Evidence map›Paper›PMID 41518457›Full record

ArticleEsophagus : official journal of the Japan Esophageal Society2026

The poorly differentiated component in endoscopic biopsy predicts submucosal invasion in superficial Barrett's esophageal adenocarcinoma.

Ken Namikawa, Junko Fujisaki, Yohei Ikenoyama, Yoshitaka Tokai, Shoichi Yoshimizu, Yusuke Horiuchi, Akiyoshi Ishiyama, Toshiyuki Yoshio, Toshiaki Hirasawa, Masayuki Watanabe and 5 more

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Article in Esophagus : official journal of the Japan Esophageal Society, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

15 authors.

Ken NamikawaDepartment of Gastroenterology, Japanese Foundation for Cancer Research, Cancer Institute Hospital, 3-8-31, Ariake, Koto-ku, Tokyo, 135-8550, Japan.
Junko FujisakiDepartment of Gastroenterology, Japanese Foundation for Cancer Research, Cancer Institute Hospital, 3-8-31, Ariake, Koto-ku, Tokyo, 135-8550, Japan. junko.fujisaki@jfcr.or.jp.
Yohei IkenoyamaDepartment of Gastroenterology, Japanese Foundation for Cancer Research, Cancer Institute Hospital, 3-8-31, Ariake, Koto-ku, Tokyo, 135-8550, Japan.
Yoshitaka TokaiDepartment of Gastroenterology, Japanese Foundation for Cancer Research, Cancer Institute Hospital, 3-8-31, Ariake, Koto-ku, Tokyo, 135-8550, Japan.
Shoichi YoshimizuDepartment of Gastroenterology, Japanese Foundation for Cancer Research, Cancer Institute Hospital, 3-8-31, Ariake, Koto-ku, Tokyo, 135-8550, Japan.
Yusuke HoriuchiDepartment of Gastroenterology, Japanese Foundation for Cancer Research, Cancer Institute Hospital, 3-8-31, Ariake, Koto-ku, Tokyo, 135-8550, Japan.
Akiyoshi IshiyamaDepartment of Gastroenterology, Japanese Foundation for Cancer Research, Cancer Institute Hospital, 3-8-31, Ariake, Koto-ku, Tokyo, 135-8550, Japan.
Toshiyuki YoshioDepartment of Gastroenterology, Japanese Foundation for Cancer Research, Cancer Institute Hospital, 3-8-31, Ariake, Koto-ku, Tokyo, 135-8550, Japan.
Toshiaki HirasawaDepartment of Gastroenterology, Japanese Foundation for Cancer Research, Cancer Institute Hospital, 3-8-31, Ariake, Koto-ku, Tokyo, 135-8550, Japan.
Masayuki WatanabeDepartment of Gastroenterological Surgery, Japanese Foundation for Cancer Research, Cancer Institute Hospital, Tokyo, Japan.
Kaoru NakanoDepartment of Pathology, Japanese Foundation for Cancer Research, Cancer Institute Hospital, Tokyo, Japan.
Manabu TakamatsuDepartment of Pathology, Japanese Foundation for Cancer Research, Cancer Institute Hospital, Tokyo, Japan.
Masahiro IkegamiDepartment of Pathology, The Jikei University School of Medicine, Tokyo, Japan.
Masayuki ShimodaDepartment of Pathology, The Jikei University School of Medicine, Tokyo, Japan.
Hiroshi KawachiDepartment of Pathology, Japanese Foundation for Cancer Research, Cancer Institute Hospital, Tokyo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimEndoscopic prediction of depth of invasion in superficial Barrett's esophageal adenocarcinoma (s-BEA) is important for treatment selection. This study aimed to evaluate the endoscopic and histopathological characteristics in s-BEA demonstrating submucosal invasion.

methodsWe retrospectively reviewed 105 tumors from 97 patients, diagnosed endoscopically and pathologically with s-BEA in short-segment Barrett's esophagus (60 lesions in 60 patients) and long-segment Barrett's esophagus (45 lesions in 37 patients); 105 s-BEA lesions were classified into 60 intramucosal and 45 submucosal tumors. We compared the clinicopathological and endoscopic characteristics of these tumors. A multivariate analysis was conducted to predict submucosal invasion based on pretreatment endoscopic and histopathological findings. The presence of the poorly differentiated component (PDC) was then assessed histologically in both pretreatment biopsy specimens (biopsy-PDC) and resected specimens.

resultsCompared to intramucosal tumors, submucosal tumors demonstrated significantly higher frequency of the following features: biopsy-PDC (21/45, 46.7%; versus 1/60, 1.7%; odds ratio = 24.9), complex macroscopic type (33/45, 73.3%; versus 15/60, 25.0%; odds ratio = 6.26), and tumor diameter > 20 mm (31/45, 68.9%; versus 13/60, 21.7%; odds ratio = 7.63). In 20 submucosal tumors with biopsy-PDC, the invasion at the biopsy site showed PDC extended to the submucosa in 95.0% (19/20) and was limited to the mucosa in 5.0% (1/20) cases.

conclusionsWe showed biopsy-PDC, tumor diameter greater than 20 mm, and complex macroscopic type independently predict submucosal invasion in Barrett's esophageal adenocarcinoma. Biopsy-PDC may predict submucosal cancer and submucosal invasion at the biopsy site more reliably, independent of endoscopic findings.

Indexed as

AdenocarcinomaBarrett EsophagusEsophageal MucosaEsophageal NeoplasmsAdultAgedAged, 80 and overBiopsyEsophagoscopyFemaleHumansMaleMiddle AgedNeoplasm InvasivenessPredictive Value of TestsRetrospective StudiesBarrett’s esophageal adenocarcinomaBiopsyDepth of invasionEndoscopyEsophageal cancer

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.