Department of Radiation Oncology, University of Michigan Medical Center, Ann Arbor, MI, USA.
Department of Radiation Oncology, Cedars-Sinai, Los Angeles, CA, USA.
Eur Urol. 2016 Jan;69(1):50-7. doi: 10.1016/j.eururo.2015.05.009. Epub 2015 May 21.
Limited data exist to guide the use of androgen deprivation therapy (ADT) for men treated with radiation therapy (RT) after radical prostatectomy (RP). The optimal duration of ADT in this setting is unknown.
To determine if the duration of ADT influences clinical outcomes for men receiving post-RP RT.
DESIGN, SETTING, AND PARTICIPANTS: A total of 680 men who received adjuvant radiation therapy (n=105) or salvage radiation therapy (n=575) between 1986 and 2010 at a single tertiary care institution were reviewed retrospectively. Median follow-up post-RT was 57.8 mo.
RT was delivered using three-dimensional conformal or intensity-modulated RT in 1.8-Gy fractions. For patients treated with ADT, >80% were treated with a gonadotropin-releasing hormone agonist with or without a nonsteroidal antiandrogen.
Biochemical failure (BF), distant metastasis (DM), prostate cancer-specific mortality (PCSM), and overall mortality were assessed using Kaplan-Meier analysis and propensity score analysis.
Overall, 144 patients (21%) received ADT with post-RP RT, most of whom had high-risk disease features such as Gleason score 8-10, seminal vesicle invasion, or pre-RT prostate-specific antigen >1 ng/ml. Median ADT duration was 12 mo (interquartile range: 6.0-23.7). Patients who received <12 mo of ADT had an association with increased BF (hazard ratio [HR]: 2.27; p=0.003) and DM (HR: 2.48; p=0.03) compared with patients receiving ≥12 mo of ADT. The 5-yr rates of DM were 6.0% and 23% for ≥12 and <12 mo of ADT, respectively. On propensity score analysis controlling for pretreatment and treatment-related factors, each month of ADT was associated with a decreased risk for BF (HR: 0.95; p=0.0004), DM (HR: 0.88; p=0.0004), and PCSM (HR: 0.90; p=0.037). These findings are limited by the retrospective nature of our analysis.
For men with high-risk disease features receiving ADT with post-RP RT, the duration of ADT is associated with clinical outcomes. Our findings suggest that for these men an extended course of ADT ≥12 mo may be preferable. Validation of our findings is needed.
We evaluated outcomes for men with high-risk disease features treated with androgen deprivation therapy (ADT) and radiotherapy after radical prostatectomy. Longer durations of ADT resulted in improved patient outcomes.
针对接受根治性前列腺切除术(RP)后接受放射治疗(RT)的男性,目前仅有少量数据可用于指导雄激素剥夺疗法(ADT)的应用。这种情况下 ADT 的最佳持续时间尚不清楚。
确定 ADT 的持续时间是否会影响接受 RP 后 RT 治疗的男性的临床结局。
设计、地点和参与者:共回顾性分析了 1986 年至 2010 年期间在一家三级医疗中心接受辅助性放疗(n=105)或挽救性放疗(n=575)的 680 例男性患者的资料。中位 RT 后随访时间为 57.8 个月。
RT 采用三维适形或调强放疗,1.8 Gy 分次。对于接受 ADT 的患者,超过 80%的患者接受促性腺激素释放激素激动剂联合或不联合非甾体类抗雄激素治疗。
采用 Kaplan-Meier 分析和倾向评分分析评估生化失败(BF)、远处转移(DM)、前列腺癌特异性死亡率(PCSM)和总死亡率。
总体而言,144 例(21%)接受了 RP 后 RT 联合 ADT,其中大多数患者具有高危疾病特征,如 Gleason 评分 8-10、精囊侵犯或 RT 前前列腺特异性抗原>1ng/ml。ADT 的中位持续时间为 12 个月(四分位间距:6.0-23.7)。与接受≥12 个月 ADT 的患者相比,接受<12 个月 ADT 的患者 BF(风险比[HR]:2.27;p=0.003)和 DM(HR:2.48;p=0.03)的风险更高。5 年 DM 发生率分别为≥12 个月和<12 个月 ADT 组的 6.0%和 23%。在基于倾向评分的分析中,控制治疗前和治疗相关因素后,ADT 每月的持续时间与 BF(HR:0.95;p=0.0004)、DM(HR:0.88;p=0.0004)和 PCSM(HR:0.90;p=0.037)的风险降低相关。这些发现受到我们分析的回顾性性质的限制。
对于接受 RP 后 RT 联合 ADT 治疗且具有高危疾病特征的男性,ADT 的持续时间与临床结局相关。我们的发现表明,对于这些男性,≥12 个月的延长 ADT 疗程可能更为理想。需要进一步验证我们的发现。
我们评估了接受雄激素剥夺治疗(ADT)和根治性前列腺切除术后放疗的高危疾病特征男性患者的结局。ADT 持续时间较长可改善患者结局。