Literature DB >> 16826316

What is the appropriate screening protocol in Lynch syndrome?

A E de Jong1, F M Nagengast, J H Kleibeuker, P C van de Meeberg, H J van Wijk, A Cats, G Griffioen, H F A Vasen.   

Abstract

INTRODUCTION: Lynch syndrome families have a substantial risk of developing colorectal cancer (CRC). The recommended surveillance protocol includes colonoscopy every 2 years from age 20-25 years. It is yet unknown whether annual screening of patients aged 40-60 years is more effective than bi-annual screening, whether patients who had an adenoma removed should be re-examined after a year and whether surveillance of second-degree relatives is indicated. The aim of this study was to address these issues.
METHODS: All carriers of a mismatch repair gene mutation who participated in the surveillance program were selected from the Dutch Lynch syndrome registry. The results of colonoscopy were prospectively collected.
RESULTS: A total of 666 mutation carriers were identified in 110 families. Fourty-one CRCs were detected during endoscopic follow-up, of which 34 (83%) were diagnosed between age 40 and 60 years. In five of 34 patients, CRC was diagnosed within 1 year after colonoscopy, eight cancers were diagnosed between 1 and 2 years and the remaining tumors more than 2 years after colonoscopy. All eight CRCs detected between 1 and 2 years were at local stage. At least one adenoma was diagnosed at 141 examinations. The risk of developing CRC during follow-up in carriers with an adenoma was similar as in carriers without an adenoma at the previous colonoscopy. 280 parent-child couples with at least one Lynch syndrome-related carcinoma were identified in 110 families. In only 19 (6.8%) of these couples, CRC developed earlier in the child than an Lynch syndrome-associated cancer in the parent.
CONCLUSION: The current surveillance protocol, i.e., bi-annual colonoscopy in first-degree relatives independent of age and endoscopic findings, appears to be appropriate.

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Year:  2006        PMID: 16826316     DOI: 10.1007/s10689-006-0008-6

Source DB:  PubMed          Journal:  Fam Cancer        ISSN: 1389-9600            Impact factor:   2.375


  23 in total

1.  Screening for hereditary non-polyposis colorectal cancer: a study of 22 kindreds in The Netherlands.

Authors:  H F Vasen; F C den Hartog Jager; F H Menko; F M Nagengast
Journal:  Am J Med       Date:  1989-03       Impact factor: 4.965

2.  Germ-line mutation of the hMSH6/GTBP gene in an atypical hereditary nonpolyposis colorectal cancer kindred.

Authors:  Y Akiyama; H Sato; T Yamada; H Nagasaki; A Tsuchiya; R Abe; Y Yuasa
Journal:  Cancer Res       Date:  1997-09-15       Impact factor: 12.701

3.  Surveillance for hereditary nonpolyposis colorectal cancer: a long-term study on 114 families.

Authors:  Wouter H de Vos tot Nederveen Cappel; Fokko M Nagengast; Gerrit Griffioen; Fred H Menko; Babs G Taal; Jan H Kleibeuker; Hans F Vasen
Journal:  Dis Colon Rectum       Date:  2002-12       Impact factor: 4.585

4.  Clues to the pathogenesis of familial colorectal cancer.

Authors:  L A Aaltonen; P Peltomäki; F S Leach; P Sistonen; L Pylkkänen; J P Mecklin; H Järvinen; S M Powell; J Jen; S R Hamilton
Journal:  Science       Date:  1993-05-07       Impact factor: 47.728

5.  The tumour spectrum in hereditary non-polyposis colorectal cancer: a study of 24 kindreds in the Netherlands.

Authors:  H F Vasen; G J Offerhaus; F C den Hartog Jager; F H Menko; F M Nagengast; G Griffioen; R B van Hogezand; A P Heintz
Journal:  Int J Cancer       Date:  1990-07-15       Impact factor: 7.396

6.  The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer.

Authors:  R Fishel; M K Lescoe; M R Rao; N G Copeland; N A Jenkins; J Garber; M Kane; R Kolodner
Journal:  Cell       Date:  1993-12-03       Impact factor: 41.582

7.  Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer.

