Cargando…

Metachronous advanced neoplasia after submucosal invasive colorectal cancer resection

Little is known about the incidence of metachronous advanced neoplasia (AN) following resection of submucosal invasive colorectal cancer (SM-CRC). Here, we aimed to assess the occurrence of metachronous AN following SM-CRC resection. We retrospectively reviewed consecutive patients who underwent SM-...

Descripción completa

Detalles Bibliográficos
Autores principales: Minamide, Tatsunori, Ikematsu, Hiroaki, Murano, Tatsuro, Kadota, Tomohiro, Shinmura, Kensuke, Yoda, Yusuke, Hori, Keisuke, Ito, Masaaki, Yano, Tomonori
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7820322/
https://www.ncbi.nlm.nih.gov/pubmed/33479474
http://dx.doi.org/10.1038/s41598-021-81645-2
_version_ 1783639186109104128
author Minamide, Tatsunori
Ikematsu, Hiroaki
Murano, Tatsuro
Kadota, Tomohiro
Shinmura, Kensuke
Yoda, Yusuke
Hori, Keisuke
Ito, Masaaki
Yano, Tomonori
author_facet Minamide, Tatsunori
Ikematsu, Hiroaki
Murano, Tatsuro
Kadota, Tomohiro
Shinmura, Kensuke
Yoda, Yusuke
Hori, Keisuke
Ito, Masaaki
Yano, Tomonori
author_sort Minamide, Tatsunori
collection PubMed
description Little is known about the incidence of metachronous advanced neoplasia (AN) following resection of submucosal invasive colorectal cancer (SM-CRC). Here, we aimed to assess the occurrence of metachronous AN following SM-CRC resection. We retrospectively reviewed consecutive patients who underwent SM-CRC resection at an academic medical center between 2005 and 2013. Among 343 patients, 250 (72.9%) underwent surgical resection or endoscopic resection followed by surgical resection and 93 (27.1%) underwent only endoscopic resection. During a median follow-up period of 61.5 months, the overall incidence of metachronous AN was 7.6%, and the cumulative incidence at 5 years was 6.1%. The cumulative incidence was significantly higher in the endoscopic resection group than in surgical resection group, in patients with colonic disease than in those with rectal disease, and in patients with synchronous AN than in those without. Multivariate analysis revealed that synchronous AN was the only significant risk factor for metachronous AN (HR 4.35; 95% CI 1.88–10.1). These findings imply that depending on synchronous AN, a surveillance protocol following SM-CRC resection can be changed for better detection of metachronous AN.
format Online
Article
Text
id pubmed-7820322
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-78203222021-01-22 Metachronous advanced neoplasia after submucosal invasive colorectal cancer resection Minamide, Tatsunori Ikematsu, Hiroaki Murano, Tatsuro Kadota, Tomohiro Shinmura, Kensuke Yoda, Yusuke Hori, Keisuke Ito, Masaaki Yano, Tomonori Sci Rep Article Little is known about the incidence of metachronous advanced neoplasia (AN) following resection of submucosal invasive colorectal cancer (SM-CRC). Here, we aimed to assess the occurrence of metachronous AN following SM-CRC resection. We retrospectively reviewed consecutive patients who underwent SM-CRC resection at an academic medical center between 2005 and 2013. Among 343 patients, 250 (72.9%) underwent surgical resection or endoscopic resection followed by surgical resection and 93 (27.1%) underwent only endoscopic resection. During a median follow-up period of 61.5 months, the overall incidence of metachronous AN was 7.6%, and the cumulative incidence at 5 years was 6.1%. The cumulative incidence was significantly higher in the endoscopic resection group than in surgical resection group, in patients with colonic disease than in those with rectal disease, and in patients with synchronous AN than in those without. Multivariate analysis revealed that synchronous AN was the only significant risk factor for metachronous AN (HR 4.35; 95% CI 1.88–10.1). These findings imply that depending on synchronous AN, a surveillance protocol following SM-CRC resection can be changed for better detection of metachronous AN. Nature Publishing Group UK 2021-01-21 /pmc/articles/PMC7820322/ /pubmed/33479474 http://dx.doi.org/10.1038/s41598-021-81645-2 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Minamide, Tatsunori
Ikematsu, Hiroaki
Murano, Tatsuro
Kadota, Tomohiro
Shinmura, Kensuke
Yoda, Yusuke
Hori, Keisuke
Ito, Masaaki
Yano, Tomonori
Metachronous advanced neoplasia after submucosal invasive colorectal cancer resection
title Metachronous advanced neoplasia after submucosal invasive colorectal cancer resection
title_full Metachronous advanced neoplasia after submucosal invasive colorectal cancer resection
title_fullStr Metachronous advanced neoplasia after submucosal invasive colorectal cancer resection
title_full_unstemmed Metachronous advanced neoplasia after submucosal invasive colorectal cancer resection
title_short Metachronous advanced neoplasia after submucosal invasive colorectal cancer resection
title_sort metachronous advanced neoplasia after submucosal invasive colorectal cancer resection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7820322/
https://www.ncbi.nlm.nih.gov/pubmed/33479474
http://dx.doi.org/10.1038/s41598-021-81645-2
work_keys_str_mv AT minamidetatsunori metachronousadvancedneoplasiaaftersubmucosalinvasivecolorectalcancerresection
AT ikematsuhiroaki metachronousadvancedneoplasiaaftersubmucosalinvasivecolorectalcancerresection
AT muranotatsuro metachronousadvancedneoplasiaaftersubmucosalinvasivecolorectalcancerresection
AT kadotatomohiro metachronousadvancedneoplasiaaftersubmucosalinvasivecolorectalcancerresection
AT shinmurakensuke metachronousadvancedneoplasiaaftersubmucosalinvasivecolorectalcancerresection
AT yodayusuke metachronousadvancedneoplasiaaftersubmucosalinvasivecolorectalcancerresection
AT horikeisuke metachronousadvancedneoplasiaaftersubmucosalinvasivecolorectalcancerresection
AT itomasaaki metachronousadvancedneoplasiaaftersubmucosalinvasivecolorectalcancerresection
AT yanotomonori metachronousadvancedneoplasiaaftersubmucosalinvasivecolorectalcancerresection