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Evaluation of D2-plus radical resection for gastric cancer with pyloric invasion

BACKGROUND: The optimal lymphadenectomy for gastric cancer (GC) with pyloric invasion is controversial because the pattern of lymph node metastasis is different from that of distal GC. The rate of lymph node metastasis into the posterior area of the pancreatic head and hepatoduodenal ligament is hig...

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Autores principales: Xu, Zhi-yuan, Hu, Can, Chen, Shangqi, Du, Yi-an, Huang, Ling, Yu, Peng-fei, Wang, Li-jing, Cheng, Xiang-dong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6868836/
https://www.ncbi.nlm.nih.gov/pubmed/31747885
http://dx.doi.org/10.1186/s12893-019-0605-6
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author Xu, Zhi-yuan
Hu, Can
Chen, Shangqi
Du, Yi-an
Huang, Ling
Yu, Peng-fei
Wang, Li-jing
Cheng, Xiang-dong
author_facet Xu, Zhi-yuan
Hu, Can
Chen, Shangqi
Du, Yi-an
Huang, Ling
Yu, Peng-fei
Wang, Li-jing
Cheng, Xiang-dong
author_sort Xu, Zhi-yuan
collection PubMed
description BACKGROUND: The optimal lymphadenectomy for gastric cancer (GC) with pyloric invasion is controversial because the pattern of lymph node metastasis is different from that of distal GC. The rate of lymph node metastasis into the posterior area of the pancreatic head and hepatoduodenal ligament is high. This study evaluated the estimated benefit of radical gastrectomy with D2-plus lymphadenectomy in patients with pyloric invasion. METHODS: All patients with GC invading the pylorus who underwent curative surgical resection with D2-plus lymphadenectomy between February 2013 and September 2015 were enrolled in the study. The index of estimated benefit from lymph node dissection (IEBLD) was calculated by multiplying the incidence of metastasis to each lymph node station by the 3-year overall survival (OS) rate of patients with metastasis to that station. RESULTS: In total, 128 patients were eligible. The rate of lymph node metastasis and the 3-year OS rate (and IEBLD) of the patients with metastasis to lymph nodes were 14.3 and 44.4% (5.56) for No. 8p, 10.9 and 35.7% (3.89) for No. 12b, 9.5 and 33.3% (3.13) for No. 12p, 18.8 and 54.2% (10.19) for No. 13, and 21.8 and 53.6% (11.68) for No. 14v, respectively. CONCLUSIONS: In radical gastrectomy for GC with pyloric invasion, some survival benefit was observed with dissection of the No. 13 and No. 14 lymph nodes, but there was no survival benefit with dissection of the No. 8p lymph nodes. The No. 12b and No. 12p lymph nodes may be better to dissect in cT3 GC patients with pyloric invasion. TRIAL REGISTRATION: http://ClinicalTrials.gov Identifier: NCT01836991. Date of registration: April 17, 2013.
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spelling pubmed-68688362019-12-12 Evaluation of D2-plus radical resection for gastric cancer with pyloric invasion Xu, Zhi-yuan Hu, Can Chen, Shangqi Du, Yi-an Huang, Ling Yu, Peng-fei Wang, Li-jing Cheng, Xiang-dong BMC Surg Research Article BACKGROUND: The optimal lymphadenectomy for gastric cancer (GC) with pyloric invasion is controversial because the pattern of lymph node metastasis is different from that of distal GC. The rate of lymph node metastasis into the posterior area of the pancreatic head and hepatoduodenal ligament is high. This study evaluated the estimated benefit of radical gastrectomy with D2-plus lymphadenectomy in patients with pyloric invasion. METHODS: All patients with GC invading the pylorus who underwent curative surgical resection with D2-plus lymphadenectomy between February 2013 and September 2015 were enrolled in the study. The index of estimated benefit from lymph node dissection (IEBLD) was calculated by multiplying the incidence of metastasis to each lymph node station by the 3-year overall survival (OS) rate of patients with metastasis to that station. RESULTS: In total, 128 patients were eligible. The rate of lymph node metastasis and the 3-year OS rate (and IEBLD) of the patients with metastasis to lymph nodes were 14.3 and 44.4% (5.56) for No. 8p, 10.9 and 35.7% (3.89) for No. 12b, 9.5 and 33.3% (3.13) for No. 12p, 18.8 and 54.2% (10.19) for No. 13, and 21.8 and 53.6% (11.68) for No. 14v, respectively. CONCLUSIONS: In radical gastrectomy for GC with pyloric invasion, some survival benefit was observed with dissection of the No. 13 and No. 14 lymph nodes, but there was no survival benefit with dissection of the No. 8p lymph nodes. The No. 12b and No. 12p lymph nodes may be better to dissect in cT3 GC patients with pyloric invasion. TRIAL REGISTRATION: http://ClinicalTrials.gov Identifier: NCT01836991. Date of registration: April 17, 2013. BioMed Central 2019-11-20 /pmc/articles/PMC6868836/ /pubmed/31747885 http://dx.doi.org/10.1186/s12893-019-0605-6 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Xu, Zhi-yuan
Hu, Can
Chen, Shangqi
Du, Yi-an
Huang, Ling
Yu, Peng-fei
Wang, Li-jing
Cheng, Xiang-dong
Evaluation of D2-plus radical resection for gastric cancer with pyloric invasion
title Evaluation of D2-plus radical resection for gastric cancer with pyloric invasion
title_full Evaluation of D2-plus radical resection for gastric cancer with pyloric invasion
title_fullStr Evaluation of D2-plus radical resection for gastric cancer with pyloric invasion
title_full_unstemmed Evaluation of D2-plus radical resection for gastric cancer with pyloric invasion
title_short Evaluation of D2-plus radical resection for gastric cancer with pyloric invasion
title_sort evaluation of d2-plus radical resection for gastric cancer with pyloric invasion
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6868836/
https://www.ncbi.nlm.nih.gov/pubmed/31747885
http://dx.doi.org/10.1186/s12893-019-0605-6
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