Prevalence of adenomas and hyperplastic polyps in mismatch repair mutation carriers among CAPP2 participants:: Report by the Colorectal Adenoma/Carcinoma Prevention Programme 2

被引:32
作者
Liljegren, Annelie
Barker, Gail
Elliott, Faye
Bertario, Lucio
Bisgaard, Marie Luise
Eccles, Diana
Evans, Gareth
Macrae, Finlay
Maher, Eamonn
Lindblom, Annika
Rotstein, Samuel
Nilsson, Bo
Mecklin, Jukka-Pekka
Moeslein, Gabriela
Jass, Jeremy
Fodde, Riccardo
Mathers, John
Burn, John
Bishop, D. Timothy
机构
[1] Karolinska Univ Hosp, Radiumhemmet, Canc Epidemiol Unit, Inst Oncol & Pathol, S-17176 Stockholm, Sweden
[2] Karolinska Univ Hosp, Dept Clin Genet, Ctr Mol Med, S-17176 Stockholm, Sweden
[3] Danderyd Hosp, Radiumhemmet, Oncol Unit, Stockholm, Sweden
[4] Univ Newcastle, Sch Clin Med Sci, Inst Human Genet Annex, Biosci Ctr, Newcastle Upon Tyne, Tyne & Wear, England
[5] Univ Newcastle, Sch Clin Med Sci, Human Nutr Res Ctr, Newcastle Upon Tyne, Tyne & Wear, England
[6] St James Univ Hosp, Leeds Inst Mol Med, Epidemiol & Biostat Sect, Leeds, W Yorkshire, England
[7] Clin Genet Unit, Southampton, Hants, England
[8] Univ Birmingham, Head Sect Med & Mol Genet, Dept Paediat & Child Hlth, Birmingham, W Midlands, England
[9] Ist Nazl Studio & Cura Tumori, I-20133 Milan, Italy
[10] Univ Copenhagen, Danish Hereditary Nonpolyposis Colorectal Canc Re, Hvidovre Hosp & Med, Genet Clin,Panum Inst 24 4, Copenhagen, Denmark
[11] Univ Melbourne, Royal Melbourne Hosp, Melbourne, Vic 3050, Australia
[12] Jyvaskyla Cent Hosp, Dept Surg, Jyvaskyla, Finland
[13] Chirurg Klin & Poliklin, Dusseldorf, Germany
[14] McGill Univ, Dept Pathol, Montreal, PQ, Canada
[15] Dept Human & Clin Genet, Leiden, Netherlands
[16] Erasmus MC, Dept Pathol, Josephine Nefkens Inst, Rotterdam, Netherlands
[17] St Marys Hosp, Dept Med Genet, Manchester M13 0JH, Lancs, England
基金
英国医学研究理事会;
关键词
D O I
10.1200/JCO.2007.13.2795
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose To determine the prevalence of adenomatous and hyperplastic polyps in a large cohort of individuals with a germline mutation in a mismatch repair (MMR) gene, the major genetic determinant of hereditary nonpolyposis colorectal cancer (HNPCC). These prevalences have been estimated previously in smaller studies, and the results have been found to be variable. Patients and Methods Colorectal Adenoma/Carcinoma Prevention Programme 2 trial is a chemoprevention trial in people classified as having HNPCC. The 695 patients with a proven germline MMR mutation and documented screening history before the chemoprevention study were the focus of this study. The number, histology, size, and location of polyps found at the participants' first ever colonoscopy were analyzed in a cross-sectional study. Results Seventy-four patients (10.6%) were found to have at least one adenoma at first colonoscopy, whereas 37 (5.3%) had at least one hyperplastic polyp. The frequency of an adenoma at first colonoscopy increased from 5.0% (95% CI, 2.8% to 8.3%) in patients younger than 35 years old to 18.9% (95% CI, 9.4% to 32.0%) in patients age at least 55 years (P = .0001 for trend). No such trend was observed for hyperplastic polyps. No sex differences were found for either type of polyp. A marginal association was found between the co-occurrence of adenomas and hyperplastic polyps. Adenomas tended to be more proximally distributed through the colon, whereas hyperplastic polyps tended to be located in the distal colon. Conclusion Adenoma prevalence increases with age among MMR mutation carriers, whereas hyperplastic polyp prevalence is consistent. No sex differences were observed for either type of lesion.
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收藏
页码:3434 / 3439
页数:6
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