Evidence map›Paper›PMID 41883970›Full record

ArticleFrontiers in oncology2026

From complex algorithms to clinical practice: a multicenter machine learning model and simplified decision tree for predicting cachexia risk in gastric cancer.

Jian Zhao, Yu Deng, Yajie Guo, Yaoyao Wu, Xiaozhou Yang, Tengyu Zeng, Yihuan Qiao, Huadong Zhao, Jiawei Song, Beilei Hou and 1 more

Abstract read
In one paragraph

Article in Frontiers in oncology, 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

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

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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

11 authors.

Jian Zhao *Department of Endocrinology, No 908th Hospital of Chinese PLA Joint Logistic Support Force, Nanchang, China.
Yu Deng *Department of Endocrinology, No 908th Hospital of Chinese PLA Joint Logistic Support Force, Nanchang, China.
Yajie Guo *Department of Digestive Surgery, Xijing Hospital of Digestive Diseases, Fourth Military Medical University, Xi'an, China.
Yaoyao WuDepartment of Endocrinology, No 908th Hospital of Chinese PLA Joint Logistic Support Force, Nanchang, China.
Xiaozhou YangDepartment of General Surgery, Tangdu Hospital, Air Force Medical University, Xi'an, China.
Tengyu ZengDepartment of General Surgery, No 908th Hospital of Chinese PLA Joint Logistic Support Force, Nanchang, China.
Yihuan QiaoDepartment of Digestive Surgery, Xijing Hospital of Digestive Diseases, Fourth Military Medical University, Xi'an, China.
Huadong ZhaoDepartment of General Surgery, Tangdu Hospital, Air Force Medical University, Xi'an, China.
Jiawei SongDepartment of Digestive Surgery, Xijing Hospital of Digestive Diseases, Fourth Military Medical University, Xi'an, China.
Beilei HouDepartment of Endocrinology, No 908th Hospital of Chinese PLA Joint Logistic Support Force, Nanchang, China.
Qianyong YangDepartment of Endocrinology, No 908th Hospital of Chinese PLA Joint Logistic Support Force, Nanchang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Cachexia is a frequent, specific metabolic syndrome that severely compromises survival in gastric cancer (GC). While early diagnosis is paramount, existing screening methods are limited by complexity and suboptimal accuracy. There is an urgent need for an efficient, data-driven tool derived from routine clinical parameters. Methods: In this multicenter retrospective study, we analyzed data from three independent hospitals. Variable selection was performed using univariable and multivariable analyses. We constructed and compared multiple machine learning (ML) models to predict cachexia risk. The models' discriminative ability, calibration, and clinical net benefit were comprehensively evaluated via AUC, calibration plots, and Decision Curve Analysis (DCA). Results: The study included 1,570 GC patients (cachexia prevalence: 30.3%). Patients were divided into training (n=920), internal testing (n=350), and external validation (n=300) cohorts. Cachexia was significantly associated with poor nutritional status, elevated inflammation, and inferior overall survival (P < 0.01). The Random Forest (RF) model yielded the best performance, maintaining excellent stability across the internal test set (AUC = 0.898) and external validation set (AUC = 0.913). To enhance clinical utility, we further derived a simplified decision tree model based on three accessible markers: CA19-9, CEA, and albumin. This simplified tool retained high diagnostic accuracy (AUC > 0.783) and demonstrated significant positive net benefits in DCA. Conclusion: We successfully established and externally validated a high-performance ML model for predicting GC-associated cachexia. Crucially, the derived simplified decision tree offers a convenient, highly generalizable tool for clinicians to identify high-risk patients using routine laboratory tests, enabling earlier precision nutritional management.

Indexed as

cachexiadecision treeexternal validationgastric cancermachine learningnutritional assessmentprediction model

Identifiers

PMID41883970
PMCPMC13008652

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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.