Authors:  F S Leach; N C Nicolaides; N Papadopoulos; B Liu; J Jen; R Parsons; P Peltomäki; P Sistonen; L A Aaltonen; M Nyström-Lahti
Journal:  Cell       Date:  1993-12-17       Impact factor: 41.582

8.  The role of mismatch repair gene defects in the development of adenomas in patients with HNPCC.

Authors:  Andrea E De Jong; Hans Morreau; Marjo Van Puijenbroek; Paul H c Eilers; Juul Wijnen; Fokko M Nagengast; Gerrit Griffioen; Annemieke Cats; Fred H Menko; Jan H Kleibeuker; Hans F A Vasen
Journal:  Gastroenterology       Date:  2004-01       Impact factor: 22.682

9.  Cancer risk in families with hereditary nonpolyposis colorectal cancer diagnosed by mutation analysis.

Authors:  H F Vasen; J T Wijnen; F H Menko; J H Kleibeuker; B G Taal; G Griffioen; F M Nagengast; E H Meijers-Heijboer; L Bertario; L Varesco; M L Bisgaard; J Mohr; R Fodde; P M Khan
Journal:  Gastroenterology       Date:  1996-04       Impact factor: 22.682

10.  Hereditary non-polyposis colorectal cancer--morphologies, genes and mutations.

Authors:  J R Jass; S M Stewart; J Stewart; M R Lane
Journal:  Mutat Res       Date:  1994-10-01       Impact factor: 2.433

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  7 in total

1.  A mobile colonoscopic unit for lynch syndrome: trends in surveillance uptake and patient experiences of screening in a developing country.

Authors:  Zandrè Bruwer; Merle Futter; Raj Ramesar
Journal:  J Genet Couns       Date:  2013-01-09       Impact factor: 2.537

2.  Quality colonoscopy and risk of interval cancer in Lynch syndrome.

Authors:  J F Haanstra; H F A Vasen; S Sanduleanu; E J van der Wouden; J J Koornstra; J H Kleibeuker; W H de Vos Tot Nederveen Cappel
Journal:  Int J Colorectal Dis       Date:  2013-07-16       Impact factor: 2.571

Review 3.  TTD consensus document on the diagnosis and management of hereditary colorectal cancer.

Authors:  Pedro Pérez Segura; Carmen Guillén Ponce; Carmen Guillén Alonso; Teresa Ramón y Cajal; Raquel Serrano Blanch; Enrique Aranda
Journal:  Clin Transl Oncol       Date:  2010-05       Impact factor: 3.405

4.  Guidelines for the management of hereditary colorectal cancer from the British Society of Gastroenterology (BSG)/Association of Coloproctology of Great Britain and Ireland (ACPGBI)/United Kingdom Cancer Genetics Group (UKCGG).

Authors:  Kevin J Monahan; Nicola Bradshaw; Sunil Dolwani; Bianca Desouza; Malcolm G Dunlop; James E East; Mohammad Ilyas; Asha Kaur; Fiona Lalloo; Andrew Latchford; Matthew D Rutter; Ian Tomlinson; Huw J W Thomas; James Hill
Journal:  Gut       Date:  2019-11-28       Impact factor: 23.059

Review 5.  Guidelines for the clinical management of Lynch syndrome (hereditary non-polyposis cancer).

Authors:  H F A Vasen; G Möslein; A Alonso; I Bernstein; L Bertario; I Blanco; J Burn; G Capella; C Engel; I Frayling; W Friedl; F J Hes; S Hodgson; J-P Mecklin; P Møller; F Nagengast; Y Parc; L Renkonen-Sinisalo; J R Sampson; A Stormorken; J Wijnen
Journal:  J Med Genet       Date:  2007-02-27       Impact factor: 6.318

6.  Body mass index in early adulthood and colorectal cancer risk for carriers and non-carriers of germline mutations in DNA mismatch repair genes.

Authors:  A K Win; J G Dowty; D R English; P T Campbell; J P Young; I Winship; F A Macrae; L Lipton; S Parry; G P Young; D D Buchanan; M E Martínez; E T Jacobs; D J Ahnen; R W Haile; G Casey; J A Baron; N M Lindor; S N Thibodeau; P A Newcomb; J D Potter; L Le Marchand; S Gallinger; J L Hopper; M A Jenkins
Journal:  Br J Cancer       Date:  2011-05-10       Impact factor: 7.640

Review 7.  Recent advances in Lynch syndrome.

Authors:  Xi Li; Guodong Liu; Wei Wu
Journal:  Exp Hematol Oncol       Date:  2021-06-12
  7 in total

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