Preston Mark A, Hong Agnes, Dufour Robert, Marden Jessica R, Kirson Noam Y, Gatoulis Sergio C, Kongara Serena, Gandhi Raj, Morgans Alicia K
Brigham and Women's Hospital, Boston, MA, USA.
Pfizer Inc., New York, NY, USA.
Eur Urol Open Sci. 2024 Jan 11;60:32-35. doi: 10.1016/j.euros.2023.12.003. eCollection 2024 Feb.
To assess the clinical impact of delayed testosterone recovery (TR) following the discontinuation of medical androgen deprivation therapy (ADT), a retrospective, longitudinal analysis was conducted in adult males with prostate cancer using the Optum® de-identified Electronic Health Record data set and Optum® Enriched Oncology Data (2010-2021). Of 3875 patients who initiated and discontinued ADT, 1553 received one or more testosterone-level tests within the 12 mo following discontinuation and were included in this study. These 1553 patients were categorized into two cohorts: 25% as TR (testosterone levels >280 ng/dl at any test within 12 mo following ADT discontinuation) and 75% as non-TR. At baseline, non-TR patients were older, had lower testosterone levels, and were more likely to have diabetes, hyperlipidemia, and hypertension, but less likely to have sexual dysfunction. After adjustment for baseline characteristics, the TR cohort had a lower risk of new-onset diabetes (hazard ratio [HR] 0.47; 95% confidence interval [CI] 0.27-0.79), trended toward a lower risk of new-onset depression (HR 0.58; 95% CI 0.33-1.02), and had a higher likelihood of seeking treatment for sexual dysfunction (HR 1.33; 95% CI 0.99-1.78) versus the non-TR cohort. These findings support monitoring testosterone levels after ADT discontinuation to manage potential long-term comorbidities in patients with prostate cancer.
This real-world analysis of males with prostate cancer who were treated with medical androgen deprivation therapy (ADT) found that most patients did not have their testosterone level checked in the 12 mo after stopping ADT. Of those who did, 75% did not achieve normal testosterone levels (>280 ng/dl), and these patients were more likely to experience new-onset diabetes than those who achieved normal testosterone levels. These results suggest that to ensure effective clinical decision-making, physicians should check patients' testosterone levels after stopping ADT.
为评估药物去势治疗(ADT)中断后睾酮恢复延迟(TR)的临床影响,利用Optum®匿名电子健康记录数据集和Optum®丰富肿瘤学数据(2010 - 2021年)对成年前列腺癌男性患者进行了一项回顾性纵向分析。在3875例开始并停止ADT治疗的患者中,1553例在停止治疗后的12个月内接受了一次或多次睾酮水平检测,并纳入本研究。这1553例患者被分为两个队列:25%为TR(ADT停止后12个月内的任何一次检测中睾酮水平>280 ng/dl),75%为非TR。在基线时,非TR患者年龄更大,睾酮水平更低,更有可能患有糖尿病、高脂血症和高血压,但性功能障碍的可能性较小。在对基线特征进行调整后,与非TR队列相比,TR队列新发糖尿病的风险较低(风险比[HR] 0.47;95%置信区间[CI] 0.27 - 0.79),新发抑郁症风险有降低趋势(HR 0.58;95% CI 0.33 - 1.02),性功能障碍寻求治疗的可能性更高(HR 1.33;95% CI 0.99 - 1.78)。这些发现支持在ADT停止后监测睾酮水平,以管理前列腺癌患者潜在的长期合并症。
这项对接受药物去势治疗(ADT)的前列腺癌男性患者的真实世界分析发现,大多数患者在停止ADT后的12个月内未检查睾酮水平。在检查了睾酮水平的患者中,75%未达到正常睾酮水平(>280 ng/dl),这些患者比达到正常睾酮水平的患者更有可能出现新发糖尿病。这些结果表明,为确保有效的临床决策,医生应在停止ADT后检查患者的睾酮水平。