Follow-up of intestinal metaplasia in the stomach: When, how and why
Gastric cancer remains the second most frequent cause of cancer-related mortality in the world. Screening programs in some Asian countries are impractical in the majority of other countries worldwide. Therefore, follow-up of precancerous lesions is advisable for secondary gastric cancer prevention....
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Veröffentlicht in: | World journal of gastrointestinal oncology 2012-03, Vol.4 (3), p.30-36 |
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description | Gastric cancer remains the second most frequent cause of cancer-related mortality in the world. Screening programs in some Asian countries are impractical in the majority of other countries worldwide. Therefore, follow-up of precancerous lesions is advisable for secondary gastric cancer prevention. Intestinal metaplasia (IM) is recognized as a precancerous lesion for gastric cancer, increasing the risk by 6-fold. IM is highly prevalent in the general population, being detected in nearly 1 of every 4 patients undergoing upper endoscopy. The IM prevalence rate is significantly higher in patients with Helicobacter pylori (H. pylori) infection, in first-degree relatives of gastric cancer patients, in smokers and it increases with patient age. IM is the "breaking point" in the gastric carcinogenesis cascade and does not appear to regress following H. pylori eradication, although the cure of infection may slow its progression. Gastric cancer risk is higher in patients with incomplete-type IM, in those with both antral and gastric body involvement, and the risk significantly increases with IM extension over 20% of the gastric mucosa. Scheduled endoscopic control could be cost-effective in IM patients, depending on the yearly incidence of gastric cancer in IM patients, the stage of gastric cancer at diagnosis discovered at surveillance, and the cost of endoscopy. As a pragmatic behavior, yearly endoscopic control would appear justified in all IM patients with at least one of these conditions: (1) IM extension > 20%; (2) the presence of incomplete type IM; (3) first-degree relative of gastric cancer patients; and (4) smokers. In the remaining IM patients, a less intensive (2-3 years) could be proposed. |
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Screening programs in some Asian countries are impractical in the majority of other countries worldwide. Therefore, follow-up of precancerous lesions is advisable for secondary gastric cancer prevention. Intestinal metaplasia (IM) is recognized as a precancerous lesion for gastric cancer, increasing the risk by 6-fold. IM is highly prevalent in the general population, being detected in nearly 1 of every 4 patients undergoing upper endoscopy. The IM prevalence rate is significantly higher in patients with Helicobacter pylori (H. pylori) infection, in first-degree relatives of gastric cancer patients, in smokers and it increases with patient age. IM is the &quot;breaking point&quot; in the gastric carcinogenesis cascade and does not appear to regress following H. pylori eradication, although the cure of infection may slow its progression. Gastric cancer risk is higher in patients with incomplete-type IM, in those with both antral and gastric body involvement, and the risk significantly increases with IM extension over 20% of the gastric mucosa. Scheduled endoscopic control could be cost-effective in IM patients, depending on the yearly incidence of gastric cancer in IM patients, the stage of gastric cancer at diagnosis discovered at surveillance, and the cost of endoscopy. As a pragmatic behavior, yearly endoscopic control would appear justified in all IM patients with at least one of these conditions: (1) IM extension &gt; 20%; (2) the presence of incomplete type IM; (3) first-degree relative of gastric cancer patients; and (4) smokers. In the remaining IM patients, a less intensive (2-3 years) could be proposed.</description><identifier>ISSN: 1948-5204</identifier><identifier>EISSN: 1948-5204</identifier><identifier>DOI: 10.4251/wjgo.v4.i3.30</identifier><identifier>PMID: 22468181</identifier><language>eng</language><publisher>China: Baishideng Publishing Group Co., Limited</publisher><subject>cancer ; factors ; Follow-up ; Gastric ; Intestinal ; metaplasia ; Prevention ; Risk ; Topic Highlight</subject><ispartof>World journal of gastrointestinal oncology, 2012-03, Vol.4 (3), p.30-36</ispartof><rights>2012 Baishideng. All rights reserved. 