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Obesity as an independent predictive factor for pathologic complete response after neoadjuvant chemoradiation in rectal cancer

PURPOSE: The predictive role of obesity on pathologic complete response (pCR) after neoadjuvant chemoradiation (nCRT) in rectal cancer remains controversial. This study aimed to evaluate the association between obesity and pathologic response in patients with rectal cancer following nCRT. METHODS: A...

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Autores principales: Lee, Soo Young, Kim, Chang Hyun, Kim, Young Jin, Kwak, Han Deok, Ju, Jae Kyun, Kim, Hyeong Rok
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Surgical Society 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6393413/
https://www.ncbi.nlm.nih.gov/pubmed/30838183
http://dx.doi.org/10.4174/astr.2019.96.3.116
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author Lee, Soo Young
Kim, Chang Hyun
Kim, Young Jin
Kwak, Han Deok
Ju, Jae Kyun
Kim, Hyeong Rok
author_facet Lee, Soo Young
Kim, Chang Hyun
Kim, Young Jin
Kwak, Han Deok
Ju, Jae Kyun
Kim, Hyeong Rok
author_sort Lee, Soo Young
collection PubMed
description PURPOSE: The predictive role of obesity on pathologic complete response (pCR) after neoadjuvant chemoradiation (nCRT) in rectal cancer remains controversial. This study aimed to evaluate the association between obesity and pathologic response in patients with rectal cancer following nCRT. METHODS: A total of 320 patients with primary rectal cancer who underwent curative resection after nCRT between January 2010 and September 2014 were enrolled in this study. Obesity was defined as body mass index of ≥25 kg/m(2). Clinicopathologic characteristics were analyzed to identify independent predictive factors for pCR. RESULTS: Among the included patients, 23.4% (n = 75) were obese, and 14.7% (n = 47) showed pCR. Baseline characteristics were generally similar between obese and nonobese patients, except that women (P = 0.001) and cT2 tumors (P = 0.001) were more common in the obese group. Multivariate logistic regression analysis revealed that obesity (odds ratio [OR] = 2.051; 95% confidence interval [CI], 1.009–4.168), cT2 (OR, 3.614; 95% CI, 1.166–11.202), and pretreatment carcinoembryonic antigen <5 ng/mL (OR, 2.921; 95% CI, 1.365–6.253) were independent predictors for pCR. Obesity was not associated with disease-free survival or local recurrence-free survival. CONCLUSION: Obesity was an independent predictive factor for pCR following nCRT in rectal cancer, but was not associated with recurrence. Further studies are needed to clarify the association between obesity and prognosis of rectal cancer after nCRT.
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spelling pubmed-63934132019-03-06 Obesity as an independent predictive factor for pathologic complete response after neoadjuvant chemoradiation in rectal cancer Lee, Soo Young Kim, Chang Hyun Kim, Young Jin Kwak, Han Deok Ju, Jae Kyun Kim, Hyeong Rok Ann Surg Treat Res Original Article PURPOSE: The predictive role of obesity on pathologic complete response (pCR) after neoadjuvant chemoradiation (nCRT) in rectal cancer remains controversial. This study aimed to evaluate the association between obesity and pathologic response in patients with rectal cancer following nCRT. METHODS: A total of 320 patients with primary rectal cancer who underwent curative resection after nCRT between January 2010 and September 2014 were enrolled in this study. Obesity was defined as body mass index of ≥25 kg/m(2). Clinicopathologic characteristics were analyzed to identify independent predictive factors for pCR. RESULTS: Among the included patients, 23.4% (n = 75) were obese, and 14.7% (n = 47) showed pCR. Baseline characteristics were generally similar between obese and nonobese patients, except that women (P = 0.001) and cT2 tumors (P = 0.001) were more common in the obese group. Multivariate logistic regression analysis revealed that obesity (odds ratio [OR] = 2.051; 95% confidence interval [CI], 1.009–4.168), cT2 (OR, 3.614; 95% CI, 1.166–11.202), and pretreatment carcinoembryonic antigen <5 ng/mL (OR, 2.921; 95% CI, 1.365–6.253) were independent predictors for pCR. Obesity was not associated with disease-free survival or local recurrence-free survival. CONCLUSION: Obesity was an independent predictive factor for pCR following nCRT in rectal cancer, but was not associated with recurrence. Further studies are needed to clarify the association between obesity and prognosis of rectal cancer after nCRT. The Korean Surgical Society 2019-03 2018-02-26 /pmc/articles/PMC6393413/ /pubmed/30838183 http://dx.doi.org/10.4174/astr.2019.96.3.116 Text en Copyright © 2019, the Korean Surgical Society http://creativecommons.org/licenses/by-nc/4.0/ Annals of Surgical Treatment and Research is an Open Access Journal. All articles are distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Lee, Soo Young
Kim, Chang Hyun
Kim, Young Jin
Kwak, Han Deok
Ju, Jae Kyun
Kim, Hyeong Rok
Obesity as an independent predictive factor for pathologic complete response after neoadjuvant chemoradiation in rectal cancer
title Obesity as an independent predictive factor for pathologic complete response after neoadjuvant chemoradiation in rectal cancer
title_full Obesity as an independent predictive factor for pathologic complete response after neoadjuvant chemoradiation in rectal cancer
title_fullStr Obesity as an independent predictive factor for pathologic complete response after neoadjuvant chemoradiation in rectal cancer
title_full_unstemmed Obesity as an independent predictive factor for pathologic complete response after neoadjuvant chemoradiation in rectal cancer
title_short Obesity as an independent predictive factor for pathologic complete response after neoadjuvant chemoradiation in rectal cancer
title_sort obesity as an independent predictive factor for pathologic complete response after neoadjuvant chemoradiation in rectal cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6393413/
https://www.ncbi.nlm.nih.gov/pubmed/30838183
http://dx.doi.org/10.4174/astr.2019.96.3.116
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