Literature DB >> 23392144

Increasing Lynch syndrome identification through establishment of a hereditary colorectal cancer registry.

Duveen Sturgeon1, Tonna McCutcheon, Timothy M Geiger, Roberta L Muldoon, Alan J Herline, Paul E Wise.   

Abstract

BACKGROUND: Lynch syndrome contributes to 5% of all colorectal cancers. Patients seen in most surgical clinics have limited or no family histories documented and are rarely assessed for hereditary syndromes. In 2007 a clinic-based hereditary colorectal cancer registry was established to screen for Lynch syndrome and facilitate genetic counseling/testing.
OBJECTIVE: To evaluate the effectiveness of the hereditary colorectal cancer registry to identify high-risk colorectal cancer patients and have them referred for genetic counseling/testing for Lynch syndrome.
DESIGN: A retrospective review and cohort comparison of both prospectively collected and retrospective data.
SETTING: The colorectal surgical clinic at Vanderbilt University Medical Center. PATIENTS: All newly diagnosed colorectal cancer patients seen between January 2006 and October 2010. MAIN OUTCOME MEASURES: To assess the identification of colorectal cancer patients at high risk for Lynch syndrome and for the occurrence of genetic counseling/testing before and after the establishment of a hereditary registry by comparing the results from the colorectal cancer patients seen the year prior to the establishment of the registry (January - December 2006, "control period") with those patients seen after initiation of the registry (January 2007 - October 2010, "registry period").
RESULTS: During the "registry period," 495 colorectal cancer patients were seen in the clinic and 257 (51.9%) were high risk for Lynch syndrome. Forty-nine patients (9.8%) underwent genetic testing, with 27 (5.4%) positive for a gene mutation, of which half were >50 years old. By comparison, in 2006, 115 colorectal cancer patients were seen in the clinic but only 4 patients (3.5%) went on for further assessment, and only 1 had genetic testing. Retrospective assessment showed that at least 22 patients (19.1%) had warranted further investigation in 2006. LIMITATIONS: This was a single-institution, retrospective review.
CONCLUSION: Establishment of a hereditary colorectal cancer registry with a clinic-based protocol improves identification of Lynch syndrome.

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Year:  2013        PMID: 23392144     DOI: 10.1097/DCR.0b013e31827edfff

Source DB:  PubMed          Journal:  Dis Colon Rectum        ISSN: 0012-3706            Impact factor:   4.585


  2 in total

1.  Clinicopathological Features and Type of Surgery for Lynch Syndrome: Changes during the Past Two Decades.

Authors:  Il Tae Son; Duck-Woo Kim; Seung-Yong Jeong; Young-Kyoung Shin; Myong Hoon Ihn; Heung-Kwon Oh; Sung-Bum Kang; Kyu Joo Park; Jae Hwan Oh; Ja-Lok Ku; Jae-Gahb Park
Journal:  Cancer Res Treat       Date:  2015-05-26       Impact factor: 4.679

2.  Knowledge of and practice patterns for hereditary colorectal cancer syndromes in korean surgical residents.

Authors:  Jangho Park; Soo Young Lee; Duck-Woo Kim; Sung-Bum Kang; Seung-Yong Jeong; Kyu Joo Park
Journal:  Ann Coloproctol       Date:  2013-10-31
  2 in total

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