Mak T, Senevrayar K, Lalloo F, Evans D G R, Hill J
Department of General Surgery, Manchester Royal Infirmary, and Academic Unit of Medical Genetics and Regional Genetics Service, St. Mary's Hospital, Manchester, UK.
Colorectal Dis. 2007 Sep;9(7):635-40. doi: 10.1111/j.1463-1318.2006.01203.x.
Screening colonoscopy has been shown to reduce mortality and cancer stage in hereditary nonpolyposis colorectal cancer (HNPCC) individuals. However, the benefit of screening in intermediate risk groups is unknown. The most recent national guidelines have recommended a reduction of screening frequency for the intermediate risk group. Therefore, this study aims to compare the results of colonoscopic screening in HNPCC and intermediate risk groups and assess the effect of the most recent screening protocol recommendations.
A total of 244 individuals; 108 from HNPCC families (28 mismatch repair gene carriers) and 136 from intermediate risk families were referred for regular colonoscopic screening by the Regional Genetics Service. Findings from 417 colonoscopies performed between 1992 and 2003 were evaluated.
A total of three cancers, 39 adenomas and 41 hyperplastic polyps were found in the HNPCC group compared with one cancer, 22 adenomas and 19 hyperplasic polyps in the intermediate risk group. If the recent screening guidelines for the intermediate group were applied, then 89 (44%) fewer colonoscopies would have been performed. Although no cancers would have been missed, six adenomas (mean size = 5.7 mm, range 2-10 mm) with two graded as severely dysplasic and six hyperplastic polyps would not have been detected.
The detection rate and distribution of adenomas were similar in both groups. If the new colonoscopic screening recommendations for the intermediate risk group had been applied, a small number of significant lesions would have been missed.
筛查结肠镜检查已被证明可降低遗传性非息肉病性结直肠癌(HNPCC)患者的死亡率并降低癌症分期。然而,中间风险组进行筛查的益处尚不清楚。最新的国家指南建议降低中间风险组的筛查频率。因此,本研究旨在比较HNPCC组和中间风险组的结肠镜筛查结果,并评估最新筛查方案建议的效果。
共有244例个体;108例来自HNPCC家族(28例错配修复基因携带者),136例来自中间风险家族,由地区遗传学服务机构转诊进行定期结肠镜筛查。对1992年至2003年间进行的417次结肠镜检查结果进行了评估。
HNPCC组共发现3例癌症、39例腺瘤和41例增生性息肉,而中间风险组发现1例癌症、22例腺瘤和19例增生性息肉。如果应用中间组的最新筛查指南,那么结肠镜检查次数将减少89次(44%)。虽然不会漏诊癌症,但6例腺瘤(平均大小=5.7毫米,范围2-10毫米),其中2例为重度发育异常,6例增生性息肉将无法检测到。
两组腺瘤的检出率和分布相似。如果应用中间风险组的新结肠镜筛查建议,将会漏诊少量重要病变。