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Adenocarcinoma with Mixed Subtypes in the Early and Advanced Gastric Cancer
OBJECTIVE: Adenocarcinoma with mixed subtypes (AM) is a histological classification based on the WHO classification. We aimed to compare the prognosis among AM, classic adenocarcinoma (CA), mucinous adenocarcinoma (MAC), and signet-ring cell carcinoma (SRCC) in early and advanced gastric cancer (EGC...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8570884/ https://www.ncbi.nlm.nih.gov/pubmed/34746042 http://dx.doi.org/10.1155/2021/8497305 |
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author | Zhao, Xixian Li, Yizhang Yang, Zhenwei Zhang, Hailin Wang, Hongling Lin, Jun Liu, Jing Zhao, Qiu |
author_facet | Zhao, Xixian Li, Yizhang Yang, Zhenwei Zhang, Hailin Wang, Hongling Lin, Jun Liu, Jing Zhao, Qiu |
author_sort | Zhao, Xixian |
collection | PubMed |
description | OBJECTIVE: Adenocarcinoma with mixed subtypes (AM) is a histological classification based on the WHO classification. We aimed to compare the prognosis among AM, classic adenocarcinoma (CA), mucinous adenocarcinoma (MAC), and signet-ring cell carcinoma (SRCC) in early and advanced gastric cancer (EGC and AGC), respectively. METHODS: The Surveillance, Epidemiology, and End Results (SEER) database was queried from 2001 to 2016. Univariate and multivariate Cox analyses were performed to compare prognosis between AM and histologic subtypes of CA, SRCC, and MAC in ECG and ACG. A nomogram was established to predict the cancer-specific survival (CSS) of gastric cancer (GC) patients with AM. C-index, calibration curves, and receiver operating characteristic (ROC) and decision curve analysis (DCA) curves were applied to examine the accuracy and clinical benefits. RESULTS: In the prognosis among these four histological subtypes in EGC patients, there are no differences. For AGC patients, AM had a significantly poorer prognosis compared with CA and MAC (P=0.003, 0.029) but similar prognosis to SRCC. A nomogram based on race, T stage, N stage, M stage, and surgical modalities was proposed to predict 1- and 3-year CSS for GC patients with AM (C-index: training cohort: 0.804, validation cohort: 0.748. 1- and 3-year CSS AUC: training cohort: 0.871 and 0.914, validation cohort: 0.810 and 0.798). 1- and 3-year CSS DCA curves showed good net benefits. CONCLUSIONS: EGC patients with AM had similar survival to those with CA, MAC, and SRCC. AM was an independent predictor of poor prognosis in AGC. A nomogram for predicting the prognosis of GC patients with AM was proposed to quantitatively assess the long-term survival. |
format | Online Article Text |
id | pubmed-8570884 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-85708842021-11-06 Adenocarcinoma with Mixed Subtypes in the Early and Advanced Gastric Cancer Zhao, Xixian Li, Yizhang Yang, Zhenwei Zhang, Hailin Wang, Hongling Lin, Jun Liu, Jing Zhao, Qiu Can J Gastroenterol Hepatol Research Article OBJECTIVE: Adenocarcinoma with mixed subtypes (AM) is a histological classification based on the WHO classification. We aimed to compare the prognosis among AM, classic adenocarcinoma (CA), mucinous adenocarcinoma (MAC), and signet-ring cell carcinoma (SRCC) in early and advanced gastric cancer (EGC and AGC), respectively. METHODS: The Surveillance, Epidemiology, and End Results (SEER) database was queried from 2001 to 2016. Univariate and multivariate Cox analyses were performed to compare prognosis between AM and histologic subtypes of CA, SRCC, and MAC in ECG and ACG. A nomogram was established to predict the cancer-specific survival (CSS) of gastric cancer (GC) patients with AM. C-index, calibration curves, and receiver operating characteristic (ROC) and decision curve analysis (DCA) curves were applied to examine the accuracy and clinical benefits. RESULTS: In the prognosis among these four histological subtypes in EGC patients, there are no differences. For AGC patients, AM had a significantly poorer prognosis compared with CA and MAC (P=0.003, 0.029) but similar prognosis to SRCC. A nomogram based on race, T stage, N stage, M stage, and surgical modalities was proposed to predict 1- and 3-year CSS for GC patients with AM (C-index: training cohort: 0.804, validation cohort: 0.748. 1- and 3-year CSS AUC: training cohort: 0.871 and 0.914, validation cohort: 0.810 and 0.798). 1- and 3-year CSS DCA curves showed good net benefits. CONCLUSIONS: EGC patients with AM had similar survival to those with CA, MAC, and SRCC. AM was an independent predictor of poor prognosis in AGC. A nomogram for predicting the prognosis of GC patients with AM was proposed to quantitatively assess the long-term survival. Hindawi 2021-10-29 /pmc/articles/PMC8570884/ /pubmed/34746042 http://dx.doi.org/10.1155/2021/8497305 Text en Copyright © 2021 Xixian Zhao et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Zhao, Xixian Li, Yizhang Yang, Zhenwei Zhang, Hailin Wang, Hongling Lin, Jun Liu, Jing Zhao, Qiu Adenocarcinoma with Mixed Subtypes in the Early and Advanced Gastric Cancer |
title | Adenocarcinoma with Mixed Subtypes in the Early and Advanced Gastric Cancer |
title_full | Adenocarcinoma with Mixed Subtypes in the Early and Advanced Gastric Cancer |
title_fullStr | Adenocarcinoma with Mixed Subtypes in the Early and Advanced Gastric Cancer |
title_full_unstemmed | Adenocarcinoma with Mixed Subtypes in the Early and Advanced Gastric Cancer |
title_short | Adenocarcinoma with Mixed Subtypes in the Early and Advanced Gastric Cancer |
title_sort | adenocarcinoma with mixed subtypes in the early and advanced gastric cancer |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8570884/ https://www.ncbi.nlm.nih.gov/pubmed/34746042 http://dx.doi.org/10.1155/2021/8497305 |
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