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Prognostic significance of tumor deposits in radically resected gastric cancer: a retrospective study of a cohort of 1915 Chinese individuals
Tumor deposits (TDs) have been identified as an independent prognostic factor in gastric cancer (GC). However, the associated clinicopathological factors and how to simply and reasonably incorporate TD into the TNM staging system remain undetermined. The aim of the current study was therefore to ass...
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Published in: | World journal of surgical oncology 2022-09, Vol.20 (1), p.304-12, Article 304 |
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description | Tumor deposits (TDs) have been identified as an independent prognostic factor in gastric cancer (GC). However, the associated clinicopathological factors and how to simply and reasonably incorporate TD into the TNM staging system remain undetermined. The aim of the current study was therefore to assess the significance of TD among radically resected GC patients.
We retrospectively reviewed 1915 patients undergoing radical resection between 2007 and 2012. The patients were classified into two groups according to TD status (absent vs. present), and the clinicopathologic characteristics, DFS, and OS were compared. Associations of TD presence with other clinicopathologic factors were evaluated by logistic regression analysis. Univariate and multivariate Cox regression analyses were performed to determine the prognostic factors for DFS and OS in the primary cohort. Propensity score matching (PSM) was performed to reduce the possibility of selection bias according to the presence of TD. External validation of previously proposed modified staging systems incorporating TD was conducted.
The detection rate of TD was 10.5% (201/1915). The presence of TD was significantly related to unfavorable clinicopathologic variables, including advanced T and N categories. According to the multivariate Cox regression analysis, the presence of TD was identified as an independent prognostic factor for DFS and OS in the primary cohort (both P < 0.001). In the after-PSM cohort, TD presence also significantly shortened DFS and OS. In the external validation, one system that incorporated TD into the pTNM stage had the best performance.
The presence of TD was significantly associated with poor survival in radically resected GC patients. The incorporation of TD into the TNM staging system can further improve the predictive capability. A multicenter cohort with a large sample size is needed to determine the appropriate method of incorporation. |
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We retrospectively reviewed 1915 patients undergoing radical resection between 2007 and 2012. The patients were classified into two groups according to TD status (absent vs. present), and the clinicopathologic characteristics, DFS, and OS were compared. Associations of TD presence with other clinicopathologic factors were evaluated by logistic regression analysis. Univariate and multivariate Cox regression analyses were performed to determine the prognostic factors for DFS and OS in the primary cohort. Propensity score matching (PSM) was performed to reduce the possibility of selection bias according to the presence of TD. External validation of previously proposed modified staging systems incorporating TD was conducted.
The detection rate of TD was 10.5% (201/1915). The presence of TD was significantly related to unfavorable clinicopathologic variables, including advanced T and N categories. According to the multivariate Cox regression analysis, the presence of TD was identified as an independent prognostic factor for DFS and OS in the primary cohort (both P < 0.001). In the after-PSM cohort, TD presence also significantly shortened DFS and OS. In the external validation, one system that incorporated TD into the pTNM stage had the best performance.
