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The potential of PIVKA-II as a treatment response biomarker in hepatocellular carcinoma: a prospective United Kingdom cohort study.
- Source :
-
Oncotarget [Oncotarget] 2021 Nov 23; Vol. 12 (24), pp. 2338-2350. Date of Electronic Publication: 2021 Nov 23 (Print Publication: 2021). - Publication Year :
- 2021
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Abstract
- Prothrombin induced by vitamin K absence II (PIVKA-II) has recently been validated internationally as a diagnostic biomarker for hepatocellular carcinoma (HCC), as part of the GALAD model. However, its role as a treatment response biomarker has been less well explored. We, therefore, undertook a prospective study at a tertiary centre in the UK to evaluate the role of PIVKA-II as a treatment response biomarker in patients with early, intermediate and advanced stage HCC. In a cohort of 141 patients, we found that PIVKA-II levels tracked concordantly with treatment response in the majority of patients, across a range of different treatment modalities. We also found that rises in PIVKA-II levels almost always predated radiological progression. Among AFP non-secretors, PIVKA-II was found to be informative in 60% of cases. In a small cohort of patients undergoing liver transplantation, pre-transplant PIVKA-II levels predicted for microvascular invasion and poorer differentiation. Our results demonstrate the potential utility of PIVKA-II as a treatment response biomarker and in predicting microvascular invasion, in a Western population. PIVKA-II demonstrated improved performance over AFP but, as a single biomarker, its performance was still limited. Further larger prospective studies are recommended to evaluate PIVKA-II as a treatment response biomarker, within the GALAD model.<br />Competing Interests: CONFLICTS OF INTEREST PP reports consultancy fees from Bayer, Eisai, MSD and Roche. SS reports consultancy fees from Faron Pharmaceuticals. YTM reports consultancy fees from Astra Zeneca, Bayer, Eisai, Faron Pharmaceuticals, Ipsen and Roche. All potential conflicts of interests were outside of the submitted work. All other authors declare no competing interests.<br /> (Copyright: © 2021 Sagar et al.)
Details
- Language :
- English
- ISSN :
- 1949-2553
- Volume :
- 12
- Issue :
- 24
- Database :
- MEDLINE
- Journal :
- Oncotarget
- Publication Type :
- Academic Journal
- Accession number :
- 34853657
- Full Text :
- https://doi.org/10.18632/oncotarget.28136