Optimizing the detection of hereditary non-polyposis colorectal cancer: An update

被引:3
|
作者
De Bruin, J. H. F. M.
Ligtenberg, M. J. L.
Nagengast, F. M.
Adang, E. M. M.
Van Krieken, J. H. J. M.
Hoogerbrugge, N.
机构
[1] Radboud Univ Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands
[2] Radboud Univ Med Ctr, Dept Pathol, NL-6500 HB Nijmegen, Netherlands
[3] Radboud Univ Med Ctr, Dept Gastroenterol, NL-6500 HB Nijmegen, Netherlands
[4] Radboud Univ Med Ctr, Dept Med Technol Assessment, NL-6500 HB Nijmegen, Netherlands
[5] Radboud Univ Med Ctr, Dept Med Oncol, NL-6500 HB Nijmegen, Netherlands
关键词
colorectal cancer; genetic testing; hereditary cancer; HNPCC; MSI;
D O I
10.1080/00365520600664508
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Hereditary non-polyposis colorectal cancer (HNPCC) is a dominant inherited disease and accounts for up to 5% of all colorectal cancer (CRC) patients. Despite the optimization of selection criteria and enhancements in molecular techniques for identifying more families with HNPCC, most cases are not recognized. Poor patient recollection of family history and inadequate family history-taking are main causative factors. We propose a new strategy for detecting HNPCC, one in which the pathologist selects patients for microsatellite instability (MSI) testing. Criteria for MSI analysis are: (1) CRC before the age of 50 years, (2) second CRC before 70 years, (3) CRC and HNPCC-associated cancer before 70 years, or (4) adenoma before 40 years. Additionally, patients with a positive MSI test and patients with a positive family history are offered referral for genetic counselling. With this strategy, at least twice the number of HNPCC patients will be identified among a population of CRC patients, and in a cost-effective, efficient and feasible way. The identification of patients with HNPCC is important because intensive surveillance can prevent death from CRC.
引用
收藏
页码:146 / 152
页数:7
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