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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.
Afiliação
  • Sagar VM; Institute of Immunology and Immunotherapy, University of Birmingham, Birmingham, UK.
  • Herring K; These authors contributed equally to this work (joint first authors).
  • Curbishley S; The Cancer Centre, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
  • Hodson J; These authors contributed equally to this work (joint first authors).
  • Fletcher P; Institute of Immunology and Immunotherapy, University of Birmingham, Birmingham, UK.
  • Karkhanis S; Institute of Translational Medicine, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
  • Mehrzad H; Cancer Research UK Clinical Trials Unit, University of Birmingham, Birmingham, UK.
  • Punia P; Department of Radiology, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
  • Shah T; Department of Radiology, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
  • Shetty S; The Cancer Centre, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
  • Ma YT; The Liver Unit, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
Oncotarget ; 12(24): 2338-2350, 2021 Nov 23.
Article em En | MEDLINE | ID: mdl-34853657
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.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Ano de publicação: 2021 Tipo de documento: Article