메뉴 건너뛰기




Volumn 25, Issue 10, 2014, Pages 2001-2007

Fourfold increased detection of Lynch syndrome by raising age limit for tumour genetic testing from 50 to 70 years is cost-effective

Author keywords

colorectal cancer; genetic; hereditary; Lynch syndrome; screening

Indexed keywords

AGED; COLORECTAL TUMOR; COMPLICATION; COST BENEFIT ANALYSIS; ECONOMICS; FEMALE; GENETICS; HEREDITARY NONPOLYPOSIS COLORECTAL CANCER; HUMAN; MALE; MIDDLE AGED; MISMATCH REPAIR; PATHOLOGY;

EID: 84930802499     PISSN: 09237534     EISSN: 15698041     Source Type: Journal    
DOI: 10.1093/annonc/mdu361     Document Type: Article
Times cited : (26)

References (31)
  • 1
    • 70350439453 scopus 로고    scopus 로고
    • Ten years after mutation testing for Lynch syndrome: cancer incidence and outcome in mutation-positive and mutation-negative family members
    • Jarvinen, H.J., Renkonen-Sinisalo, L., Aktan-Collan, K., et al. Ten years after mutation testing for Lynch syndrome: cancer incidence and outcome in mutation-positive and mutation-negative family members. J Clin Oncol 27 (2009), 4793–4797.
    • (2009) J Clin Oncol , vol.27 , pp. 4793-4797
    • Jarvinen, H.J.1    Renkonen-Sinisalo, L.2    Aktan-Collan, K.3
  • 2
    • 84876900933 scopus 로고    scopus 로고
    • Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts
    • Vasen, H.F., Blanco, I., Aktan-Collan, K., et al. Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts. Gut 62 (2013), 812–823.
    • (2013) Gut , vol.62 , pp. 812-823
    • Vasen, H.F.1    Blanco, I.2    Aktan-Collan, K.3
  • 3
    • 10744233937 scopus 로고    scopus 로고
    • Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability
    • Umar, A., Boland, C.R., Terdiman, J.P., et al. Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability. J Natl Cancer Inst 96 (2004), 261–268.
    • (2004) J Natl Cancer Inst , vol.96 , pp. 261-268
    • Umar, A.1    Boland, C.R.2    Terdiman, J.P.3
  • 4
    • 0033063711 scopus 로고    scopus 로고
    • New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative group on HNPCC
    • 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 116 (1999), 1453–1456.
    • (1999) Gastroenterology , vol.116 , pp. 1453-1456
    • Vasen, H.F.1    Watson, P.2    Mecklin, J.P.3    Lynch, H.T.4
  • 5
    • 84875667429 scopus 로고    scopus 로고
    • Familial colorectal cancer risk assessment needs improvement for more effective cancer prevention in relatives
    • discussion e185
    • Dekker, N., Hermens, R.P., Nagengast, F.M., et al. Familial colorectal cancer risk assessment needs improvement for more effective cancer prevention in relatives. Colorectal Dis 15 (2013), e175–e185 discussion e185.
    • (2013) Colorectal Dis , vol.15 , pp. e175-e185
    • Dekker, N.1    Hermens, R.P.2    Nagengast, F.M.3
  • 6
    • 67650924286 scopus 로고    scopus 로고
    • Review of the Lynch syndrome: history, molecular genetics, screening, differential diagnosis, and medicolegal ramifications
    • Lynch, H.T., Lynch, P.M., Lanspa, S.J., et al. Review of the Lynch syndrome: history, molecular genetics, screening, differential diagnosis, and medicolegal ramifications. Clin Genet 76 (2009), 1–18.
    • (2009) Clin Genet , vol.76 , pp. 1-18
    • Lynch, H.T.1    Lynch, P.M.2    Lanspa, S.J.3
  • 7
    • 58149144567 scopus 로고    scopus 로고
    • Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3′ exons of TACSTD1
    • Ligtenberg, M.J., Kuiper, R.P., Chan, T.L., et al. Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3′ exons of TACSTD1. Nat Genet 41 (2009), 112–117.
    • (2009) Nat Genet , vol.41 , pp. 112-117
    • Ligtenberg, M.J.1    Kuiper, R.P.2    Chan, T.L.3
  • 8
    • 0032534069 scopus 로고    scopus 로고
    • A National Cancer Institute Workshop on Microsatellite Instability for cancer detection and familial predisposition: development of international criteria for the determination of microsatellite instability in colorectal cancer
