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Association of T Stage and Serum CEA Levels in Determining Survival of Rectal Cancer

Purpose: To investigate the association of T stage and serum carcinoembryonic antigen (CEA) levels in determining oncologic outcomes of rectal cancer. Methods: Patients diagnosed with stage I–II rectal cancer patients were identified from the Surveillance, Epidemiology, and End Results database. Res...

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Autores principales: Wu, Shengwen, Gu, Wenlong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6965058/
https://www.ncbi.nlm.nih.gov/pubmed/31998724
http://dx.doi.org/10.3389/fmed.2019.00270
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author Wu, Shengwen
Gu, Wenlong
author_facet Wu, Shengwen
Gu, Wenlong
author_sort Wu, Shengwen
collection PubMed
description Purpose: To investigate the association of T stage and serum carcinoembryonic antigen (CEA) levels in determining oncologic outcomes of rectal cancer. Methods: Patients diagnosed with stage I–II rectal cancer patients were identified from the Surveillance, Epidemiology, and End Results database. Results: In stage T1N0M0 disease, elevated level of serum CEA (C1) was associated with 227.6% increased risk of mortality compared to normal level of serum CEA (C0; hazard ratio = 3.276, 95% confidence interval = 2.781–3.858, P < 0.001). Conclusions: Stage T1N0M0 rectal cancer, when involved in preoperative serum CEA elevation, may be a surrogate of biologically aggressive disease and correlate with unfavorable oncologic outcomes. Moreover, this subgroup of rectal cancer deserves more clinical attention of oncologists.
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spelling pubmed-69650582020-01-29 Association of T Stage and Serum CEA Levels in Determining Survival of Rectal Cancer Wu, Shengwen Gu, Wenlong Front Med (Lausanne) Medicine Purpose: To investigate the association of T stage and serum carcinoembryonic antigen (CEA) levels in determining oncologic outcomes of rectal cancer. Methods: Patients diagnosed with stage I–II rectal cancer patients were identified from the Surveillance, Epidemiology, and End Results database. Results: In stage T1N0M0 disease, elevated level of serum CEA (C1) was associated with 227.6% increased risk of mortality compared to normal level of serum CEA (C0; hazard ratio = 3.276, 95% confidence interval = 2.781–3.858, P < 0.001). Conclusions: Stage T1N0M0 rectal cancer, when involved in preoperative serum CEA elevation, may be a surrogate of biologically aggressive disease and correlate with unfavorable oncologic outcomes. Moreover, this subgroup of rectal cancer deserves more clinical attention of oncologists. Frontiers Media S.A. 2020-01-10 /pmc/articles/PMC6965058/ /pubmed/31998724 http://dx.doi.org/10.3389/fmed.2019.00270 Text en Copyright © 2020 Wu and Gu. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Medicine
Wu, Shengwen
Gu, Wenlong
Association of T Stage and Serum CEA Levels in Determining Survival of Rectal Cancer
title Association of T Stage and Serum CEA Levels in Determining Survival of Rectal Cancer
title_full Association of T Stage and Serum CEA Levels in Determining Survival of Rectal Cancer
title_fullStr Association of T Stage and Serum CEA Levels in Determining Survival of Rectal Cancer
title_full_unstemmed Association of T Stage and Serum CEA Levels in Determining Survival of Rectal Cancer
title_short Association of T Stage and Serum CEA Levels in Determining Survival of Rectal Cancer
title_sort association of t stage and serum cea levels in determining survival of rectal cancer
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6965058/
https://www.ncbi.nlm.nih.gov/pubmed/31998724
http://dx.doi.org/10.3389/fmed.2019.00270
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