School of Medicine and Dentistry, Griffith University, Sunshine Coast, Queensland, Australia; Institute for Evidence based health care, Bond University, Queensland, Australia.
Faculty of Health Sciences and Medicine, Bond University, Queensland, Australia.
Cancer Epidemiol. 2022 Apr;77:102093. doi: 10.1016/j.canep.2021.102093. Epub 2022 Jan 11.
Population trends in PSA testing and prostate cancer incidence do not perfectly correspond. We aimed to better understand relationships between trends in PSA testing, prostate cancer incidence and mortality in Australia and factors that influence them.
We calculated and described standardised time trends in PSA tests, prostate biopsies, treatment of benign prostatic hypertrophy (BPH) and prostate cancer incidence and mortality in Australia in men aged 45-74, 75-84, and 85 + years.
PSA testing increased from its introduction in 1989 to a peak in 2008 before declining in men aged 45-84 years. Prostate biopsies and cancer incidence fell from 1995 to 2000 in parallel with decrease in trans-urethral resections of the prostate (TURP) and, latterly, changes in pharmaceutical management of BPH. After 2000, changes in biopsies and incidence paralleled changes in PSA screening in men 45-84 years, while in men ≥85 years biopsy rates stabilised, and incidence fell. Prostate cancer mortality in men aged 45-74 years remained low throughout. Mortality in men 75-84 years gradually increased until mid 1990s, then gradually decreased. Mortality in men ≥ 85 years increased until mid 1990s, then stabilised.
Age specific prostate cancer incidence largely mirrors PSA testing rates. Most deviation from this pattern may be explained by less use of TURP in management of BPH and consequent less incidental cancer detection in TURP tissue specimens. Mortality from prostate cancer initially rose and then fell below what it was when PSA testing began. Its initial rise and fall may be explained by a possible initial tendency to over-attribute deaths of uncertain cause in older men with a diagnosis of prostate cancer to prostate cancer. Decreases in mortality rates were many fold smaller than the increases in incidence, suggesting substantial overdiagnosis of prostate cancer after introduction of PSA testing.
前列腺特异性抗原(PSA)检测和前列腺癌发病率的人口趋势并不完全一致。我们旨在更好地了解澳大利亚 PSA 检测、前列腺癌发病率和死亡率的趋势以及影响这些趋势的因素之间的关系。
我们计算并描述了澳大利亚 45-74 岁、75-84 岁和 85 岁及以上男性中 PSA 检测、前列腺活检、良性前列腺增生(BPH)治疗以及前列腺癌发病率和死亡率的标准化时间趋势。
从 1989 年 PSA 检测引入到 2008 年达到峰值,然后在 45-84 岁男性中下降。前列腺活检和癌症发病率从 1995 年到 2000 年下降,与经尿道前列腺切除术(TURP)的减少以及后来 BPH 药物治疗的变化同时发生。2000 年后,45-84 岁男性的活检和发病率变化与 PSA 筛查变化平行,而 85 岁以上男性的活检率稳定,发病率下降。45-74 岁男性的前列腺癌死亡率一直较低。75-84 岁男性的死亡率在 20 世纪 90 年代中期逐渐上升,然后逐渐下降。85 岁以上男性的死亡率在 20 世纪 90 年代中期上升,然后稳定。
特定年龄的前列腺癌发病率在很大程度上反映了 PSA 检测率。这种模式的大多数偏差可以用 TURP 在 BPH 管理中的应用减少以及由此导致 TURP 组织标本中偶然发现的癌症减少来解释。前列腺癌死亡率最初上升,然后降至 PSA 检测开始时的水平以下。其最初的上升和下降可能是由于最初倾向于将不确定病因的老年男性的前列腺癌死亡归因于前列腺癌。死亡率的下降幅度远小于发病率的上升幅度,表明 PSA 检测引入后前列腺癌的过度诊断明显。