Department of Radiation Oncology, UCLA Medical Center, Los Angeles, CA, USA.
Ahmanson Translational Theranostics Division, Department of Molecular and Medical Pharmacology, UCLA Medical Center, Los Angeles, CA, USA.
Eur Urol Oncol. 2022 Feb;5(1):100-103. doi: 10.1016/j.euo.2021.01.006. Epub 2021 Feb 16.
Prostate-specific membrane antigen (PSMA) positron emission tomography (PET)/computed tomography (CT) is an emerging imaging modality with greater sensitivity and specificity over conventional imaging for prostate cancer (PCa) staging. Using data from two prospective trials (NCT03368547 and NCT04050215), we explored predictors of overall upstaging (nodal and metastatic) by PSMA PET/CT among patients with cN0M0 National Comprehensive Cancer Network high-risk PCa on conventional imaging (n = 213). Overall, 21.1%, 8.9%, and 23.9% of patients experienced nodal, metastatic, and overall upstaging, respectively, without histologic confirmation. On multivariable analysis, Gleason grade group (GG) and percent positive core (PPC) on systematic biopsy significantly predict overall upstaging (odds ratio [OR] 2.15, 95% confidence interval [CI] 1.33-3.45; p = 0.002; and OR 1.03, 95% CI 1.01-1.04; p < 0.001). Overall upstaging was significantly more frequent among men with GG 5 disease (33.0% vs. 17.6%; p = 0.0097) and PPC ≥50% (33.0% vs 15.0%; p = 0.0020). We constructed a nomogram that predicts overall upstaging using initial prostate-specific antigen, PPC, GG, and cT stage, with coefficients estimated from a standard logistic regression model (using maximum likelihood estimation). It is internally validated with a tenfold cross-validated area under the receiver operating characteristic curve estimated at 0.74 (95% CI 0.67-0.82). In our cohort, 90% of patients who had a nomogram-estimated risk below the cutoff of 22% for overall upstaging could have been spared PSMA PET/CT as our model correctly predicted no upstaging. In other words, the predictive model only missed 10% of patients who would otherwise have benefitted from PSMA PET/CT. PATIENT SUMMARY: We analyzed predictors of overall upstaging (lymph node or/and metastasis) by prostate-specific membrane antigen (PSMA) positron emission tomography/computed tomography (PET/CT) from conventional imaging in men with high-risk prostate cancer undergoing initial staging deemed free of disease in the lymph nodes and distant metastasis by conventional imaging techniques. We found that the pathologic grade and disease burden in a prostate biopsy are associated with upstaging. We also developed a tool that predicts the probability of upstaging according to an individual patient's characteristics. Our study may help in defining patient groups who are most likely to benefit from the addition of a PSMA PET/CT scan.
前列腺特异性膜抗原(PSMA)正电子发射断层扫描(PET)/计算机断层扫描(CT)是一种新兴的成像方式,与传统的前列腺癌(PCa)分期成像相比,具有更高的敏感性和特异性。使用来自两项前瞻性试验(NCT03368547 和 NCT04050215)的数据,我们探讨了在传统影像学检查中,前列腺特异性膜抗原(PSMA)PET/CT 对 cN0M0 美国国家综合癌症网络高危 PCa 患者总体升级(淋巴结和转移)的预测因素(n=213)。总体而言,分别有 21.1%、8.9%和 23.9%的患者出现淋巴结、转移和总体升级,但未经组织学证实。多变量分析显示,系统活检的 Gleason 分级组(GG)和阳性核心百分比(PPC)显著预测总体升级(优势比[OR]2.15,95%置信区间[CI]1.33-3.45;p=0.002;和 OR 1.03,95%CI 1.01-1.04;p<0.001)。GG 5 疾病(33.0%比 17.6%;p=0.0097)和 PPC≥50%(33.0%比 15.0%;p=0.0020)的患者总体升级更为频繁。我们构建了一个使用初始前列腺特异性抗原、PPC、GG 和 cT 期的预测总体升级的列线图,系数由标准逻辑回归模型(使用最大似然估计)估计。它通过十折交叉验证的接收者操作特征曲线下面积进行内部验证,估计值为 0.74(95%CI 0.67-0.82)。在我们的队列中,90%的列线图估计风险低于总体升级 22%截断值的患者可以避免 PSMA PET/CT,因为我们的模型正确预测没有升级。换句话说,预测模型仅漏掉了 10%否则可能受益于 PSMA PET/CT 的患者。患者总结:我们分析了在传统影像学检查中被认为无淋巴结和远处转移疾病的高危前列腺癌患者中,前列腺特异性膜抗原(PSMA)正电子发射断层扫描/计算机断层扫描(PET/CT)对总体升级(淋巴结和/或转移)的预测因素。我们发现,病理分级和前列腺活检中的疾病负担与升级有关。我们还开发了一种工具,可以根据个体患者的特征预测升级的概率。我们的研究可能有助于确定最有可能从 PSMA PET/CT 扫描中获益的患者群体。