The presence of TD was significantly associated with poor survival in radically resected GC patients. The incorporation of TD into the TNM staging system can further improve the predictive capability. A multicenter cohort with a large sample size is needed to determine the appropriate method of incorporation.</description><identifier>ISSN: 1477-7819</identifier><identifier>EISSN: 1477-7819</identifier><identifier>DOI: 10.1186/s12957-022-02773-1</identifier><identifier>PMID: 36138439</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Analysis ; Cancer ; Cancer therapies ; Care and treatment ; Chemotherapy ; China - epidemiology ; Colorectal cancer ; Diagnosis ; Extranodal Extension ; Gastric cancer ; Humans ; Lymphatic system ; Medical prognosis ; Metastasis ; Methods ; Multivariate analysis ; Neoplasm Staging ; Patients ; Prognosis ; Propensity score ; Propensity scores ; Radiation therapy ; Regression analysis ; Retrospective Studies ; Stomach cancer ; Stomach Neoplasms - pathology ; Surgery ; Tumor deposit ; Tumor staging ; Tumors ; Variables</subject><ispartof>World journal of surgical oncology, 2022-09, Vol.20 (1), p.304-12, Article 304</ispartof><rights>2022. The Author(s).</rights><rights>COPYRIGHT 2022 BioMed Central Ltd.</rights><rights>2022. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c594t-711c6f2cb2579a56d484a8172eea1aa7bc616f322d3e51d7cb2484ff290e3db43</citedby><cites>FETCH-LOGICAL-c594t-711c6f2cb2579a56d484a8172eea1aa7bc616f322d3e51d7cb2484ff290e3db43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9502614/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2726137272?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36138439$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhou, Menglong</creatorcontrib><creatorcontrib>Yang, Wang</creatorcontrib><creatorcontrib>Zou, Wei</creatorcontrib><creatorcontrib>Yang, Jianing</creatorcontrib><creatorcontrib>Zhou, Changming</creatorcontrib><creatorcontrib>Zhang, Zhiyuan</creatorcontrib><creatorcontrib>Wang, Yaqi</creatorcontrib><creatorcontrib>Zhang, Jing</creatorcontrib><creatorcontrib>Wang, Yan</creatorcontrib><creatorcontrib>Li, Guichao</creatorcontrib><creatorcontrib>Zhang, Zhen</creatorcontrib><creatorcontrib>Xia, Fan</creatorcontrib><title>Prognostic significance of tumor deposits in radically resected gastric cancer: a retrospective study of a cohort of 1915 Chinese individuals</title><title>World journal of surgical oncology</title><addtitle>World J Surg Oncol</addtitle><description>Tumor deposits (TDs) have been identified as an independent prognostic factor in gastric cancer (GC). However, the associated clinicopathological factors and how to simply and reasonably incorporate TD into the TNM staging system remain undetermined. The aim of the current study was therefore to assess the significance of TD among radically resected GC patients.
We retrospectively reviewed 1915 patients undergoing radical resection between 2007 and 2012. The patients were classified into two groups according to TD status (absent vs. present), and the clinicopathologic characteristics, DFS, and OS were compared. Associations of TD presence with other clinicopathologic factors were evaluated by logistic regression analysis. Univariate and multivariate Cox regression analyses were performed to determine the prognostic factors for DFS and OS in the primary cohort. Propensity score matching (PSM) was performed to reduce the possibility of selection bias according to the presence of TD. External validation of previously proposed modified staging systems incorporating TD was conducted.
The detection rate of TD was 10.5% (201/1915). The presence of TD was significantly related to unfavorable clinicopathologic variables, including advanced T and N categories. According to the multivariate Cox regression analysis, the presence of TD was identified as an independent prognostic factor for DFS and OS in the primary cohort (both P < 0.001). In the after-PSM cohort, TD presence also significantly shortened DFS and OS. In the external validation, one system that incorporated TD into the pTNM stage had the best performance.