    • Boland, C.R., Thibodeau, S.N., Hamilton, S.R., et al. A National Cancer Institute Workshop on Microsatellite Instability for cancer detection and familial predisposition: development of international criteria for the determination of microsatellite instability in colorectal cancer. Cancer Res 58 (1998), 5248–5257.
    • (1998) Cancer Res , vol.58 , pp. 5248-5257
    • Boland, C.R.1    Thibodeau, S.N.2    Hamilton, S.R.3
  • 9
    • 79957554816 scopus 로고    scopus 로고
    • Young age and a positive family history of colorectal cancer are complementary selection criteria for the identification of Lynch syndrome
    • Manders, P., Spruijt, L., Kets, C.M., et al. Young age and a positive family history of colorectal cancer are complementary selection criteria for the identification of Lynch syndrome. Eur J Cancer 47 (2011), 1407–1413.
    • (2011) Eur J Cancer , vol.47 , pp. 1407-1413
    • Manders, P.1    Spruijt, L.2    Kets, C.M.3
  • 10
    • 19944397798 scopus 로고    scopus 로고
    • Cost effectiveness of a new strategy to identify HNPCC patients
    • Kievit, W., de Bruin, J.H., Adang, E.M., et al. Cost effectiveness of a new strategy to identify HNPCC patients. Gut 54 (2005), 97–102.
    • (2005) Gut , vol.54 , pp. 97-102
    • Kievit, W.1    de Bruin, J.H.2    Adang, E.M.3
  • 11
    • 84885337474 scopus 로고    scopus 로고
    • Familial risk-colorectal cancer: ESMO Clinical Practice Guidelines
    • Balmana, J., Balaguer, F., Cervantes, A., et al. Familial risk-colorectal cancer: ESMO Clinical Practice Guidelines. Ann Oncol 24:Suppl 6 (2013), vi73–vi80.
    • (2013) Ann Oncol , vol.24 , pp. vi73-vi80
    • Balmana, J.1    Balaguer, F.2    Cervantes, A.3
  • 12
    • 85081956719 scopus 로고    scopus 로고
    • Genetic/Familial High-Risk Assessment: Colorectal (Version 2.2013)
    • NCCN Guidelines: Genetic/Familial High-Risk Assessment: Colorectal (Version 2.2013).
    • Guidelines, N.C.C.N.1
  • 13
    • 84867499525 scopus 로고    scopus 로고
    • Identification of Lynch syndrome among patients with colorectal cancer
    • Moreira, L., Balaguer, F., Lindor, N., et al. Identification of Lynch syndrome among patients with colorectal cancer. JAMA 308 (2012), 1555–1565.
    • (2012) JAMA , vol.308 , pp. 1555-1565
    • Moreira, L.1    Balaguer, F.2    Lindor, N.3
  • 17
    • 57449097359 scopus 로고    scopus 로고
    • Feasibility of screening for Lynch syndrome among patients with colorectal cancer
    • Hampel, H., Frankel, W.L., Martin, E., et al. Feasibility of screening for Lynch syndrome among patients with colorectal cancer. J Clin Oncol 26 (2008), 5783–5788.
    • (2008) J Clin Oncol , vol.26 , pp. 5783-5788
    • Hampel, H.1    Frankel, W.L.2    Martin, E.3
  • 18
    • 17944362664 scopus 로고    scopus 로고
    • Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer)
    • Hampel, H., Frankel, W.L., Martin, E., et al. Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer). N Engl J Med 352 (2005), 1851–1860.
    • (2005) N Engl J Med , vol.352 , pp. 1851-1860
    • Hampel, H.1    Frankel, W.L.2    Martin, E.3
  • 19
    • 84857993554 scopus 로고    scopus 로고
    • Yield of routine molecular analyses in colorectal cancer patients
    • van Lier, M.G., Leenen, C.H., Wagner, A., et al. Yield of routine molecular analyses in colorectal cancer patients
    • (2012) J Pathol , vol.226 , pp. 764-774
    • van Lier, M.G.1    Leenen, C.H.2    Wagner, A.3
  • 20
    • 55349099844 scopus 로고    scopus 로고
    • Identification in daily practice of patients with Lynch syndrome (hereditary nonpolyposis colorectal cancer): revised Bethesda guidelines-based approach versus molecular screening
    • quiz 2836
    • Julie, C., Tresallet, C., Brouquet, A., et al. Identification in daily practice of patients with Lynch syndrome (hereditary nonpolyposis colorectal cancer): revised Bethesda guidelines-based approach versus molecular screening. Am J Gastroenterol 103 (2008), 2825–2835 quiz 2836.
    • (2008) Am J Gastroenterol , vol.103 , pp. 2825-2835
    • Julie, C.1    Tresallet, C.2    Brouquet, A.3
  • 21
    • 85081966817 scopus 로고    scopus 로고
