Efficacy of Annual Colonoscopic Surveillance in Individuals With Hereditary Nonpolyposis Colorectal Cancer

被引:143
作者
Engel, Christoph [1 ]
Rahner, Nils [2 ]
Schulmann, Karsten [3 ]
Holinski-Feder, Elke [4 ,5 ]
Goecke, Timm O. [6 ]
Schackert, Hans K. [7 ]
Kloor, Matthias [8 ]
Steinke, Verena [2 ]
Vogelsang, Holger [9 ]
Moeslein, Gabriela [10 ]
Goergens, Heike [7 ]
Dechant, Stefan [11 ]
Doeberitz, Magnus Von Knebel [8 ]
Rueschoff, Josef [12 ,13 ]
Friedrichs, Nicolaus [14 ]
Buettner, Reinhard [14 ]
Loeffler, Markus [1 ]
Propping, Peter [2 ]
Schmiegel, Wolff [3 ]
机构
[1] Univ Leipzig, Inst Med Informat Stat & Epidemiol, D-04107 Leipzig, Germany
[2] Univ Bonn, Inst Human Genet, D-5300 Bonn, Germany
[3] Ruhr Univ Bochum, Dept Med, Knappschaftskrankenhaus, Bochum, Germany
[4] Ctr Med Genet, Munich, Germany
[5] Univ Munich, Dept Internal Med, Univ Hosp, Munich, Germany
[6] Univ Dusseldorf, Inst Human Genet, Dusseldorf, Germany
[7] Tech Univ Dresden, Dept Surg Res, Dresden, Germany
[8] Univ Heidelberg, Inst Pathol, Dept Appl Tumour Biol, D-6900 Heidelberg, Germany
[9] Tech Univ Munich, Dept Surg, Munich, Germany
[10] St Josefs Hosp, Dept Surg, Bochum, Germany
[11] Univ Regensburg, Dept Surg, Regensburg, Germany
[12] Nordhessen & Targos Mol Pathol GmbH, Inst Pathol, Kassel, Germany
[13] Univ Regensburg, Inst Pathol, Regensburg, Germany
[14] Univ Bonn, Inst Pathol, D-5300 Bonn, Germany
关键词
POPULATION-BASED ANALYSIS; LYNCH-SYNDROME; MUTATION CARRIERS; COLON-CANCER; FAMILIES; RISK; HNPCC; PREVENTION; GUIDELINES; CARCINOMA;
D O I
10.1016/j.cgh.2009.10.003
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
BACKGROUND & AIMS: Individuals with hereditary non-polyposis colorectal cancer (HNPCC; Lynch syndrome) have a high risk for developing colorectal cancer (CRC). We evaluated the efficacy of annual surveillance colonoscopies to detect adenomas and CRCs. METHODS: In a prospective, multicenter cohort study, 1126 individuals underwent 3474 colonoscopies. We considered individuals from 3 groups of HNPCC families: those with a pathogenic germline mutation in a mismatch repair gene (MUT group), those without a mutation but with microsatellite instability (MSI group), and those who fufilled the Amsterdam criteria without microsatellite instability (MSS group). RESULTS: Compliance to annual intervals was good, with 81% of colonoscopies completed within 15 months. Ninety-nine CRC events were observed in 90 patients. Seventeen CRCs (17%) were detected through symptoms (8 before baseline colonoscopy, 8 at intervals >15 months to the preceding colonoscopy, and 1 interval cancer). Only 2 of 43 CRCs detected by follow-up colonoscopy were regionally advanced. Tumor stages were significantly lower among CRCs detected by follow-up colonoscopies compared with CRCs detected by symptoms (P = .01). Cumulative CRC risk at the age of 60 years was similar in the MUT and MSI groups (23.0% combined; 95% confidence interval [CI], 14.8%-31.2%) but considerably lower in the MSS group (1.8%; 95% CI, 0.0%-5.1%). Adenomas at baseline colonoscopy predicted an earlier occurrence of subsequent adenoma (hazard ratio, 2.6; 95% CI, 1.7-4.0) and CRC (hazard ratio, 3.9; 95% CI, 1.7-8.5), providing information about inter-individual heterogeneity of adenomas and kinetics of CRC formation. CONCLUSIONS: Annual colonoscopic surveillance is recommended for individuals with HNPCC. Less intense surveillance might be appropriate for MSS families.
引用
收藏
页码:174 / 182
页数:9
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