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Tytuł pozycji:

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).

Tytuł:
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).
Autorzy:
Monahan KJ; Family Cancer Clinic, St Mark's Hospital, London, UK .; Faculty of Medicine, Imperial College, London, UK.
Bradshaw N; Clinical Genetics, West of Scotland Genetics Services, Glasgow, Glasgow, UK.
Dolwani S; Gastroenterology, Cardiff and Vale NHS Trust, Cardiff, UK.
Desouza B; Clinical Genetics, Guy's and St Thomas' NHS Foundation Trust, London, UK.
Dunlop MG; CCGG, University of Edinburgh, Edinburgh, UK.
East JE; Translational Gastroenterology Unit, John Radcliffe Hospital, Oxford, UK.; Oxford NIHR Biomedical Research Centre, University of Oxford, Oxford, UK.
Ilyas M; Faculty of Medicine & Health Sciences, Nottingham University, Nottingham, UK.
Kaur A; Head of Policy and Campaigns, Bowel Cancer UK, London, UK.
Lalloo F; Genetic Medicine, Central Manchester University Hospitals Foundation Trust, Manchester, UK.
Latchford A; Polyposis Registry, St Mark's Hospital, London, UK.
Rutter MD; Gastroenterology, University Hospital of North Tees, Stockton-on-Tees, UK.; Northern Institute for Cancer Research, Newcastle University, Newcastle upon Tyne, UK.
Tomlinson I; Nuffield Department of Clinical Medicine, Wellcome Trust Centre for Human Genetics, Birmingham, UK.; Cancer Research Centre, University of Edinburgh, Edinburgh, UK.
Thomas HJW; Family Cancer Clinic, St Mark's Hospital, London, UK.; Faculty of Medicine, Imperial College, London, UK.
Hill J; Genetic Medicine, Central Manchester University Hospitals Foundation Trust, Manchester, UK.
Corporate Authors:
Hereditary CRC guidelines eDelphi consensus group
Źródło:
Gut [Gut] 2020 Mar; Vol. 69 (3), pp. 411-444. Date of Electronic Publication: 2019 Nov 28.
Typ publikacji:
Journal Article; Practice Guideline; Research Support, Non-U.S. Gov't
Język:
English
Imprint Name(s):
Original Publication: London, British Medical Assn.
MeSH Terms:
Population Surveillance*
Colorectal Neoplasms/*genetics
Colorectal Neoplasms/*therapy
Adenomatous Polyposis Coli/genetics ; Adenomatous Polyposis Coli/prevention & control ; Adenomatous Polyposis Coli/therapy ; Colonoscopy ; Colorectal Neoplasms/pathology ; Colorectal Neoplasms/prevention & control ; Colorectal Neoplasms, Hereditary Nonpolyposis/genetics ; Colorectal Neoplasms, Hereditary Nonpolyposis/prevention & control ; Colorectal Neoplasms, Hereditary Nonpolyposis/therapy ; DNA Glycosylases/genetics ; Family Health ; Humans ; Intestinal Polyposis/congenital ; Intestinal Polyposis/genetics ; Intestinal Polyposis/therapy ; Ireland ; Life Style ; Neoplastic Syndromes, Hereditary/genetics ; Neoplastic Syndromes, Hereditary/therapy ; Peutz-Jeghers Syndrome/genetics ; Peutz-Jeghers Syndrome/therapy ; Referral and Consultation/standards ; Risk Factors ; United Kingdom
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Grant Information:
12076 United Kingdom CRUK_ Cancer Research UK; MC_U127527198 United Kingdom MRC_ Medical Research Council; United Kingdom DH_ Department of Health; 18927 United Kingdom CRUK_ Cancer Research UK; 27327 United Kingdom CRUK_ Cancer Research UK; MC_UU_00007/1 United Kingdom MRC_ Medical Research Council; MC_PC_U127527198 United Kingdom MRC_ Medical Research Council
Contributed Indexing:
Investigator: T Seppälä; S Clark; O Faiz; F Balaguer; MV Leerdam; D Gareth Evans; R Jover; M Tischkowitz; H Hanson; S Gibson; A Taylor; G Moeslein; A Wagner; JC Saurin; T Smith; J Ashford; J Martin; J Gunningham; M Cooper
Keywords: colorectal cancer; colorectal surgery; genetic testing; inherited cancers; surveillance
Substance Nomenclature:
EC 3.2.2.- (DNA Glycosylases)
EC 3.2.2.- (mutY adenine glycosylase)
SCR Disease Name:
Juvenile polyposis syndrome
Entry Date(s):
Date Created: 20191130 Date Completed: 20200414 Latest Revision: 20240210
Update Code:
20240210
PubMed Central ID:
PMC7034349
DOI:
10.1136/gutjnl-2019-319915
PMID:
31780574
Czasopismo naukowe
Heritable factors account for approximately 35% of colorectal cancer (CRC) risk, and almost 30% of the population in the UK have a family history of CRC. The quantification of an individual's lifetime risk of gastrointestinal cancer may incorporate clinical and molecular data, and depends on accurate phenotypic assessment and genetic diagnosis. In turn this may facilitate targeted risk-reducing interventions, including endoscopic surveillance, preventative surgery and chemoprophylaxis, which provide opportunities for cancer prevention. This guideline is an update from the 2010 British Society of Gastroenterology/Association of Coloproctology of Great Britain and Ireland (BSG/ACPGBI) guidelines for colorectal screening and surveillance in moderate and high-risk groups; however, this guideline is concerned specifically with people who have increased lifetime risk of CRC due to hereditary factors, including those with Lynch syndrome, polyposis or a family history of CRC. On this occasion we invited the UK Cancer Genetics Group (UKCGG), a subgroup within the British Society of Genetic Medicine (BSGM), as a partner to BSG and ACPGBI in the multidisciplinary guideline development process. We also invited external review through the Delphi process by members of the public as well as the steering committees of the European Hereditary Tumour Group (EHTG) and the European Society of Gastrointestinal Endoscopy (ESGE). A systematic review of 10 189 publications was undertaken to develop 67 evidence and expert opinion-based recommendations for the management of hereditary CRC risk. Ten research recommendations are also prioritised to inform clinical management of people at hereditary CRC risk.
Competing Interests: Competing interests: KJM: Medical advisory board of Bowel Cancer UK, Lynch Syndrome UK. JH and FL: FAP trial (now closed) with funding awarded to NHS trust research facility. JE: Advisory board Lumendi, Boston Scientific; Speaker fees Olympus, Falk. MDR: Speaker fees: SwissSCWeb, Pentax; Research Grant: Olympus; Consultancy: Norgine.
(© Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.)
Comment in: Gut. 2021 Mar;70(3):624-626. (PMID: 32571974)

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