The presence of TD was significantly associated with poor survival in radically resected GC patients. The incorporation of TD into the TNM staging system can further improve the predictive capability. A multicenter cohort with a large sample size is needed to determine the appropriate method of incorporation.</description><subject>Analysis</subject><subject>Cancer</subject><subject>Cancer therapies</subject><subject>Care and treatment</subject><subject>Chemotherapy</subject><subject>China - epidemiology</subject><subject>Colorectal cancer</subject><subject>Diagnosis</subject><subject>Extranodal Extension</subject><subject>Gastric cancer</subject><subject>Humans</subject><subject>Lymphatic system</subject><subject>Medical prognosis</subject><subject>Metastasis</subject><subject>Methods</subject><subject>Multivariate analysis</subject><subject>Neoplasm Staging</subject><subject>Patients</subject><subject>Prognosis</subject><subject>Propensity score</subject><subject>Propensity scores</subject><subject>Radiation therapy</subject><subject>Regression analysis</subject><subject>Retrospective Studies</subject><subject>Stomach cancer</subject><subject>Stomach Neoplasms - pathology</subject><subject>Surgery</subject><subject>Tumor deposit</subject><subject>Tumor staging</subject><subject>Tumors</subject><subject>Variables</subject><issn>1477-7819</issn><issn>1477-7819</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkt-K1DAUxoso7rr6Al5IQBBvujZJ07ReCMvgn4UFvdDrkCannQydZEzSgXkI39kzM-s6IxLKCTnf90tz-IriJa2uKW2bd4myTsiyYgw_KXlJHxWXtJaylC3tHp_sL4pnKa2qinEu-NPigjeUtzXvLotf32IYfUjZGZLc6N3gjPYGSBhIntchEgubkFxOxHkStcX2NO1IhAQmgyWjTjmi-eCK74nGVo4hbbDttkBSnu1uT9PEhGWIeb-nHRVksXQeKci1buvsrKf0vHgyYIEX9_Wq-PHp4_fFl_Lu6-fbxc1daURX51JSapqBmZ4J2WnR2LqtdUslA9BUa9mbhjYDZ8xyENRKFKJiGFhXAbd9za-K2yPXBr1Sm-jWOu5U0E4dDkIclY44kglUw6XuGbLqHvCSXveybQ0IMKavG2qQ9eHI2sz9GqwBn6OezqDnHe-Wagxb1YmKNXT_M2_vATH8nCFltXbJwDRpD2FOikkqm1bUokPp63-kqzBHj6NCFcK4xPJXNWp8gPNDwHvNHqpuJO1YTUXXoOr6PypcFtbOBA-Dw_Mzw5sTwxL0lJcpTHN2wadzITsKDeYgRRgehkErtU-uOiZXYXLVIbmKounV6RgfLH-iyn8DzBHp2A</recordid><startdate>20220923</startdate><enddate>20220923</enddate><creator>Zhou, Menglong</creator><creator>Yang, Wang</creator><creator>Zou, Wei</creator><creator>Yang, Jianing</creator><creator>Zhou, Changming</creator><creator>Zhang, Zhiyuan</creator><creator>Wang, Yaqi</creator><creator>Zhang, Jing</creator><creator>Wang, Yan</creator><creator>Li, Guichao</creator><creator>Zhang, Zhen</creator><creator>Xia, Fan</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><general>BMC</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QL</scope><scope>7QO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FD</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20220923</creationdate><title>Prognostic significance of tumor deposits in radically resected gastric cancer: a retrospective study of a cohort of 1915 Chinese individuals</title><author>Zhou, Menglong ; Yang, Wang ; Zou, Wei ; Yang, Jianing ; Zhou, Changming ; Zhang, Zhiyuan ; Wang, Yaqi ; Zhang, Jing ; Wang, Yan ; Li, Guichao ; Zhang, Zhen ; Xia, Fan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c594t-711c6f2cb2579a56d484a8172eea1aa7bc616f322d3e51d7cb2484ff290e3db43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Analysis</topic><topic>Cancer</topic><topic>Cancer therapies</topic><topic>Care and treatment</topic><topic>Chemotherapy</topic><topic>China - epidemiology</topic><topic>Colorectal cancer</topic><topic>Diagnosis</topic><topic>Extranodal Extension</topic><topic>Gastric cancer</topic><topic>Humans</topic><topic>Lymphatic system</topic><topic>Medical prognosis</topic><topic>Metastasis</topic><topic>Methods</topic><topic>Multivariate analysis</topic><topic>Neoplasm Staging</topic><topic>Patients</topic><topic>Prognosis</topic><topic>Propensity score</topic><topic>Propensity scores</topic><topic>Radiation therapy</topic><topic>Regression analysis</topic><topic>Retrospective Studies</topic><topic>Stomach cancer</topic><topic>Stomach Neoplasms - pathology</topic><topic>Surgery</topic><topic>Tumor deposit</topic><topic>Tumor