Dana-Farber Cancer Institute, Boston, Massachusetts.
Boston University School of Public Health, Boston, Massachusetts.
Cancer. 2020 Mar 1;126(5):986-993. doi: 10.1002/cncr.32630. Epub 2019 Nov 26.
An older age at the diagnosis of prostate cancer has been linked to worse prostate cancer-specific survival (PCSS). However, these studies were conducted before the approval of many life-prolonging drugs. This study was aimed at describing outcomes in a contemporary cohort of men diagnosed with de novo metastatic prostate cancer (mPCa) and assessing associations with the age at diagnosis while controlling for known prognostic factors.
The Surveillance, Epidemiology, and End Results registry was used to identify men diagnosed with mPCa from 2004 to 2014. Men were classified by 4 age groups: ≤54, 55 to 64, 65 to 74, and ≥75 years. The median overall survival, PCSS, and restricted mean survival times for any-cause mortality and prostate cancer-specific mortality (PCSM) were calculated. Multivariable and subdistribution hazard ratios for PCSM according to age group and with controlling for race, marital status, and income were estimated.
Compared with men aged ≤54 years, men aged ≥75 years experienced a mean PCSS at 5 years that was 6.7 months shorter (95% confidence interval [CI], 5.5-7.8 months). In multivariable analyses, men aged ≥75 years had a 49% increase in the rate of PCSM in comparison with those aged ≤54 years (95% CI, 1.39-1.60). The subdistribution hazard ratio for PCSM between these groups was 1.41 (95% CI, 1.32-1.50).
Age was found to be an independent predictor of shorter PCSS in men diagnosed with de novo mPCa even in an era with more effective therapies. Further work is needed to determine the reason for poor outcomes in older men with mPCa.
前列腺癌诊断年龄较大与前列腺癌特异性生存(PCSS)较差相关。然而,这些研究是在许多延长寿命的药物获得批准之前进行的。本研究旨在描述一组新诊断为转移性前列腺癌(mPCa)的男性的结局,并评估与诊断年龄相关的关联,同时控制已知的预后因素。
使用监测、流行病学和最终结果登记处(Surveillance, Epidemiology, and End Results registry)来确定 2004 年至 2014 年间新诊断为 mPCa 的男性。根据 4 个年龄组对男性进行分类:≤54 岁、55 至 64 岁、65 至 74 岁和≥75 岁。计算中位总生存期、PCSS 以及任何原因死亡率和前列腺癌特异性死亡率(PCSM)的限制平均生存时间。根据年龄组和控制种族、婚姻状况和收入,估计多变量和亚分布 PCSS 死亡风险比。
与≤54 岁的男性相比,≥75 岁的男性在 5 年内的 PCSS 短 6.7 个月(95%置信区间[CI],5.5-7.8 个月)。在多变量分析中,≥75 岁的男性与≤54 岁的男性相比,PCSM 发生率增加了 49%(95%CI,1.39-1.60)。两组之间的 PCSM 亚分布风险比为 1.41(95%CI,1.32-1.50)。
即使在治疗效果更有效的时代,年龄也是新诊断为 mPCa 的男性 PCSS 较短的独立预测因素。需要进一步研究以确定 mPCa 老年男性预后不良的原因。