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通过前列腺特异性抗原筛查在高危前列腺癌家族的无症状男性中检测亚临床癌症。

Detection of subclinical cancers by prostate-specific antigen screening in asymptomatic men from high-risk prostate cancer families.

作者信息

Matikainen M P, Schleutker J, Mörsky P, Kallioniemi O P, Tammela T L

机构信息

Laboratory of Cancer Genetics, Institute of Medical Technology, University of Tampere and Tampere University Hospital, Finland.

出版信息

Clin Cancer Res. 1999 Jun;5(6):1275-9.

PMID:10389909
Abstract

Positive family history is a significant risk factor for prostate cancer. Improved knowledge of the epidemiology and molecular basis of hereditary prostate cancer has led to a need for counseling and clinical follow-up for men with a positive family history of prostate cancer. However, very little information is available on the efficacy of early screening procedures, such as serum prostate-specific antigen (PSA) measurements, in the management of genetically predisposed, high-risk individuals. In a nationwide study, we obtained family histories from 2099 Finnish prostate cancer patients and identified 302 families with two or more affected cases. Here, 209 asymptomatic 45-75-year-old males from these families were included in a study to determine the frequency of serum PSA positivity and the prevalence of subclinical prostate cancers. Serum PSA was elevated in 21 (10.0%) of these high-risk individuals. Seven prostate cancers (3.3%) and two high-grade prostatic intraepithelial neoplasia lesions were diagnosed, with three cancers occurring in men ages < or = 59 years. Men from prostate cancer families with an average age of onset of < 60 years had a significantly higher frequency of PSA positivity (28.6%, P = 0.01) as well as cancers (14.3%, P = 0.02) than those with a later age of onset. The results suggest that prostate cancer development in genetically predisposed individuals is preceded by a subclinical period when PSA detection is possible. Serum PSA screening may be particularly useful in men with a family history of early-onset prostate cancer.

摘要

家族史阳性是前列腺癌的一个重要危险因素。对遗传性前列腺癌的流行病学和分子基础的认识不断提高,使得有前列腺癌家族史阳性的男性需要接受咨询和临床随访。然而,关于早期筛查程序(如血清前列腺特异性抗原(PSA)检测)在遗传易感性高风险个体管理中的效果,目前可用信息非常少。在一项全国性研究中,我们从2099名芬兰前列腺癌患者那里获取了家族史,并确定了302个有两例或更多患病病例的家庭。在此,来自这些家庭的209名无症状的45 - 75岁男性被纳入一项研究,以确定血清PSA阳性的频率和亚临床前列腺癌的患病率。这些高风险个体中有21人(10.0%)血清PSA升高。诊断出7例前列腺癌(3.3%)和2例高级别前列腺上皮内瘤变病变,其中3例癌症发生在年龄≤59岁的男性中。前列腺癌家族中平均发病年龄<60岁的男性,其PSA阳性频率(28.6%,P = 0.01)和癌症患病率(14.3%,P = 0.02)显著高于发病年龄较晚的男性。结果表明,在遗传易感性个体中,前列腺癌的发展在PSA检测可行的亚临床期之前。血清PSA筛查对有早发性前列腺癌家族史的男性可能特别有用。

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Targeted prostate cancer screening in men with mutations in BRCA1 and BRCA2 detects aggressive prostate cancer: preliminary analysis of the results of the IMPACT study.
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