Evidence map›Paper›PMID 35600083›Full record

ArticleEuropean journal of radiology open2022

Noninvasively predict the micro-vascular invasion and histopathological grade of hepatocellular carcinoma with CT-derived radiomics.

Xu Tong, Jing Li

Abstract read
In one paragraph

Article in European journal of radiology open, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

11 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  11. [Research progress in radiomics based on CT and MRI images for prediction of microvascular invasion in hepatocellular carcinoma].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2022
    Article
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

2 authors.

Xu TongDepartment of Radiotherapy, the Third Affiliated Hospital of Qiqihar Medical University, Qiqihar City, Heilongjiang Province, China.
Jing LiDepartment of Radiotherapy, the Third Affiliated Hospital of Qiqihar Medical University, Qiqihar City, Heilongjiang Province, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: This research aims to predict the micro-vascular invasion and histopathologic grade of hepatocellular carcinoma with the CT-derived radiomics. Methods: The clinical and image data of 82 patients were accessed from the TCGA-LIHC collection in The Cancer Imaging Archive. Then the radiomics features were extracted from the CT images. For obtaining the appropriate feature subset, the redundant features were removed by means of intra-class agreement analysis, the Student t test, LASSO-regression and support vector machine (SVM) Recursive feature elimination (SVM-RFE). Then several machine-learning-based classifiers including SVM and random forest (RF) were established. To accurately evaluate the tumor grade and MVI with the integration of the Radiomics and clinical insights, the nomogram-based clinical models were constructed. The diagnostic performance was evaluated with ROC analysis. Results: 7 and 10 radiomics features were selected via LASSO regression and SVM-RFE for identifying the tumor grade with regard to 13 and 10 features selected via LASSO regression and SVM-RFE for evaluating the MVI. The combination of the classifier-RF and the selection strategy of SVM-RFE yielded the best performance for grading HCC (AUC: 0.898). Differently, the combination of the classifier-RF and the selection strategy of LASSO regression resulted in the best performance for identifying MVI (AUC: 0.876). Finally, two nomograms were constructed with radiomics score (Rscore) and clinical risk factors, which showed excellent predictive value for both tumor grade (AUC: 0.928) and MVI (AUC: 0.945). Conclusion: CT-derived radiomics were valuable for noninvasively assessing the micro-vascular invasion and histopathologic grade of hepatocellular carcinoma.

Indexed as

CT-RadiomicsHepatocellular carcinomaMachine LearningPrognostic factors

Identifiers

PMID35600083
PMCPMC9120240

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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 OpenQuestion graph.