Department of Radiation Oncology, University of Toronto, Toronto, Canada; Radiation Medicine Program, Princess Margaret Cancer Centre, University Health Network, Canada; Department of Radiation Oncology, Hospital Clinico San Carlos, Madrid, Spain.
Department of Radiation Oncology, University of Toronto, Toronto, Canada.
Urol Oncol. 2020 Nov;38(11):848.e1-848.e7. doi: 10.1016/j.urolonc.2020.04.019. Epub 2020 Jun 16.
To assess the impact of RTOG-9601 and GETUG-AFU-16 on the routine use of combination androgen deprivation therapy (ADT) with postoperative radiotherapy (PORT) for prostate cancer (CaP).
Patients with localized CaP treated with radical prostatectomy (RP) and PORT with or without ADT at a comprehensive cancer center from January 2006 to June 2007 (Period 1 = P1), July 2011 to December 2012 (Period 2 = P2), and January 2017 to June 2018 (Period 3 = P3) were included. Clinicopathologic features and treatment characteristics were analyzed and compared. Multivariable logistic regression was used to assess prognostic factors and association with ADT use. Statistical tests were two-sided and a P value <0.05 was considered significant. To validate the findings, United States National Cancer Database (NCDB) and Surveillance, Epidemiology, and End Results (SEER) data were collected to assess rates of combined ADT and PORT from 2004 to 2015.
Five hundred and two patients were included: 152 (P1), 185 (P2), and 165 (P3). PORT was most commonly delivered as early SRT (delivered >1 year post-RP with undetectable PSA or PSA >0.05 and ≤0.5 ng/ml) in all periods. The use of combination PORT and ADT increased over time: 14.5% (P1), 32% (P2), and 41% (P3) (P < 0.001). The proportion of patients that met eligibility criteria for either GETUG-AFU-16 or RTOG-9601 decreased from 47% (P1) to 35% (P3) (P = 0.04). International Society of Urological Pathology grade ≥4 (P < 0.002) and pre-PORT PSA >0.5 ng/ml (P < 0.001) were associated with use of ADT. Positive surgical margin status had a negative association (RR 0.5, P < 0.002). The NCDB demonstrated similar trends for use of combined ADT with PORT, increasing from 37% to 49% from 2004 to 2015.
The use of combined ADT with PORT increased over time. However, only a third of contemporary patients undergoing PORT are represented in the major trials supporting the evidence for combination treatment, highlighting the need to characterize the modern impact of this intensification strategy.
评估 RTOG-9601 和 GETUG-AFU-16 对前列腺癌(CaP)术后放疗(PORT)联合雄激素剥夺治疗(ADT)常规应用的影响。
本研究纳入了 2006 年 1 月至 2007 年 6 月(第 1 期,P1)、2011 年 7 月至 2012 年 12 月(第 2 期,P2)和 2017 年 1 月至 2018 年 6 月(第 3 期,P3)期间在综合癌症中心接受根治性前列腺切除术(RP)和 PORT 联合或不联合 ADT 治疗的局限性 CaP 患者。分析并比较了临床病理特征和治疗特征。采用多变量逻辑回归评估预后因素与 ADT 使用的相关性。统计检验为双侧,P 值<0.05 认为差异有统计学意义。为了验证研究结果,还收集了美国国家癌症数据库(NCDB)和监测、流行病学和最终结果(SEER)的数据,以评估 2004 年至 2015 年联合 ADT 和 PORT 的比率。
共纳入 502 例患者:152 例(P1)、185 例(P2)和 165 例(P3)。在所有阶段,PORT 最常作为早期 SRT(在 RP 后 >1 年,PSA 不可检测或 PSA>0.05 且≤0.5ng/ml 时)进行。联合 PORT 和 ADT 的使用随时间推移而增加:14.5%(P1)、32%(P2)和 41%(P3)(P<0.001)。符合 GETUG-AFU-16 或 RTOG-9601 入组标准的患者比例从 47%(P1)降至 35%(P3)(P=0.04)。国际泌尿病理学会(ISUP)分级≥4(P<0.002)和 PORT 前 PSA>0.5ng/ml(P<0.001)与 ADT 的使用相关。切缘阳性状态与 ADT 的使用呈负相关(RR 0.5,P<0.002)。NCDB 显示了联合 ADT 和 PORT 使用的类似趋势,从 2004 年到 2015 年,联合使用的比例从 37%增加到 49%。
联合 ADT 和 PORT 的使用随时间推移而增加。然而,只有三分之一接受 PORT 治疗的当代患者在支持联合治疗证据的主要试验中得到了体现,这突出表明需要描述这种强化策略的现代影响。