Evergreen Health Hospitalist Services, Kirkland, Washington.
Urology Section, Department of Surgery, Veterans Affairs Medical Centers, Durham, North Carolina.
J Urol. 2018 Mar;199(3):713-718. doi: 10.1016/j.juro.2017.08.107. Epub 2017 Sep 1.
Short prostate specific antigen doubling time following recurrence after radical prostatectomy portends a poor prognosis. Prostate specific antigen doubling time is traditionally calculated using prostate specific antigen values 0.2 ng/ml or greater. We determined whether early prostate specific antigen doubling time, calculated from the first detectable postoperative prostate specific antigen up to and including the first recurrence value, correlates with prostate cancer outcomes.
Cox models were used to examine the association between early prostate specific antigen doubling time and castration resistant prostate cancer, metastases, and all cause and prostate cancer specific mortality in 674 men who underwent radical prostatectomy between 1988 and 2014 and had a biochemical recurrence. Early prostate specific antigen doubling time was examined as a log transformed continuous and a categorical variable.
After adjusting for multiple clinicopathological characteristics, log transformed early prostate specific antigen doubling time was not associated with any outcome. However, when early doubling time was categorized as 15 or greater, 9 to 14.9, 3 to 8.9 and less than 3 months, on multivariable analysis men with early doubling time less than 3 months were at increased risk for castration resistant prostate cancer (HR 6.20, p = 0.004), metastases (HR 5.26, p = 0.001), prostate cancer specific mortality (HR 5.06, p = 0.026) and all cause mortality (HR 1.63, p = 0.065) compared to those with an early doubling time of 15 months or greater. However, the association with all cause mortality was not significant. Those with an early prostate specific antigen doubling time of 3 to 8.9 months were at increased risk for castration resistant prostate cancer (HR 3.56, p = 0.015), all cause mortality (HR 1.67, p = 0.006) and prostate cancer specific mortality (HR 3.17, p = 0.044) but not metastases (p = 0.13).
Early prostate specific antigen doubling time less than 9 months, calculated using prostate specific antigen values before and up to biochemical recurrence, is associated with an increased risk of castration resistant prostate cancer, metastases, and prostate cancer specific and all cause mortality among men with biochemical recurrence after radical prostatectomy. Early prostate specific antigen doubling time allows for risk stratification at biochemical recurrence and before prostate specific antigen doubling time is calculable, enabling these men to be referred for early aggressive secondary treatment and/or clinical trials.
根治性前列腺切除术后复发后前列腺特异抗原倍增时间短预示预后不良。前列腺特异抗原倍增时间传统上是使用前列腺特异抗原值 0.2ng/ml 或更高来计算的。我们确定了从第一次可检测到的术后前列腺特异抗原开始,包括第一次复发值在内的早期前列腺特异抗原倍增时间是否与前列腺癌的结果相关。
使用 Cox 模型来研究 674 名于 1988 年至 2014 年期间接受根治性前列腺切除术且生化复发的患者中,早期前列腺特异抗原倍增时间与去势抵抗性前列腺癌、转移以及全因和前列腺癌特异性死亡率之间的关系。早期前列腺特异抗原倍增时间被检查为对数转换的连续变量和分类变量。
在调整了多个临床病理特征后,对数转换的早期前列腺特异抗原倍增时间与任何结果均无关。然而,当早期倍增时间被分类为 15 个月或以上、9 至 14.9 个月、3 至 8.9 个月和小于 3 个月时,多变量分析显示,早期倍增时间小于 3 个月的患者发生去势抵抗性前列腺癌(HR 6.20,p=0.004)、转移(HR 5.26,p=0.001)、前列腺癌特异性死亡率(HR 5.06,p=0.026)和全因死亡率(HR 1.63,p=0.065)的风险增加与早期倍增时间为 15 个月或更长的患者相比。然而,与全因死亡率的相关性并不显著。早期前列腺特异抗原倍增时间为 3 至 8.9 个月的患者发生去势抵抗性前列腺癌(HR 3.56,p=0.015)、全因死亡率(HR 1.67,p=0.006)和前列腺癌特异性死亡率(HR 3.17,p=0.044)的风险增加,但转移的风险没有增加(p=0.13)。
在根治性前列腺切除术生化复发后,使用前列腺特异抗原值在生化复发前和至生化复发时计算的早期前列腺特异抗原倍增时间小于 9 个月,与去势抵抗性前列腺癌、转移以及前列腺癌特异性和全因死亡率的风险增加相关。早期前列腺特异抗原倍增时间可在生化复发前进行风险分层,且在可计算前列腺特异抗原倍增时间之前,使这些患者能够接受早期积极的辅助治疗和/或临床试验。