Division of Urology, Department of Surgical Oncology, Princess Margaret Cancer Centre, University of Toronto, Toronto, ON, Canada.
Division of Urology, Department of Surgical Oncology, Mount Sinai Hospital and University Health Network, University of Toronto, Toronto, ON, Canada.
Prostate Cancer Prostatic Dis. 2021 Mar;24(1):69-76. doi: 10.1038/s41391-020-0218-2. Epub 2020 Mar 9.
Although 5-alpha-reductase inhibitors (5ARIs) have been shown to benefit men with prostate cancer (PCa) on active surveillance (AS), their long-term safety remains controversial. Our objective is to describe the long-term association of 5ARI use with PCa progression in men on AS.
MATERIALS/SUBJECTS AND METHODS: The cohort of men with low-risk PCa was derived from a prospectively maintained AS database at the Princess Margaret (1995-2016). Pathologic, grade, and volume progression were the primary end points. Kaplan-Meier time-to-event analysis was performed and Cox proportional hazards regression was used to determine predictors of progression where 5ARI exposure was analyzed as a time-dependent variable. Patients who came off AS prior to any progression events were censored at that time.
The cohort included 288 men with median follow-up of 82 months (interquartile range: 37-120 months). Among non-5ARI users (n = 203); 114 men (56.2%) experienced pathologic progression compared with 24 men (28.2%) in the 5ARI group (n = 85), (p < 0.001). Grade and volume progression were higher in the non-5ARI group compared with the 5ARI group (n = 82; 40.4% vs. n = 19; 22.4% respectively, p = 0.003 for grade progression; n = 87; 43.1% and n = 15; 17.7%, respectively for volume progression p < 0.001). Lack of 5ARI use was independently positively associated with pathologic progression (HR: 2.65; CI: 1.65-4.24), grade progression (HR: 2.75; CI: 1.49-5.06), and volume progression (HR: 3.15; CI: 1.78-5.56). The frequency of progression to high-grade (Grade Group 4-5) tumors was not significantly different between the groups.
Use of 5ARIs diminished both grade and volume progression without an increased risk of developing Grade Groups 4-5 disease.
尽管 5α-还原酶抑制剂(5ARIs)已被证明可使接受主动监测(AS)的前列腺癌(PCa)患者受益,但它们的长期安全性仍存在争议。我们的目的是描述 5ARI 使用与 AS 男性 PCa 进展之间的长期关联。
材料/受试者和方法:该低危 PCa 队列来自玛格丽特公主医院(1995-2016 年)前瞻性维护的 AS 数据库。病理、分级和体积进展是主要终点。进行 Kaplan-Meier 时间事件分析,并使用 Cox 比例风险回归来确定进展的预测因素,其中 5ARI 暴露被分析为时间依赖性变量。在任何进展事件之前退出 AS 的患者在该时间点被删失。
该队列包括 288 名中位随访 82 个月(四分位距:37-120 个月)的患者。在非 5ARI 使用者(n=203)中,114 名男性(56.2%)经历了病理进展,而 5ARI 组(n=85)中有 24 名男性(28.2%)(p<0.001)。与 5ARI 组相比,非 5ARI 组的分级和体积进展更高(n=82;40.4%与 n=19;22.4%,分别为 p=0.003;n=87;43.1%和 n=15;17.7%,分别为体积进展 p<0.001)。未使用 5ARI 与病理进展(HR:2.65;CI:1.65-4.24)、分级进展(HR:2.75;CI:1.49-5.06)和体积进展(HR:3.15;CI:1.78-5.56)独立呈正相关。两组之间高级别(分级组 4-5)肿瘤进展的频率没有显著差异。
5ARI 的使用减少了分级和体积的进展,而不会增加发展为 4-5 级疾病的风险。