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Favorable Long-Term Outcomes of Endoscopic Submucosal Dissection for Differentiated-Type-Predominant Early Gastric Cancer with Histological Heterogeneity

It remains unclear whether endoscopic submucosal dissection (ESD) can be indicated for differentiated-type-predominant early gastric cancer mixed with a minor undifferentiated component (EGC with histological heterogeneity (HH)). Here, we reviewed and compared clinicopathologic characteristics and l...

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Autores principales: Kim, Tae-Se, Shin, Hyeong Chan, Min, Byung-Hoon, Kim, Kyoung-Mee, Min, Yang Won, Lee, Hyuk, Lee, Jun Haeng, Rhee, Poong-Lyul, Kim, Jae J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7231251/
https://www.ncbi.nlm.nih.gov/pubmed/32283696
http://dx.doi.org/10.3390/jcm9041064
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author Kim, Tae-Se
Shin, Hyeong Chan
Min, Byung-Hoon
Kim, Kyoung-Mee
Min, Yang Won
Lee, Hyuk
Lee, Jun Haeng
Rhee, Poong-Lyul
Kim, Jae J.
author_facet Kim, Tae-Se
Shin, Hyeong Chan
Min, Byung-Hoon
Kim, Kyoung-Mee
Min, Yang Won
Lee, Hyuk
Lee, Jun Haeng
Rhee, Poong-Lyul
Kim, Jae J.
author_sort Kim, Tae-Se
collection PubMed
description It remains unclear whether endoscopic submucosal dissection (ESD) can be indicated for differentiated-type-predominant early gastric cancer mixed with a minor undifferentiated component (EGC with histological heterogeneity (HH)). Here, we reviewed and compared clinicopathologic characteristics and long-term outcomes of ESD of 257 patients with EGC-HH and those of 2386 patients with pure differentiated-type EGC (PuD-EGC). After ESD, EGC-HH was managed in the same way as PuD-EGC. EGC-HHs were significantly associated with larger tumor size, more frequent submucosal invasion, and lymphovascular invasion compared to PuD-EGCs. Despite these aggressive features of EGC-HH, no local recurrence or gastric cancer-related death occurred during a median of 58 months of follow up after ESD for EGC-HH, if curative resection was achieved. After curative ESD for EGC-HH, six patients had metachronous recurrence (5.0%) and one patient underwent extragastric recurrence in a regional lymph node (0.8%). All these recurrence cases were curatively treated with ESD or gastrectomy. For patients with EGC-HH, five-year overall survival and recurrence-free survival rates after curative ESD were 97.0% and 94.8%, respectively, which were comparable to those of patients with PuD-EGC. In conclusion, ESD showed favorable long-term outcomes after curative resection and may be an acceptable treatment option for EGC-HH meeting curative endoscopic resection criteria.
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spelling pubmed-72312512020-05-22 Favorable Long-Term Outcomes of Endoscopic Submucosal Dissection for Differentiated-Type-Predominant Early Gastric Cancer with Histological Heterogeneity Kim, Tae-Se Shin, Hyeong Chan Min, Byung-Hoon Kim, Kyoung-Mee Min, Yang Won Lee, Hyuk Lee, Jun Haeng Rhee, Poong-Lyul Kim, Jae J. J Clin Med Article It remains unclear whether endoscopic submucosal dissection (ESD) can be indicated for differentiated-type-predominant early gastric cancer mixed with a minor undifferentiated component (EGC with histological heterogeneity (HH)). Here, we reviewed and compared clinicopathologic characteristics and long-term outcomes of ESD of 257 patients with EGC-HH and those of 2386 patients with pure differentiated-type EGC (PuD-EGC). After ESD, EGC-HH was managed in the same way as PuD-EGC. EGC-HHs were significantly associated with larger tumor size, more frequent submucosal invasion, and lymphovascular invasion compared to PuD-EGCs. Despite these aggressive features of EGC-HH, no local recurrence or gastric cancer-related death occurred during a median of 58 months of follow up after ESD for EGC-HH, if curative resection was achieved. After curative ESD for EGC-HH, six patients had metachronous recurrence (5.0%) and one patient underwent extragastric recurrence in a regional lymph node (0.8%). All these recurrence cases were curatively treated with ESD or gastrectomy. For patients with EGC-HH, five-year overall survival and recurrence-free survival rates after curative ESD were 97.0% and 94.8%, respectively, which were comparable to those of patients with PuD-EGC. In conclusion, ESD showed favorable long-term outcomes after curative resection and may be an acceptable treatment option for EGC-HH meeting curative endoscopic resection criteria. MDPI 2020-04-09 /pmc/articles/PMC7231251/ /pubmed/32283696 http://dx.doi.org/10.3390/jcm9041064 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kim, Tae-Se
Shin, Hyeong Chan
Min, Byung-Hoon
Kim, Kyoung-Mee
Min, Yang Won
Lee, Hyuk
Lee, Jun Haeng
Rhee, Poong-Lyul
Kim, Jae J.
Favorable Long-Term Outcomes of Endoscopic Submucosal Dissection for Differentiated-Type-Predominant Early Gastric Cancer with Histological Heterogeneity
title Favorable Long-Term Outcomes of Endoscopic Submucosal Dissection for Differentiated-Type-Predominant Early Gastric Cancer with Histological Heterogeneity
title_full Favorable Long-Term Outcomes of Endoscopic Submucosal Dissection for Differentiated-Type-Predominant Early Gastric Cancer with Histological Heterogeneity
title_fullStr Favorable Long-Term Outcomes of Endoscopic Submucosal Dissection for Differentiated-Type-Predominant Early Gastric Cancer with Histological Heterogeneity
title_full_unstemmed Favorable Long-Term Outcomes of Endoscopic Submucosal Dissection for Differentiated-Type-Predominant Early Gastric Cancer with Histological Heterogeneity
title_short Favorable Long-Term Outcomes of Endoscopic Submucosal Dissection for Differentiated-Type-Predominant Early Gastric Cancer with Histological Heterogeneity
title_sort favorable long-term outcomes of endoscopic submucosal dissection for differentiated-type-predominant early gastric cancer with histological heterogeneity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7231251/
https://www.ncbi.nlm.nih.gov/pubmed/32283696
http://dx.doi.org/10.3390/jcm9041064
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