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Gastric xanthoma is a predictive marker for metachronous and synchronous gastric cancer

AIM: To investigate predictive markers for metachronous and synchronous gastric cancer (GC), which can develop after endoscopic submucosal dissection (ESD). METHODS: A total of 352 patients underwent ESD for early GC at NTT West Osaka Hospital between June 2006 and February 2016. Exclusion criteria...

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Autores principales: Shibukawa, Narihiro, Ouchi, Shohei, Wakamatsu, Shuji, Wakahara, Yuhei, Kaneko, Akira
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5561044/
https://www.ncbi.nlm.nih.gov/pubmed/28868113
http://dx.doi.org/10.4251/wjgo.v9.i8.327
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author Shibukawa, Narihiro
Ouchi, Shohei
Wakamatsu, Shuji
Wakahara, Yuhei
Kaneko, Akira
author_facet Shibukawa, Narihiro
Ouchi, Shohei
Wakamatsu, Shuji
Wakahara, Yuhei
Kaneko, Akira
author_sort Shibukawa, Narihiro
collection PubMed
description AIM: To investigate predictive markers for metachronous and synchronous gastric cancer (GC), which can develop after endoscopic submucosal dissection (ESD). METHODS: A total of 352 patients underwent ESD for early GC at NTT West Osaka Hospital between June 2006 and February 2016. Exclusion criteria were as follows: Remnant stomach, unknown Helicobacter pylori status, and endoscopic observation of the whole stomach outside our hospital. We analyzed data from 192 patients comprising 109 patients with solitary GC (Group A) and 83 with metachronous and synchronous GC (Group B). We retrospectively investigated the clinicopathological and endoscopic characteristics, and endoscopic risk score as predictive markers for GC. RESULTS: The median age of Group B [72 years (interquartile range 63-78)] was significantly higher than that of Group A [66 years (interquartile range 61-74), respectively, P = 0.0009]. The prevalence of intestinal metaplasia in Group B tended to be higher than that in Group A (57.8% vs 45.0%, P = 0.08). The prevalence of gastric xanthoma (GX) in Group B was significantly higher than that in Group A (54.2% vs 32.1%, P = 0.003). The atrophy score in Group B was significantly higher than that in Group A (P = 0.005). Multivariate analysis revealed that higher age and the presence of GX were independently related to metachronous and synchronous GC [OR = 1.04 (1.01-1.08), P = 0.02; and OR = 2.11 (1.14-3.99), P = 0.02, respectively]. CONCLUSION: The presence of GX is a useful predictive marker for metachronous and synchronous GC.
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spelling pubmed-55610442017-09-01 Gastric xanthoma is a predictive marker for metachronous and synchronous gastric cancer Shibukawa, Narihiro Ouchi, Shohei Wakamatsu, Shuji Wakahara, Yuhei Kaneko, Akira World J Gastrointest Oncol Observational Study AIM: To investigate predictive markers for metachronous and synchronous gastric cancer (GC), which can develop after endoscopic submucosal dissection (ESD). METHODS: A total of 352 patients underwent ESD for early GC at NTT West Osaka Hospital between June 2006 and February 2016. Exclusion criteria were as follows: Remnant stomach, unknown Helicobacter pylori status, and endoscopic observation of the whole stomach outside our hospital. We analyzed data from 192 patients comprising 109 patients with solitary GC (Group A) and 83 with metachronous and synchronous GC (Group B). We retrospectively investigated the clinicopathological and endoscopic characteristics, and endoscopic risk score as predictive markers for GC. RESULTS: The median age of Group B [72 years (interquartile range 63-78)] was significantly higher than that of Group A [66 years (interquartile range 61-74), respectively, P = 0.0009]. The prevalence of intestinal metaplasia in Group B tended to be higher than that in Group A (57.8% vs 45.0%, P = 0.08). The prevalence of gastric xanthoma (GX) in Group B was significantly higher than that in Group A (54.2% vs 32.1%, P = 0.003). The atrophy score in Group B was significantly higher than that in Group A (P = 0.005). Multivariate analysis revealed that higher age and the presence of GX were independently related to metachronous and synchronous GC [OR = 1.04 (1.01-1.08), P = 0.02; and OR = 2.11 (1.14-3.99), P = 0.02, respectively]. CONCLUSION: The presence of GX is a useful predictive marker for metachronous and synchronous GC. Baishideng Publishing Group Inc 2017-08-15 2017-08-15 /pmc/articles/PMC5561044/ /pubmed/28868113 http://dx.doi.org/10.4251/wjgo.v9.i8.327 Text en ©The Author(s) 2017. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ Open-Access: This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is 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 and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Observational Study
Shibukawa, Narihiro
Ouchi, Shohei
Wakamatsu, Shuji
Wakahara, Yuhei
Kaneko, Akira
Gastric xanthoma is a predictive marker for metachronous and synchronous gastric cancer
title Gastric xanthoma is a predictive marker for metachronous and synchronous gastric cancer
title_full Gastric xanthoma is a predictive marker for metachronous and synchronous gastric cancer
title_fullStr Gastric xanthoma is a predictive marker for metachronous and synchronous gastric cancer
title_full_unstemmed Gastric xanthoma is a predictive marker for metachronous and synchronous gastric cancer
title_short Gastric xanthoma is a predictive marker for metachronous and synchronous gastric cancer
title_sort gastric xanthoma is a predictive marker for metachronous and synchronous gastric cancer
topic Observational Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5561044/
https://www.ncbi.nlm.nih.gov/pubmed/28868113
http://dx.doi.org/10.4251/wjgo.v9.i8.327
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