Fürst Laboratories, Department of Clinical Chemistry, Oslo, Norway.
Department of Urology, Institute of Clinical Sciences, Gothenburg University, Gothenburg, Sweden; Department of Urology, Sahlgrenska University Hospital, Gothenburg, Sweden.
Eur Urol. 2024 Jul;86(1):20-26. doi: 10.1016/j.eururo.2023.04.028. Epub 2023 May 9.
Prostate-specific antigen (PSA) levels in midlife are strongly associated with the long-term risk of lethal prostate cancer in cohorts not subject to screening. This is the first study evaluating the association between PSA levels drawn as part of routine medical care in the Norwegian population and prostate cancer incidence and mortality. The objective of the study was to determine the association between midlife PSA levels <4.0 ng/ml, drawn aspart of routine medical care, and long-term risk of prostate cancer death.
The Norwegian Prostate Cancer Consortium collected >8 million PSA results from >1 million Norwegian males (more than or equal to) 40 yr of age. We studied 176 099 men (predefined age strata: 40-54 and 55-69 yr) without a prior prostate cancer diagnosis who had a nonelevated baseline PSA level (<4.0 ng/ml) between January 1,1995 and December 31, 2005. We assessed the 16-yr risk of prostate cancer mortality. We calculated the discrimination (C-index) between predefined PSA strata (<0.5, 0.5-0.9, 1.0-1.9, 2.0-2.9, and 3.0-3.9 ng/ml) and subsequent prostate cancer death. Survival curves were plotted using the Kaplan-Meier method.
The median follow-up time of men who did not get prostate cancer was 17.9 yr. Overall, 84% of men had a baseline PSA level of <2.0 ng/ml and 1346 men died from prostate cancer, with 712 deaths (53%) occurring in the 16% of men with the highest baseline PSA of 2.0-3.9 ng/ml. Baseline PSA levels were associated with prostate cancer mortality (C-index 0.72 for both age groups, 40-54 and 55-69 yr). The fact that the reason for any given PSA measurement remains unknown represents a limitation.
We replicated prior studies that baseline PSA at age 40-69 yr can be used to stratify a man's risk of dying from prostate cancer within the next 15-20 yr.
A prostate-specific antigen level obtained as part of routine medical care is strongly associated with a man's risk of dying from prostate cancer in the next two decades.
在未接受筛查的队列中,中年时的前列腺特异性抗原(PSA)水平与致命性前列腺癌的长期风险密切相关。这是第一项评估作为挪威人群常规医疗一部分抽取的 PSA 水平与前列腺癌发病率和死亡率之间关联的研究。本研究的目的是确定中年时抽取的 PSA 水平<4.0ng/ml 与前列腺癌死亡的长期风险之间的关联,这些 PSA 水平是作为常规医疗的一部分抽取的。
挪威前列腺癌联合会从>100 万 40 岁及以上的挪威男性中收集了超过 800 万个 PSA 结果。我们研究了 176099 名(年龄分层预设:40-54 岁和 55-69 岁)无先前前列腺癌诊断且基线 PSA 水平正常(<4.0ng/ml)的男性,他们在 1995 年 1 月 1 日至 2005 年 12 月 31 日期间进行了检测。我们评估了 16 年的前列腺癌死亡率风险。我们计算了预定义 PSA 分层(<0.5、0.5-0.9、1.0-1.9、2.0-2.9 和 3.0-3.9ng/ml)和随后的前列腺癌死亡之间的区分度(C 指数)。使用 Kaplan-Meier 方法绘制生存曲线。
未患前列腺癌的男性中位随访时间为 17.9 年。总体而言,84%的男性基线 PSA 水平<2.0ng/ml,有 1346 人死于前列腺癌,其中 16%的男性基线 PSA 水平为 2.0-3.9ng/ml,有 712 人(53%)死于前列腺癌。基线 PSA 水平与前列腺癌死亡率相关(40-54 岁和 55-69 岁两个年龄组的 C 指数均为 0.72)。由于任何特定 PSA 测量的原因仍然未知,这是一个局限性。
我们复制了先前的研究结果,即 40-69 岁时的基线 PSA 可用于分层预测男性在未来 15-20 年内死于前列腺癌的风险。
作为常规医疗的一部分抽取的前列腺特异性抗原水平与男性在未来二十年死于前列腺癌的风险密切相关。