Evidence map›Paper›PMID 41840268›Full record

ArticleThe Kaohsiung journal of medical sciences2026

Construction of a Non-Invasive Predictive Model Based on PIVKA-II Combined With MRI Imaging Features for Evaluating Microvascular Invasion in Hepatocellular Carcinoma.

Di Gao, Rui-Qi Jin, Hong-Wei Wang

Abstract read
In one paragraph

Article in The Kaohsiung journal of medical sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Di GaoDepartment of Radiology, Harbin Medical University Cancer Hospital, Harbin, Heilongjiang, China.
Rui-Qi JinDepartment of Radiology, Harbin Medical University Cancer Hospital, Harbin, Heilongjiang, China.
Hong-Wei WangDepartment of Radiology, Harbin Medical University Cancer Hospital, Harbin, Heilongjiang, China.ORCID https://orcid.org/0009-0006-7739-7474

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study developed a non-invasive model using PIVKA-II and MRI features to predict microvascular invasion in hepatocellular carcinoma, providing a reliable tool for early risk assessment and personalized treatment planning. The study included 98 patients with pathologically confirmed HCC (Child-Pugh A, BCLC stage A), comprising 43 MVI-positive and 55 MVI-negative cases. Baseline clinical characteristics and MRI features were collected. Univariate analysis identified candidate variables associated with MVI, which were subsequently included in multivariate logistic regression analysis to identify independent influencing factors. A nomogram prediction model was developed based on the independent factors. The model's diagnostic performance, calibration, and clinical applicability were evaluated. The diagnostic value of PIVKA-II alone for MVI was analyzed. The MVI-positive group showed significantly higher alpha-fetoprotein ≥ 400 ng/mL, PIVKA-II levels, and aspartate aminotransferase levels. ROC curve analysis showed that PIVKA-II alone had an AUC of 0.682 for diagnosing MVI, with a maximum Youden's index of 33.57, a cut-off value of 741.5 mAU/mL, 37.21% sensitivity, 96.36% specificity. Tumor diameter, peritumoral abnormal enhancement, intratumoral arteries, and mean tumor ADC value showed significant differences between the two groups. Elevated PIVKA-II, intratumoral arteries, and mean tumor ADC value were independent influencing factors for MVI in HCC. A nomogram incorporating these factors achieved an AUC of 0.81, outperforming PIVKA-II alone. The model demonstrated good calibration and clinical utility. The non-invasive predictive nomogram constructed by combining PIVKA-II with MRI features demonstrates good predictive value and clinical applicability for assessing MVI in HCC patients. [Correction added on 25 March 2026, after first online publication: In the sentence "A nomogram incorporating these factors achieved......." the value "0.85" is changed to "0.81" in this version.].

Indexed as

BiomarkersCarcinoma, HepatocellularLiver NeoplasmsMagnetic Resonance ImagingMicrovesselsProtein PrecursorsProthrombinAdultAgedalpha-FetoproteinsFemaleHumansMaleMiddle AgedNeoplasm InvasivenessNomogramsacarboxyprothrombinalpha-FetoproteinsBiomarkersProtein PrecursorsProthrombinhepatocellular carcinomamagnetic resonance imagingmicrovascular invasionnon‐invasive prediction modelprothrombin induced by vitamin K absence or antagonist‐II (PIVKA‐II)

Identifiers

PMID41840268
PMCPMC13399812

What Socratic holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.