Department of Urology, University of Heidelberg, Im Neuenheimer Feld 110, 69120, Heidelberg, Germany.
World J Urol. 2012 Feb;30(1):91-5. doi: 10.1007/s00345-010-0631-6. Epub 2010 Dec 31.
To investigate prostate-specific antigen density as a predictor for pathologic upstaging in patients initially thought to have unilateral prostate cancer.
We analyzed 438 patients with unilateral prostate cancer in prostate biopsy samples that were treated with radical prostatectomy. Bilateral or extracapsular growth in the final surgical specimens was defined as upstaging. Using Kaplan-Meier curves and a multivariate Cox proportional hazard model, we evaluated the oncologic effect of pathologic upstaging on biochemical recurrence-free survival. Prostate-specific antigen density was evaluated as a diagnostic tool to predict upstaging using ROC-curve analysis.
Of the patients, 30.8% had bilateral prostate cancer or extracapsular extension in the surgical specimen. Prostate-specific antigen density was a diagnostic predictor for pathologic upstaging in patients initially thought to have unilateral prostate cancer (AUC 0.62, P < 0.001). Using a lower cutoff value of PSA density <0.056 ng/ml/cm3, upstaging could be excluded in patients with a sensitivity of >98%.
A considerable amount of patients that are initially diagnosed with unilateral prostate cancer on biopsy are underdiagnosed and are upstaged in the radical prostatectomy specimen. In general, AUC of PSA density is too low to use PSA density as diagnostic tool to predict pathologic upstaging in all patients. Nonetheless, PSA density could be used for hemiablative focal therapy decision making using a lower cutoff value of <0.056 ng/ml/cm3.
探讨前列腺特异性抗原密度(PSAD)作为预测初始单侧前列腺癌患者病理升级的指标。
我们分析了 438 例接受根治性前列腺切除术治疗的单侧前列腺癌患者的前列腺活检样本。最终手术标本中双侧或包膜外生长定义为升级。通过 Kaplan-Meier 曲线和多变量 Cox 比例风险模型,我们评估了病理升级对生化无复发生存的肿瘤学影响。使用 ROC 曲线分析,评估 PSAD 作为预测升级的诊断工具的效能。
在这些患者中,30.8%的患者在手术标本中存在双侧前列腺癌或包膜外延伸。PSAD 是初始单侧前列腺癌患者病理升级的诊断预测指标(AUC 0.62,P < 0.001)。使用 PSA 密度 <0.056ng/ml/cm3 的较低截断值,可以排除具有>98%敏感性的患者发生升级。
相当数量的在活检时被诊断为单侧前列腺癌的患者被低估,并且在根治性前列腺切除标本中被升级。一般来说,PSA 密度的 AUC 太低,无法将 PSA 密度用作预测所有患者病理升级的诊断工具。然而,PSA 密度可以用于半破坏性的局灶性治疗决策,使用较低的截断值<0.056ng/ml/cm3。