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Comparison of outcomes between rectal squamous cell carcinoma and adenocarcinoma

Large, population‐based analyses of rectal squamous cell carcinoma (SCC) have not been previously conducted. We assessed patterns of care, prognostic factors, and outcomes of rectal SCC and adenocarcinoma (AC) in population‐based cohorts. Surveillance, Epidemiology, and End Results (SEER) registry s...

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Autores principales: Chiu, Max S., Verma, Vivek, Bennion, Nathan R., Bhirud, Abhijeet R., Li, Jinluan, Charlton, Mary E., Are, Chandrakanth, Lin, Chi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5224838/
https://www.ncbi.nlm.nih.gov/pubmed/27781400
http://dx.doi.org/10.1002/cam4.927
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author Chiu, Max S.
Verma, Vivek
Bennion, Nathan R.
Bhirud, Abhijeet R.
Li, Jinluan
Charlton, Mary E.
Are, Chandrakanth
Lin, Chi
author_facet Chiu, Max S.
Verma, Vivek
Bennion, Nathan R.
Bhirud, Abhijeet R.
Li, Jinluan
Charlton, Mary E.
Are, Chandrakanth
Lin, Chi
author_sort Chiu, Max S.
collection PubMed
description Large, population‐based analyses of rectal squamous cell carcinoma (SCC) have not been previously conducted. We assessed patterns of care, prognostic factors, and outcomes of rectal SCC and adenocarcinoma (AC) in population‐based cohorts. Surveillance, Epidemiology, and End Results (SEER) registry searches were performed (1998–2011), producing 42,308 nonmetastatic rectal cancer patients (999 SCC and 41,309 AC). Patient, tumor, and treatment characteristics were compared. Based on risk factors, SCC/AC groups were subdivided into low‐, intermediate‐, and high‐risk groups. Overall survival (OS) was compared between histological and risk groups using Kaplan–Meier method and log‐rank test. Multivariate logistic regression models evaluated prognostic factors for 5‐year survival. Cox regression modeling was performed on propensity‐matched data. Rectal SCC, more common in females and associated with larger tumors of higher grade, was more often treated with radiotherapy (RT) than surgery. Surgery was associated with higher OS in AC but not SCC, and RT had proportionally greater benefits in SCC. These effects of RT and surgery were retained when stratified into risk groups (particularly high/intermediate‐risk). Favorable prognostic factors for survival included younger age, non‐black race, SCC histology, size ≤3.9 cm, localized stage, lower grade, surgery, and RT. For SCC, race, tumor grade, and surgery were not prognostic factors for survival. Cox regression modeling of propensity‐matched data showed that AC histology increased risk of death versus SCC. In the largest analysis of rectal SCC to date, and in the notable absence (and unlikelihood) of prospective data, nonsurgical and RT‐based treatment is recommended.
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spelling pubmed-52248382017-01-17 Comparison of outcomes between rectal squamous cell carcinoma and adenocarcinoma Chiu, Max S. Verma, Vivek Bennion, Nathan R. Bhirud, Abhijeet R. Li, Jinluan Charlton, Mary E. Are, Chandrakanth Lin, Chi Cancer Med Clinical Cancer Research Large, population‐based analyses of rectal squamous cell carcinoma (SCC) have not been previously conducted. We assessed patterns of care, prognostic factors, and outcomes of rectal SCC and adenocarcinoma (AC) in population‐based cohorts. Surveillance, Epidemiology, and End Results (SEER) registry searches were performed (1998–2011), producing 42,308 nonmetastatic rectal cancer patients (999 SCC and 41,309 AC). Patient, tumor, and treatment characteristics were compared. Based on risk factors, SCC/AC groups were subdivided into low‐, intermediate‐, and high‐risk groups. Overall survival (OS) was compared between histological and risk groups using Kaplan–Meier method and log‐rank test. Multivariate logistic regression models evaluated prognostic factors for 5‐year survival. Cox regression modeling was performed on propensity‐matched data. Rectal SCC, more common in females and associated with larger tumors of higher grade, was more often treated with radiotherapy (RT) than surgery. Surgery was associated with higher OS in AC but not SCC, and RT had proportionally greater benefits in SCC. These effects of RT and surgery were retained when stratified into risk groups (particularly high/intermediate‐risk). Favorable prognostic factors for survival included younger age, non‐black race, SCC histology, size ≤3.9 cm, localized stage, lower grade, surgery, and RT. For SCC, race, tumor grade, and surgery were not prognostic factors for survival. Cox regression modeling of propensity‐matched data showed that AC histology increased risk of death versus SCC. In the largest analysis of rectal SCC to date, and in the notable absence (and unlikelihood) of prospective data, nonsurgical and RT‐based treatment is recommended. John Wiley and Sons Inc. 2016-10-26 /pmc/articles/PMC5224838/ /pubmed/27781400 http://dx.doi.org/10.1002/cam4.927 Text en © 2016 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Cancer Research
Chiu, Max S.
Verma, Vivek
Bennion, Nathan R.
Bhirud, Abhijeet R.
Li, Jinluan
Charlton, Mary E.
Are, Chandrakanth
Lin, Chi
Comparison of outcomes between rectal squamous cell carcinoma and adenocarcinoma
title Comparison of outcomes between rectal squamous cell carcinoma and adenocarcinoma
title_full Comparison of outcomes between rectal squamous cell carcinoma and adenocarcinoma
title_fullStr Comparison of outcomes between rectal squamous cell carcinoma and adenocarcinoma
title_full_unstemmed Comparison of outcomes between rectal squamous cell carcinoma and adenocarcinoma
title_short Comparison of outcomes between rectal squamous cell carcinoma and adenocarcinoma
title_sort comparison of outcomes between rectal squamous cell carcinoma and adenocarcinoma
topic Clinical Cancer Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5224838/
https://www.ncbi.nlm.nih.gov/pubmed/27781400
http://dx.doi.org/10.1002/cam4.927
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