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首页> 外文期刊>Urology >Men (aged 40-49 years) with a single baseline prostate-specific antigen below 1.0 ng/mL have a very low long-term risk of prostate cancer: Results from a prospectively screened population cohort
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Men (aged 40-49 years) with a single baseline prostate-specific antigen below 1.0 ng/mL have a very low long-term risk of prostate cancer: Results from a prospectively screened population cohort

机译:单一基线前列腺特异性抗原低于1.0 ng / mL的男性(40-49岁)长期患前列腺癌的风险非常低:前瞻性筛查人群的结果

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Objective To study the use of a baseline prostate-specific antigen (PSA) and digital rectal examination in men (aged 40-49 years) in predicting long-term prostate cancer risk in a prospectively followed, representative population cohort. Patients and Methods Since 1990, a random sample of men in Olmsted County (aged 40-49 years) has been followed up prospectively (n = 268), with biennial visits, including a urologic questionnaire, PSA screening, and physical examination. The ensuing risk of prostate cancer (CaP) was compared using survival analyses. Results Median follow-up was 16.3 years (interquartile range 14.0-17.3, max 19.1). For men with a baseline PSA <1.0 ng/mL (n = 195), the risk of subsequent Gleason 6 CaP diagnosis by 55 years was 0.6% (95% confidence interval [CI] 0%-1.7%) and 15.7% (95% CI 6.5%-24.9%) for men with a baseline PSA ≥1.0 ng/mL. No man with a low baseline PSA developed an intermediate or high risk CaP, whereas 2.6% of men with a higher baseline PSA did (95% CI 0.58%-4.6%). Conclusion Men (aged 40-49 years) can be stratified with a baseline PSA. If it is below 1.0 ng/mL, there is very little risk for developing a lethal CaP, and as many as 75% of men might be able to avoid additional PSA screening until 55 years. Conversely, men aged 40-49 years with a baseline PSA level >1.0 ng/mL had a significant risk of CaP diagnosis and should be monitored more closely.
机译:目的研究基线前列腺特异性抗原(PSA)和直肠指检在男性(40-49岁)中的应用,以预测未来人群中长期前列腺癌的风险。患者和方法自1990年以来,对Olmsted县(年龄40-49岁)的男性随机样本进行了随访(n = 268),每两年一次,包括泌尿科问卷,PSA筛查和体检。使用生存分析比较了随之而来的前列腺癌(CaP)风险。结果中位随访时间为16.3年(四分位间距为14.0-17.3,最大值为19.1)。对于基线PSA <1.0 ng / mL(n = 195)的男性,随后55年诊断为Gleason 6 CaP的风险分别为0.6%(95%置信区间[CI] 0%-1.7%)和15.7%(95)基线PSA≥1.0ng / mL的男性的CI为6.5%-24.9%。基线PSA较低的男性中,没有人出现中度或高风险的CaP,基线PSA较高的男性中有2.6%发生了CaP(95%CI 0.58%-4.6%)。结论40-49岁的男性可以使用基线PSA进行分层。如果浓度低于1.0 ng / mL,则致死性CaP的风险很小,多达55%的男性可能能够避免进行额外的PSA筛查,直至55岁。相反,基线PSA水平> 1.0 ng / mL的40-49岁男性有很大的CaP诊断风险,应进行更密切的监测。

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