    • Comprehensive Cancer Centres, the Netherlands. Amsterdam, The Netherlands: Netherlands Cancer Registry. 2013
    • Comprehensive Cancer Centres, the Netherlands. Amsterdam, The Netherlands: Netherlands Cancer Registry. 2013.
  • 22
    • 85081953338 scopus 로고    scopus 로고
    • Netherlands Foundation for the Detection of Hereditary Tumours (STOET). 2005. Leiden, The Netherlands
    • Netherlands Foundation for the Detection of Hereditary Tumours (STOET). 2005. Leiden, The Netherlands.
  • 24
    • 10744233669 scopus 로고    scopus 로고
    • Decision analysis in the surgical treatment of colorectal cancer due to a mismatch repair gene defect
    • de Vos tot Nederveen Cappel, W.H., Buskens, E., van Duijvendijk, P., et al. Decision analysis in the surgical treatment of colorectal cancer due to a mismatch repair gene defect. Gut 52 (2003), 1752–1755.
    • (2003) Gut , vol.52 , pp. 1752-1755
    • de Vos tot Nederveen Cappel, W.H.1    Buskens, E.2    van Duijvendijk, P.3
  • 25
    • 29144505362 scopus 로고    scopus 로고
    • Long term follow-up of HNPCC gene mutation carriers: compliance with screening and satisfaction with counseling and screening procedures
    • Wagner, A., van Kessel, I., Kriege, M.G., et al. Long term follow-up of HNPCC gene mutation carriers: compliance with screening and satisfaction with counseling and screening procedures. Fam Cancer 4 (2005), 295–300.
    • (2005) Fam Cancer , vol.4 , pp. 295-300
    • Wagner, A.1    van Kessel, I.2    Kriege, M.G.3
  • 26
    • 0034011564 scopus 로고    scopus 로고
    • Controlled 15-year trial on screening for colorectal cancer in families with hereditary nonpolyposis colorectal cancer
    • Jarvinen, H.J., Aarnio, M., Mustonen, H., et al. Controlled 15-year trial on screening for colorectal cancer in families with hereditary nonpolyposis colorectal cancer. Gastroenterology 118 (2000), 829–834.
    • (2000) Gastroenterology , vol.118 , pp. 829-834
    • Jarvinen, H.J.1    Aarnio, M.2    Mustonen, H.3
  • 28
    • 77149122082 scopus 로고    scopus 로고
    • The cost-effectiveness of genetic testing strategies for Lynch syndrome among newly diagnosed patients with colorectal cancer
    • Mvundura, M., Grosse, S.D., Hampel, H., Palomaki, G.E., The cost-effectiveness of genetic testing strategies for Lynch syndrome among newly diagnosed patients with colorectal cancer. Genet Med 12 (2010), 93–104.
    • (2010) Genet Med , vol.12 , pp. 93-104
    • Mvundura, M.1    Grosse, S.D.2    Hampel, H.3    Palomaki, G.E.4
  • 29
    • 79960604164 scopus 로고    scopus 로고
    • Strategies to identify the Lynch syndrome among patients with colorectal cancer: a cost-effectiveness analysis
    • Ladabaum, U., Wang, G., Terdiman, J., et al. Strategies to identify the Lynch syndrome among patients with colorectal cancer: a cost-effectiveness analysis. Ann Intern Med 155 (2011), 69–79.
    • (2011) Ann Intern Med , vol.155 , pp. 69-79
    • Ladabaum, U.1    Wang, G.2    Terdiman, J.3
  • 30
    • 0032533172 scopus 로고    scopus 로고
    • Benefits of colonoscopic surveillance and prophylactic colectomy in patients with hereditary nonpolyposis colorectal cancer mutations
    • Syngal, S., Weeks, J.C., Schrag, D., et al. Benefits of colonoscopic surveillance and prophylactic colectomy in patients with hereditary nonpolyposis colorectal cancer mutations. Ann Intern Med 129 (1998), 787–796.
    • (1998) Ann Intern Med , vol.129 , pp. 787-796
    • Syngal, S.1    Weeks, J.C.2    Schrag, D.3
  • 31
    • 49249104185 scopus 로고    scopus 로고
    • Interpretation of immunohistochemistry for mismatch repair proteins is only reliable in a specialized setting
    • Overbeek, L.I., Ligtenberg, M.J., Willems, R.W., et al. Interpretation of immunohistochemistry for mismatch repair proteins is only reliable in a specialized setting. Am J Surg Pathol 32 (2008), 1246–1251.
    • (2008) Am J Surg Pathol , vol.32 , pp. 1246-1251
    • Overbeek, L.I.1    Ligtenberg, M.J.2    Willems, R.W.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.