Evidence map›Paper›PMID 37442945›Full record

ArticleBMC cancer2023

HER2-low breast cancer: evolution of HER2 expression from primary tumor to distant metastases.

Mengyuan Cai, Ming Li, Hong Lv, Shuling Zhou, Xiaoli Xu, Ruohong Shui, Wentao Yang

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2023. 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
3.2field-weighted citation impact, top 7% 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

10 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. HER2-Low Breast Cancer: Now and in the Future.Cancer research and treatment · 2024
    Review
  9. Article
  10. 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

7 authors at 3 institutions in 1 country.

Mengyuan CaiDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Ming LiDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Hong LvDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Shuling ZhouDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Xiaoli XuDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Ruohong ShuiDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Wentao YangDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China. yangwt2000@163.com.
Fudan University Shanghai Cancer Center · CNShanghai Medical College of Fudan University · CNFudan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBreast cancer (BC) with low human epidermal growth factor receptor 2 (HER2) expression is attracting much attention due to the breakthrough progress of novel anti-HER2 antibody-drug conjugates. HER2 expression is examined in patients with HER2-low BC and their distant metastases in this study, so as to further clarify the dynamic characteristics of HER2 low status in the process of disease progression.

methodsPatients diagnosed with HER2 low breast cancer (defined as IHC1+ or IHC2+/ISH-) between 2012 and 2021 were included in this study. We evaluated HER2 expression of primary sites and metastatic sites, compared the impact of different clinicopathological parameters on HER2 status of metastases and compared the overall survival and disease-free survival of patients with different HER2 status in metastases.

resultsNinety-eight patients were included. All HER2 IHC scores were confirmed and the consistent rate with the original pathological report was 81.1%. 27.6% of the patients showed different HER2 status in metastases. The HER2 discordance rate differed among different metastatic sites (p = 0.040). The higher the T stage of the primary BC, the higher the rate of HER2 discordance was observed (p = 0.042). For the specimen type of metastasis, HER2 discordant rate was higher in surgical specimen than biopsy (p = 0.050). No difference of HER2 discordance rate was found between HER2-1+ and HER2-2+ patients. But comparing HER2 IHC score, HER2-2+ patients were less likely to have consistent metastatic HER2 levels than HER2-1+ patients (p = 0.006). No difference in survival outcomes was observed between patients with different HER2 status in metastases.

conclusionsThere is a possibility of HER2 expression alteration in the metastases of HER2-low breast cancer. And the rate of altered HER2 low expression was different among different metastatic sites, different T stages of primary BC and specimen type of metastasis. No prognostic significance was observed.

Indexed as

Antineoplastic AgentsBreast NeoplasmsBiomarkers, TumorBiopsyDisease ProgressionErb-b2 Receptor Tyrosine KinasesFemaleHumansPrognosisAntineoplastic AgentsBiomarkers, TumorErb-b2 Receptor Tyrosine KinasesAnti-HER2 antibody-drug conjugatesBreast cancerHER2 discordanceHER2-low expressionMetastasis

Identifiers

PMID37442945
PMCPMC10347880
OpenAlexW4384200286

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.