Evidence map›Paper›PMID 36847918›Full record

ArticleJournal of gastroenterology2023

Characteristics of synchronous and metachronous duodenal tumors and association with colorectal cancer: a supplementary analysis.

Yasushi Yamasaki, Motohiko Kato, Yoji Takeuchi, Shu Hoteya, Tsuneo Oyama, Satoru Nonaka, Shoichi Yoshimizu, Masao Yoshida, Ken Ohata, Yoshimasa Miura and 11 more

Erratum issuedAbstract read
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In one paragraph

Article in Journal of gastroenterology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 28% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 2 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors at 17 institutions in 1 country.

Yasushi YamasakiDepartment of Gastroenterology, Okayama University Hospital, 2-5-1 Shikata-Cho, Kita-Ku, Okayama, 700-8558, Japan. yasshifive@yahoo.co.jp.ORCID http://orcid.org/0000-0002-2992-9863
Motohiko KatoDivision of Research and Development for Minimally Invasive Treatment, Cancer Center, Keio University School of Medicine, Tokyo, Japan.
Yoji TakeuchiDepartment of Gastrointestinal Oncology and Department of Genetic Oncology, Division of Hereditary Tumors, Osaka International Cancer Institute, Osaka, Japan.
Shu HoteyaDepartment of Gastroenterology, Toranomon Hospital, Tokyo, Japan.
Tsuneo OyamaDepartment of Endoscopy, Saku Central Hospital Advanced Care Center, Nagano, Japan.
Satoru NonakaEndoscopy Division, National Cancer Center Hospital, Tokyo, Japan.
Shoichi YoshimizuDepartment of Gastroenterology, Cancer Institute Hospital of the Japanese Foundation for Cancer Research, Tokyo, Japan.
Masao YoshidaDivision of Endoscopy, Shizuoka Cancer Center, Shizuoka, Japan.
Ken OhataDepartment of Gastrointestinal Endoscopy, NTT Medical Center Tokyo, Tokyo, Japan.
Yoshimasa MiuraDepartment of Medicine, Division of Gastroenterology, Jichi Medical University, Shimotsuke, Japan.
Yuko HaraDepartment of Endoscopy, The Jikei University School of Medicine, Tokyo, Japan.
Shigetsugu TsujiDepartment of Gastroenterology, Ishikawa Prefectural Central Hospital, Kanazawa, Japan.
Osamu DohiMolecular Gastroenterology and Hepatology, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Hiroya UeyamaDepartment of Gastroenterology, Juntendo University School of Medicine, Tokyo, Japan.
Koichi KuraharaDivision of Gastroenterology, Matsuyama Red Cross Hospital, Matsuyama, Japan.
Tomoaki TashimaDepartment of Gastroenterology, Saitama Medical University International Medical Center, Saitama, Japan.
Nobutsugu AbeDepartment of Gastroenterological and General Surgery, Faculty of Medicine, Kyorin University, Tokyo, Japan.
Toshiharu MitsuhashiCenter for Innovative Clinical Medicine, Okayama University Hospital, Okayama, Japan.
Atsushi NakayamaDivision of Research and Development for Minimally Invasive Treatment, Cancer Center, Keio University School of Medicine, Tokyo, Japan.
Ichiro OdaEndoscopy Division, National Cancer Center Hospital, Tokyo, Japan.
Naohisa YahagiDivision of Research and Development for Minimally Invasive Treatment, Cancer Center, Keio University School of Medicine, Tokyo, Japan.
Keio University · JPNational Cancer Center Hospital East · JPOkayama University Hospital · JPIshikawa Prefectural Central Hospital · JPJapanese Foundation For Cancer Research · JPJichi Medical University · JPJikei University School of Medicine · JPJuntendo University · JPKyorin University · JPKyoto Prefectural University of Medicine · JPMatsuyama Red Cross Hospital · JPNTT Medical Center · JPOsaka International Cancer Institute · JPSaitama Medical University · JPSaku Central Hospital · JPShizuoka Cancer Center · JPToranomon Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWe previously reported outcomes of endoscopic resection for duodenal tumors in a large cohort. This study investigated the frequency and characteristics of synchronous and metachronous lesions, and their association with colorectal advanced adenoma (CAA) and colorectal cancer (CRC).

methodsPatients underwent duodenal endoscopic resection during January 2008 to December 2018. Background and characteristics, incidence of synchronous and metachronous lesions, and incidence of CAA and CRC were investigated. Patients without synchronous lesions were classified as the single group, and those with synchronous lesions as the synchronous group. Patients were also classified as the metachronous and non-metachronous groups. The characteristics among the groups were compared.

resultsWe included 2658 patients with 2881 duodenal tumors: 2472 (93.0%) patients had single, 186 (7.0%) had synchronous, and 54 (2.0%) had metachronous lesions. The 5-year cumulative incidence of metachronous lesions was 4.1%. In total, 208 (7.8%) had CAA and 127 (4.8%) patients had CRC, and colonoscopy was performed in 936 (35.2%) patients. The incidence of CAA in the synchronous groups tended to be higher compared with that in the single groups (11.8% vs 7.5%, adjusted risk ratio 1.56), and the incidence of CRC in the metachronous groups tended to be higher compared with that in the non-metachronous groups (13.0% vs 4.6%, adjusted risk ratio 2.75), but there was no difference after adjusting for colonoscopy.

conclusionsThis study showed the incidence of synchronous and metachronous duodenal lesions. There was no significant difference in incidence of CAA and CRC among each group, but further studies are warranted.

Indexed as

Colorectal NeoplasmsDuodenal NeoplasmsNeoplasms, Multiple PrimaryNeoplasms, Second PrimaryColonoscopyHumansRetrospective StudiesRisk FactorsColorectal cancerDuodenal tumorMetachronous lesionSynchronous lesion

Identifiers

PMID36847918
OpenAlexW4322496118

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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.