Evidence map›Paper›PMID 39211554›Full record

ArticleFrontiers in oncology2024

Preliminary study on DCE-MRI radiomics analysis for differentiation of HER2-low and HER2-zero breast cancer.

Liang Yin, Yun Zhang, Xi Wei, Zakari Shaibu, Lingling Xiang, Ting Wu, Qing Zhang, Rong Qin, Xiuhong Shan

Abstract read
In one paragraph

Article in Frontiers in oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

10 citing papers in PubMed.

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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

9 authors.

Liang YinDepartment of Breast Surgery, Jiangsu University Affiliated People's Hospital, Zhenjiang, China.
Yun ZhangSchool of Medical Imaging, Jiangsu University, Zhenjiang, China.
Xi WeiZhenjiang Clinical Medical College of Nanjing Medical University, Zhenjiang, China.
Zakari ShaibuSchool of Medicine, Jiangsu University, Zhenjiang, Jiangsu, China.
Lingling XiangZhenjiang Clinical Medical College of Nanjing Medical University, Zhenjiang, China.
Ting WuDepartment of Pathology, Jiangsu University Affiliated People's Hospital, Zhenjiang, China.
Qing ZhangZhenjiang Clinical Medical College of Nanjing Medical University, Zhenjiang, China.
Rong QinZhenjiang Clinical Medical College of Nanjing Medical University, Zhenjiang, China.
Xiuhong ShanZhenjiang Clinical Medical College of Nanjing Medical University, Zhenjiang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: This study aims to evaluate the utility of radiomic features from dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) in distinguishing HER2-low from HER2-zero breast cancer. Patients and methods: We retrospectively analyzed 118 MRI cases, including 78 HER2-low and 40 HER2-zero patients confirmed by immunohistochemistry or fluorescence Results: The radiomics model, clinical model, and nomogram successfully distinguished between HER2-low and HER2-zero. The radiomics model showed excellent performance, with area under the curve (AUC) values of 0.875 in the training set and 0.845 in the test set, outperforming the clinical model (AUC = 0.691 and 0.672, respectively). HER2 status correlated with increased rad-score and Time Intensity Curve (TIC). The nomogram outperformed both models, with AUC, sensitivity, and specificity values of 0.892, 79.6%, and 82.8% in the training set, and 0.886, 83.3%, and 90.9% in the test set. Conclusions: The DCE-MRI-based nomogram shows promising potential in differentiating HER2-low from HER2-zero status in breast cancer patients.

Indexed as

breast cancerDCE-MRIHER2-lowHER2-zeronomogramradiomics analysis

Identifiers

PMID39211554
PMCPMC11357957

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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.