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Risk factors for early metachronous tumor development after endoscopic resection for early gastric cancer

BACKGROUND: Metachronous gastric tumor (MGT) is one of major concerns after endoscopic submucosal dissection (ESD) for early gastric cancer (EGC). Optimal follow-up strategy has not been yet well-established. The aim of this study was to identify the different clinical features of the patients accor...

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Autores principales: Park, Jae Yong, Kim, Sang Gyun, Kim, Jung, Han, Seung Jun, Oh, Sooyeon, Choi, Ji Min, Lim, Joo Hyun, Chung, Hyunsoo, Jung, Hyun Chae
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5614623/
https://www.ncbi.nlm.nih.gov/pubmed/28950014
http://dx.doi.org/10.1371/journal.pone.0185501
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author Park, Jae Yong
Kim, Sang Gyun
Kim, Jung
Han, Seung Jun
Oh, Sooyeon
Choi, Ji Min
Lim, Joo Hyun
Chung, Hyunsoo
Jung, Hyun Chae
author_facet Park, Jae Yong
Kim, Sang Gyun
Kim, Jung
Han, Seung Jun
Oh, Sooyeon
Choi, Ji Min
Lim, Joo Hyun
Chung, Hyunsoo
Jung, Hyun Chae
author_sort Park, Jae Yong
collection PubMed
description BACKGROUND: Metachronous gastric tumor (MGT) is one of major concerns after endoscopic submucosal dissection (ESD) for early gastric cancer (EGC). Optimal follow-up strategy has not been yet well-established. The aim of this study was to identify the different clinical features of the patients according to the time interval to development of MGT. METHODS: Among 1,780 consecutive patients with EGC who underwent ESD between 2005 and 2014, 115 patients with MGT were retrospectively reviewed. MGT was defined as secondary gastric cancer or dysplasia detected > 1 year after initial ESD. Clinicopathological factors associated with early development of MGT were evaluated. RESULTS: The median interval to development of MGT was 37 months. In univariate analysis, the median interval to MGT was shorter if EGC lesion was non-elevated type (39.4 vs 57.0 months, p = 0.011), or synchronous primary lesion was absent (39.8 vs 51.4 months, p = 0.050). In multivariate Cox’s proportional hazards analysis, the hazard ratios for early occurrence of MGT were 1.966 (95% CI: 1.141–3.386, p = 0.015) and 1.911 (95% CI: 1.163–3.141, p = 0.011), respectively. There was no significant difference in overall survival after diagnosis of MGT between the early occurrence group and the late occurrence group. CONCLUSIONS: Non-elevated gross type and absence of synchronous gastric tumor were independent risk factors for early development of MGT. Meticulous endoscopic inspection is especially important for the detection of MGT during the early follow-up period in patients with these initial tumor characteristics.
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spelling pubmed-56146232017-10-09 Risk factors for early metachronous tumor development after endoscopic resection for early gastric cancer Park, Jae Yong Kim, Sang Gyun Kim, Jung Han, Seung Jun Oh, Sooyeon Choi, Ji Min Lim, Joo Hyun Chung, Hyunsoo Jung, Hyun Chae PLoS One Research Article BACKGROUND: Metachronous gastric tumor (MGT) is one of major concerns after endoscopic submucosal dissection (ESD) for early gastric cancer (EGC). Optimal follow-up strategy has not been yet well-established. The aim of this study was to identify the different clinical features of the patients according to the time interval to development of MGT. METHODS: Among 1,780 consecutive patients with EGC who underwent ESD between 2005 and 2014, 115 patients with MGT were retrospectively reviewed. MGT was defined as secondary gastric cancer or dysplasia detected > 1 year after initial ESD. Clinicopathological factors associated with early development of MGT were evaluated. RESULTS: The median interval to development of MGT was 37 months. In univariate analysis, the median interval to MGT was shorter if EGC lesion was non-elevated type (39.4 vs 57.0 months, p = 0.011), or synchronous primary lesion was absent (39.8 vs 51.4 months, p = 0.050). In multivariate Cox’s proportional hazards analysis, the hazard ratios for early occurrence of MGT were 1.966 (95% CI: 1.141–3.386, p = 0.015) and 1.911 (95% CI: 1.163–3.141, p = 0.011), respectively. There was no significant difference in overall survival after diagnosis of MGT between the early occurrence group and the late occurrence group. CONCLUSIONS: Non-elevated gross type and absence of synchronous gastric tumor were independent risk factors for early development of MGT. Meticulous endoscopic inspection is especially important for the detection of MGT during the early follow-up period in patients with these initial tumor characteristics. Public Library of Science 2017-09-26 /pmc/articles/PMC5614623/ /pubmed/28950014 http://dx.doi.org/10.1371/journal.pone.0185501 Text en © 2017 Park et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Park, Jae Yong
Kim, Sang Gyun
Kim, Jung
Han, Seung Jun
Oh, Sooyeon
Choi, Ji Min
Lim, Joo Hyun
Chung, Hyunsoo
Jung, Hyun Chae
Risk factors for early metachronous tumor development after endoscopic resection for early gastric cancer
title Risk factors for early metachronous tumor development after endoscopic resection for early gastric cancer
title_full Risk factors for early metachronous tumor development after endoscopic resection for early gastric cancer
title_fullStr Risk factors for early metachronous tumor development after endoscopic resection for early gastric cancer
title_full_unstemmed Risk factors for early metachronous tumor development after endoscopic resection for early gastric cancer
title_short Risk factors for early metachronous tumor development after endoscopic resection for early gastric cancer
title_sort risk factors for early metachronous tumor development after endoscopic resection for early gastric cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5614623/
https://www.ncbi.nlm.nih.gov/pubmed/28950014
http://dx.doi.org/10.1371/journal.pone.0185501
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