Suppr超能文献

家族性前列腺癌及可能相关的恶性肿瘤:瑞典全国性登记队列研究

Familial prostate cancer and possible associated malignancies: nation-wide register cohort study in Sweden.

作者信息

Damber L, Grönberg H, Damber J E

机构信息

Department of Oncology, Umeå University, Sweden.

出版信息

Int J Cancer. 1998 Oct 29;78(3):293-7. doi: 10.1002/(SICI)1097-0215(19981029)78:3<293::AID-IJC5>3.0.CO;2-Q.

Abstract

There is a familial aggregation of prostate cancer, and 5 to 10% of all prostate cancers are estimated to be inherited in an autosomal-dominant mode. A population-based cohort study was performed in order to study familial prostate cancer and associated malignancies. A nation-wide register cohort study was conducted using an unselected study population. The cohort of 5,595 sons and 5,089 daughters of Swedish men found to have prostate cancer between 1959 and 1963 was identified. All types of cancer reported between 1958 and 1992 in this cohort were identified through linkage to the Swedish Cancer Registry. The expected number of different cancers was calculated using incidence rates obtained from the Registry. A highly significant increased overall standardized incidence ratio (SIR) of 1.65 (95% CI, 1.49-1.83) was obtained for prostate cancer, with 370 observed cases compared with 224 expected prostate cancers. The SIR was 3.18 among cases 45 to 49 years old at diagnosis, with the risk gradually decreasing to a SIR of 1.45 among cases over 80 years of age. Among sons and daughters with a father whose prostate cancer was diagnosed at an early age (<70 years), an increased risk for colorectal cancer SIR 1.48 (1.10-1.95) was observed. No significant difference in cancer risk for other sites was observed among the daughters and sons of men with prostate cancer. This cohort study confirms earlier studies that a positive family history of prostate cancer is an important risk factor for developing this disease. Though increased risk was found for all ages, it was more pronounced in younger men. Since no other malignancy was significantly associated with prostate cancer, it is most likely that familial prostate cancer is "site-specific".

摘要

前列腺癌存在家族聚集性,据估计,所有前列腺癌中有5%至10%是以常染色体显性模式遗传的。为了研究家族性前列腺癌及相关恶性肿瘤,开展了一项基于人群的队列研究。使用未经过筛选的研究人群进行了一项全国性登记队列研究。确定了1959年至1963年间被发现患有前列腺癌的瑞典男性的5595名儿子和5089名女儿组成的队列。通过与瑞典癌症登记处的链接,确定了该队列在1958年至1992年间报告的所有癌症类型。使用从登记处获得的发病率计算不同癌症的预期数量。前列腺癌的总体标准化发病率(SIR)显著升高,为1.65(95%可信区间,1.49 - 1.83),观察到370例病例,而预期前列腺癌为224例。在诊断时年龄为45至49岁的病例中,SIR为3.18,风险逐渐降低,80岁以上病例的SIR为1.45。在父亲前列腺癌在早年(<70岁)被诊断的儿子和女儿中,观察到结直肠癌风险增加,SIR为1.48(1.10 - 1.95)。前列腺癌男性的女儿和儿子在其他部位的癌症风险未观察到显著差异。这项队列研究证实了早期研究,即前列腺癌的阳性家族史是患此病的一个重要风险因素。虽然在所有年龄段都发现风险增加,但在年轻男性中更为明显。由于没有其他恶性肿瘤与前列腺癌有显著关联,家族性前列腺癌很可能是“部位特异性的”。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验