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Adenocarcinoma with mixed subtypes is a rare but aggressive histologic subtype in colorectal cancer
BACKGROUND: Although numerous studies have investigated the clinicopathologic and prognostic relevance of mucinous adenocarcinoma (MAC) and signet-ring cell carcinoma (SRCC) compared with classic adenocarcinoma (CA), little is known about the prognosis of adenocarcinoma with mixed subtypes (AM) and...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6842229/ https://www.ncbi.nlm.nih.gov/pubmed/31703713 http://dx.doi.org/10.1186/s12885-019-6245-5 |
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author | Sheng, Hui Wei, Xiaoli Mao, Minjie He, Jincan Luo, Tianqi Lu, Shilin Zhou, Liye Huang, Zhixin Yang, Anli |
author_facet | Sheng, Hui Wei, Xiaoli Mao, Minjie He, Jincan Luo, Tianqi Lu, Shilin Zhou, Liye Huang, Zhixin Yang, Anli |
author_sort | Sheng, Hui |
collection | PubMed |
description | BACKGROUND: Although numerous studies have investigated the clinicopathologic and prognostic relevance of mucinous adenocarcinoma (MAC) and signet-ring cell carcinoma (SRCC) compared with classic adenocarcinoma (CA), little is known about the prognosis of adenocarcinoma with mixed subtypes (AM) and the differences among these four subtypes. METHODS: The statistics of colorectal cancer registered in the Surveillance, Epidemiology and End Results (SEER) database were retrieved and analyzed. We also compared the clinicopathologic and prognostic relevance between CA, SRCC, MAC, and AM. RESULTS: The frequencies of these four subtypes were 69.9% (CA, n = 15,812), 25.1% (MAC, n = 5689), 3.6% (SRCC, n = 814) and 1.4% (AM, n = 321), respectively. All of MAC, SRCC, and AM were significantly related with aggressive features. Only SRCC and AM were identified as independent poor prognostic markers for overall survival by multivariate analysis. The aggressiveness of AM was between MAC and SRCC according to the clinicopathologic associations. The prognosis of AM was significantly worse than MAC but comparable with SRCC. CONCLUSIONS: We confirmed the clinicopathologic relevance with aggressive features of MAC and SRCC, as well as poor prognostic relevance of SRCC by analyzing a large study population data set. Furthermore, we identified AM as a rare but aggressive histologic subtype in colorectal cancer, to which particular attention should be given in clinical practice. |
format | Online Article Text |
id | pubmed-6842229 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-68422292019-11-14 Adenocarcinoma with mixed subtypes is a rare but aggressive histologic subtype in colorectal cancer Sheng, Hui Wei, Xiaoli Mao, Minjie He, Jincan Luo, Tianqi Lu, Shilin Zhou, Liye Huang, Zhixin Yang, Anli BMC Cancer Research Article BACKGROUND: Although numerous studies have investigated the clinicopathologic and prognostic relevance of mucinous adenocarcinoma (MAC) and signet-ring cell carcinoma (SRCC) compared with classic adenocarcinoma (CA), little is known about the prognosis of adenocarcinoma with mixed subtypes (AM) and the differences among these four subtypes. METHODS: The statistics of colorectal cancer registered in the Surveillance, Epidemiology and End Results (SEER) database were retrieved and analyzed. We also compared the clinicopathologic and prognostic relevance between CA, SRCC, MAC, and AM. RESULTS: The frequencies of these four subtypes were 69.9% (CA, n = 15,812), 25.1% (MAC, n = 5689), 3.6% (SRCC, n = 814) and 1.4% (AM, n = 321), respectively. All of MAC, SRCC, and AM were significantly related with aggressive features. Only SRCC and AM were identified as independent poor prognostic markers for overall survival by multivariate analysis. The aggressiveness of AM was between MAC and SRCC according to the clinicopathologic associations. The prognosis of AM was significantly worse than MAC but comparable with SRCC. CONCLUSIONS: We confirmed the clinicopathologic relevance with aggressive features of MAC and SRCC, as well as poor prognostic relevance of SRCC by analyzing a large study population data set. Furthermore, we identified AM as a rare but aggressive histologic subtype in colorectal cancer, to which particular attention should be given in clinical practice. BioMed Central 2019-11-08 /pmc/articles/PMC6842229/ /pubmed/31703713 http://dx.doi.org/10.1186/s12885-019-6245-5 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 Sheng, Hui Wei, Xiaoli Mao, Minjie He, Jincan Luo, Tianqi Lu, Shilin Zhou, Liye Huang, Zhixin Yang, Anli Adenocarcinoma with mixed subtypes is a rare but aggressive histologic subtype in colorectal cancer |
title | Adenocarcinoma with mixed subtypes is a rare but aggressive histologic subtype in colorectal cancer |
title_full | Adenocarcinoma with mixed subtypes is a rare but aggressive histologic subtype in colorectal cancer |
title_fullStr | Adenocarcinoma with mixed subtypes is a rare but aggressive histologic subtype in colorectal cancer |
title_full_unstemmed | Adenocarcinoma with mixed subtypes is a rare but aggressive histologic subtype in colorectal cancer |
title_short | Adenocarcinoma with mixed subtypes is a rare but aggressive histologic subtype in colorectal cancer |
title_sort | adenocarcinoma with mixed subtypes is a rare but aggressive histologic subtype in colorectal cancer |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6842229/ https://www.ncbi.nlm.nih.gov/pubmed/31703713 http://dx.doi.org/10.1186/s12885-019-6245-5 |
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