Protein Induced by Vitamin K Absence or Antagonist-II Versus Alpha-Fetoprotein in the Diagnosis of Hepatocellular Carcinoma: A Systematic Review With Meta-Analysis.

Alpha-fetoprotein Hepatitis B virus Hepatitis C virus Hepatocellular carcinoma Vitamin K absence or antagonist-II

Journal

Journal of clinical medicine research
ISSN: 1918-3003
Titre abrégé: J Clin Med Res
Pays: Canada
ID NLM: 101538301

Informations de publication

Date de publication:
Jul 2023
Historique:
received: 13 05 2023
accepted: 09 06 2023
medline: 14 8 2023
pubmed: 14 8 2023
entrez: 14 8 2023
Statut: ppublish

Résumé

Protein induced by vitamin K absence or antagonist-II (PIVKA-II) and α-fetoprotein (AFP) are promising tumor markers for the diagnosis of hepatocellular carcinoma (HCC). Yet, their diagnostic performance differs throughout HCC investigations. The aim of this meta-analysis was to assess the effectiveness of PIVKA-II and AFP in the diagnosis of HCC. A systematic literature search was performed to identify relevant studies from eight databases, which were published up to February 2023, in order to compare the diagnostic performance of PIVKA-II and AFP for HCC. Pooled sensitivity and specificity were calculated. Summary receiver operating characteristic (SROC) curve was performed to assess the diagnostic accuracy of each biomarker. Fifty-three studies were identified. The pooled sensitivity (95% confidence interval (CI)) of PIVKA-II and AFP was 0.71 (0.70 - 0.72) and 0.64 (0.63 - 0.65), respectively in diagnosis of HCC, and the corresponding pooled specificity (95% CI) was 0.90 (0.89 - 0.90) and 0.87 (0.87 - 0.88), respectively. The area under the ROC curve (AUC) of PIVKA-II and AFP was 0.89 (0.88 - 0.90) and 0.78 (0.77 - 0.79), respectively. Subgroup analysis demonstrated that PIVKA-II presented higher AUC values compared to AFP in terms of ethnic group (African, European, Asian, and American patients), etiology (mixed-type HCC, hepatitis C virus (HCV)-related, and hepatitis B virus (HBV)-related) and sample size of cases (≤ 100 and > 100). This study reveals that PIVKA-II is a promising biomarker for identifying and tracking HCC, exhibiting greater accuracy than AFP. Our findings indicate that PIVKA-II outperforms AFP in detecting HCC across diverse racial groups and sample sizes, as well as in cases of HBV-related, HCV-related, or mixed-etiology HCC.

Sections du résumé

Background UNASSIGNED
Protein induced by vitamin K absence or antagonist-II (PIVKA-II) and α-fetoprotein (AFP) are promising tumor markers for the diagnosis of hepatocellular carcinoma (HCC). Yet, their diagnostic performance differs throughout HCC investigations. The aim of this meta-analysis was to assess the effectiveness of PIVKA-II and AFP in the diagnosis of HCC.
Methods UNASSIGNED
A systematic literature search was performed to identify relevant studies from eight databases, which were published up to February 2023, in order to compare the diagnostic performance of PIVKA-II and AFP for HCC. Pooled sensitivity and specificity were calculated. Summary receiver operating characteristic (SROC) curve was performed to assess the diagnostic accuracy of each biomarker.
Results UNASSIGNED
Fifty-three studies were identified. The pooled sensitivity (95% confidence interval (CI)) of PIVKA-II and AFP was 0.71 (0.70 - 0.72) and 0.64 (0.63 - 0.65), respectively in diagnosis of HCC, and the corresponding pooled specificity (95% CI) was 0.90 (0.89 - 0.90) and 0.87 (0.87 - 0.88), respectively. The area under the ROC curve (AUC) of PIVKA-II and AFP was 0.89 (0.88 - 0.90) and 0.78 (0.77 - 0.79), respectively. Subgroup analysis demonstrated that PIVKA-II presented higher AUC values compared to AFP in terms of ethnic group (African, European, Asian, and American patients), etiology (mixed-type HCC, hepatitis C virus (HCV)-related, and hepatitis B virus (HBV)-related) and sample size of cases (≤ 100 and > 100).
Conclusion UNASSIGNED
This study reveals that PIVKA-II is a promising biomarker for identifying and tracking HCC, exhibiting greater accuracy than AFP. Our findings indicate that PIVKA-II outperforms AFP in detecting HCC across diverse racial groups and sample sizes, as well as in cases of HBV-related, HCV-related, or mixed-etiology HCC.

Identifiants

pubmed: 37575350
doi: 10.14740/jocmr4951
pmc: PMC10416192
doi:

Banques de données

Dryad
['10.5061/dryad.3n901']

Types de publication

Journal Article

Langues

eng

Pagination

343-359

Informations de copyright

Copyright 2023, Kobeissy et al.

Déclaration de conflit d'intérêts

All other authors have no conflict of interest to disclose.

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Auteurs

Abdallah Kobeissy (A)

Department of Gastroenterology, The University of Toledo, Toledo, OH, USA.

Nooraldin Merza (N)

Department of Internal Medicine, The University of Toledo, Toledo, OH, USA.

Alsadiq Al-Hillan (A)

Gastroenterology Department, Corewell Health/Willam Beaumont University Hospital, Royal Oak, MI, USA.

Safa Boujemaa (S)

Biotechnology Development, Institute Pasteur De Tunis, Universite De Tunis El Manar, Tunis, Tunisia.

Zohaib Ahmed (Z)

Department of Internal Medicine, The University of Toledo, Toledo, OH, USA.

Mohamad Nawras (M)

The University of Toledo, College of Medicine and Life Sciences, Toledo, OH, USA.

Mohammed Albaaj (M)

Department of Pharmacology and Experimental Therapeutics, University of Toledo, Toledo, OH, USA.

Dushyant Singh Dahiya (DS)

Division of Gastroenterology, University of Kansas School of Medicine, Kansas City, KS, USA.

Yaseen Alastal (Y)

Department of Gastroenterology, The University of Toledo, Toledo, OH, USA.

Mona Hassan (M)

Department of Gastroenterology, The University of Toledo, Toledo, OH, USA.

Classifications MeSH