Evidence map›Paper›PMID 38346865›Full record

ArticleJournal of clinical pathology2025

Response to anti-HER2 neoadjuvant chemotherapy in HER2-positive invasive breast cancers with different HER2 FISH patterns.

Hong Lv, Qian-Ming Bai, Ming Li, Meng-Yuan Cai, Shu-Ling Zhou, Yin Liu, Zhong-Hua Wang, Ruo-Hong Shui, Hong-Fen Lu, Xiao-Li Xu and 7 more

Abstract read
In one paragraph

Article in Journal of clinical pathology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

17 authors.

Hong Lv *Department of Pathology, Fudan University Shanghai Cancer Center, Shanghai, China.ORCID http://orcid.org/0000-0002-2129-2781
Qian-Ming Bai *Department of Pathology, Fudan University Shanghai Cancer Center, Shanghai, China.
Ming LiDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, China.
Meng-Yuan CaiDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, China.
Shu-Ling ZhouDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, China.
Yin LiuDepartment of Breast Surgery, Fudan University Shanghai Cancer Center, Shanghai, China.
Zhong-Hua WangDepartment of Medical Oncology, Fudan University Shanghai Cancer Center, Shanghai, China.
Ruo-Hong ShuiDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, China.ORCID http://orcid.org/0000-0001-5464-1741
Hong-Fen LuDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, China.
Xiao-Li XuDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, China.ORCID http://orcid.org/0000-0001-9788-1534
Bao-Hua YuDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, China.ORCID http://orcid.org/0000-0003-4433-4136
Xiao-Yu TuDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, China.
Rui BiDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, China.ORCID http://orcid.org/0000-0003-1217-1838
Yu-Fan ChengDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, China.
Xiao-Yan ZhouDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, China.ORCID http://orcid.org/0000-0001-5999-7237
Zhi-Min ShaoDepartment of Breast Surgery, Fudan University Shanghai Cancer Center, Shanghai, China.
Wen-Tao YangDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, China yangwt2000@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsHuman epidermal growth factor receptor 2 (HER2)-positive patients with breast cancer may have different HER2/CEP17 ratios and HER2 copy numbers, with inconsistent responses to anti-HER2 neoadjuvant chemotherapy (NACT). Our study aimed to explore the relationship between different HER2 fluorescence in situ hybridisation (FISH) patterns in HER2-positive patients with breast cancer and responses to anti-HER2 NACT.

methods527 patients with HER2-positive invasive breast cancer who received anti-HER2 NACT from 2015 to 2022 were included and divided into three groups by FISH results, namely group A: HER2/CEP17<2.0 and HER2 copy numbers ≥6.0, HER2 immunohistochemistry 2/3+; group B: HER2/CEP17≥2.0 and HER2 copy numbers ≥4.0 and <6.0; group C: HER2/CEP17≥2.0 and HER2 copy numbers ≥6.0. We compared clinicopathological characteristics and pathological complete response (pCR) rates of different groups.

resultsAccording to HER2 FISH results, 12 patients (2.3%, 12/527) were in group A, 40 (7.6%, 40/527) were in group B and 475 (90.1%, 475/527) were in group C. The pCR rate was the lowest in group B (5.0%), while the pCR rates in group A and group C were 33.3% and 44.4%, respectively (p

conclusionsPatients with HER2/CEP17≥2.0 and HER2 copy numbers ≥4.0 and <6.0 do not benefit to the same extent from current anti-HER2 therapies as FISH-positive patients with other patterns.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsBiomarkers, TumorBreast NeoplasmsErb-b2 Receptor Tyrosine KinasesIn Situ Hybridization, FluorescenceAdultAgedChemotherapy, AdjuvantFemaleHumansMiddle AgedNeoadjuvant TherapyNeoplasm InvasivenessRetrospective StudiesTreatment OutcomeBiomarkers, TumorERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesBREASTCARCINOMAPathology, Molecular

Identifiers

PMID38346865
PMCPMC12322473

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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.