Aglan Mostafa, Kong Yixin, Connell Brendan
General Internal Medicine, Lahey Hospital & Medical Center, Burlington, MA, USA.
Department of Medicine, Lahey Hospital & Medical Center, Burlington, MA, USA.
Transl Androl Urol. 2025 Feb 28;14(2):250-257. doi: 10.21037/tau-24-422. Epub 2025 Feb 25.
In locoregional prostate cancer (PC), androgen deprivation therapy (ADT) is combined with radiation therapy (RT) for 4-24 months. Post-ADT, some men remain hypogonadal. Sparse data exist regarding the safety and prostate cancer recurrence risk with testosterone therapy (TTh) after prior ADT/RT. The aim of the study is to share Lahey Hospital & Medical Center's experience with patients receiving TTh after previous treatment with ADT and RT, with the goal of contributing to the existing literature on TTh safety in this population to set the stage for a prospective trial.
We abstracted clinical data in patients with stage I-IVA PC, treated with ADT and RT and subsequently received TTh between 2014-2023. The co-primary endpoints were change in prostate-specific antigen (PSA) and incidence of PC recurrence.
Twenty-one patients met criteria. Grade groups (GG) results included: GG1, n=2; GG2, n=2; GG3, n=8; GG4, n=2; and GG5, n=7. American Joint Committee on Cancer (AJCC) stages were: I, n=2; II, n=7; III, n=7; IVA, n=5. Median interval from RT to TTh was 19 months. Prior to TTh, median testosterone was 38 ng/dL. Median follow-up was 15 months. TTh was ongoing in 15 (71.4%) patients and discontinued in 6 (28.6%). Reasons for discontinuation included testosterone recovery (n=1), hospice (not PC-related) (n=2), no perceived benefit (n=2), and physician concern for PSA rise (n=1). After TTh, median testosterone level was 318 ng/dL. Mean PSA pre- and post-TTh were 0.086 and 0.193 ng/dL (P=0.008). No patients experienced PC recurrence. One patient showed PSA bounce without recurrence.
In men with locoregional PC who remained hypogonadal after prior ADT and RT, we found that TTh was not associated with a clinically significant rise in mean PSA and no cases of PC recurrence were documented. These findings support the case for a prospective trial in this setting.
在局部区域前列腺癌(PC)中,雄激素剥夺疗法(ADT)与放射治疗(RT)联合应用4 - 24个月。ADT治疗后,部分男性仍存在性腺功能减退。关于先前接受ADT/RT治疗后使用睾酮治疗(TTh)的安全性及前列腺癌复发风险的数据稀少。本研究的目的是分享拉希医院及医疗中心对先前接受ADT和RT治疗后接受TTh治疗患者的经验,旨在为该人群中TTh安全性的现有文献做出贡献,为前瞻性试验奠定基础。
我们提取了2014年至2023年间接受ADT和RT治疗且随后接受TTh治疗的I - IVA期PC患者的临床数据。共同主要终点为前列腺特异性抗原(PSA)的变化及PC复发率。
21例患者符合标准。分级组(GG)结果包括:GG1,n = 2;GG2,n = 2;GG3,n = 8;GG4,n = 2;GG5,n = 7。美国癌症联合委员会(AJCC)分期为:I期,n = 2;II期,n = 7;III期,n = 7;IVA期,n = 5。从RT到TTh的中位间隔时间为19个月。在TTh之前,中位睾酮水平为38 ng/dL。中位随访时间为15个月。15例(71.4%)患者仍在接受TTh治疗,6例(28.6%)患者停药。停药原因包括睾酮恢复(n = 1)、临终关怀(与PC无关)(n = 2)、未观察到益处(n = 2)以及医生担心PSA升高(n = 1)。TTh治疗后,中位睾酮水平为318 ng/dL。TTh治疗前后的平均PSA分别为0.086和0.193 ng/dL(P = 0.008)。无患者发生PC复发。1例患者出现PSA反弹但未复发。
在先前接受ADT和RT治疗后仍性腺功能减退的局部区域PC男性患者中我们发现,TTh与平均PSA的临床显著升高无关,且未记录到PC复发病例。这些发现支持在这种情况下进行前瞻性试验。