Cargando…

The Risk of Metachronous Advanced Colorectal Neoplasia Rises in Parallel with an Increasing Number of High-Risk Findings at Baseline

BACKGROUND/AIMS: Colorectal adenomas that are ≥10 mm have villous histology or high-grade dysplasia, or that are associated with ≥3 adenomas are considered high-risk for metachronous advanced neoplasia. We evaluated the cumulative incidence of metachronous advanced neoplasia according to the total n...

Descripción completa

Detalles Bibliográficos
Autores principales: Lee, Seung Min, Kim, Jeong Hwan, Sung, In Kyung, Hong, Sung Noh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial Office of Gut and Liver 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4625703/
https://www.ncbi.nlm.nih.gov/pubmed/25963078
http://dx.doi.org/10.5009/gnl14210
_version_ 1782398019350560768
author Lee, Seung Min
Kim, Jeong Hwan
Sung, In Kyung
Hong, Sung Noh
author_facet Lee, Seung Min
Kim, Jeong Hwan
Sung, In Kyung
Hong, Sung Noh
author_sort Lee, Seung Min
collection PubMed
description BACKGROUND/AIMS: Colorectal adenomas that are ≥10 mm have villous histology or high-grade dysplasia, or that are associated with ≥3 adenomas are considered high-risk for metachronous advanced neoplasia. We evaluated the cumulative incidence of metachronous advanced neoplasia according to the total number of high-risk findings detected on baseline colonoscopy. METHODS: This was a retrospective cohort study performed in 862 patients who underwent removal of colorectal adenomas between 2005 and 2009. At least one surveillance colonoscopy had been conducted at Konkuk University Medical Center, Seoul, Korea. RESULTS: The cumulative incidence of metachronous advanced neoplasia in patients with 0, 1, 2, and 3–4 high-risk findings at 1 year were 0.7%, 1.3%, 2.8%, and 8.0%; at 3 years, those were 5.9%, 11.9%, 15.5%, and 24.7%; and at 5 years, those were 8.5%, 18.7%, 26.3%, and 37.2%, respectively. In a multivariate model, the risk of metachronous advanced neoplasia was significantly higher for the multiple high-risk findings group when compared with the 0 high-risk findings group (1 high-risk (+): hazard ratio, 1.86 [95% confidence interval, 1.00–3.44]; 2 high-risk (+): 1.84 [0.88–3.84]; and 3–4 high-risk (+): 3.29 [1.54–7.01]; p(trend)=0.020). CONCLUSIONS: The presence of overlapping multiple high-risk findings was associated with an increased risk of advanced neoplasia during surveillance.
format Online
Article
Text
id pubmed-4625703
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Editorial Office of Gut and Liver
record_format MEDLINE/PubMed
spelling pubmed-46257032015-11-01 The Risk of Metachronous Advanced Colorectal Neoplasia Rises in Parallel with an Increasing Number of High-Risk Findings at Baseline Lee, Seung Min Kim, Jeong Hwan Sung, In Kyung Hong, Sung Noh Gut Liver Original Article BACKGROUND/AIMS: Colorectal adenomas that are ≥10 mm have villous histology or high-grade dysplasia, or that are associated with ≥3 adenomas are considered high-risk for metachronous advanced neoplasia. We evaluated the cumulative incidence of metachronous advanced neoplasia according to the total number of high-risk findings detected on baseline colonoscopy. METHODS: This was a retrospective cohort study performed in 862 patients who underwent removal of colorectal adenomas between 2005 and 2009. At least one surveillance colonoscopy had been conducted at Konkuk University Medical Center, Seoul, Korea. RESULTS: The cumulative incidence of metachronous advanced neoplasia in patients with 0, 1, 2, and 3–4 high-risk findings at 1 year were 0.7%, 1.3%, 2.8%, and 8.0%; at 3 years, those were 5.9%, 11.9%, 15.5%, and 24.7%; and at 5 years, those were 8.5%, 18.7%, 26.3%, and 37.2%, respectively. In a multivariate model, the risk of metachronous advanced neoplasia was significantly higher for the multiple high-risk findings group when compared with the 0 high-risk findings group (1 high-risk (+): hazard ratio, 1.86 [95% confidence interval, 1.00–3.44]; 2 high-risk (+): 1.84 [0.88–3.84]; and 3–4 high-risk (+): 3.29 [1.54–7.01]; p(trend)=0.020). CONCLUSIONS: The presence of overlapping multiple high-risk findings was associated with an increased risk of advanced neoplasia during surveillance. Editorial Office of Gut and Liver 2015-11 2015-05-13 /pmc/articles/PMC4625703/ /pubmed/25963078 http://dx.doi.org/10.5009/gnl14210 Text en Copyright © 2015 by The Korean Society of Gastroenterology, the Korean Society of Gastrointestinal Endoscopy, the Korean Society of Neurogastroenterology and Motility, Korean College of Helicobacter and Upper Gastrointestinal Research, Korean Association the Study of Intestinal Diseases, the Korean Association for the Study of the Liver, Korean Pancreatobiliary Association, and Korean Society of Gastrointestinal Cancer. 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
Lee, Seung Min
Kim, Jeong Hwan
Sung, In Kyung
Hong, Sung Noh
The Risk of Metachronous Advanced Colorectal Neoplasia Rises in Parallel with an Increasing Number of High-Risk Findings at Baseline
title The Risk of Metachronous Advanced Colorectal Neoplasia Rises in Parallel with an Increasing Number of High-Risk Findings at Baseline
title_full The Risk of Metachronous Advanced Colorectal Neoplasia Rises in Parallel with an Increasing Number of High-Risk Findings at Baseline
title_fullStr The Risk of Metachronous Advanced Colorectal Neoplasia Rises in Parallel with an Increasing Number of High-Risk Findings at Baseline
title_full_unstemmed The Risk of Metachronous Advanced Colorectal Neoplasia Rises in Parallel with an Increasing Number of High-Risk Findings at Baseline
title_short The Risk of Metachronous Advanced Colorectal Neoplasia Rises in Parallel with an Increasing Number of High-Risk Findings at Baseline
title_sort risk of metachronous advanced colorectal neoplasia rises in parallel with an increasing number of high-risk findings at baseline
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4625703/
https://www.ncbi.nlm.nih.gov/pubmed/25963078
http://dx.doi.org/10.5009/gnl14210
work_keys_str_mv AT leeseungmin theriskofmetachronousadvancedcolorectalneoplasiarisesinparallelwithanincreasingnumberofhighriskfindingsatbaseline
AT kimjeonghwan theriskofmetachronousadvancedcolorectalneoplasiarisesinparallelwithanincreasingnumberofhighriskfindingsatbaseline
AT sunginkyung theriskofmetachronousadvancedcolorectalneoplasiarisesinparallelwithanincreasingnumberofhighriskfindingsatbaseline
AT hongsungnoh theriskofmetachronousadvancedcolorectalneoplasiarisesinparallelwithanincreasingnumberofhighriskfindingsatbaseline
AT leeseungmin riskofmetachronousadvancedcolorectalneoplasiarisesinparallelwithanincreasingnumberofhighriskfindingsatbaseline
AT kimjeonghwan riskofmetachronousadvancedcolorectalneoplasiarisesinparallelwithanincreasingnumberofhighriskfindingsatbaseline
AT sunginkyung riskofmetachronousadvancedcolorectalneoplasiarisesinparallelwithanincreasingnumberofhighriskfindingsatbaseline
AT hongsungnoh riskofmetachronousadvancedcolorectalneoplasiarisesinparallelwithanincreasingnumberofhighriskfindingsatbaseline