Department of Urology, University of Miami Miller School of Medicine, Miami, FL, USA.
Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, FL, USA.
Eur Urol Focus. 2021 Jan;7(1):142-147. doi: 10.1016/j.euf.2019.04.021. Epub 2019 May 15.
The challenge of managing non-muscle-invasive bladder cancer (NMIBC) is its high recurrence rate. Clinical investigations have begun to explore the role of androgen suppression as an adjunct to bladder cancer (BC) treatment.
To examine the effect of androgen suppression therapy (AST) on recurrence and progression rate of risk-stratified NMIBC.
DESIGN, SETTING, AND PARTICIPANTS: Male patients with NMIBC were identified retrospectively from a US institutional database between 2001 and 2017. AST included 5α-reductase inhibitor, gonadotropin-releasing hormone agonist, and antiandrogen. Patients who were exposed to AST prior to documented recurrence/progression were included in the treatment arm. BC was risk stratified to investigate the differential response to AST.
Hazard ratios (HRs) for NMIBC recurrence and progression were estimated using Cox proportional hazards multivariate regression models with stepwise method. Recurrence-free survival (RFS) and progression-free survival (PFS) were compared between groups with and without AST.
We identified a total of 274 males with a median follow-up period of 3.1 yr (interquartile range [IQR] 1.5-5.2). Thirty-six patients were exposed to AST with a median duration of 1.7 yr (IQR 0.7-2.6). AST was associated with a lower risk of recurrence (HR 0.53, 95% confidence interval 0.30-0.88) as well as improved RFS (p = 0.014). However, no significant reduction of progression or improvement of PFS (p = 0.23) was found with AST. After risk stratification, all five patients who progressed in the AST cohort had high-risk disease on initial transurethral resection (TUR), whereas no patients with low/intermediate-risk disease progressed on AST. Limitations of the study include nonstandardized initiation of AST in relation to initial TUR, lack of androgen level quantification, and small sample size in the treatment arm.
In this retrospective, single-institution study, AST was associated with a lower risk of recurrence in NMIBC. No significant association between AST and progression was found. Further investigation is warranted to define the role of AST as an adjunctive therapy for NMIBC.
Non-muscle-invasive bladder cancer is a highly recurrent disease that often requires patients to undergo repeated surgical treatments. This single-institution report suggests that medical suppression of androgen may be a potential preventive therapy to reduce recurrence in certain patients.
管理非肌肉浸润性膀胱癌(NMIBC)的挑战在于其高复发率。临床研究已经开始探索雄激素抑制作为膀胱癌(BC)治疗的辅助手段。
研究雄激素抑制疗法(AST)对风险分层的 NMIBC 复发和进展率的影响。
设计、地点和参与者:从 2001 年至 2017 年,我们从美国的一个机构数据库中回顾性地确定了患有 NMIBC 的男性患者。AST 包括 5α-还原酶抑制剂、促性腺激素释放激素激动剂和抗雄激素。在记录复发/进展之前接受 AST 的患者被纳入治疗组。BC 进行风险分层以研究 AST 的差异反应。
使用逐步法 Cox 比例风险多变量回归模型估计 NMIBC 复发和进展的风险比(HRs)。比较有无 AST 组之间的无复发生存率(RFS)和无进展生存率(PFS)。
我们共确定了 274 名男性患者,中位随访时间为 3.1 年(四分位距 [IQR] 1.5-5.2)。36 名患者接受 AST 治疗,中位治疗时间为 1.7 年(IQR 0.7-2.6)。AST 与较低的复发风险(HR 0.53,95%置信区间 0.30-0.88)以及更好的 RFS(p=0.014)相关。然而,AST 并没有显著降低进展或改善 PFS(p=0.23)。在风险分层后,AST 组中所有 5 名进展的患者在初始经尿道切除术(TUR)时均患有高危疾病,而在 AST 组中没有低/中危疾病进展的患者。研究的局限性包括与初始 TUR 相关的 AST 起始非标准化、雄激素水平定量缺乏以及治疗组的样本量小。
在这项回顾性单机构研究中,AST 与 NMIBC 较低的复发风险相关。AST 与进展之间没有显著关联。需要进一步研究来确定 AST 作为 NMIBC 辅助治疗的作用。
非肌肉浸润性膀胱癌是一种高度复发性疾病,通常需要患者反复接受手术治疗。这项单机构报告表明,医学抑制雄激素可能是一种降低某些患者复发风险的潜在预防疗法。