staging</topic><topic>Tumors</topic><topic>Variables</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhou, Menglong</creatorcontrib><creatorcontrib>Yang, Wang</creatorcontrib><creatorcontrib>Zou, Wei</creatorcontrib><creatorcontrib>Yang, Jianing</creatorcontrib><creatorcontrib>Zhou, Changming</creatorcontrib><creatorcontrib>Zhang, Zhiyuan</creatorcontrib><creatorcontrib>Wang, Yaqi</creatorcontrib><creatorcontrib>Zhang, Jing</creatorcontrib><creatorcontrib>Wang, Yan</creatorcontrib><creatorcontrib>Li, Guichao</creatorcontrib><creatorcontrib>Zhang, Zhen</creatorcontrib><creatorcontrib>Xia, Fan</creatorcontrib><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>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Technology Research Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>World journal of surgical oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhou, Menglong</au><au>Yang, Wang</au><au>Zou, Wei</au><au>Yang, Jianing</au><au>Zhou, Changming</au><au>Zhang, Zhiyuan</au><au>Wang, Yaqi</au><au>Zhang, Jing</au><au>Wang, Yan</au><au>Li, Guichao</au><au>Zhang, Zhen</au><au>Xia, Fan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prognostic significance of tumor deposits in radically resected gastric cancer: a retrospective study of a cohort of 1915 Chinese individuals</atitle><jtitle>World journal of surgical oncology</jtitle><addtitle>World J Surg Oncol</addtitle><date>2022-09-23</date><risdate>2022</risdate><volume>20</volume><issue>1</issue><spage>304</spage><epage>12</epage><pages>304-12</pages><artnum>304</artnum><issn>1477-7819</issn><eissn>1477-7819</eissn><abstract>Tumor deposits (TDs) have been identified as an independent prognostic factor in gastric cancer (GC). However, the associated clinicopathological factors and how to simply and reasonably incorporate TD into the TNM staging system remain undetermined. The aim of the current study was therefore to assess the significance of TD among radically resected GC patients.
We retrospectively reviewed 1915 patients undergoing radical resection between 2007 and 2012. The patients were classified into two groups according to TD status (absent vs. present), and the clinicopathologic characteristics, DFS, and OS were compared. Associations of TD presence with other clinicopathologic factors were evaluated by logistic regression analysis. Univariate and multivariate Cox regression analyses were performed to determine the prognostic factors for DFS and OS in the primary cohort. Propensity score matching (PSM) was performed to reduce the possibility of selection bias according to the presence of TD. External validation of previously proposed modified staging systems incorporating TD was conducted.
The detection rate of TD was 10.5% (201/1915). The presence of TD was significantly related to unfavorable clinicopathologic variables, including advanced T and N categories. According to the multivariate Cox regression analysis, the presence of TD was identified as an independent prognostic factor for DFS and OS in the primary cohort (both P < 0.001). In the after-PSM cohort, TD presence also significantly shortened DFS and OS. In the external validation, one system that incorporated TD into the pTNM stage had the best performance.
The presence of TD was significantly associated with poor survival in radically resected GC patients. The incorporation of TD into the TNM staging system can further improve the predictive capability. A multicenter cohort with a large sample size is needed to determine the appropriate method of incorporation.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>36138439</pmid><doi>10.1186/s12957-022-02773-1</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Analysis Cancer Cancer therapies Care and treatment Chemotherapy China - epidemiology Colorectal cancer Diagnosis Extranodal Extension Gastric cancer Humans Lymphatic system Medical prognosis Metastasis Methods Multivariate analysis Neoplasm Staging Patients Prognosis Propensity score Propensity scores Radiation therapy Regression analysis Retrospective Studies Stomach cancer Stomach Neoplasms - pathology Surgery Tumor deposit Tumor staging Tumors Variables |
title | Prognostic significance of tumor deposits in radically resected gastric cancer: a retrospective study of a cohort of 1915 Chinese individuals |
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