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

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.

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Publication Details

Journal
iScience
Published
2026-04-22
DOI
https://doi.org/10.1016/j.isci.2026.115833
Primary Topic
Cancer Genomics and Diagnostics
Type
article
Field-Weighted Citation Impact
0.00

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article

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

Wei Liu, Hanqing Zhang, Liulin Luo, YUZHI LIU et al.
iScience
Cancer Genomics and Diagnostics
article

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

Wei Liu, Hanqing Zhang, Liulin Luo, YUZHI LIU, Haiqi Liao, Ziao Lin, Songxiao Xu, Beilong He, Wenjia Liu, Yongyi Chen, Dingding Hou, Miao Luo, Jiangang Jin
article en

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.

iScienceVol. 29(6)
Sichuan University (CN), West China Hospital of Sichuan University (CN), Zhejiang Cancer Hospital (CN), Jinhua Academy of Agricultural Sciences (CN), First People's Hospital of Chongqing (CN), Jinhua Central Hospital (CN), Chongqing Dazu District People's Hospital (CN), Sichuan Center for Disease Control and Prevention (CN), Hangzhou Cancer Hospital (CN), Yangpu Hospital of Tongji University (CN), Zhejiang University (CN), University of California, Davis (US)
National Natural Science Foundation of China, China Postdoctoral Science Foundation
Good health and well-being
Openalex Percentile: Top 19%
Cancer Genomics and Diagnostics
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