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Early screening, diagnosis and recurrence monitoring of hepatocellular carcinoma in patients with chronic hepatitis B based on serum N-glycomics analysis: A cohort study.

Hepatology (Baltimore, Md.) 2026 Vol.83(1) p. 40-56

Su R, Tao X, Yan L, Liu Y, Chen CC, Li P, Li J, Miao J, Liu F, Kuai W, Hou J, Liu M, Mi Y, Xu L

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[BACKGROUND AND AIMS] HCC poses a significant global health burden, with HBV being the predominant etiology in China.

🔬 핵심 임상 통계 (초록에서 자동 추출 — 원문 검증 권장)
  • 표본수 (n) 12
  • 95% CI 0.930-1.000

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BibTeX ↓ RIS ↓
APA Su R, Tao X, et al. (2026). Early screening, diagnosis and recurrence monitoring of hepatocellular carcinoma in patients with chronic hepatitis B based on serum N-glycomics analysis: A cohort study.. Hepatology (Baltimore, Md.), 83(1), 40-56. https://doi.org/10.1097/HEP.0000000000001316
MLA Su R, et al.. "Early screening, diagnosis and recurrence monitoring of hepatocellular carcinoma in patients with chronic hepatitis B based on serum N-glycomics analysis: A cohort study.." Hepatology (Baltimore, Md.), vol. 83, no. 1, 2026, pp. 40-56.
PMID 40117651

Abstract

[BACKGROUND AND AIMS] HCC poses a significant global health burden, with HBV being the predominant etiology in China. However, current diagnostic markers lack the requisite sensitivity and specificity. This study aims to develop and validate serum N-glycomics-based models for the diagnosis and prognosis of HCC in patients with chronic hepatitis B-related cirrhosis.

[APPROACH AND RESULTS] This study enrolled a total of 397 patients with chronic hepatitis B-related cirrhosis and HCC for clinical management. N-glycomics profiling was conducted on all participants, and clinical data were collected. First, machine learning-based models, Hepatocellular Carcinoma Glycomics Random Forest model and Hepatocellular Carcinoma Glycomics Support Vector Machine model, were established for early screening and diagnosis of HCC using N-glycomics. The AUC values in the validation set were 0.967 (95% CI: 0.930-1.000) and 0.908 (0.840-0.976) for Hepatocellular Carcinoma Glycomics Random Forest model and Hepatocellular Carcinoma Glycomics Support Vector Machine model, respectively, outperforming AFP (0.687 [0.575-0.765]) and Protein Induced by Vitamin K Absence or Antagonist-II (PIVKA-II) (0.665 [0.507-0.823]). It also showed superiority in subgroup analysis and external validation. Calibration and decision curve analysis also showed good predictive performance. Additionally, we developed a prognostic model, the prog-G model, based on N-glycans to monitor recurrence in patients with HCC after curative treatment. During the follow-up period, it was observed that this model correlated with the clinical condition of the patients and could identify all recurrent HCC cases (n=12) prior to imaging findings, outperforming AFP (n=7) and PIVKA-II (n=9), while also detecting recurrent lesions earlier than imaging.

[CONCLUSIONS] N-glycomics models can effectively predict the occurrence and recurrence of HCC to improving the efficiency of clinical decision-making and promoting the precision treatment of HCC.

MeSH Terms

Humans; Carcinoma, Hepatocellular; Liver Neoplasms; Hepatitis B, Chronic; Male; Female; Middle Aged; Glycomics; Early Detection of Cancer; Neoplasm Recurrence, Local; Adult; Liver Cirrhosis; Cohort Studies; Prognosis; Biomarkers, Tumor; Support Vector Machine; alpha-Fetoproteins; China; Protein Precursors; Prothrombin; Biomarkers

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