Department of Urology, Miller School of Medicine, University of Miami, Miami, FL, USA.
Prostate Cancer Prostatic Dis. 2016 Dec;19(4):385-389. doi: 10.1038/pcan.2016.27. Epub 2016 Jul 19.
Our goal was to compare the ability of active surveillance (AS) criteria and preoperative nomograms to identify patients with pathologically low-risk prostate cancer.
The study cohort consisted of 402 radical prostatectomy patients with Gleason 6 prostate cancer on at least 10-core biopsy. In this group, we analyzed the ability of Kattan and Truong nomograms to select patients with Gleason 3+3 or 3+4 organ-confined prostate cancer, and compared it with that of AS criteria of John Hopkins (JH) and University of California at San Francisco (UCSF) medical centers, and Prostate Cancer Research International: Active Surveillance (PRIAS) study. The performance of each tool was evaluated with respect to discrimination and predictive accuracy.
About 30% of patients were upgraded and 8% were upstaged in the final pathology. The nomograms demonstrated slightly higher discrimination in detecting organ-confined Gleason 3+3 and 3+4 disease. The predictive accuracy of the nomograms in selecting patients with low-grade organ-confined prostate cancer was superior to that of JH and UCSF criteria but not to PRIAS criteria. Furthermore, the nomograms were unable to select larger subgroups of patients with the same prevalence of Gleason 3+3 organ-confined prostate cancer as in men who met the PRIAS criteria. No difference was seen between the studied nomograms and AS criteria in their ability to identify patients with Gleason 3+4 organ-confined prostate cancer.
PRIAS criteria demonstrate optimal balance between sensitivity and specificity and are not inferior to the available pathological nomograms in selecting patients with low-grade organ-confined prostate cancer.
我们的目标是比较主动监测(AS)标准和术前列线图识别低危前列腺癌患者的能力。
研究队列包括 402 例接受根治性前列腺切除术的 Gleason 6 前列腺癌患者,这些患者至少接受了 10 针核心活检。在该组中,我们分析了 Kattan 和 Truong 列线图选择 Gleason 3+3 或 3+4 器官局限性前列腺癌患者的能力,并将其与约翰霍普金斯大学(JH)和加利福尼亚大学旧金山分校(UCSF)医学中心的 AS 标准以及前列腺癌研究国际:主动监测(PRIAS)研究进行比较。每种工具的性能均通过区分度和预测准确性进行评估。
约 30%的患者在最终病理检查中升级,8%的患者分期升高。列线图在检测器官局限性 Gleason 3+3 和 3+4 疾病方面显示出略高的区分度。列线图在选择低分级器官局限性前列腺癌患者方面的预测准确性优于 JH 和 UCSF 标准,但不如 PRIAS 标准。此外,列线图无法选择与符合 PRIAS 标准的男性相同的 Gleason 3+3 器官局限性前列腺癌患病率的更大亚组患者。在识别 Gleason 3+4 器官局限性前列腺癌患者方面,研究中的列线图与 AS 标准之间没有差异。
PRIAS 标准在敏感性和特异性之间表现出最佳平衡,在选择低分级器官局限性前列腺癌患者方面并不逊于现有的病理列线图。