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Clinical Significance of Signet-Ring-Cell Colorectal Cancer as a Prognostic Factor

PURPOSE: The aim of this study is to evaluate the prognosis for patients with a signet-ring-cell carcinoma (SRCC) who undergo curative surgery by comparing them to patients with an adenocarcinoma (ADC), excluding a mucinous ADC. METHODS: Between September 1994 and December 2013, 14,110 patients with...

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Autores principales: Yun, Sang-Oh, Cho, Yong Beom, Lee, Woo Yong, Kim, Hee Cheol, Yun, Seong Hyeon, Park, Yoon Ah, Huh, Jung Wook
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Coloproctology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5768478/
https://www.ncbi.nlm.nih.gov/pubmed/29354606
http://dx.doi.org/10.3393/ac.2017.33.6.232
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author Yun, Sang-Oh
Cho, Yong Beom
Lee, Woo Yong
Kim, Hee Cheol
Yun, Seong Hyeon
Park, Yoon Ah
Huh, Jung Wook
author_facet Yun, Sang-Oh
Cho, Yong Beom
Lee, Woo Yong
Kim, Hee Cheol
Yun, Seong Hyeon
Park, Yoon Ah
Huh, Jung Wook
author_sort Yun, Sang-Oh
collection PubMed
description PURPOSE: The aim of this study is to evaluate the prognosis for patients with a signet-ring-cell carcinoma (SRCC) who undergo curative surgery by comparing them to patients with an adenocarcinoma (ADC), excluding a mucinous ADC. METHODS: Between September 1994 and December 2013, 14,110 patients with colorectal cancer underwent surgery and among them, 12,631 patients were enrolled in this study. 71 patients with a SRCC and 12,570 patients with a ADC were identified. We analyzed the disease-free survival and the overall survival rates before and after a 1:2 propensity score matching and evaluated those rates after stage stratification. RESULTS: The median follow-up durations were 48.5 months for the SRC group and 48.6 months for the ADC group. The disease-free survival rates and the overall survival rates were significantly lower in the SRC group before and after propensity score matching (P < 0.001). After stratification by stage, no differences were observed between the SRC and the ADC groups for the disease-free survival (DFS) and the overall survival (OS) rates for patients with cancer in its early stages (P = 0.913 and P = 0.380 for the DFS and the OS, respectively, in stages 0 and I, and P = 0.223 and P = 0.991 for the DFS and the OS, respectively, in stage II), but those rates were significantly lower in the SRC group for cancer in its later stages (P < 0.001, respectively in stages III and IV). CONCLUSION: For cancer in advanced stages, patients with a resectable colorectal SRCC had a poorer prognosis after propensity score matching than those with an ADC did. Therefore, more intensive surveillance and closer observation should be offered to such patients.
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spelling pubmed-57684782018-01-21 Clinical Significance of Signet-Ring-Cell Colorectal Cancer as a Prognostic Factor Yun, Sang-Oh Cho, Yong Beom Lee, Woo Yong Kim, Hee Cheol Yun, Seong Hyeon Park, Yoon Ah Huh, Jung Wook Ann Coloproctol Original Article PURPOSE: The aim of this study is to evaluate the prognosis for patients with a signet-ring-cell carcinoma (SRCC) who undergo curative surgery by comparing them to patients with an adenocarcinoma (ADC), excluding a mucinous ADC. METHODS: Between September 1994 and December 2013, 14,110 patients with colorectal cancer underwent surgery and among them, 12,631 patients were enrolled in this study. 71 patients with a SRCC and 12,570 patients with a ADC were identified. We analyzed the disease-free survival and the overall survival rates before and after a 1:2 propensity score matching and evaluated those rates after stage stratification. RESULTS: The median follow-up durations were 48.5 months for the SRC group and 48.6 months for the ADC group. The disease-free survival rates and the overall survival rates were significantly lower in the SRC group before and after propensity score matching (P < 0.001). After stratification by stage, no differences were observed between the SRC and the ADC groups for the disease-free survival (DFS) and the overall survival (OS) rates for patients with cancer in its early stages (P = 0.913 and P = 0.380 for the DFS and the OS, respectively, in stages 0 and I, and P = 0.223 and P = 0.991 for the DFS and the OS, respectively, in stage II), but those rates were significantly lower in the SRC group for cancer in its later stages (P < 0.001, respectively in stages III and IV). CONCLUSION: For cancer in advanced stages, patients with a resectable colorectal SRCC had a poorer prognosis after propensity score matching than those with an ADC did. Therefore, more intensive surveillance and closer observation should be offered to such patients. The Korean Society of Coloproctology 2017-12 2017-12-31 /pmc/articles/PMC5768478/ /pubmed/29354606 http://dx.doi.org/10.3393/ac.2017.33.6.232 Text en © 2017 The Korean Society of Coloproctology http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article 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
Yun, Sang-Oh
Cho, Yong Beom
Lee, Woo Yong
Kim, Hee Cheol
Yun, Seong Hyeon
Park, Yoon Ah
Huh, Jung Wook
Clinical Significance of Signet-Ring-Cell Colorectal Cancer as a Prognostic Factor
title Clinical Significance of Signet-Ring-Cell Colorectal Cancer as a Prognostic Factor
title_full Clinical Significance of Signet-Ring-Cell Colorectal Cancer as a Prognostic Factor
title_fullStr Clinical Significance of Signet-Ring-Cell Colorectal Cancer as a Prognostic Factor
title_full_unstemmed Clinical Significance of Signet-Ring-Cell Colorectal Cancer as a Prognostic Factor
title_short Clinical Significance of Signet-Ring-Cell Colorectal Cancer as a Prognostic Factor
title_sort clinical significance of signet-ring-cell colorectal cancer as a prognostic factor
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5768478/
https://www.ncbi.nlm.nih.gov/pubmed/29354606
http://dx.doi.org/10.3393/ac.2017.33.6.232
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