Serial increase and high alpha-fetoprotein levels predict the development of hepatocellular carcinoma in 6 months.

AFP biomarker liver cancer prediction surveillance

Journal

Hepatology research : the official journal of the Japan Society of Hepatology
ISSN: 1386-6346
Titre abrégé: Hepatol Res
Pays: Netherlands
ID NLM: 9711801

Informations de publication

Date de publication:
Oct 2023
Historique:
revised: 23 05 2023
received: 31 01 2023
accepted: 05 06 2023
medline: 9 6 2023
pubmed: 9 6 2023
entrez: 8 6 2023
Statut: ppublish

Résumé

Alpha-fetoprotein (AFP) checkup with abdominal ultrasonography for hepatocellular carcinoma (HCC) surveillance remains controversial. We evaluated a serial AFP-increase and high AFP levels in the prediction of HCC. At-risk patients with chronic liver disease underwent HCC surveillance with trimonthly AFP measurement were included and categorized into HCC and non-HCC groups. Their AFP levels at 12, 9, and 6 months (-6M) before the outcome date were evaluated. Group-based trajectory analysis and multivariable regression analysis were performed to identify AFP trajectories as risk predictors for HCC. Overall, 2776 patients were included in the HCC (n = 326) and non-HCC (n = 2450) groups. Serial AFP levels were significantly higher in the HCC than the non-HCC groups. Trajectory analysis identified AFP-increase group (11%) increased 24-fold risks of HCC compared with the AFP-stable (89%) group. Compared with patients without the AFP-increase, a serial 3-month AFP-increase ≥10% elevated HCC risk by 12.1-fold (95% CI: 6.5-22.4) in 6 months, and the HCC risks increased 13-60 fold in patients with cirrhosis, hepatitis B, or C receiving antiviral therapy, or AFP levels <20 ng/ml. Combining serial AFP-increase ≥10% and AFP ≥20 ng/ml at -6M significantly increased 41.7-fold (95% CI: 13.8-126.2) HCC risks. In patients who underwent biannual AFP checkups, those with both 6-month AFP-increase ≥10% and AFP ≥20 ng/ml increased 22.1-fold (95% CI: 12.52-39.16) HCC risks in 6 months. Most HCCs were detected at an early stage. Serial 3-6-month AFP-increase of ≥10% previously and AFP level of ≥20 ng/ml significantly increased HCC risks in 6 months.

Identifiants

pubmed: 37291079
doi: 10.1111/hepr.13932
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1021-1030

Subventions

Organisme : National Taiwan University Hospital
Organisme : Liver Disease Prevention & Treatment Research Foundation, Taiwan
Organisme : Ministry of Science and Technology, Taiwan
Organisme : Ministry of Health and Welfare

Informations de copyright

© 2023 Japan Society of Hepatology.

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Auteurs

Tung-Hung Su (TH)

Department of Internal Medicine, Division of Gastroenterology and Hepatology, National Taiwan University Hospital, Taipei, Taiwan.
Hepatitis Research Center, National Taiwan University Hospital, Taipei, Taiwan.

Shan-Han Chang (SH)

Department of Internal Medicine, Division of Gastroenterology and Hepatology, National Taiwan University Hospital Yunlin Branch, Yunlin County, Taiwan.

Chi-Ling Chen (CL)

Graduate Institute of Clinical Medicine, National Taiwan University College of Medicine, Taipei, Taiwan.

Sih-Han Liao (SH)

Department of Medicine, Section of Gastroenterology, National Taiwan University Cancer Center, Taipei, Taiwan.

Tai-Chung Tseng (TC)

Hepatitis Research Center, National Taiwan University Hospital, Taipei, Taiwan.
Department of Medical Research, National Taiwan University Hospital, Taipei, Taiwan.

Shih-Jer Hsu (SJ)

Department of Internal Medicine, Division of Gastroenterology and Hepatology, National Taiwan University Hospital, Taipei, Taiwan.
Hepatitis Research Center, National Taiwan University Hospital, Taipei, Taiwan.

Chun-Ming Hong (CM)

Department of Internal Medicine, Division of Hospital Medicine, National Taiwan University Hospital, Taipei, Taiwan.

Chen-Hua Liu (CH)

Department of Internal Medicine, Division of Gastroenterology and Hepatology, National Taiwan University Hospital, Taipei, Taiwan.
Hepatitis Research Center, National Taiwan University Hospital, Taipei, Taiwan.

Hung-Chih Yang (HC)

Department of Internal Medicine, Division of Gastroenterology and Hepatology, National Taiwan University Hospital, Taipei, Taiwan.

Chun-Jen Liu (CJ)

Department of Internal Medicine, Division of Gastroenterology and Hepatology, National Taiwan University Hospital, Taipei, Taiwan.
Hepatitis Research Center, National Taiwan University Hospital, Taipei, Taiwan.

Pei-Jer Chen (PJ)

Department of Internal Medicine, Division of Gastroenterology and Hepatology, National Taiwan University Hospital, Taipei, Taiwan.
Hepatitis Research Center, National Taiwan University Hospital, Taipei, Taiwan.
Graduate Institute of Clinical Medicine, National Taiwan University College of Medicine, Taipei, Taiwan.
Department of Medicine, Section of Gastroenterology, National Taiwan University Cancer Center, Taipei, Taiwan.

Jia-Horng Kao (JH)

Department of Internal Medicine, Division of Gastroenterology and Hepatology, National Taiwan University Hospital, Taipei, Taiwan.
Hepatitis Research Center, National Taiwan University Hospital, Taipei, Taiwan.
Graduate Institute of Clinical Medicine, National Taiwan University College of Medicine, Taipei, Taiwan.
Department of Medicine, Section of Gastroenterology, National Taiwan University Cancer Center, Taipei, Taiwan.

Classifications MeSH