Evidence map›Paper›PMID 37264417›Full record

ArticleJournal of translational medicine2023

Analysis of clinical features, genomic landscapes and survival outcomes in HER2-low breast cancer.

Juan Jin, Bin Li, Jianing Cao, Ting Li, Jian Zhang, Jun Cao, Mingchuan Zhao, Leiping Wang, Biyun Wang, Zhonghua Tao and 1 more

Open access · goldAbstract read
In one paragraph

Article in Journal of translational medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
6.9field-weighted citation impact, top 3% of its field
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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 30 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Utilization of MRI-based radiomics nomogram for predicting HER2-zero, -low, and -overexpression breast cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
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  6. Redefining breast cancer: therapeutic opportunities in HER2-low and emerging molecular subtypes.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
  7. Is the risk of brain metastasis and prognosis different in HER2-low breast cancer?Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
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  18. Effect of HER2-low status on brain metastasis-free survival and survival after brain metastasis in patients with breast cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2025
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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

11 authors at 1 institution in 1 country.

Juan Jin *Department of Breast and Urologic Medical Oncology, Fudan University Shanghai Cancer Center, Shanghai, China.
Bin Li *Department of Breast and Urologic Medical Oncology, Fudan University Shanghai Cancer Center, Shanghai, China.
Jianing CaoDepartment of Breast and Urologic Medical Oncology, Fudan University Shanghai Cancer Center, Shanghai, China.
Ting LiDepartment of Breast and Urologic Medical Oncology, Fudan University Shanghai Cancer Center, Shanghai, China.
Jian ZhangDepartment of Breast and Urologic Medical Oncology, Fudan University Shanghai Cancer Center, Shanghai, China.
Jun CaoDepartment of Breast and Urologic Medical Oncology, Fudan University Shanghai Cancer Center, Shanghai, China.
Mingchuan ZhaoDepartment of Breast and Urologic Medical Oncology, Fudan University Shanghai Cancer Center, Shanghai, China.
Leiping WangDepartment of Breast and Urologic Medical Oncology, Fudan University Shanghai Cancer Center, Shanghai, China.
Biyun WangDepartment of Breast and Urologic Medical Oncology, Fudan University Shanghai Cancer Center, Shanghai, China. pro_wangbiyun@163.com.
Zhonghua TaoDepartment of Breast and Urologic Medical Oncology, Fudan University Shanghai Cancer Center, Shanghai, China. drtaozhh@126.com.
Xichun HuDepartment of Breast and Urologic Medical Oncology, Fudan University Shanghai Cancer Center, Shanghai, China. huxichun2017@163.com.ORCID 0000-0001-6148-9186
Shanghai Medical College of Fudan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNovel human epidermal growth factor receptor 2 (HER2)-directed antibody-drug conjugates prompt the identification of the HER2-low subtype. However, the biological significance of HER2-low expression in breast cancer is unclear.

methodsClinical and genomic data of 579 metastatic breast cancer patients were reviewed from our next-generation sequencing (NGS) database and genomic analysis of early breast cancer patients from TCGA was also analyzed.

findingsFirst, the clinicopathological characteristics of HER2-low patients were profoundly influenced by HR status and no difference of prognosis was observed between HER2-low and HER2-zero patients when paired by HR status, but notably HER2-low patients showed similar metastatic patterns to HER2-positive patients in the HR-positive (HR+ ) subgroup, with more brain and initial lung metastases and more cases of de novo stage IV breast cancer than HER2-zero patients. Second, among patients with primary HER2-low or HER2-zero tumors, the discordance of HER2 status between primary and metastatic tumors was significant, with 48.4% of patients with HER2-zero primary tumors exhibiting HER2-low phenotype in metastatic tumors in the HR+ subgroup. Third, within HR+ and HR-negative subtypes, HER2-low and HER2-zero tumors showed no substantial differences in mutation alterations and copy number variations. Forth, germline BRCA2 mutations were observed only in HER2-low patients in our NGS database, especially in HR+ HER2-low tumors. Finally, three molecular subtypes based on genomic alterations in HER2-low breast cancer were identified, which provided novel insights into heterogeneity in HER2-low breast cancer.

conclusionsAfter correcting for HR expression, only marginal differences in clinical and molecular phenotypes were determined between HER2-low and HER2-zero breast cancer. Therefore, HER2-low breast cancer is insufficient to be defined as a distinct molecular entity, but rather a heterogenous disease.

Indexed as

Breast NeoplasmsBiomarkers, TumorDNA Copy Number VariationsErb-b2 Receptor Tyrosine KinasesFemaleGenomicsHumansPrognosisBiomarkers, TumorErb-b2 Receptor Tyrosine KinasesAntibody–drug conjugatesHER2 dynamicsHER2 expressionHER2-low breast cancerHeterogeneityMetastatic breast cancer

Identifiers

PMID37264417
PMCPMC10236705
OpenAlexW4378974924

What OpenQuestion holds

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LicenceCC BY
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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.