British Society of Gastroenterology guidelines on the diagnosis and management of patients at risk of gastric adenocarcinoma

Gastric adenocarcinoma carries a poor prognosis, in part due to the late stage of diagnosis. Risk factors include Helicobacter pylori infection, family history of gastric cancer—in particular, hereditary diffuse gastric cancer and pernicious anaemia. The stages in the progression to cancer include c...

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Veröffentlicht in:Gut 2019-09, Vol.68 (9), p.1545-1575
Hauptverfasser: Banks, Matthew, Graham, David, Jansen, Marnix, Gotoda, Takuji, Coda, Sergio, di Pietro, Massimiliano, Uedo, Noriya, Bhandari, Pradeep, Pritchard, D Mark, Kuipers, Ernst J, Rodriguez-Justo, Manuel, Novelli, Marco R, Ragunath, Krish, Shepherd, Neil, Dinis-Ribeiro, Mario
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container_end_page 1575
container_issue 9
container_start_page 1545
container_title Gut
container_volume 68
creator Banks, Matthew
Graham, David
Jansen, Marnix
Gotoda, Takuji
Coda, Sergio
di Pietro, Massimiliano
Uedo, Noriya
Bhandari, Pradeep
Pritchard, D Mark
Kuipers, Ernst J
Rodriguez-Justo, Manuel
Novelli, Marco R
Ragunath, Krish
Shepherd, Neil
Dinis-Ribeiro, Mario
description Gastric adenocarcinoma carries a poor prognosis, in part due to the late stage of diagnosis. Risk factors include Helicobacter pylori infection, family history of gastric cancer—in particular, hereditary diffuse gastric cancer and pernicious anaemia. The stages in the progression to cancer include chronic gastritis, gastric atrophy (GA), gastric intestinal metaplasia (GIM) and dysplasia. The key to early detection of cancer and improved survival is to non-invasively identify those at risk before endoscopy. However, although biomarkers may help in the detection of patients with chronic atrophic gastritis, there is insufficient evidence to support their use for population screening. High-quality endoscopy with full mucosal visualisation is an important part of improving early detection. Image-enhanced endoscopy combined with biopsy sampling for histopathology is the best approach to detect and accurately risk-stratify GA and GIM. Biopsies following the Sydney protocol from the antrum, incisura, lesser and greater curvature allow both diagnostic confirmation and risk stratification for progression to cancer. Ideally biopsies should be directed to areas of GA or GIM visualised by high-quality endoscopy. There is insufficient evidence to support screening in a low-risk population (undergoing routine diagnostic oesophagogastroduodenoscopy) such as the UK, but endoscopic surveillance every 3 years should be offered to patients with extensive GA or GIM. Endoscopic mucosal resection or endoscopic submucosal dissection of visible gastric dysplasia and early cancer has been shown to be efficacious with a high success rate and low rate of recurrence, providing that specific quality criteria are met.
doi_str_mv 10.1136/gutjnl-2018-318126
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Risk factors include Helicobacter pylori infection, family history of gastric cancer—in particular, hereditary diffuse gastric cancer and pernicious anaemia. The stages in the progression to cancer include chronic gastritis, gastric atrophy (GA), gastric intestinal metaplasia (GIM) and dysplasia. The key to early detection of cancer and improved survival is to non-invasively identify those at risk before endoscopy. However, although biomarkers may help in the detection of patients with chronic atrophic gastritis, there is insufficient evidence to support their use for population screening. High-quality endoscopy with full mucosal visualisation is an important part of improving early detection. Image-enhanced endoscopy combined with biopsy sampling for histopathology is the best approach to detect and accurately risk-stratify GA and GIM. Biopsies following the Sydney protocol from the antrum, incisura, lesser and greater curvature allow both diagnostic confirmation and risk stratification for progression to cancer. Ideally biopsies should be directed to areas of GA or GIM visualised by high-quality endoscopy. There is insufficient evidence to support screening in a low-risk population (undergoing routine diagnostic oesophagogastroduodenoscopy) such as the UK, but endoscopic surveillance every 3 years should be offered to patients with extensive GA or GIM. Endoscopic mucosal resection or endoscopic submucosal dissection of visible gastric dysplasia and early cancer has been shown to be efficacious with a high success rate and low rate of recurrence, providing that specific quality criteria are met.