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A comparative prognostic performance of definitions of Crohn-like lymphoid reaction in colorectal carcinoma

BACKGROUND: The prognostic potential of Crohn-like lymphoid reaction (CLR) in colorectal carcinoma (CRC) has been investigated through the assessment of different criteria. METHODS: The prognostic impact of CLR was investigated in 636 CRC patients to compare methods from previously published article...

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Autores principales: Kim, Younghoon, Bae, Jeong Mo, Kim, Jung Ho, Cho, Nam-Yun, Kang, Gyeong Hoon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Pathologists and the Korean Society for Cytopathology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7829571/
https://www.ncbi.nlm.nih.gov/pubmed/33238662
http://dx.doi.org/10.4132/jptm.2020.10.06
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author Kim, Younghoon
Bae, Jeong Mo
Kim, Jung Ho
Cho, Nam-Yun
Kang, Gyeong Hoon
author_facet Kim, Younghoon
Bae, Jeong Mo
Kim, Jung Ho
Cho, Nam-Yun
Kang, Gyeong Hoon
author_sort Kim, Younghoon
collection PubMed
description BACKGROUND: The prognostic potential of Crohn-like lymphoid reaction (CLR) in colorectal carcinoma (CRC) has been investigated through the assessment of different criteria. METHODS: The prognostic impact of CLR was investigated in 636 CRC patients to compare methods from previously published articles. These methods included CLR measured by number of lymphoid aggregates (LAs) (CLR count), LA size greater than or equal to 1 mm (CLR size), CLR density with a cutoff value of 0.38, and subjective criteria as defined by intense CLR. RESULTS: In univariate survival analysis, CLR-positive CRC as defined by the four aforementioned methods was associated with better overall survival (OS) (hazard ratio [HR], 0.463; 95% confidence interval [CI], 0.305 to 0.702; p < .001; HR, 0.656; 95% CI, 0.411 to 1.046; p = .077; HR, 0.363; 95% CI, 0.197 to 0.669; p = .001; and HR, 0.433; 95% CI, 0.271 to 0.690; p < .001, respectively) and disease-free survival (DFS) (HR, 0.411; 95% CI, 0.304 to 0.639; p < .001; HR, 0.528; 95% CI, 0.340 to 0.821; p = .004; HR, 0.382; 95% CI, 0.226 to 0.645, p = .004; and HR, 0.501; 95% CI, 0.339 to 0.741; p < .001, respectively) than CLR-negative CRC, regardless of criteria with the exception of OS for CLR density. In multivariate analysis, two objective criteria (CLR count and CLR density) and one subjective criterion (intense CLR) for defining CLR were considered independent prognostic factors of OS and DFS in CRC patients. CONCLUSIONS: CLR has similar traits regardless of criteria, but CLR-positivity should be defined by objective criteria for better reproducibility and prognostic value.
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spelling pubmed-78295712021-02-01 A comparative prognostic performance of definitions of Crohn-like lymphoid reaction in colorectal carcinoma Kim, Younghoon Bae, Jeong Mo Kim, Jung Ho Cho, Nam-Yun Kang, Gyeong Hoon J Pathol Transl Med Original Article BACKGROUND: The prognostic potential of Crohn-like lymphoid reaction (CLR) in colorectal carcinoma (CRC) has been investigated through the assessment of different criteria. METHODS: The prognostic impact of CLR was investigated in 636 CRC patients to compare methods from previously published articles. These methods included CLR measured by number of lymphoid aggregates (LAs) (CLR count), LA size greater than or equal to 1 mm (CLR size), CLR density with a cutoff value of 0.38, and subjective criteria as defined by intense CLR. RESULTS: In univariate survival analysis, CLR-positive CRC as defined by the four aforementioned methods was associated with better overall survival (OS) (hazard ratio [HR], 0.463; 95% confidence interval [CI], 0.305 to 0.702; p < .001; HR, 0.656; 95% CI, 0.411 to 1.046; p = .077; HR, 0.363; 95% CI, 0.197 to 0.669; p = .001; and HR, 0.433; 95% CI, 0.271 to 0.690; p < .001, respectively) and disease-free survival (DFS) (HR, 0.411; 95% CI, 0.304 to 0.639; p < .001; HR, 0.528; 95% CI, 0.340 to 0.821; p = .004; HR, 0.382; 95% CI, 0.226 to 0.645, p = .004; and HR, 0.501; 95% CI, 0.339 to 0.741; p < .001, respectively) than CLR-negative CRC, regardless of criteria with the exception of OS for CLR density. In multivariate analysis, two objective criteria (CLR count and CLR density) and one subjective criterion (intense CLR) for defining CLR were considered independent prognostic factors of OS and DFS in CRC patients. CONCLUSIONS: CLR has similar traits regardless of criteria, but CLR-positivity should be defined by objective criteria for better reproducibility and prognostic value. The Korean Society of Pathologists and the Korean Society for Cytopathology 2021-01 2020-12-03 /pmc/articles/PMC7829571/ /pubmed/33238662 http://dx.doi.org/10.4132/jptm.2020.10.06 Text en © 2021 The Korean Society of Pathologists/The Korean Society for Cytopathology This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://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
Kim, Younghoon
Bae, Jeong Mo
Kim, Jung Ho
Cho, Nam-Yun
Kang, Gyeong Hoon
A comparative prognostic performance of definitions of Crohn-like lymphoid reaction in colorectal carcinoma
title A comparative prognostic performance of definitions of Crohn-like lymphoid reaction in colorectal carcinoma
title_full A comparative prognostic performance of definitions of Crohn-like lymphoid reaction in colorectal carcinoma
title_fullStr A comparative prognostic performance of definitions of Crohn-like lymphoid reaction in colorectal carcinoma
title_full_unstemmed A comparative prognostic performance of definitions of Crohn-like lymphoid reaction in colorectal carcinoma
title_short A comparative prognostic performance of definitions of Crohn-like lymphoid reaction in colorectal carcinoma
title_sort comparative prognostic performance of definitions of crohn-like lymphoid reaction in colorectal carcinoma
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7829571/
https://www.ncbi.nlm.nih.gov/pubmed/33238662
http://dx.doi.org/10.4132/jptm.2020.10.06
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