2012</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c344t-a34ac6e2b9f7c44755e81eabd45476a9719e57eecbbe784950fcf30c0c9504483</citedby><cites>FETCH-LOGICAL-c344t-a34ac6e2b9f7c44755e81eabd45476a9719e57eecbbe784950fcf30c0c9504483</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/71425X/71425X.jpg</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3312926/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3312926/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22468181$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zullo, Angelo</creatorcontrib><creatorcontrib>Hassan, Cesare</creatorcontrib><creatorcontrib>Romiti, Adriana</creatorcontrib><creatorcontrib>Giusto, Michela</creatorcontrib><creatorcontrib>Guerriero, Carmine</creatorcontrib><creatorcontrib>Lorenzetti, Roberto</creatorcontrib><creatorcontrib>Campo, Salvatore Ma</creatorcontrib><creatorcontrib>Tomao, Silverio</creatorcontrib><title>Follow-up of intestinal metaplasia in the stomach: When, how and why</title><title>World journal of gastrointestinal oncology</title><addtitle>World Journal of Gastrointestinal Oncology</addtitle><description>Gastric cancer remains the second most frequent cause of cancer-related mortality in the world. Screening programs in some Asian countries are impractical in the majority of other countries worldwide. Therefore, follow-up of precancerous lesions is advisable for secondary gastric cancer prevention. Intestinal metaplasia (IM) is recognized as a precancerous lesion for gastric cancer, increasing the risk by 6-fold. IM is highly prevalent in the general population, being detected in nearly 1 of every 4 patients undergoing upper endoscopy. The IM prevalence rate is significantly higher in patients with Helicobacter pylori (H. pylori) infection, in first-degree relatives of gastric cancer patients, in smokers and it increases with patient age. IM is the &quot;breaking point&quot; in the gastric carcinogenesis cascade and does not appear to regress following H. pylori eradication, although the cure of infection may slow its progression. Gastric cancer risk is higher in patients with incomplete-type IM, in those with both antral and gastric body involvement, and the risk significantly increases with IM extension over 20% of the gastric mucosa. Scheduled endoscopic control could be cost-effective in IM patients, depending on the yearly incidence of gastric cancer in IM patients, the stage of gastric cancer at diagnosis discovered at surveillance, and the cost of endoscopy. As a pragmatic behavior, yearly endoscopic control would appear justified in all IM patients with at least one of these conditions: (1) IM extension &gt; 20%; (2) the presence of incomplete type IM; (3) first-degree relative of gastric cancer patients; and (4) smokers. In the remaining IM patients, a less intensive (2-3 years) could be proposed.</description><subject>cancer</subject><subject>factors</subject><subject>Follow-up</subject><subject>Gastric</subject><subject>Intestinal</subject><subject>metaplasia</subject><subject>Prevention</subject><subject>Risk</subject><subject>Topic Highlight</subject><issn>1948-5204</issn><issn>1948-5204</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNpVkN9LwzAQx4Mobsw9-ioBX21NmusvHwSZToWBL4qPIc3SNqNNatut7L83Y3PMe7nj7nufO74IXVPiQxDS-2FVWH8DvmY-I2doTFNIvDAgcH5Sj9C061bEBUBMKLlEoyCAKKEJHaPnua0qO3jrBtsca9OrrtdGVLhWvWgq0WnhurgvFe56WwtZPuDvUpk7XNoBC7PEQ7m9Qhe5qDo1PeQJ-pq_fM7evMXH6_vsaeFJBtB7goGQkQqyNI-l-yUMVUKVyJYQQhyJNKapCmOlZJapOIE0JLnMGZFEuhIgYRP0uOc266xWS6lM34qKN62uRbvlVmj-f2J0yQu74YzRIA0iB_D2ANnarmtVftylhO8c5TtH-Qa4ZpwRp785PXhU__nnBLcHYGlN8aNNcUIkjkDcXfYLPzt_bQ</recordid><startdate>20120315</startdate><enddate>20120315</enddate><creator>Zullo, Angelo</creator><creator>Hassan, Cesare</creator><creator>Romiti, Adriana</creator><creator>Giusto, Michela</creator><creator>Guerriero, Carmine</creator><creator>Lorenzetti, Roberto</creator><creator>Campo, Salvatore Ma</creator><creator>Tomao, Silverio</creator><general>Baishideng Publishing Group