</description><identifier>ISSN: 0017-5749</identifier><identifier>EISSN: 1468-3288</identifier><identifier>DOI: 10.1136/gutjnl-2018-318126</identifier><identifier>PMID: 31278206</identifier><language>eng</language><publisher>England: BMJ Publishing Group Ltd and British Society of Gastroenterology</publisher><subject>Adenocarcinoma ; Adenocarcinoma - diagnosis ; Adenocarcinoma - microbiology ; Adenocarcinoma - surgery ; Agreements ; Anemia ; Atrophy ; Biomarkers, Tumor - blood ; Biopsy ; Diagnosis ; Disease Management ; Disease Progression ; Dysplasia ; Early Detection of Cancer - methods ; Endoscopy ; Evidence-Based Medicine - methods ; gastric adenocarcinoma ; Gastric cancer ; gastric pre-cancer ; Gastritis ; Gastritis, Atrophic - diagnosis ; Gastritis, Atrophic - microbiology ; Gastritis, Atrophic - surgery ; Gastroenterology ; Gastroscopy - methods ; Guidelines ; Helicobacter Infections - complications ; Helicobacter Infections - drug therapy ; Helicobacter pylori ; helicobacter pylori-gastritis ; Humans ; Intestine ; Medical research ; Metaplasia ; Mucosa ; Pernicious anemia ; Precancerous Conditions - diagnosis ; Precancerous Conditions - microbiology ; Precancerous Conditions - surgery ; Quality ; Risk Assessment - methods ; Risk factors ; Stomach Neoplasms - diagnosis ; Stomach Neoplasms - microbiology ; Stomach Neoplasms - surgery ; Surveillance ; University colleges</subject><ispartof>Gut, 2019-09, Vol.68 (9), p.1545-1575</ispartof><rights>Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.</rights><rights>2019 Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ . Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b573t-3c0a06a9f19a799a4e635cf97066381e299508b80973958abb41e36c30a755723</citedby><cites>FETCH-LOGICAL-b573t-3c0a06a9f19a799a4e635cf97066381e299508b80973958abb41e36c30a755723</cites><orcidid>0000-0003-0645-564X ; 0000-0002-9137-2779</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6709778/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6709778/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31278206$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Banks, Matthew</creatorcontrib><creatorcontrib>Graham, David</creatorcontrib><creatorcontrib>Jansen, Marnix</creatorcontrib><creatorcontrib>Gotoda, Takuji</creatorcontrib><creatorcontrib>Coda, Sergio</creatorcontrib><creatorcontrib>di Pietro, Massimiliano</creatorcontrib><creatorcontrib>Uedo, Noriya</creatorcontrib><creatorcontrib>Bhandari, Pradeep</creatorcontrib><creatorcontrib>Pritchard, D Mark</creatorcontrib><creatorcontrib>Kuipers, Ernst J</creatorcontrib><creatorcontrib>Rodriguez-Justo, Manuel</creatorcontrib><creatorcontrib>Novelli, Marco R</creatorcontrib><creatorcontrib>Ragunath, Krish</creatorcontrib><creatorcontrib>Shepherd, Neil</creatorcontrib><creatorcontrib>Dinis-Ribeiro, Mario</creatorcontrib><title>British Society of Gastroenterology guidelines on the diagnosis and management of patients at risk of gastric adenocarcinoma</title><title>Gut</title><addtitle>Gut</addtitle><addtitle>Gut</addtitle><description>Gastric adenocarcinoma carries a poor prognosis, in part due to the late stage of diagnosis. 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Graham, David ; Jansen, Marnix ; Gotoda, Takuji ; Coda, Sergio ; di Pietro, Massimiliano ; Uedo, Noriya ; Bhandari, Pradeep ; Pritchard, D Mark ; Kuipers, Ernst J ; Rodriguez-Justo, Manuel ; Novelli, Marco R ; Ragunath, Krish ; Shepherd, Neil ; Dinis-Ribeiro, Mario</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b573t-3c0a06a9f19a799a4e635cf97066381e299508b80973958abb41e36c30a755723</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Adenocarcinoma</topic><topic>Adenocarcinoma - diagnosis</topic><topic>Adenocarcinoma - microbiology</topic><topic>Adenocarcinoma - surgery</topic><topic>Agreements</topic><topic>Anemia</topic><topic>Atrophy</topic><topic>Biomarkers, Tumor - blood</topic><topic>Biopsy</topic><topic>Diagnosis</topic><topic>Disease Management</topic><topic>Disease Progression</topic><topic>Dysplasia</topic><topic>Early Detection of Cancer - methods</topic><topic>Endoscopy</topic><topic>Evidence-Based Medicine - methods</topic><topic>gastric adenocarcinoma</topic><topic>Gastric cancer</topic><topic>gastric pre-cancer</topic><topic>Gastritis</topic><topic>Gastritis, Atrophic - diagnosis</topic><topic>Gastritis, Atrophic - microbiology</topic><topic>Gastritis, Atrophic - surgery</topic><topic>Gastroenterology</topic><topic>Gastroscopy - methods</topic><topic>Guidelines</topic><topic>Helicobacter Infections - complications</topic><topic>Helicobacter Infections - drug therapy</topic><topic>Helicobacter pylori</topic><topic>helicobacter pylori-gastritis</topic><topic>Humans</topic><topic>Intestine</topic><topic>Medical research</topic><topic>Metaplasia</topic><topic>Mucosa</topic><topic>Pernicious anemia</topic><topic>Precancerous Conditions - diagnosis</topic><topic>Precancerous Conditions - microbiology</topic><topic>Precancerous Conditions - surgery</topic><topic>Quality</topic><topic>Risk Assessment - methods</topic><topic>Risk factors</topic><topic>Stomach Neoplasms - diagnosis</topic><topic>Stomach Neoplasms - microbiology</topic><topic>Stomach Neoplasms - surgery</topic><topic>Surveillance</topic><topic>University colleges</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Banks, Matthew</creatorcontrib><creatorcontrib>Graham, David</creatorcontrib><creatorcontrib>Jansen, Marnix</creatorcontrib><creatorcontrib>Gotoda, Takuji</creatorcontrib><creatorcontrib>Coda, Sergio</creatorcontrib><creatorcontrib>di Pietro, Massimiliano</creatorcontrib><creatorcontrib>Uedo, Noriya</creatorcontrib><creatorcontrib>Bhandari, Pradeep</creatorcontrib><creatorcontrib>Pritchard, D Mark</creatorcontrib><creatorcontrib>Kuipers, Ernst J</creatorcontrib><creatorcontrib>Rodriguez-Justo, Manuel</creatorcontrib><creatorcontrib>Novelli, Marco R</creatorcontrib><creatorcontrib>Ragunath, Krish</creatorcontrib><creatorcontrib>Shepherd, Neil</creatorcontrib><creatorcontrib>Dinis-Ribeiro, Mario</creatorcontrib><collection>BMJ Open Access Journals</collection><collection>BMJ Journals:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health &amp; 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Biopsies following the Sydney protocol from the antrum, incisura, lesser and greater curvature allow both diagnostic confirmation and risk stratification for progression to cancer. Ideally biopsies should be directed to areas of GA or GIM visualised by high-quality endoscopy. There is insufficient evidence to support screening in a low-risk population (undergoing routine diagnostic oesophagogastroduodenoscopy) such as the UK, but endoscopic surveillance every 3 years should be offered to patients with extensive GA or GIM. 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source MEDLINE; PubMed Central
subjects Adenocarcinoma
Adenocarcinoma - diagnosis
Adenocarcinoma - microbiology
Adenocarcinoma - surgery
Agreements
Anemia
Atrophy
Biomarkers, Tumor - blood
Biopsy
Diagnosis
Disease Management
Disease Progression
Dysplasia
Early Detection of Cancer - methods
Endoscopy
Evidence-Based Medicine - methods
gastric adenocarcinoma
Gastric cancer
gastric pre-cancer
Gastritis
Gastritis, Atrophic - diagnosis
Gastritis, Atrophic - microbiology
Gastritis, Atrophic - surgery
Gastroenterology
Gastroscopy - methods
Guidelines
Helicobacter Infections - complications
Helicobacter Infections - drug therapy
Helicobacter pylori
helicobacter pylori-gastritis
Humans
Intestine
Medical research
Metaplasia
Mucosa
Pernicious anemia
Precancerous Conditions - diagnosis
Precancerous Conditions - microbiology
Precancerous Conditions - surgery
Quality
Risk Assessment - methods
Risk factors
Stomach Neoplasms - diagnosis
Stomach Neoplasms - microbiology
Stomach Neoplasms - surgery
Surveillance
University colleges
title British Society of Gastroenterology guidelines on the diagnosis and management of patients at risk of gastric adenocarcinoma
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