Evidence map›Paper›PMID 38726477›Full record

ArticleJournal of magnetic resonance imaging : JMRI2025

Preoperative Differentiation of HER2-Zero and HER2-Low from HER2-Positive Invasive Ductal Breast Cancers Using BI-RADS MRI Features and Machine Learning Modeling.

Jiejie Zhou, Yang Zhang, Haiwei Miao, Ga Young Yoon, Jinhao Wang, Yezhi Lin, Hailing Wang, Yan-Lin Liu, Jeon-Hor Chen, Zhifang Pan and 2 more

Abstract read
In one paragraph

Article in Journal of magnetic resonance imaging : JMRI, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
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  5. Review
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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

12 authors.

Jiejie ZhouDepartment of Radiology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.ORCID https://orcid.org/0000-0002-4299-8046
Yang ZhangDepartment of Radiological Sciences, University of California, Irvine, California, USA.
Haiwei MiaoDepartment of Radiology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Ga Young YoonDepartment of Radiological Sciences, University of California, Irvine, California, USA.
Jinhao WangGuangxi Normal University, Guilin, China.
Yezhi LinThe First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Hailing WangGuangxi Normal University, Guilin, China.
Yan-Lin LiuDepartment of Radiological Sciences, University of California, Irvine, California, USA.
Jeon-Hor ChenDepartment of Radiological Sciences, University of California, Irvine, California, USA.
Zhifang PanThe First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.ORCID https://orcid.org/0000-0002-3683-6657
Min-Ying SuDepartment of Radiological Sciences, University of California, Irvine, California, USA.ORCID https://orcid.org/0000-0002-3069-0271
Meihao WangDepartment of Radiology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.ORCID https://orcid.org/0000-0002-7055-993X

Funding

Univ.of Calif., Irvine Cancer Center Support GrantP30CA062203 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI Melanie Funes · 1994 to 2026
$57.9M
Key Laboratory of Intelligent Medical Imaging of Wenzhou 2021HZSY0057NCI NIH HHS P30 CA062203Wenzhou Science & Technology Bureau Y20210232Zhejiang Provincial Natural Science Foundation of China LY21F020030
6 · The paper itself

Abstract

backgroundAccurate determination of human epidermal growth factor receptor 2 (HER2) is important for choosing optimal HER2 targeting treatment strategies. HER2-low is currently considered HER2-negative, but patients may be eligible to receive new anti-HER2 drug conjugates. PURPOSE: To use breast MRI BI-RADS features for classifying three HER2 levels, first to distinguish HER2-zero from HER2-low/positive (Task-1), and then to distinguish HER2-low from HER2-positive (Task-2). STUDY TYPE: Retrospective. POPULATION: 621 invasive ductal cancer, 245 HER2-zero, 191 HER2-low, and 185 HER2-positive. For Task-1, 488 cases for training and 133 for testing. For Task-2, 294 cases for training and 82 for testing. FIELD STRENGTH/SEQUENCE: 3.0 T; 3D T1-weighted DCE, short time inversion recovery T2, and single-shot EPI DWI. ASSESSMENT: Pathological information and BI-RADS features were compared. Random Forest was used to select MRI features, and then four machine learning (ML) algorithms: decision tree (DT), support vector machine (SVM), k-nearest neighbors (k-NN), and artificial neural nets (ANN), were applied to build models. STATISTICAL TESTS: Chi-square test, one-way analysis of variance, and Kruskal-Wallis test were performed. The P values <0.05 were considered statistically significant. For ML models, the generated probability was used to construct the ROC curves.

resultsPeritumoral edema, the presence of multiple lesions and non-mass enhancement (NME) showed significant differences. For distinguishing HER2-zero from non-zero (low + positive), multiple lesions, edema, margin, and tumor size were selected, and the k-NN model achieved the highest AUC of 0.86 in the training set and 0.79 in the testing set. For differentiating HER2-low from HER2-positive, multiple lesions, edema, and margin were selected, and the DT model achieved the highest AUC of 0.79 in the training set and 0.69 in the testing set. DATA

conclusionBI-RADS features read by radiologists from preoperative MRI can be analyzed using more sophisticated feature selection and ML algorithms to build models for the classification of HER2 status and identify HER2-low. LEVEL OF EVIDENCE: 4: TECHNICAL EFFICACY: Stage 2.

Indexed as

Breast NeoplasmsCarcinoma, Ductal, BreastErb-b2 Receptor Tyrosine KinasesMachine LearningMagnetic Resonance ImagingAdultAgedAlgorithmsBreastFemaleHumansImage Interpretation, Computer-AssistedMiddle AgedReproducibility of ResultsRetrospective StudiesROC CurveERBB2 protein, humanErb-b2 Receptor Tyrosine Kinasesbreast cancerHER2 lowHER2 positivemagnetic resonance imaging

Identifiers

PMID38726477
PMCPMC11550260

What OpenQuestion holds

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Registered trials

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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.