Department of Urology, Seoul National University Bundang Hospital, Seongnam, Korea.
Department of Urology, Seoul National University Bundang Hospital, Seongnam, Korea; Department of Urology, Seoul National University College of Medicine, Seoul, Korea.
Clin Genitourin Cancer. 2017 Dec;15(6):e1117-e1122. doi: 10.1016/j.clgc.2017.07.020. Epub 2017 Aug 3.
To investigate the feasibility of active surveillance (AS) in biopsy Gleason score (GS) 3 + 4 prostate cancer (PCa), we compared the outcomes of biopsy GS 3 + 3 and 3 + 4 PCa after radical prostatectomy.
We analyzed the data of 1491 patients undergoing radical prostatectomy for biopsy GS 3 + 3 or 3 + 4 PCa who fulfilled the low-risk criteria of the National Comprehensive Cancer Network guidelines regardless of GS. The favorable GS 3 + 4 group was defined as having core involvement ≤ 50%, prostate-specific antigen density ≤ 0.2 ng/mL/cm, and number of positive cores ≤ 2 (maximal 1 core of GS 3 + 4).
The GS 3 + 4 group showed significantly worse pathologic outcomes, including pathologic GS, pathologic stage, and seminal vesicle invasion rate (all P < .001), as well as worse biochemical recurrence-free survival (P < .001) than the GS 3 + 3 group. However, the favorable GS 3 + 4 subgroup showed no significant differences in the pathologic outcomes (all P > .05) and in biochemical recurrence-free survival (P = .817) compared to the GS 3 + 3 group.
Despite the application of low-risk criteria, GS 3 + 4 PCa patients showed significantly worse outcomes than GS 3 + 3 patients. However, favorable GS 3 + 4 patients showed comparable clinicopathologic outcomes with GS 3 + 3 patients, suggesting possible expansion of AS for the favorable GS 3 + 4 group.
为了研究在活检 Gleason 评分(GS)3+4 前列腺癌(PCa)中进行主动监测(AS)的可行性,我们比较了根治性前列腺切除术后活检 GS 3+3 和 3+4 PCa 的结果。
我们分析了 1491 例接受根治性前列腺切除术治疗活检 GS 3+3 或 3+4 PCa 的患者的数据,这些患者符合国家综合癌症网络指南的低危标准,而与 GS 无关。有利的 GS 3+4 组定义为核心受累≤50%、前列腺特异性抗原密度≤0.2ng/mL/cm 和阳性核心数≤2(最大 1 个 GS 3+4 核心)。
GS 3+4 组的病理结果明显较差,包括病理 GS、病理分期和精囊侵犯率(均 P<0.001),以及生化无复发生存率(P<0.001)较差,与 GS 3+3 组相比。然而,有利的 GS 3+4 亚组在病理结果(均 P>0.05)和生化无复发生存率(P=0.817)方面与 GS 3+3 组无显著差异。
尽管应用了低危标准,但 GS 3+4 PCa 患者的结果明显差于 GS 3+3 患者。然而,有利的 GS 3+4 患者的临床病理结果与 GS 3+3 患者相当,提示有利的 GS 3+4 组可能扩大 AS 的应用。