Co., Limited</general><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>W91</scope><scope>~WA</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope></search><sort><creationdate>20120315</creationdate><title>Follow-up of intestinal metaplasia in the stomach: When, how and why</title><author>Zullo, Angelo ; Hassan, Cesare ; Romiti, Adriana ; Giusto, Michela ; Guerriero, Carmine ; Lorenzetti, Roberto ; Campo, Salvatore Ma ; Tomao, Silverio</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c344t-a34ac6e2b9f7c44755e81eabd45476a9719e57eecbbe784950fcf30c0c9504483</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>cancer</topic><topic>factors</topic><topic>Follow-up</topic><topic>Gastric</topic><topic>Intestinal</topic><topic>metaplasia</topic><topic>Prevention</topic><topic>Risk</topic><topic>Topic Highlight</topic><toplevel>online_resources</toplevel><creatorcontrib>Zullo, Angelo</creatorcontrib><creatorcontrib>Hassan, Cesare</creatorcontrib><creatorcontrib>Romiti, Adriana</creatorcontrib><creatorcontrib>Giusto, Michela</creatorcontrib><creatorcontrib>Guerriero, Carmine</creatorcontrib><creatorcontrib>Lorenzetti, Roberto</creatorcontrib><creatorcontrib>Campo, Salvatore Ma</creatorcontrib><creatorcontrib>Tomao, Silverio</creatorcontrib><collection>中文科技期刊数据库</collection><collection>中文科技期刊数据库-CALIS站点</collection><collection>中文科技期刊数据库-7.0平台</collection><collection>中文科技期刊数据库-医药卫生</collection><collection>中文科技期刊数据库- 镜像站点</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>World journal of gastrointestinal oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zullo, Angelo</au><au>Hassan, Cesare</au><au>Romiti, Adriana</au><au>Giusto, Michela</au><au>Guerriero, Carmine</au><au>Lorenzetti, Roberto</au><au>Campo, Salvatore Ma</au><au>Tomao, Silverio</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Follow-up of intestinal metaplasia in the stomach: When, how and why</atitle><jtitle>World journal of gastrointestinal oncology</jtitle><addtitle>World Journal of Gastrointestinal Oncology</addtitle><date>2012-03-15</date><risdate>2012</risdate><volume>4</volume><issue>3</issue><spage>30</spage><epage>36</epage><pages>30-36</pages><issn>1948-5204</issn><eissn>1948-5204</eissn><abstract>Gastric cancer remains the second most frequent cause of cancer-related mortality in the world. Screening programs in some Asian countries are impractical in the majority of other countries worldwide. Therefore, follow-up of precancerous lesions is advisable for secondary gastric cancer prevention. Intestinal metaplasia (IM) is recognized as a precancerous lesion for gastric cancer, increasing the risk by 6-fold. IM is highly prevalent in the general population, being detected in nearly 1 of every 4 patients undergoing upper endoscopy. The IM prevalence rate is significantly higher in patients with Helicobacter pylori (H. pylori) infection, in first-degree relatives of gastric cancer patients, in smokers and it increases with patient age. IM is the &quot;breaking point&quot; in the gastric carcinogenesis cascade and does not appear to regress following H. pylori eradication, although the cure of infection may slow its progression. Gastric cancer risk is higher in patients with incomplete-type IM, in those with both antral and gastric body involvement, and the risk significantly increases with IM extension over 20% of the gastric mucosa. Scheduled endoscopic control could be cost-effective in IM patients, depending on the yearly incidence of gastric cancer in IM patients, the stage of gastric cancer at diagnosis discovered at surveillance, and the cost of endoscopy. As a pragmatic behavior, yearly endoscopic control would appear justified in all IM patients with at least one of these conditions: (1) IM extension &gt; 20%; (2) the presence of incomplete type IM; (3) first-degree relative of gastric cancer patients; and (4) smokers. In the remaining IM patients, a less intensive (2-3 years) could be proposed.</abstract><cop>China</cop><pub>Baishideng Publishing Group Co., Limited</pub><pmid>22468181</pmid><doi>10.4251/wjgo.v4.i3.30</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | cancer factors Follow-up Gastric Intestinal metaplasia Prevention Risk Topic Highlight |
title | Follow-up of intestinal metaplasia in the stomach: When, how and why |
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