Department of Surgery, Monash University, Melbourne, Australia; Australian Urology Associates, Malvern, Australia; Department of Urology, University of Minnesota, Minneapolis, MN, USA.
Healthcare Imaging Services, Richmond, Australia.
Eur Urol Oncol. 2022 Jun;5(3):314-320. doi: 10.1016/j.euo.2021.02.006. Epub 2021 Mar 23.
Gallium-labelled prostate-specific membrane antigen positron emission tomography (Ga-PSMA-11 PET) is a valuable staging tool, but its utility in characterising primary prostate cancer remains unclear. The maximum standardised uptake value (SUVmax) is a quantification measure of highest radiotracer uptake within PET-avid lesions.
To assess the utility of SUVmax in detecting clinically significant prostate cancer (csPCa) on biopsy alone and in combination with multiparametric magnetic resonance imaging (mpMRI).
DESIGN, SETTING, AND PARTICIPANTS: This was a retrospective analysis of 200 men who underwent Ga-PSMA-11 PET/CT, mpMRI, and transperineal template prostate biopsy between 2016 and 2018.
The primary and secondary outcomes were detection of grade group (GG) 3-5 and GG 2-5 prostate cancer, respectively. We used the Mann-Whitney U test to compare SUVmax by GG, and calculated sensitivity and specificity for csPCa detection via Ga-PSMA-11 PET/CT, mpMRI, and both. Multivariable logistic regression analyses were used to identify predictors of csPCa on biopsy.
The median SUVmax was greater for GG 3-5 tumours (6.40, interquartile range [IQR] 4.47-11.0) than for benign and GG 1-2 tumours (3.14, IQR 2.55-3.91; p < 0.001). The median SUVmax was greater for GG 3 (5.70, IQR 3.68-8.67) than for GG 2 (3.47, IQR 2.70-4.74; p < 0.001). For GG 3-5 disease, sensitivity was 86.5%, 95.9%, and 98.6%, and the negative predictive value (NPV) was 88.4%, 88.5%, and 93.3% using SUVmax ≥4, a Prostate Imaging-Reporting and Data System (PI-RADS) score of 3-5, and both, respectively. This combined model detected more GG 3-5 disease than mpMRI alone (98.6% vs 95.9%; p = 0.04). SUVmax was an independent predictor of csPCa for GG 3-5 disease only (odds ratio 1.27 per unit, 95% confidence interval 1.13-1.45). Our results are limited by the retrospective study design.
Greater SUVmax on Ga-PSMA-11 PET/CT is associated with detection of GG 3-5 cancer on biopsy. The combination of PI-RADS score and SUVmax provides higher sensitivity and NPV than either alone. Ga-PSMA-11 PET/CT may be useful alongside mpMRI in improving risk stratification for localised disease.
The amount of a radioactive tracer taken up in the prostate during a type of scan called PET (positron emission tomography) can predict whether aggressive prostate cancer is likely to be found on biopsy. This may complement the more usual type of scan, MRI (magnetic resonance imaging), used to detect prostate cancer.
镓标记前列腺特异性膜抗原正电子发射断层扫描(Ga-PSMA-11 PET)是一种有价值的分期工具,但它在描绘原发性前列腺癌中的作用仍不清楚。最大标准化摄取值(SUVmax)是一种对 PET 阳性病变内最高放射性示踪剂摄取进行量化的测量方法。
评估 SUVmax 在单独活检以及与多参数磁共振成像(mpMRI)联合检测临床显著前列腺癌(csPCa)的效用。
设计、地点和参与者:这是一项回顾性分析,纳入了 200 名 2016 年至 2018 年间接受 Ga-PSMA-11 PET/CT、mpMRI 和经会阴模板前列腺活检的男性。
主要和次要结果分别为检测 GG 3-5 和 GG 2-5 前列腺癌。我们使用曼-惠特尼 U 检验比较了按 GG 分组的 SUVmax,并计算了 Ga-PSMA-11 PET/CT、mpMRI 及两者联合检测 csPCa 的灵敏度和特异性。多变量逻辑回归分析用于识别活检中 csPCa 的预测因素。
GG 3-5 肿瘤的 SUVmax 中位数(6.40,四分位距[IQR] 4.47-11.0)大于良性和 GG 1-2 肿瘤(3.14,IQR 2.55-3.91;p<0.001)。GG 3 的 SUVmax 中位数(5.70,IQR 3.68-8.67)大于 GG 2(3.47,IQR 2.70-4.74;p<0.001)。对于 GG 3-5 疾病,SUVmax≥4、PI-RADS 评分 3-5 和两者联合的灵敏度分别为 86.5%、95.9%和 98.6%,阴性预测值(NPV)分别为 88.4%、88.5%和 93.3%。该联合模型检测到的 GG 3-5 疾病多于 mpMRI 单独检测(98.6% vs 95.9%;p=0.04)。SUVmax 是 GG 3-5 疾病 csPCa 的独立预测因素(每单位的优势比为 1.27,95%置信区间 1.13-1.45)。我们的结果受到回顾性研究设计的限制。
Ga-PSMA-11 PET/CT 上的 SUVmax 增加与活检中 GG 3-5 癌症的检出相关。PI-RADS 评分和 SUVmax 的组合比单独使用任何一种方法都具有更高的灵敏度和 NPV。Ga-PSMA-11 PET/CT 可能与 mpMRI 联合使用,以改善局限性疾病的风险分层。
一种名为 PET(正电子发射断层扫描)的扫描类型中,放射性示踪剂在前列腺中的摄取量可以预测活检中是否可能发现侵袭性前列腺癌。这可能补充了通常用于检测前列腺癌的 MRI(磁共振成像)扫描类型。