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Clinicopathological characteristics and prognostic analysis of Lauren classification in gastric adenocarcinoma in China

BACKGROUND: According to the Lauren classification, gastric adenocarcinomas are divided into diffuse and intestinal types. The causative attribution explaining the dismal prognosis of diffuse-type remains unknown. METHODS: We examined the archive of 1000 patients with gastric adenocarcinomas who rec...

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Autores principales: Qiu, Miao-zhen, Cai, Mu-yan, Zhang, Dong-sheng, Wang, Zhi-qiang, Wang, De-shen, Li, Yu-hong, Xu, Rui-hua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3600019/
https://www.ncbi.nlm.nih.gov/pubmed/23497313
http://dx.doi.org/10.1186/1479-5876-11-58
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author Qiu, Miao-zhen
Cai, Mu-yan
Zhang, Dong-sheng
Wang, Zhi-qiang
Wang, De-shen
Li, Yu-hong
Xu, Rui-hua
author_facet Qiu, Miao-zhen
Cai, Mu-yan
Zhang, Dong-sheng
Wang, Zhi-qiang
Wang, De-shen
Li, Yu-hong
Xu, Rui-hua
author_sort Qiu, Miao-zhen
collection PubMed
description BACKGROUND: According to the Lauren classification, gastric adenocarcinomas are divided into diffuse and intestinal types. The causative attribution explaining the dismal prognosis of diffuse-type remains unknown. METHODS: We examined the archive of 1000 patients with gastric adenocarcinomas who received radical gastrectomy in our center and assessed the effect of the Lauren classification on survival in a multivariate approach. Moreover we compared the variation of clinical features between the diffuse-type and intestinal-type and explored the contributing factors for the prognostic difference. RESULTS: There were 805 resectable patients for the final analysis. Diffuse-type comprised of 48.7% in the gastric carcinoma in our group and showed poorer prognosis than intestinal-type (P=0.013). Multivariate analysis revealed that independent prognostic factors for gastric carcinoma patients were T stage (P<0.001), N stage (P<0.001) tumor size (P<0.001) and Lauren classification (P=0.003). For the clinical features, diffuse-type was significantly associated with younger age (p<0.001), female preponderance (p <0.001), distal location (P<0.001), advanced pT (p < 0.001), advanced pN (p < 0.001) and advanced TNM stage (p = 0.027). CONCLUSIONS: Diffuse type adenocarcinoma carries a worse prognosis that may be partially explained by the tendency of this subtype to present at more advanced T and N stage. However, Lauren classification has prognostic significance that is independent of T and N stage as well as other prognostic variables based on the multivariate cox analysis.
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spelling pubmed-36000192013-03-17 Clinicopathological characteristics and prognostic analysis of Lauren classification in gastric adenocarcinoma in China Qiu, Miao-zhen Cai, Mu-yan Zhang, Dong-sheng Wang, Zhi-qiang Wang, De-shen Li, Yu-hong Xu, Rui-hua J Transl Med Research BACKGROUND: According to the Lauren classification, gastric adenocarcinomas are divided into diffuse and intestinal types. The causative attribution explaining the dismal prognosis of diffuse-type remains unknown. METHODS: We examined the archive of 1000 patients with gastric adenocarcinomas who received radical gastrectomy in our center and assessed the effect of the Lauren classification on survival in a multivariate approach. Moreover we compared the variation of clinical features between the diffuse-type and intestinal-type and explored the contributing factors for the prognostic difference. RESULTS: There were 805 resectable patients for the final analysis. Diffuse-type comprised of 48.7% in the gastric carcinoma in our group and showed poorer prognosis than intestinal-type (P=0.013). Multivariate analysis revealed that independent prognostic factors for gastric carcinoma patients were T stage (P<0.001), N stage (P<0.001) tumor size (P<0.001) and Lauren classification (P=0.003). For the clinical features, diffuse-type was significantly associated with younger age (p<0.001), female preponderance (p <0.001), distal location (P<0.001), advanced pT (p < 0.001), advanced pN (p < 0.001) and advanced TNM stage (p = 0.027). CONCLUSIONS: Diffuse type adenocarcinoma carries a worse prognosis that may be partially explained by the tendency of this subtype to present at more advanced T and N stage. However, Lauren classification has prognostic significance that is independent of T and N stage as well as other prognostic variables based on the multivariate cox analysis. BioMed Central 2013-03-06 /pmc/articles/PMC3600019/ /pubmed/23497313 http://dx.doi.org/10.1186/1479-5876-11-58 Text en Copyright ©2013 Qiu et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Qiu, Miao-zhen
Cai, Mu-yan
Zhang, Dong-sheng
Wang, Zhi-qiang
Wang, De-shen
Li, Yu-hong
Xu, Rui-hua
Clinicopathological characteristics and prognostic analysis of Lauren classification in gastric adenocarcinoma in China
title Clinicopathological characteristics and prognostic analysis of Lauren classification in gastric adenocarcinoma in China
title_full Clinicopathological characteristics and prognostic analysis of Lauren classification in gastric adenocarcinoma in China
title_fullStr Clinicopathological characteristics and prognostic analysis of Lauren classification in gastric adenocarcinoma in China
title_full_unstemmed Clinicopathological characteristics and prognostic analysis of Lauren classification in gastric adenocarcinoma in China
title_short Clinicopathological characteristics and prognostic analysis of Lauren classification in gastric adenocarcinoma in China
title_sort clinicopathological characteristics and prognostic analysis of lauren classification in gastric adenocarcinoma in china
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3600019/
https://www.ncbi.nlm.nih.gov/pubmed/23497313
http://dx.doi.org/10.1186/1479-5876-11-58
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