Roobol Monique J, Grenabo Anna, Schröder Fritz H, Hugosson Jonas
Department of Urology, Erasmus Medical Centre, Rm NH 224, PO Box 2040, 3000 CA Rotterdam, The Netherlands.
J Natl Cancer Inst. 2007 Sep 5;99(17):1296-303. doi: 10.1093/jnci/djm101. Epub 2007 Aug 28.
The incidence of prostate cancer has increased substantially since it became common practice to screen asymptomatic men for the disease. The European Randomized Study of Screening for Prostate Cancer (ERSPC) was initiated in 1993 to determine how prostate-specific antigen (PSA) screening affects prostate cancer mortality. Variations in the screening algorithm, such as the interval between screening rounds, likely influence the morbidity, mortality, and quality of life of the screened population.
We compared the number and characteristics of interval cancers, defined as those diagnosed during the screening interval but not detected by screening, in men in the screening arm of the ERSPC who were aged 55-65 years at the time of the first screening and were participating through two centers of the ERSPC: Gothenburg (2-year screening interval, n = 4202) and Rotterdam (4-year screening interval, n = 13301). All participants who were diagnosed with prostate cancer through December 31, 2005, but at most 10 years after the initial screening were ascertained by linkage with the national cancer registries. A potentially life-threatening (aggressive) interval cancer was defined as one with at least one of the following characteristics at diagnosis: stage M1 or N1, plasma PSA concentration greater than 20.0 ng/mL, or Gleason score greater than 7. We used Mantel Cox regression to assess differences between rates of interval cancers and aggressive interval cancers at the two centers. All statistical tests were two-sided.
The 10-year cumulative incidence of all prostate cancers in Rotterdam versus Gothenburg was 1118 (8.41%) versus 552 (13.14%) (P<.001), the cumulative incidence of interval cancer was 57 (0.43%) versus 31 (0.74%) (P = .51), and the cumulative incidence of aggressive interval cancer was 15 (0.11%) versus 5 (0.12%) (P = .72).
The rate of interval cancer, especially aggressive interval cancer, was low in this study. The 2-year screening interval had higher detection rates than the 4-year interval but did not lead to lower rates of interval and aggressive interval prostate cancers.
自从对无症状男性进行前列腺癌筛查成为普遍做法以来,前列腺癌的发病率大幅上升。欧洲前列腺癌筛查随机研究(ERSPC)于1993年启动,以确定前列腺特异性抗原(PSA)筛查如何影响前列腺癌死亡率。筛查算法的变化,如筛查轮次之间的间隔,可能会影响筛查人群的发病率、死亡率和生活质量。
我们比较了ERSPC筛查组中55至65岁男性的间期癌(定义为在筛查间隔期内诊断出但未通过筛查检测到的癌症)的数量和特征,这些男性在首次筛查时年龄为55 - 65岁,通过ERSPC的两个中心参与研究:哥德堡(筛查间隔为2年,n = 4202)和鹿特丹(筛查间隔为4年,n = 13301)。通过与国家癌症登记处进行关联,确定了所有在2005年12月31日前被诊断为前列腺癌,但在初次筛查后最多10年的参与者。潜在危及生命(侵袭性)的间期癌定义为在诊断时具有以下至少一项特征的癌症:M1或N1期、血浆PSA浓度大于20.0 ng/mL或Gleason评分大于7。我们使用Mantel Cox回归来评估两个中心之间间期癌和侵袭性间期癌发生率的差异。所有统计检验均为双侧检验。
鹿特丹与哥德堡所有前列腺癌的10年累积发病率分别为每1118例(8.41%)和552例(13.%)(P <.001),间期癌的累积发病率分别为每57例(0.43%)和31例(0.74%)(P =.51),侵袭性间期癌的累积发病率分别为每15例(0.11%)和5例(0.12%)(P =.72)。
本研究中间期癌,尤其是侵袭性间期癌的发生率较低。2年的筛查间隔比4年的筛查间隔具有更高的检出率,但并未导致更低的间期和侵袭性间期前列腺癌发生率。