丹麦遗传性非息肉性结直肠癌(HNPCC)登记中结直肠癌登记的完整性。

IF 2 4区 医学 Q3 GENETICS & HEREDITY
Lars Joachim Lindberg, Inge Bernstein, Henrik Møller, Lone Sunde, Christina Therkildsen
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引用次数: 0

摘要

丹麦遗传性非息肉病性结直肠癌登记册(HNPCC-R)已成为支持风险分层和国家和国际监测指南的许多流行病学研究的基础。然而,HNPCC-R是基于自愿报告的,登记的完整性尚不清楚。因此,我们旨在评估HNPCC-R中结直肠癌(CRC)登记的有效性和完整性。我们将HNPCC-R中的登记与丹麦国家癌症登记处(DCR)中的登记结合起来,该登记处经过验证并基于强制性报告,并使用基于唯一的国家中央人口登记号、诊断日期、位置和形态学的13步算法匹配每个登记处的病例,从而在49,799个人中识别出9160例经过验证的crc。注册者之间的总体一致性为85%,HNPCC-R的完整性为95%。DCR在1975年之前登记的人数最多,而HNPCC-R在1985年之后登记的人数最多,特别是更多的同步和异时病例。总之,HNPCC-R关于结直肠癌的数据是有效的,应该优先用于研究遗传性结直肠癌风险增加的家庭的结直肠癌,特别是Lynch综合征,该综合征以多种结直肠癌而闻名,尽管两种登记的组合将确保最优的数据集。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Completeness of colorectal cancer registration in the Danish hereditary non-polyposis colorectal cancer (HNPCC) register.

Completeness of colorectal cancer registration in the Danish hereditary non-polyposis colorectal cancer (HNPCC) register.

Completeness of colorectal cancer registration in the Danish hereditary non-polyposis colorectal cancer (HNPCC) register.

Completeness of colorectal cancer registration in the Danish hereditary non-polyposis colorectal cancer (HNPCC) register.

The Danish Hereditary Non-Polyposis Colorectal Cancer Register (HNPCC-R) has formed the basis for many epidemiologic studies supporting risk stratification and both national and international guidelines on surveillance. However, the HNPCC-R is based on voluntary reporting and the completeness of registration is unknown. Hence, we aimed to assess the validity and completeness of the colorectal cancer (CRC) registrations in the HNPCC-R. We combined the registrations in the HNPCC-R with the registrations in the national Danish Cancer Registry (DCR), which is validated and based on mandatory reporting, and matched the cases from each register using a 13-step algorithm based on unique, national Central Population Registration number, date of diagnosis, location, and morphology thus identifying 9160 verified CRCs in 49,799 individuals. The overall agreement between the registers was 85%, and the completeness of the HNPCC-R was 95%. The DCR had the highest number of registrations before 1975, and the HNPCC-R had the highest number of registrations after 1985-especially more synchronous and metachronous cases. In conclusion, data from the HNPCC-R on CRC are valid and should be preferred for studies on CRC in families with a heritable increased risk of colorectal cancer-especially in Lynch syndrome, which is known for multiple CRCs, though a combination of both registers would secure the most optimal dataset.

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来源期刊
Familial Cancer
Familial Cancer 医学-遗传学
CiteScore
4.10
自引率
4.50%
发文量
36
审稿时长
6-12 weeks
期刊介绍: In recent years clinical cancer genetics has become increasingly important. Several events, in particular the developments in DNA-based technology, have contributed to this evolution. Clinical cancer genetics has now matured to a medical discipline which is truly multidisciplinary in which clinical and molecular geneticists work together with clinical and medical oncologists as well as with psycho-social workers. Due to the multidisciplinary nature of clinical cancer genetics most papers are currently being published in a wide variety of journals on epidemiology, oncology and genetics. Familial Cancer provides a forum bringing these topics together focusing on the interests and needs of the clinician. The journal mainly concentrates on clinical cancer genetics. Most major areas in the field shall be included, such as epidemiology of familial cancer, molecular analysis and diagnosis, clinical expression, treatment and prevention, counselling and the health economics of familial cancer.
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