Evidence map›Paper›PMID 41765898›Full record

ArticleBMC medicine2026

Is random biopsy necessary for normal esophageal mucosa during chromoendoscopy? Evidence from a population-based cohort study.

Wenlei Yang, Mengfei Liu, Zifan Qi, Yi Huang, Zhen Liu, Chuanhai Guo, Anxiang Liu, Haijun Yang, Fenglei Li, Ying Liu and 5 more

Abstract read
In one paragraph

Article in BMC medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

15 authors.

Wenlei Yang *Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Genetics, Peking University Cancer Hospital & Institute, Beijing, 100142, China.
Mengfei Liu *Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Genetics, Peking University Cancer Hospital & Institute, Beijing, 100142, China.
Zifan Qi *Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Genetics, Peking University Cancer Hospital & Institute, Beijing, 100142, China.
Yi Huang *Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Genetics, Peking University Cancer Hospital & Institute, Beijing, 100142, China.
Zhen LiuKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Genetics, Peking University Cancer Hospital & Institute, Beijing, 100142, China.
Chuanhai GuoKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Genetics, Peking University Cancer Hospital & Institute, Beijing, 100142, China.
Anxiang LiuAnyang Cancer Hospital, Anyang, Henan Province, 455006, China.
Haijun YangAnyang Cancer Hospital, Anyang, Henan Province, 455006, China.
Fenglei LiHua County People's Hospital, Hua County, Anyang, Henan Province, 456463, China.
Ying LiuKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Genetics, Peking University Cancer Hospital & Institute, Beijing, 100142, China.
Fangfang LiuKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Genetics, Peking University Cancer Hospital & Institute, Beijing, 100142, China.
Yaqi PanKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Genetics, Peking University Cancer Hospital & Institute, Beijing, 100142, China.
Hong CaiKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Genetics, Peking University Cancer Hospital & Institute, Beijing, 100142, China.
Zhonghu HeState Key Laboratory of Molecular Oncology, Department of Genetics, Peking University Cancer Hospital & Institute, Beijing, 100142, China. zhonghuhe@foxmail.com.
Yang KeState Key Laboratory of Molecular Oncology, Department of Genetics, Peking University Cancer Hospital & Institute, Beijing, 100142, China. keyang@bjmu.edu.cn.

Funding

National Key R&D Program of China 2021YFC2500405National Natural Science Foundation of China 81773501National Natural Science Foundation of China 82073626National Natural Science Foundation of China 82303952Science and Technology Planning Project of Tibet Autonomous Region XZ202501JD0021
6 · The paper itself

Abstract

backgroundEsophageal squamous intraepithelial neoplasia could be detected in normally stained mucosa under Lugol's chromoendoscopy. We aim to determine whether an active biopsy should be performed on such mucosa.

methodsThis study was based on a population-based screening cohort where participants underwent Lugol's chromoendoscopy with biopsies taken from abnormal-unstaining areas and normally stained standard site. A total of 641 participants with esophageal squamous intraepithelial neoplasia or more severe lesions were included in the analysis. The cumulative incidence of high-grade intraepithelial neoplasia/esophageal squamous cell carcinoma (HGIN/ESCC) and ESCC-specific mortality were compared between participants biopsied from iodine unstained and stained areas. Additionally, paired eligible tissues were utilized for comparative genomic analysis.

resultsFor participants diagnosed with low-grade intraepithelial neoplasia (LGIN), HGIN, and ESCC, 292 (54.8%), 11 (14.9%), and 1 (2.9%) cases, respectively, were biopsied from normal-staining mucosa. Over a median 9.5-year follow-up, no incident HGIN/ESCC cases were identified among individuals with LGIN diagnosed from normal-staining esophageal mucosa. In contrast, LGIN cases detected in unstained lesions exhibited a cumulative incidence of HGIN/ESCC of 15.8 (95% CI, 11.4-21.0) per 100 persons. No ESCC-related deaths occurred in patients having normal-staining lesions, irrespective of pathological grade. Contrastingly, cumulative ESCC-specific mortality per 100 persons for LGIN, HGIN, and ESCC patients of unstained lesions were 2.1 (95% CI, 0.7-4.8), 14.3 (95% CI, 6.7-25.4), and 36.4 (95% CI, 20.4-54.9), respectively. Genomic analysis revealed minimal copy number variants in normally stained lesions compared to substantial alterations in unstained lesions.

conclusionsRandom biopsies of normally stained esophageal mucosa under Lugol's chromoendoscopy should be unnecessary for population-level ESCC screening.

Indexed as

Esophageal MucosaEsophageal NeoplasmsEsophageal Squamous Cell CarcinomaEsophagoscopyAgedBiopsyCohort StudiesColoring AgentsFemaleHumansIodidesMaleMiddle AgedColoring AgentsIodidesLugol's solutionEsophageal cancer screeningEsophageal squamous intraepithelial neoplasiaLugol-unstained lesionsRandom biopsy

Identifiers

PMID41765898
PMCPMC13059622

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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.