ArticleClinical hemorheology and microcirculation2025
The value of clinical indicators combined with imaging tumor burden score in predicting microvascular invasion of hepatocellular carcinoma.
Article in Clinical hemorheology and microcirculation, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 1 paper.
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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.
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Who cites it
1 citing paper in PubMed.
- Protein Induced by Vitamin K Absence or Antagonist II in Primary Liver Cancer: Basic Research Insights and Clinical Applications.Journal of clinical and translational hepatology · 2025Review
Corrections and comments
- Retraction · 2025-11-23Compromised Peer Review · Concerns/Issues about Referencing/Attributions · Concerns/Issues about Third Party Involvement · Investigation by Journal/Publisher ·
- Retracted
Authors and funding
8 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
objectiveTo explore the value of a new clinical prediction model combined serological indicators and tumor burden score (TBS) in predicting microvascular invasion (MVI) in hepatocellular carcinoma (HCC) patients.
methodsThis study retrospectively analyzed a total of 605 patients who underwent liver tumor resection at our hospital from January 2021 to December 2023. The required clinical data before surgery were collected from the electronic medical record system. All patients were randomly divided into a training group and a validation group according to the ratio of 7 : 3. Univariate and multivariate analyses were conducted to identify factors associated with MVI. Based on the combined factors, a nomogram for predicting MVI was constructed and its diagnostic performance was evaluated.
resultsThere were 123 (20.3%) female patients and 482 (79.7%) male patients were enrolled, with an average age of 59 years. There were 182 (30.1%) patients with positive MVI and 423 (69.9%) patients with negative MVI. On multivariate logistic analysis, prealbumin (0.993 [0.986, 1.000]), AFP (0.993 [0.987, 1.000]), PIVKA-II (1.000 [1.000, 1.000]) were independently associated with MVI. The nomogram constructed based on the aforementioned variables and TBS exhibited area under the curve (AUC) of 0.804 and 0.742 in the training group and a validation group, respectively. The calibration curves in both training group and a validation group showed good fit, and the decision curve analysis revealed a net benefit across a wide range of threshold probabilities.
conclusionsThe newly developed nomogram was an independent biomarker for predict MVI, which might take precision medicine one step further.
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