行 3-T 多参数 MRI 检查。两名放射科医生在不了解病理结果的情况下,分别使用前列腺影像报告和数据系统(PI-RADS)第 2 版独立评估多参数 MRI 图像。由第三位盲法放射科医生从配准的 ADC 和 RP 图中提取全病变 ADC 平均值、百分位数和纹理特征。采用卡方检验、多变量逻辑回归和 ROC 分析进行比较。
RP 后,30 名男性中有 30.0%(9/30)的肿瘤降为中危(GS 4+3[n=7]和 GS 3+4[n=2])PCa。两组间在年龄(p=0.028)、前列腺特异抗原水平(p=0.018)或临床分期(p=0.021)方面无统计学差异。两组的 PI-RADS 第 2 版评分无差异(p=0.035,p=0.091),具有中度一致性(κ=0.48)。两组间 ADC 平均值或百分位数无差异(p=0.269-0.634)。降级肿瘤的 ADC 熵显著降低(5.542±0.721[SD]比 8.089±1.237,p<0.001),但峰度和偏度无差异(p=0.133,p=0.296)。ADC 熵<6.31 时,诊断降级的 ROC AUC 为 0.93(95%CI,0.84-1.00),灵敏度为 85.7%,特异性为 88.9%。
通过非靶向经直肠超声引导活检诊断的 GS 9 和 10 级肿瘤,在 RP 后降为中危(GS 7)级的肿瘤中,ADC 熵显著降低。ADC 纹理分析可能有助于进一步对活检诊断的 PCa 进行危险分层。