Evidence map›Paper›PMID 42103307›Full record

Trial reportEndoscopy2026

Generative chromoendoscopy for gastric neoplasms: a multicenter prospective study.

Sho Suzuki, Yusuke Monno, Hiroyuki Yamamoto, Ayaka Takasu, Toshiaki Hirasawa, Toshihiro Nishizawa, Shun Ito, Fumiaki Ishibashi, Masatoshi Okutomi, Tomohiro Tada

Abstract readMulticenter StudyClinical Trial
In one paragraph

Trial report in Endoscopy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. How Does Artificial Intelligence-Assisted Endoscopy Impact Upper Gastrointestinal Screening?Digestive endoscopy : official journal of the Japan Gastroenterological Endoscopy Society · 2026
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Sho SuzukiInternational University of Health and Welfare Ichikawa Hospital, Department of Gastroenterology, Chiba, Japan, Ichikawa.ORCID 0000-0003-4831-1409
Yusuke MonnoInstitute of Science Tokyo, Department of Systems and Control Engineering, School of Engineering, Japan, Tokyo.
Hiroyuki YamamotoCancer Institute Hospital, Japanese Foundation for Cancer Research, Department of Gastroenterology, Japan, Tokyo.
Ayaka TakasuCancer Institute Hospital, Japanese Foundation for Cancer Research, Department of Gastroenterology, Japan, Tokyo.ORCID 0000-0003-0130-7170
Toshiaki HirasawaCancer Institute Hospital, Japanese Foundation for Cancer Research, Department of Gastroenterology, Japan, Tokyo.
Toshihiro NishizawaInternational University of Health and Welfare, Faculty of Medicine, Graduate School of Medicine, Japan, Narita.ORCID 0000-0003-4876-3384
Shun ItoInternational University of Health and Welfare Ichikawa Hospital, Department of Gastroenterology, Chiba, Japan, Ichikawa.
Fumiaki IshibashiInternational University of Health and Welfare Ichikawa Hospital, Department of Gastroenterology, Chiba, Japan, Ichikawa.ORCID 0000-0003-4065-7958
Masatoshi OkutomiInstitute of Science Tokyo, Department of Systems and Control Engineering, School of Engineering, Japan, Tokyo.
Tomohiro TadaAI Medical Service Inc., Japan, Tokyo.

Funding

Japan Agency for Medical Research and Development (AMED 24hma922022h0001,25hma322042h0001Japan Agency for Medical Research and Development (AMED) 24hma922022h0001Japan Agency for Medical Research and Development (AMED) 25hma322042h0001Japan Society for the Promotion of Science (JSPS) KAKENHI JP24K15772
6 · The paper itself

Abstract

Background: Generative indigo carmine chromoendoscopy (generative chromoendoscopy), produced using deep learning-based synthetic image transformation, is a novel image-enhanced endoscopic approach, whose clinical feasibility has not been validated. This proof-of-concept study evaluated whether generative chromoendoscopy improves the visibility of gastric neoplasms compared with conventional white-light imaging (WLI) and real chromoendoscopy. Methods: This prospective multicenter study was conducted at three Japanese institutions between January and August 2025. A deep neural network-based program converted WLI into generative chromoendoscopy images. Patients with early gastric cancer or adenoma sequentially underwent endoscopy using WLI, generative chromoendoscopy, and real chromoendoscopy. During live endoscopy, two endoscopists independently assessed lesion visibility using a 7-point Likert-type scale (-3 to +3). The primary end point was visibility of gastric neoplasms with generative chromoendoscopy relative to WLI, with comparison to real chromoendoscopy. Secondary end points included clinicopathologic factors associated with improved visibility. Results: 60 patients were included. Mean (SD) visibility scores were 0.67 (0.93) for generative chromoendoscopy and 0.51 (1.00) for real chromoendoscopy. The mean difference was 0.16 (95%CI 0.01 to 0.30). Differentiated-type histology (odds ratio [OR] 2.19, 95%CI 1.03 to 4.62), current Conclusions: Generative chromoendoscopy was feasible during live endoscopic procedures. It improved visibility of pre-identified gastric neoplasms compared with WLI and achieved visibility comparable to real chromoendoscopy.

Indexed as

AdenomaGastroscopyImage EnhancementStomach NeoplasmsAgedColoring AgentsDeep LearningFemaleGenerative Artificial IntelligenceHumansIndigo CarmineMaleMiddle AgedProspective StudiesColoring AgentsIndigo Carmine

Identifiers

PMID42103307
PMCPMC13494756

What OpenQuestion holds

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Registered trials

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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.