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The potential of PIVKA-II as a treatment response biomarker in hepatocellular carcinoma: a prospective United Kingdom cohort study

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 pro...

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Autores principales: Sagar, Vandana M., Herring, Kathyrn, Curbishley, Stuart, Hodson, James, Fletcher, Peter, Karkhanis, Salil, Mehrzad, Homoyon, Punia, Pankaj, Shah, Tahir, Shetty, Shishir, Ma, Yuk Ting
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8629402/
https://www.ncbi.nlm.nih.gov/pubmed/34853657
http://dx.doi.org/10.18632/oncotarget.28136
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author Sagar, Vandana M.
Herring, Kathyrn
Curbishley, Stuart
Hodson, James
Fletcher, Peter
Karkhanis, Salil
Mehrzad, Homoyon
Punia, Pankaj
Shah, Tahir
Shetty, Shishir
Ma, Yuk Ting
author_facet Sagar, Vandana M.
Herring, Kathyrn
Curbishley, Stuart
Hodson, James
Fletcher, Peter
Karkhanis, Salil
Mehrzad, Homoyon
Punia, Pankaj
Shah, Tahir
Shetty, Shishir
Ma, Yuk Ting
author_sort Sagar, Vandana M.
collection PubMed
description 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.
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spelling pubmed-86294022021-11-30 The potential of PIVKA-II as a treatment response biomarker in hepatocellular carcinoma: a prospective United Kingdom cohort study Sagar, Vandana M. Herring, Kathyrn Curbishley, Stuart Hodson, James Fletcher, Peter Karkhanis, Salil Mehrzad, Homoyon Punia, Pankaj Shah, Tahir Shetty, Shishir Ma, Yuk Ting Oncotarget Research Paper 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. Impact Journals LLC 2021-11-23 /pmc/articles/PMC8629402/ /pubmed/34853657 http://dx.doi.org/10.18632/oncotarget.28136 Text en Copyright: © 2021 Sagar et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Sagar, Vandana M.
Herring, Kathyrn
Curbishley, Stuart
Hodson, James
Fletcher, Peter
Karkhanis, Salil
Mehrzad, Homoyon
Punia, Pankaj
Shah, Tahir
Shetty, Shishir
Ma, Yuk Ting
The potential of PIVKA-II as a treatment response biomarker in hepatocellular carcinoma: a prospective United Kingdom cohort study
title The potential of PIVKA-II as a treatment response biomarker in hepatocellular carcinoma: a prospective United Kingdom cohort study
title_full The potential of PIVKA-II as a treatment response biomarker in hepatocellular carcinoma: a prospective United Kingdom cohort study
title_fullStr The potential of PIVKA-II as a treatment response biomarker in hepatocellular carcinoma: a prospective United Kingdom cohort study
title_full_unstemmed The potential of PIVKA-II as a treatment response biomarker in hepatocellular carcinoma: a prospective United Kingdom cohort study
title_short The potential of PIVKA-II as a treatment response biomarker in hepatocellular carcinoma: a prospective United Kingdom cohort study
title_sort potential of pivka-ii as a treatment response biomarker in hepatocellular carcinoma: a prospective united kingdom cohort study
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8629402/
https://www.ncbi.nlm.nih.gov/pubmed/34853657
http://dx.doi.org/10.18632/oncotarget.28136
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