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林奇综合征患者结直肠癌后发生原发性结外癌症的风险。

Risks of primary extracolonic cancers following colorectal cancer in lynch syndrome.

机构信息

Centre for Molecular, Environmental, Genetic and Analytic Epidemiology, Melbourne School of Population Health, Level 3, 207 Bouverie Street, The University of Melbourne, VIC 3010, Australia.

出版信息

J Natl Cancer Inst. 2012 Sep 19;104(18):1363-72. doi: 10.1093/jnci/djs351. Epub 2012 Aug 28.

Abstract

BACKGROUND

Lynch syndrome is a highly penetrant cancer predisposition syndrome caused by germline mutations in DNA mismatch repair (MMR) genes. We estimated the risks of primary cancers other than colorectal cancer following a diagnosis of colorectal cancer in mutation carriers.

METHODS

We obtained data from the Colon Cancer Family Registry for 764 carriers of an MMR gene mutation (316 MLH1, 357 MSH2, 49 MSH6, and 42 PMS2), who had a previous diagnosis of colorectal cancer. The Kaplan-Meier method was used to estimate their cumulative risk of cancers 10 and 20 years after colorectal cancer. We estimated the age-, sex-, country- and calendar period-specific standardized incidence ratios (SIRs) of cancers following colorectal cancer, compared with the general population.

RESULTS

Following colorectal cancer, carriers of MMR gene mutations had the following 10-year risk of cancers in other organs: kidney, renal pelvis, ureter, and bladder (2%, 95% confidence interval [CI] = 1% to 3%); small intestine, stomach, and hepatobiliary tract (1%, 95% CI = 0.2% to 2%); prostate (3%, 95% CI = 1% to 5%); endometrium (12%, 95% CI = 8% to 17%); breast (2%, 95% CI = 1% to 4%); and ovary (1%, 95% CI = 0% to 2%). They were at elevated risk compared with the general population: cancers of the kidney, renal pelvis, and ureter (SIR = 12.54, 95% CI = 7.97 to 17.94), urinary bladder (SIR = 7.22, 95% CI = 4.08 to 10.99), small intestine (SIR = 72.68, 95% CI = 39.95 to 111.29), stomach (SIR = 5.65, 95% CI = 2.32 to 9.69), and hepatobiliary tract (SIR = 5.94, 95% CI = 1.81 to 10.94) for both sexes; cancer of the prostate (SIR = 2.05, 95% CI = 1.23 to 3.01), endometrium (SIR = 40.23, 95% CI = 27.91 to 56.06), breast (SIR = 1.76, 95% CI = 1.07 to 2.59), and ovary (SIR = 4.19, 95% CI = 1.28 to 7.97).

CONCLUSION

Carriers of MMR gene mutations who have already had a colorectal cancer are at increased risk of a greater range of cancers than the recognized spectrum of Lynch syndrome cancers, including breast and prostate cancers.

摘要

背景

林奇综合征是一种由 DNA 错配修复(MMR)基因突变引起的高外显率癌症易感性综合征。我们估计了突变携带者在诊断出结直肠癌后发生其他原发性癌症的风险。

方法

我们从结肠癌家族登记处获得了 764 名 MMR 基因突变携带者(316 名 MLH1、357 名 MSH2、49 名 MSH6 和 42 名 PMS2)的数据,这些人之前曾被诊断患有结直肠癌。我们使用 Kaplan-Meier 法估计了他们在结直肠癌后 10 年和 20 年内癌症的累积风险。我们估计了与一般人群相比,结直肠癌后癌症的年龄、性别、国家和日历期特定标准化发病比(SIR)。

结果

结直肠癌后,MMR 基因突变携带者的其他器官癌症 10 年风险如下:肾脏、肾盂、输尿管和膀胱(2%,95%置信区间[CI] = 1%至 3%);小肠、胃和肝胆道(1%,95%CI = 0.2%至 2%);前列腺(3%,95%CI = 1%至 5%);子宫内膜(12%,95%CI = 8%至 17%);乳房(2%,95%CI = 1%至 4%);和卵巢(1%,95%CI = 0%至 2%)。与一般人群相比,他们的风险增加:肾脏、肾盂和输尿管的癌症(SIR = 12.54,95%CI = 7.97 至 17.94)、膀胱癌(SIR = 7.22,95%CI = 4.08 至 10.99)、小肠(SIR = 72.68,95%CI = 39.95 至 111.29)、胃(SIR = 5.65,95%CI = 2.32 至 9.69)和肝胆道(SIR = 5.94,95%CI = 1.81 至 10.94)(男女);前列腺癌(SIR = 2.05,95%CI = 1.23 至 3.01)、子宫内膜癌(SIR = 40.23,95%CI = 27.91 至 56.06)、乳腺癌(SIR = 1.76,95%CI = 1.07 至 2.59)和卵巢癌(SIR = 4.19,95%CI = 1.28 至 7.97)。

结论

已经患有结直肠癌的 MMR 基因突变携带者发生其他癌症的风险高于林奇综合征癌症的公认范围,包括乳腺癌和前列腺癌。

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