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DOI 10.1093/jnci/djs351

Медицинская библиотека · Journal of the National Cancer Institute · 2012

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

Win Aung Ko, Lindor Noralane M, Young Joanne P, Macrae Finlay A, Young Graeme P, Williamson Elizabeth, Parry Susan, Goldblatt Jack, Lipton Lara, Winship Ingrid, Leggett Barbara, Tucker Katherine M, Giles Graham G, Buchanan Daniel D, Clendenning Mark, Rosty Christophe, Arnold Julie, Levine A Joan, Haile Robert W, Gallinger Steven, Le Marchand Loïc, Newcomb Polly A, Hopper John L, Jenkins Mark A

СтатьяПоддержка NIH: внешняя программаПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

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.

Для цитирования: Win Aung Ko, Lindor Noralane M, Young Joanne P, Macrae Finlay A, Young Graeme P, Williamson Elizabeth, Parry Susan, Goldblatt Jack, Lipton Lara, Winship Ingrid, Leggett Barbara, Tucker Katherine M, Giles Graham G, Buchanan Daniel D, Clendenning Mark, Rosty Christophe, Arnold Julie, Levine A Joan, Haile Robert W, Gallinger Steven, Le Marchand Loïc, Newcomb Polly A, Hopper John L, Jenkins Mark A. Risks of primary extracolonic cancers following colorectal cancer in lynch syndrome.. Journal of the National Cancer Institute. 2012. DOI: 10.1093/jnci/djs351.

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