Sebastian Nikhil T, Goyal Subir, Liu Yuan, Dhere Vishal, Jani Ashesh B, Hershatter Bruce, Patel Pretesh R, Shelton Jay W, Hanasoge Sheela, Godette Karen D, Patel Sagar A
Department of Radiation Oncology, Winship Cancer Institute, Emory University, Atlanta, GA, USA.
Biostatistics and Bioinformatics Shared Resource, Winship Cancer Institute, Emory University, Atlanta, GA, USA.
J Contemp Brachytherapy. 2024 Aug;16(4):268-272. doi: 10.5114/jcb.2024.143130. Epub 2024 Sep 12.
While the benefit of short-term androgen deprivation therapy (ADT) has been established for patients with intermediate-risk (IR) prostate cancer (PCa) receiving dose-escalated external beam radiation therapy (EBRT), the role of ADT for patients treated with brachytherapy (BT) with or without supplemental EBRT (sEBRT) is less clear.
We conducted a single-institution retrospective analysis of men with National Comprehensive Cancer Network (NCCN) unfavorable IR (UIR) PCa. All patients received BT with or without sEBRT, and were stratified by the receipt of 4-6 months of ADT. Kaplan-Meier method was used to measure biochemical progression- free survival (bPFS) between men who did vs. did not receive ADT. Multivariable Cox proportional hazards with backward selection was utilized to determine association of concomitant ADT with bPFS accounting for confounding variables.
We identified 201 eligible patients treated between 2002 and 2019, 78 (38.8%) of whom received ADT. Median follow-up was 15 years. On univariable analysis, there was no significant association of ADT use with bPFS (HR = 0.95, 95% CI: 0.34-2.63, = 0.92). Only PSA ≥ 10 was significant for association with worse bPFS (HR = 3.51, 95% CI: 1.29-9.52, = 0.014). On multivariable analysis, there was no association of ADT use with bPFS (HR = 0.97, 95% CI: 0.34-2.78, = 0.96).
Short-course ADT was not associated with improved bPFS in our study among men with UIR PCa treated with BT with or without sEBRT. These findings suggest that dose intensification achieved with BT may alone be sufficient in treating selected patients with UIR disease, but prospective studies are warranted.
虽然对于接受剂量递增外照射放疗(EBRT)的中危(IR)前列腺癌(PCa)患者,短期雄激素剥夺治疗(ADT)的益处已得到证实,但ADT在接受近距离放疗(BT)联合或不联合补充外照射放疗(sEBRT)的患者中的作用尚不清楚。
我们对患有美国国立综合癌症网络(NCCN)不良IR(UIR)PCa的男性进行了单机构回顾性分析。所有患者均接受了BT联合或不联合sEBRT,并根据是否接受4 - 6个月的ADT进行分层。采用Kaplan - Meier方法测量接受与未接受ADT的男性之间的生化无进展生存期(bPFS)。利用多变量Cox比例风险模型和向后选择法来确定伴随ADT与bPFS之间的关联,并考虑混杂变量。
我们确定了2002年至2019年间接受治疗的201例符合条件的患者,其中78例(38.8%)接受了ADT。中位随访时间为15年。单变量分析显示,使用ADT与bPFS无显著关联(HR = 0.95,95% CI:0.34 - 2.63,P = 0.92)。只有PSA≥10与较差的bPFS显著相关(HR = 3.51,95% CI:1.29 - 9.52,P = 0.014)。多变量分析显示,使用ADT与bPFS无关联(HR = 0.97,95% CI:0.34 - 2.78,P = 0.96)。
在我们的研究中,对于接受BT联合或不联合sEBRT治疗的UIR PCa男性患者,短期ADT与改善bPFS无关。这些发现表明,BT实现的剂量强化可能单独就足以治疗部分UIR疾病患者,但仍需要进行前瞻性研究。