Evidence map›Paper›PMID 42666212›Full record

ArticleJournal of hepatocellular carcinoma2026

Individualized Risk Stratification for Early Recurrence of Hepatocellular Carcinoma: A Clinical Tool Derived from a Large-Scale (n=3084) Cohort Study.

Xuanyi Zhu, Yiteng Zhao, Muyan Li, Shugeng Zhang

Abstract read
In one paragraph

Article in Journal of hepatocellular carcinoma, 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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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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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

4 authors.

Xuanyi ZhuDepartment of Graduate School, Bengbu Medical University, Bengbu, Anhui Province, 233000, People's Republic of China.
Yiteng ZhaoDepartment of Graduate School, Bengbu Medical University, Bengbu, Anhui Province, 233000, People's Republic of China.ORCID 0009-0003-0493-7976
Muyan LiDepartment of Graduate School, Bengbu Medical University, Bengbu, Anhui Province, 233000, People's Republic of China.
Shugeng ZhangDepartment of Liver Transplantation, The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui, 230000, People's Republic of China.ORCID 0000-0001-9832-9784

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Early recurrence (typically within 2 years) following curative liver resection remains the primary obstacle to long-term survival in patients with hepatocellular carcinoma (HCC). Traditional linear staging systems frequently fail to capture the non-linear clinical and biological interactions driving early relapse. This study aimed to develop and validate a methodologically rigorous machine learning framework for precision post-hepatectomy risk stratification, and to deploy an interactive clinical tool. Patients and Methods: In this large-scale retrospective cohort study, we analyzed 3084 HCC patients who underwent curative resection. To strictly prevent data leakage and ensure generalizability, the cohort was partitioned into training (60%), validation (20%), and independent test (20%) sets prior to any preprocessing. Six ML algorithms were evaluated, and SHapley Additive exPlanations (SHAP) were employed to decode model transparency. A web-based calculator was subsequently deployed for clinical use. Results: XGBoost emerged as the optimal model, achieving an area under the curve (AUC) of 0.891 (95% CI: 0.865-0.915) on the independent test set, significantly outperforming traditional logistic regression (P < 0.0001). Using a rigorously optimized probability threshold of 0.310, the model yielded a sensitivity of 87.6% (95% CI: 83.5%-91.4%) and a specificity of 70.3% (95% CI: 65.4%-75.2%), with all confidence intervals derived from 2,000 bootstrap resamples. SHAP analysis identified tumor capsule integrity, neutrophil-to-eosinophil ratio (NER), and alpha-fetoprotein (AFP) as the most critical predictors of recurrence. Conclusion: This methodologically rigorous ML framework provides a highly sensitive, data-driven tool for individual risk stratification. By identifying high-risk patients, the web-based calculator can guide clinicians in implementing intensified postoperative surveillance and selecting candidates for targeted adjuvant interventions, ultimately improving oncological outcomes in HCC.

Indexed as

early predictionhepatocellular carcinomamachine learningprediction modelSHAP

Identifiers

PMID42666212
PMCPMC13521810

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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.