Institute of Urologic Oncology, Department of Urology, David Geffen School of Medicine at UCLA, Los Angeles, CA 90024, USA.
Eur Urol. 2012 Jun;61(6):1119-28. doi: 10.1016/j.eururo.2012.01.045. Epub 2012 Feb 1.
Previous studies demonstrate that androgen-deprivation therapy (ADT) with gonadotropin-releasing hormone (GnRH) agonists and orchiectomy for prostate cancer (PCa) is associated with cardiovascular disease. However, few studies have examined its effect on the peripheral vascular system.
To study the risk of peripheral artery disease (PAD) and venous thromboembolism associated with ADT for PCa.
DESIGN, SETTINGS, AND PARTICIPANTS: This was a population-based observational study of 182 757 US men ≥ 66 yr of age who were diagnosed with nonmetastatic PCa from 1992 to 2007, with a median follow-up of 5.1 yr, of whom 47.8% received GnRH agonists and 2.2% orchiectomy.
We used Cox proportional hazards models with time-varying treatment variables to adjust for demographic and tumor characteristics in assessing whether treatment with GnRH agonists or orchiectomy were associated with PAD and/or venous thromboembolism.
GnRH agonist use was associated with an increased risk of incident PAD (adjusted hazard ratio [HR]: 1.16; 95% confidence interval [CI], 1.12-1.21) and incident venous thromboembolism (adjusted HR: 1.10; 95% CI, 1.04-1.15). In addition, orchiectomy was associated with an increased risk of peripheral arterial disease (adjusted HR: 1.13; 95% CI, 1.02-1.26) and venous thromboembolism (adjusted HR: 1.27; 95% CI, 1.11-1.45). Limitations include the observational study design and the inability to assess the use of oral antiandrogens.
ADT for nonmetastatic PCa is associated with an increased risk of PAD and venous thromboembolism. Additional research is needed to better understand the potential risks and benefits of ADT, so that this treatment can be targeted to patients for whom the benefits are clearest.
先前的研究表明,促性腺激素释放激素(GnRH)激动剂联合去势治疗前列腺癌(PCa)与心血管疾病相关。然而,很少有研究探讨其对周围血管系统的影响。
研究 PCa 的去势治疗与外周动脉疾病(PAD)和静脉血栓栓塞(VTE)风险的相关性。
设计、地点和参与者:这是一项基于人群的观察性研究,纳入了 1992 年至 2007 年间被诊断为非转移性 PCa 的 182757 名年龄≥66 岁的美国男性,中位随访时间为 5.1 年,其中 47.8%接受了 GnRH 激动剂治疗,2.2%接受了去势治疗。
我们使用时变治疗变量的 Cox 比例风险模型,根据人口统计学和肿瘤特征进行调整,以评估 GnRH 激动剂或去势治疗是否与 PAD 和/或 VTE 相关。
GnRH 激动剂的使用与 PAD(调整后的风险比[HR]:1.16;95%置信区间[CI]:1.12-1.21)和 VTE(调整后的 HR:1.10;95% CI:1.04-1.15)的发病风险增加相关。此外,去势治疗与 PAD(调整后的 HR:1.13;95% CI:1.02-1.26)和 VTE(调整后的 HR:1.27;95% CI:1.11-1.45)的发病风险增加相关。局限性包括观察性研究设计和无法评估口服抗雄激素的使用。
非转移性 PCa 的去势治疗与 PAD 和 VTE 的风险增加相关。需要进一步研究以更好地了解去势治疗的潜在风险和获益,以便使这种治疗能够针对获益最明确的患者。