Evidence map›Paper›PMID 42819146›Full record

ArticleFrontiers in pharmacology2026

GDF15-integrated blood biomarker panel for risk stratification of digestive malignancies: a multicenter retrospective study.

Ranliang Cui, Yue Cao, Yueguo Li

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

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Ranliang Cui *Department of Laboratory, Tianjin Medical University Cancer Institute & Hospital, National Clinical Research Center for Cancer, Tianjin Key Laboratory of Digestive Cancer, State Key Laboratory of Druggability Evaluation and Systematic Translational Medicine, Tianjin's Clinical Research Center for Cancer, Tianjin, China.
Yue Cao *Department of Laboratory, Tianjin First Central Hospital, School of Medicine, Nankai University, Tianjin, China.
Yueguo LiDepartment of Laboratory, Tianjin Medical University Cancer Institute & Hospital, National Clinical Research Center for Cancer, Tianjin Key Laboratory of Digestive Cancer, State Key Laboratory of Druggability Evaluation and Systematic Translational Medicine, Tianjin's Clinical Research Center for Cancer, Tianjin, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Digestive malignancies remain a major cause of cancer-related mortality worldwide. Current diagnostic approaches are often limited by invasiveness, cost, and accessibility. We aimed to develop a blood-based risk stratification model for identifying individuals at increased risk of digestive malignancies. Methods: We retrospectively collected clinical data from 667 patients with digestive malignancies and 795 non-cancer controls. A machine learning model was developed by integrating GDF15 with selected routine blood biomarkers. Model performance was evaluated using measures of discrimination, risk reclassification, and SHAP analysis. Blood GDF15 levels were measured by chemiluminescent immunoassay, and tissue expression was assessed by immunohistochemistry. Results: The GDF15-based machine learning model showed favourable performance in the independent validation cohort (AUROC = 0.886). Compared with conventional tumor markers alone, the addition of GDF15 improved model discrimination (AUROC, 0.856 vs. 0.777; Conclusion: Integrating GDF15 with routine blood biomarkers enables effective risk stratification of individuals at increased risk of digestive malignancies. This blood-based model may provide a practical approach for risk stratification and help identify individuals who may benefit from further diagnostic evaluation.

Indexed as

blood-based risk stratificationblood biomarkersdigestive malignanciesGDF15machine learning

Identifiers

PMID42819146
PMCPMC13623688

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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.