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Original Research

Open Access

Lynch syndrome in patients treated for endometrial cancer

  • K. Cetinkaya1
  • E. Yuce2,*,

1Ankara Oncology Education and Research Hospital, Ankara

2Department of Gynecology and Obstetrics, Koru Hospital, Ankara (Turkey)

DOI: 10.12892/ejgo3654.2017 Vol.38,Issue 4,August 2017 pp.607-613

Published: 10 August 2017

*Corresponding Author(s): E. Yuce E-mail: dr.ebruk@gmail.com

Abstract

Objective: To evaluate the patients with familial Lynch syndrome, who were treated for endometrial cancer in Gynecology Department of Ankara Oncology Education and Research Hospital. Materials and Methods: Staging surgery was performed in all patients diagnosed with endometrial cancer. Total abdominal hysterectomy (TAH), bilateral salpingo-oophorectomy (BSO), omentectomy, bilateral pelvic-para-aortic lymph node dissection (BPPLND), and peritoneal cytology were performed. The patients were referred to radiation oncology clinic with their final pathology report, postoperatively. Adjuvant radiotherapy was performed in patients deemed necessary. Results: Familial Lynch syndrome was detected in four of 93 patients. All of the Lynch cases were diagnosed with FIGO Stage I endometrial adenocarcinoma. The mean age of Lynch syndrome patients was 51.5 years. Two of these 93 patients were synchronous colon and endometrial cancer and one of these 93 patients was metachronous colon and endometrial cancer, but Lynch syndrome was not diagnosed in these three patients according to Amsterdam criteria. Conclusion: Diagnosis of patients with Lynch syndrome and identification of at-risk people is very important because if it is diagnosed at early stage, better survival rates could be expected.

Keywords

Lynch syndrome; Endometrial cancer; Colon cancer.


Cite and Share

K. Cetinkaya,E. Yuce. Lynch syndrome in patients treated for endometrial cancer. European Journal of Gynaecological Oncology. 2017. 38(4);607-613.

References

[1] Lynch H.T., de la Chapelle A.: “Hereditary colorectal cancer”. N. Engl. J. Med., 2003, 348, 919.

[2] Vasen H.F., Watson P., Mecklin J.P., Lynch H.T.: “New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative Group on HNPCC”. Gastroenterology, 1999, 116, 1453.

[3] Pinol V., Castells A., Andreu M., Castellvi-Bel S., Alenda C., Llor X., et al.: “Gastrointestinal Oncology Group of the Spanish Gastroenterological Association. Accuracy of revised Bethesda guidelines, microsatellite instability, and immunohistochemistry for the identification of patients with hereditary nonpolyposis colorectal cancer”. JAMA, 2005, 293, 1986.

[4] de la Chapelle A.: “The incidence of Lynch Syndrome”. Fam. Cancer, 2005, 4, 233.

[5] Dunlop M.G., Farrington S.M., Nicholl I., Aaltonen L., Petersen G., Porteous M., et al.: “Population carrier frequency of hMSH2 and hMLH1 mutations”. Br. J. Cancer, 2000, 83, 1643.

[6] Hampel H., Frankel W., Panescu J., Lockman J., Sotamaa K., Fix D., et al.: “Screening for Lynch syndrome (hereditary nonpolyposis colorectal cancer) among endometrial cancer patients”. Cancer Res., 2006, 66, 7810.

[7] Hampel H., Frankel W.L., Martin E., Arnold M., Khanduja K., Kuebler P., et al.: “Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer)”. N. Engl. J. Med., 2005, 352, 1851.

[8] Lu K.H., Berchuck A., Kauff N.D.: “Hereditary gynecologic cancers”. In: Barakat R., Berchuck A., Markman M., Randall M.E. (eds). Principles and practice of gynecologic oncology. 6th ed. Philadelphia: Lippincott Williams & Wilkins, 2013, 60.

[9] Lindor N.M., Petersen G.M., Hadley D.W., Kinney A.Y., Miesfeldt S., Lu K.H., et al.: “Recommendations for the care of individuals with an inherited predisposition to Lynch syndrome: a systematic review”. JAMA, 2006, 296, 1507.

[10] Celentano V., Luglio G., Antonelli G., Tarquini R., Bucci L.: “Prophylactic surgery in Lynch syndrome”. Tech. Coloproctol., 2011, 15, 129.

[11] Marra G., Boland C.: “Hereditary nonpolyposis colorectal cancer”. J. Natl. Cancer Inst., 1995, 87, 1114.

[12] Aarnio M., Sankila R., Pukkala E., Salovaara R., Aaltonen L.A., de la Chapelle A., et al.: “Cancer risk in mutation carriers of DNA- mismatch-repair genes”. Int. J. Cancer, 1999, 81, 214.

[13] Dunlop M.G., Farrington S.M., Carothers A.D., Wyllie A.H., Sharp L., Burn J., et al.: “Cancer risk associated with germline DNA mismatch repair gene mutations”. Hum. Mol. Genet., 1997, 6, 105.

