Martini-Klinik Prostate Cancer Center, University Hospital Hamburg-Eppendorf, Martinistraße 52, 20246, Hamburg, Germany.
Cancer Prognostics and Health Outcomes Unit, Division of Urology, University of Montreal Health Center, Montreal, QC, Canada.
Cancer Causes Control. 2020 Mar;31(3):283-290. doi: 10.1007/s10552-020-01273-5. Epub 2020 Feb 7.
To test the effect of age on cancer-specific mortality (CSM) in most contemporary prostate cancer (PCa) patients of all stages and across all treatment modalities.
Within the Surveillance, Epidemiology, and End Results database (2004-2016), we identified 579,369 PCa patients. Cumulative incidence plots and multivariable competing-risks regression analyses (MCR) were used. Subgroup analyses were performed according to ethnicity (African-Americans), clinical stage (T1-2N0M0, T3-4N0M0, TanyN1M0, and TanyNanyM1), as well as treatment modalities.
Patient distribution was as follows: 142,338 (24.6%) < 60 years; 113,064 (19.5%) 60-64 years; 127,158 (21.9%) 65-69 years; 94,782 (16.4%) 70-74 years; and 102,027 (17.6%) ≥ 75 years. Older patients harbored worse tumor characteristics and more frequently received no local treatment. Overall, 10-year CSM rates were 4.8, 5.3, 5.9, 7.6, and 14.6%, respectively, in patients aged < 60, 60-64, 65-69, 70-74 ,and ≥ 75 years (p < 0.001). In MCR focusing on the overall cohort and T1-2N0M0 patients, older age independently predicted higher CSM, but not in T3-4N0-1M0-1 patients.
Older age was associated with higher grade and stage and independently predicted higher CSM in T1-2N0M0 patients, but not in higher stages. Differences in diagnostics and therapeutics seem to affect elderly patients within T1-2N0M0 PCa and should be avoided if possible.
测试年龄对所有阶段和所有治疗方式的前列腺癌(PCa)患者的癌症特异性死亡率(CSM)的影响。
在监测、流行病学和结果数据库(2004-2016 年)中,我们确定了 579369 例 PCa 患者。使用累积发病率图和多变量竞争风险回归分析(MCR)。根据种族(非裔美国人)、临床分期(T1-2N0M0、T3-4N0M0、TanyN1M0 和 TanyNanyM1)以及治疗方式进行亚组分析。
患者分布如下:<60 岁 142338 例(24.6%);60-64 岁 113064 例(19.5%);65-69 岁 127158 例(21.9%);70-74 岁 94782 例(16.4%);≥75 岁 102027 例(17.6%)。老年患者具有更差的肿瘤特征,并且更频繁地未接受局部治疗。总体而言,<60 岁、60-64 岁、65-69 岁、70-74 岁和≥75 岁的患者 10 年 CSM 率分别为 4.8%、5.3%、5.9%、7.6%和 14.6%(p<0.001)。在针对整个队列和 T1-2N0M0 患者的 MCR 中,年龄较大与更高的 CSM 独立相关,但在 T3-4N0-1M0-1 患者中则没有。
年龄较大与更高的分级和分期相关,并且与 T1-2N0M0 患者的 CSM 独立相关,但与更高的分期无关。诊断和治疗方法的差异似乎会影响 T1-2N0M0 PCa 中的老年患者,如果可能的话,应避免这种情况。