Evidence map›Paper›PMID 42109851›Full record

ArticleiScience2026

Early detection and subtyping of gastric cancer: A cell-free DNA fragmentome-based liquid biopsy method.

Yongyi Chen, Haiqi Liao, Yuzhi Liu, Liulin Luo, Jiangang Jin, Dingding Hou, Wenjia Liu, Hanqing Zhang, Beilong He, Miao Luo and 3 more

Abstract read
In one paragraph

Article in iScience, 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
–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

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

13 authors.

Yongyi ChenDepartment of Clinical Laboratory, Zhejiang Cancer Hospital, Hangzhou Institute of Medicine (HIM), Chinese Academy of Sciences, Hangzhou, China.
Haiqi LiaoDepartment of Clinical Laboratory, Zhejiang Cancer Hospital, Hangzhou Institute of Medicine (HIM), Chinese Academy of Sciences, Hangzhou, China.
Yuzhi LiuDepartment of Gastroenterology and Hepatology, West China Hospital, Sichuan University, Chengdu, China.
Liulin LuoDepartment of Clinical Laboratory, Shanghai Yangpu Hospital, Tongji University School of Medicine, Shanghai, China.
Jiangang JinDepartment of Clinical Laboratory, Zhejiang Cancer Hospital, Hangzhou Institute of Medicine (HIM), Chinese Academy of Sciences, Hangzhou, China.
Dingding HouDepartment of Clinical Laboratory, Zhejiang Cancer Hospital, Hangzhou Institute of Medicine (HIM), Chinese Academy of Sciences, Hangzhou, China.
Wenjia LiuOmixScience Research Institute, OmixScience Co., Ltd., Hangzhou, China.
Hanqing ZhangUniversity of California, Davis, Davis, CA, USA.
Beilong HeOmixScience Research Institute, OmixScience Co., Ltd., Hangzhou, China.
Miao LuoDepartment of Clinical Laboratory, People's Hospital of Yubei District of Chongqing, Chongqing, China.
Wei LiuDepartment of Infectious Disease, People's Hospital of Yubei District of Chongqing, Chongqing, China.
Ziao LinOmixScience Research Institute, OmixScience Co., Ltd., Hangzhou, China.
Songxiao XuDepartment of Clinical Laboratory, Zhejiang Cancer Hospital, Hangzhou Institute of Medicine (HIM), Chinese Academy of Sciences, Hangzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cell-free DNA (cfDNA) in plasma provides attractive opportunities for early cancer diagnosis. This study aimed to establish gastric cancer (GC) artificial intelligence algorithms (GC-AIAs) based on cfDNA fragmentome for GC's early detection and subtyping. Whole-genome sequencing data were obtained from the training cohort of 404 participants, the internal testing cohort of 173 participants, and the independent validation cohort of 299 participants. Seven classes of cfDNA fragmentomic features were analyzed and employed to build the GC-AIA employing a stack ensemble model. The model's AUC in the internal testing cohort was 0.958 (95% confidence interval [CI]: 0.931-0.985) and that in the independent validation cohort was 0.951 (95% CI: 0.926-0.975). The GC-AIA showed high performance for various staged/differentiated GC detection and molecular subtyping. The stage shift analysis showed a notable increase in diagnosed stage Ⅰ patients. Our methodology built on the cfDNA fragmentomics exhibited encouraging preliminary performance in early detection and subtyping of GC patients.

Indexed as

cancerdiagnostic proceduremachine learning

Identifiers

PMID42109851
PMCPMC13156687

What OpenQuestion holds

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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.