Delgado Jessica, Ory Jesse, Loloi Justin, Deebel Nicholas A, Bernstein Ari, Nackeeran Sirpi, Zucker Isaac, Ramasamy Ranjith
Urology, University of Miami, Miami, USA.
Urology, Dalhousie University, Halifax, CAN.
Cureus. 2022 Dec 19;14(12):e32699. doi: 10.7759/cureus.32699. eCollection 2022 Dec.
Introduction Many men receiving temporary androgen deprivation therapy (ADT) for localized prostate cancer fail to achieve baseline testosterone levels after cessation. Testosterone recovery in men with localized prostate cancer receiving temporary ADT was assessed. Methods A global federated health research network (TriNetX) was used to identify men diagnosed with prostate cancer undergoing temporary ADT. Two cohorts were identified: men receiving luteinizing hormone-releasing hormone (LHRH) antagonists or LHRH agonists, and men receiving combined ADT (LHRH agonist and antiandrogens). Further stratification was based on a treatment duration of six months (short-term) or 18 months (long-term) to compare testosterone (T) recovery profiles five years after ADT cessation. Results A total of 28,583 men received LHRH agonist or antagonist therapy alone, and 20,188 men received combination ADT. A total of 46.7% of men who received short-term LHRH agonists or antagonists and 40.6% of men who received short-term combined ADT, recovered to mean baseline T levels at five years. Only men who received short-term LHRH agonists/antagonists recovered to eugonadal levels at the five-year follow-up. Around 50% of men who received long-term LHRH agonist/antagonist therapy and 10.7% of men who received combined ADT, recovered to mean baseline T levels at five years. However, neither group recovered to eugonadal T levels. Conclusions At the five-year follow-up after ADT cessation, most patients failed to recover to their mean baseline and eugonadal T levels. Given that testosterone deficiency is associated with metabolically adverse changes in body composition, increased insulin resistance, impaired bone health, and hypogonadal symptoms, serum T levels must be closely monitored in men receiving ADT following treatment cessation.
引言 许多接受局部前列腺癌临时雄激素剥夺疗法(ADT)的男性在治疗停止后未能恢复到基线睾酮水平。本研究评估了接受局部前列腺癌临时ADT治疗的男性的睾酮恢复情况。方法 利用一个全球联合健康研究网络(TriNetX)来识别被诊断为前列腺癌且正在接受临时ADT治疗的男性。确定了两个队列:接受促黄体生成素释放激素(LHRH)拮抗剂或LHRH激动剂的男性,以及接受联合ADT(LHRH激动剂和抗雄激素药物)的男性。进一步根据治疗持续时间为6个月(短期)或18个月(长期)进行分层,以比较ADT停止后五年的睾酮(T)恢复情况。结果 共有28583名男性单独接受LHRH激动剂或拮抗剂治疗,20188名男性接受联合ADT治疗。接受短期LHRH激动剂或拮抗剂治疗的男性中,共有46.7%在五年时恢复到平均基线T水平;接受短期联合ADT治疗的男性中,这一比例为40.6%。只有接受短期LHRH激动剂/拮抗剂治疗的男性在五年随访时恢复到正常性腺功能水平。接受长期LHRH激动剂/拮抗剂治疗的男性中约50%,以及接受联合ADT治疗的男性中10.7%,在五年时恢复到平均基线T水平。然而,两组均未恢复到正常性腺功能T水平。结论 在ADT停止后的五年随访中,大多数患者未能恢复到其平均基线和正常性腺功能T水平。鉴于睾酮缺乏与身体成分的代谢不良变化、胰岛素抵抗增加、骨骼健康受损和性腺功能减退症状相关,在治疗停止后接受ADT的男性中必须密切监测血清T水平。