[14] Schmeler K.M., Lynch H.T., Chen L.M., Munsell M.F., Soliman P.T., Clark M.B., et al.: “Prophylactic surgery to reduce the risk of gynecologic cancers in the Lynch syndrome”. N. Engl. J. Med., 2006, 354, 261.

[15] Barrow E., Hill J., Evans D.G.: ‘Cancer risk in Lynch Syndrome”. Fam. Cancer, 2013, 12, 229.

[16] American College of Obstetricians and Gynecologists, ACOG Committee on Practice Bulletins--Gynecology, ACOG Committee on Genetics, Society of Gynecologic Oncologists: “ACOG Practice Bulletin No. 103: Hereditary breast and ovarian cancer syndrome”. Obstet. Gynecol., 2009, 113, 957.

[17] Boks D.E., Trujillo A.P., Voogd A.C., Morrearu H., Kenter G.G., Vasen H.F.: “Survival analysis of endometrial carcinoma associated with hereditary nonpolyposis colorectal cancer”. Int. J. Cancer, 2002, 102, 198.

[18] Lu K.H., Dinh M., Kohlmann W., Watson P., Green J., Syngal S., et al.: “Gynecologic cancer as a “sentinel cancer” for women with hereditary nonpolyposis colorectal cancer syndrome”. Obstet. Gynecol., 2005, 105, 569.

[19] Broaddus R.R., Lynch H.T., Chen L.M., Daniels M.S., Conrad P., Munsell M.F., et al.: ‘Pathologic features of endometrial carcinoma associated with HNPCC: a comparison with sporadic endometrial carcinoma”. Cancer, 2006, 106, 87.

[20] Koehler-Santos P., Izetti P., Abud J., Pitroski C.E, Cossio S.L, Camey S.A, et al.: “Identification of patients at-risk for Lynch syndrome in a hospital- based colorectal surgery clinic”. World J. Gastroenterol., 2011, 17, 766.

[21] Ishii N., Arai M., Koyama Y., Ueno M., Yamaguchi T., Kazuma K., et al.: “Factors affecting encouragement of relatives among families with Lynch syndrome to seek medical assessment”. Fam. Cancer, 2011, 10, 649.

[22] Backes F.J. Cohn D.E.: “Lynch syndrome”. Clin. Obstet. Gynecol., 2011, 54, 199.

[23] Vasen H.F., Mecklin J.P., Khan P.M., Lynch H.T.: “The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC)”. Dis. Colon Rectum, 1991, 34, 424.

[24] Umar A., Boland C.R., Terdiman J.P., Syngal S., de la Chapelle A., Ruschoff J., et al.: “Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability”. J. Natl. Cancer Inst., 2004, 96, 261.

[25] Lancaster J.M., Powell C.B., Kauff N.D., Cass I., Chen L.M., Lu K.H., et al.: “Society of Gynecologic Oncologists Education Committee statement on risk assessment for inherited gynecologic cancer predispositions”. Gynecol. Oncol., 2007, 107, 159.

[26] Gruber S.B.: “New developments in Lynch syndrome (hereditary nonpolyposis colorectal cancer) and mismatch repair gene testing”. Gastroenterology, 2006, 130, 577.

[27] Carcangiu M.L., Radice P., Casalini P., Bertario L., Merola M., Sala P.: “Lynch syndrome—related endometrial carcinomas show a high frequency of nonendometrioid types and of high FIGO grade endometrioid types”. Int. J. Surg. Pathol., 2010, 18, 21.

[28] Westin S.N., Lacour R.A., Urbauer D.L., Luthra R., Bodurka D.C., Lu K.H., et al.: “Carcinoma of the lower uterine segment: a newly described association with Lynch syndrome”. J. Clin. Oncol., 2008, 26, 5965.

[29] Vasen H.F., Möslein G., Alonso A., Bernstein I., Bertario L., Blanco I., et al.: “Guidelines for the clinical management of Lynch syndrome (hereditary non-polyposis cancer)”. J. Med. Genet., 2007, 44, 353.

[30] National Comprehensive Cancer Network: “NCCN Clinical Practice Guidelines in Oncology-Colorectal Cancer Screening. Version 2.2012”. Available at: http://www.nccn.org.2012

[31] Dove-Edwin I., Boks D., Goff S., Kenter G.G., Carpenter R., Vasen H.F., et al.: “The outcome of endometrial carcinoma surveillance by ultrasound scan in women at risk of hereditary nonpolyposis colorectal carcinoma and familial colorectal carcinoma”. Cancer, 2002, 94, 1708.

[32] Rijcken F.E., Mourits M.J., Kleibeuker J.H., Hollema H., van der Zee A.G.: “Gynecologic screening in hereditary nonpolyposis colorectal cancer”. Gynecol. Oncol., 2003, 91, 74.

[33] Renkonen-Sinisalo L., Butzow R., Leminen A., Lehtovirta P., Mecklin J.P., Jarvinen H.J.: “Surveillance for endometrial cancer in hereditary nonpolyposis colorectal cancer syndrome”. Int. J. Cancer, 2007, 120, 821.

[34] Hampel H., de la Chapelle A.: “The search for unaffected individuals with Lynch syndrome: do the ends justify the means?” Cancer Prev. Res., (Phila.), 2011, 4, 1.

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