Evidence map›Paper›PMID 36910643›Full record

ArticleFrontiers in oncology2023

Evolution and clinical significance of HER2-low status after neoadjuvant therapy for breast cancer.

Jiuyan Shang, Xuemei Sun, Zihang Xu, Lijing Cai, Chang Liu, Si Wu, Yueping Liu

Abstract read
In one paragraph

Article in Frontiers in oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

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

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

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. HER2-Low Breast Cancer: Now and in the Future.Cancer research and treatment · 2024
    Review
  12. Article
  13. Insights Into the Emerging Entity of HER2-Low Breast Cancer.International journal of breast cancer · 2024
    Review
  14. Article
  15. Review
  16. 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.

Jiuyan ShangDepartment of Pathology, Hebei Medical University, The Fourth Affiliated Hospital and Hebei Provincial Tumor Hospital, Shijiazhuang, China.
Xuemei SunDepartment of Pathology, Hebei Medical University, The Fourth Affiliated Hospital and Hebei Provincial Tumor Hospital, Shijiazhuang, China.
Zihang XuAnesthesia Class, School of Basic Medicine, Hebei Medical University, Shijiazhuang, China.
Lijing CaiDepartment of Pathology, Hebei Medical University, The Fourth Affiliated Hospital and Hebei Provincial Tumor Hospital, Shijiazhuang, China.
Chang LiuDepartment of Pathology, Hebei Medical University, The Fourth Affiliated Hospital and Hebei Provincial Tumor Hospital, Shijiazhuang, China.
Si WuDepartment of Pathology, Hebei Medical University, The Fourth Affiliated Hospital and Hebei Provincial Tumor Hospital, Shijiazhuang, China.
Yueping LiuDepartment of Pathology, Hebei Medical University, The Fourth Affiliated Hospital and Hebei Provincial Tumor Hospital, Shijiazhuang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The emergence of HER2 antibody-drug conjugates provides new treatment decisions for breast cancer patients, especially those with HER2-low expression. In order to explore the biological characteristics of breast cancer with HER2-low expression, the HER2-low category in primary breast cancer and residual tumor after neoadjuvant therapy was investigated to reflect the evolution of HER2 expression. Methods: HER2 was assessed according to the latest ASCO/CAP guidelines. The cut-off value for staining of HER2-positive cells was >10%. HER2-negative cases were divided into HER2-low (IHC=1+/2+ and no ISH amplification) and HER2-zero (IHC-0), and the clinicopathological characteristics of the cases were collected. Results: This study included 1140 patients with invasive breast cancer who received preoperative neoadjuvant therapy from 2018 to 2021, of which 365 patients achieved pCR and 775 were non-pCR. In the non-pCR cohort, HER2-low cases accounted for 59.61% of primary tumors and 55.36% of residual tumors. Among HER2-negative cases, HR-positive tumors had a higher incidence of low HER2 expression compared with triple-negative tumors (80.27% vs 60.00% in primary tumors and 72.68% vs 50.77% in residual tumors). The inconsistency rate of HER2 expression was 21.42%, mainly manifested as the conversion of HER2-low cases to HER2-zero (10.19%) and the conversion of HER2-zero to HER2-low (6.45%). Among the HER2-negative cases in the primary tumor, the HER2 discordance rate of HR-positive cases was lower than that of triple-negative cases (23.34% VS 36.92%). This difference was mainly caused by the case switching from HER2-low to HER2-zero. Compared with HER2-zero cases, there were statistically significant differences in RCB grade, MP grade and the number of metastatic lymph nodes in HER2-low cases. Patients with low HER2 expression had a lower pathological response rate and a higher number of metastatic lymph nodes. Conclusion: HER2-low breast cancer is highly unstable during disease evolution and has certain biological characteristics. HER2-low breast cancer is not only correlated with positive HR, but also has a certain correlation with positive AR. Re-detection of HER2 in breast cancer after neoadjuvant therapy may lead to new treatment opportunities for a certain proportion of patients.

Indexed as

breast cancerhormone receptorhuman epidermal growth factor receptor 2neoadjuvant therapypathological complete response

Identifiers

PMID36910643
PMCPMC9992719

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.