Harvard Radiation Oncology Program, Dana-Farber Cancer Institute and Brigham and Women's Hospital, Boston, Massachusetts.
Department of Radiation Oncology, Dana-Farber Cancer Institute and Brigham and Women's Hospital, Boston, Massachusetts.
Cancer. 2021 Aug 1;127(15):2623-2630. doi: 10.1002/cncr.33543. Epub 2021 Apr 6.
Although both PSA nadir (PSAn) and testosterone levels at PSA failure are known prognostic factors in men undergoing radiation therapy (RT) and androgen deprivation therapy (ADT) for unfavorable-risk prostate cancer (PC), it is unclear whether their prognostic significance is independent or overlapping.
Seventy-five men treated with RT with or without 6 months of ADT for unfavorable-risk nonmetastatic PC enrolled in 2 prospective clinical trials between 1986 and 2001 formed the study cohort. Competing risks and Cox multivariable regression were used to assess whether low versus normal serum testosterone at the time of PSA failure and higher PSAn after initial therapy were independently associated with the risk of PC-specific (PCSM) and all-cause mortality (ACM) adjusting for PC prognostic factors.
After a median follow-up of 15.34 years (interquartile range, 6.66-16.88 years), there were 53 deaths (73.3%): 30 (56.6%) were from PC. Low testosterone at PSA failure was significantly associated with an increased risk of PCSM (adjusted HR [AHR], 7.77; 95% CI, 1.14-52.99; P = .04) and ACM (AHR, 3.01; 95% CI, 1.01-8.96; P = .05), as was higher PSAn (PCSM AHR, 1.03; 95% CI, 1.01-1.05; P < .01; ACM AHR, 1.04; 95% CI, 1.02-1.07; P < .01), although the prognostic significance of PSAn was only noted in men with a normal testosterone at PSA failure.
Low testosterone level at PSA failure in high-risk patients with PC treated with RT is associated with increased PCSM and ACM risk. In men with normal testosterone levels at the time of PSA failure, an elevated PSAn was associated with worse PCSM and ACM risk.
This study investigates whether the prostate-specific antigen (PSA) nadir and normal versus low testosterone at the time of PSA failure provide mutually exclusive or overlapping prognostic information following treatment with radiation and androgen deprivation therapy for unfavorable-risk patients with prostate cancer using data from 2 prospective clinical trials. It was found that both provided prognostic information; however, higher PSA nadir was only found to be of prognostic significance in men with normal testosterone levels at PSA failure.
在接受放疗(RT)和雄激素剥夺治疗(ADT)治疗不利风险前列腺癌(PC)的男性中,PSA 无进展期(PSAn)和 PSA 失败时的睾酮水平是已知的预后因素,但尚不清楚它们的预后意义是否独立或重叠。
1986 年至 2001 年间,75 名接受 RT 联合或不联合 6 个月 ADT 治疗的不利风险非转移性 PC 男性患者入组了 2 项前瞻性临床试验,形成了研究队列。使用竞争风险和 Cox 多变量回归来评估 PSA 失败时血清睾酮水平低与正常以及初始治疗后 PSAn 较高是否与 PC 特异性(PCSM)和全因死亡率(ACM)风险相关,调整 PC 预后因素后。
中位随访 15.34 年(四分位距,6.66-16.88 年)后,有 53 人死亡(73.3%):30 人(56.6%)死于 PC。PSA 失败时睾酮水平低与 PCSM(调整后的 HR [AHR],7.77;95%CI,1.14-52.99;P=0.04)和 ACM(AHR,3.01;95%CI,1.01-8.96;P=0.05)风险增加显著相关,PSAn 较高也是如此(PCSM AHR,1.03;95%CI,1.01-1.05;P<.01;ACM AHR,1.04;95%CI,1.02-1.07;P<.01),尽管 PSAn 的预后意义仅在 PSA 失败时睾酮水平正常的男性中得到了证实。
接受 RT 治疗的高危 PC 患者 PSA 失败时的低睾酮水平与 PCSM 和 ACM 风险增加相关。在 PSA 失败时睾酮水平正常的男性中,升高的 PSAn 与更差的 PCSM 和 ACM 风险相关。
本研究使用来自 2 项前瞻性临床试验的数据,探讨 PSA 无进展期和 PSA 失败时正常与低睾酮水平是否为接受放疗和雄激素剥夺治疗的不利风险前列腺癌患者提供相互排斥或重叠的预后信息。结果表明,两者均提供了预后信息;然而,仅发现较高的 PSA 无进展期在 PSA 失败时睾酮水平正常的男性中具有预后意义。