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PIVKA-II作为肝细胞癌治疗反应生物标志物的潜力:一项英国前瞻性队列研究。

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

作者信息

Sagar Vandana M, Herring Kathyrn, Curbishley Stuart, Hodson James, Fletcher Peter, Karkhanis Salil, Mehrzad Homoyon, Punia Pankaj, Shah Tahir, Shetty Shishir, Ma Yuk Ting

机构信息

Institute of Immunology and Immunotherapy, University of Birmingham, Birmingham, UK.

These authors contributed equally to this work (joint first authors).

出版信息

Oncotarget. 2021 Nov 23;12(24):2338-2350. doi: 10.18632/oncotarget.28136.


DOI:10.18632/oncotarget.28136
PMID:34853657
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8629402/
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.

摘要

维生素K缺乏诱导蛋白II(PIVKA-II)最近在国际上被确认为肝细胞癌(HCC)的一种诊断生物标志物,是GALAD模型的一部分。然而,其作为治疗反应生物标志物的作用尚未得到充分研究。因此,我们在英国一家三级中心进行了一项前瞻性研究,以评估PIVKA-II作为早期、中期和晚期HCC患者治疗反应生物标志物的作用。在一个由141名患者组成的队列中,我们发现,在一系列不同的治疗方式中,大多数患者的PIVKA-II水平与治疗反应呈一致变化。我们还发现,PIVKA-II水平升高几乎总是先于影像学进展。在甲胎蛋白(AFP)非分泌者中,60%的病例中PIVKA-II具有参考价值。在一小群接受肝移植的患者中,移植前的PIVKA-II水平可预测微血管侵犯和较差的分化程度。我们的结果表明,在西方人群中,PIVKA-II作为治疗反应生物标志物以及预测微血管侵犯具有潜在效用。PIVKA-II的表现优于AFP,但作为单一生物标志物,其性能仍然有限。建议开展进一步的大型前瞻性研究,在GALAD模型中评估PIVKA-II作为治疗反应生物标志物的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38c4/8629402/ffe6852dfc8e/oncotarget-12-2338-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38c4/8629402/8a9ee0e5e72e/oncotarget-12-2338-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38c4/8629402/205009291d2e/oncotarget-12-2338-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38c4/8629402/99ce4e4ce4e4/oncotarget-12-2338-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38c4/8629402/c4cbda3a8650/oncotarget-12-2338-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38c4/8629402/ffe6852dfc8e/oncotarget-12-2338-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38c4/8629402/8a9ee0e5e72e/oncotarget-12-2338-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38c4/8629402/205009291d2e/oncotarget-12-2338-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38c4/8629402/99ce4e4ce4e4/oncotarget-12-2338-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38c4/8629402/c4cbda3a8650/oncotarget-12-2338-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38c4/8629402/ffe6852dfc8e/oncotarget-12-2338-g005.jpg

相似文献

[1]
The potential of PIVKA-II as a treatment response biomarker in hepatocellular carcinoma: a prospective United Kingdom cohort study.

Oncotarget. 2021-11-23

[2]
PIVKA-II serves as a potential biomarker that complements AFP for the diagnosis of hepatocellular carcinoma.

BMC Cancer. 2021-4-13

[3]
Utility of combining PIVKA-II and AFP in the surveillance and monitoring of hepatocellular carcinoma in the Asia-Pacific region.

Clin Mol Hepatol. 2023-4

[4]
Diagnostic and prognostic performances of GALAD score in staging and 1-year mortality of hepatocellular carcinoma: A prospective study.

World J Gastroenterol. 2024-5-7

[5]
Alpha-fetoprotein, protein induced by vitamin K absence or antagonist-II, lens culinaris agglutinin-reactive fraction of alpha-fetoprotein alone and in combination for early detection of hepatocellular carcinoma from nonalcoholic fatty liver disease: A multicenter analysis.

Hepatobiliary Pancreat Dis Int. 2022-12

[6]
PIVKA-II as a surrogate biomarker for therapeutic response in Non-AFP-secreting hepatocellular carcinoma.

BMC Cancer. 2025-2-4

[7]
Diagnostic value of serum PIVKA-II levels for BCLC early hepatocellular carcinoma and correlation with HBV DNA.

Cancer Biomark. 2018

[8]
Performance of PIVKA-II for early hepatocellular carcinoma diagnosis and prediction of microvascular invasion.

J Hepatol. 2014-11-11

[9]
Diagnostic value of prothrombin induced by the absence of vitamin K or antagonist-II (PIVKA-II) for early stage HBV related hepatocellular carcinoma.

Infect Agent Cancer. 2017-8-23

[10]
Diagnostic value of gamma-glutamyltransferase/aspartate aminotransferase ratio, protein induced by vitamin K absence or antagonist II, and alpha-fetoprotein in hepatitis B virus-related hepatocellular carcinoma.

World J Gastroenterol. 2019-9-28

引用本文的文献

[1]
Prediction of the efficacy of first transarterial chemoembolization for advanced hepatocellular carcinoma a clinical-radiomics model.

World J Clin Cases. 2025-8-16

[2]
PIVKA-II as a surrogate biomarker for therapeutic response in Non-AFP-secreting hepatocellular carcinoma.

BMC Cancer. 2025-2-4

[3]
Prognostic Role of Serum Vascular Endothelial Growth Factor and Hepatocyte Growth Factor Post Stereotactic Body Radiation in Advanced Hepatocellular Carcinoma.

J Clin Exp Hepatol. 2025

[4]
Biological variation of PIVKA-II in blood serum of healthy subjects measured by automated electrochemiluminescent assay.

Pract Lab Med. 2024-3-19

[5]
The GALAD score and the BALAD-2 score correlate with transarterial and systemic treatment response and survival in patients with hepatocellular carcinoma.

J Cancer Res Clin Oncol. 2024-2-6

[6]
Preoperative assessment of microvascular invasion risk using gadoxetate-enhanced MRI for predicting outcomes after liver transplantation for single hepatocellular carcinoma within the Milan criteria.

Eur Radiol. 2024-1

[7]
Updating the Clinical Application of Blood Biomarkers and Their Algorithms in the Diagnosis and Surveillance of Hepatocellular Carcinoma: A Critical Review.

Int J Mol Sci. 2023-2-21

[8]
PIVKA-II or AFP has better diagnostic properties for hepatocellular carcinoma diagnosis in high-risk patients.

J Circ Biomark. 2023-2-17

本文引用的文献

[1]
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CA Cancer J Clin. 2021-5

[2]
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Am J Clin Oncol. 2020-11

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J Hepatol. 2020-11

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Clin Chim Acta. 2020-10

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Protein induced by vitamin K absence or antagonist-II versus alpha-fetoprotein in the diagnosis of hepatocellular carcinoma: A systematic review with meta-analysis.

Hepatobiliary Pancreat Dis Int. 2018-9-15

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Chirurgia (Bucur). 2018

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Serum ARCHITECT PIVKA-II reference interval in healthy Chinese adults: Sub-analysis from a prospective multicenter study.

Clin Biochem. 2018-4

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