Evidence map›Paper›PMID 34251757›Full record

ReviewCancer communications (London, England)2021

Estrogen receptor-low breast cancer: Biology chaos and treatment paradox.

Ke-Da Yu, Yu-Wen Cai, Song-Yang Wu, Ruo-Hong Shui, Zhi-Ming Shao

Abstract readReview
In one paragraph

Review in Cancer communications (London, England), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing 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

39 citing papers in PubMed.

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  12. Predictive and prognostic value ofEuropean journal of nuclear medicine and molecular imaging · 2025
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  18. Molecular Basis of Breast Tumor Heterogeneity.Advances in experimental medicine and biology · 2025
    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

5 authors.

Ke-Da YuDepartment of Breast Surgery, Fudan University Shanghai Cancer Center, Shanghai, 200032, P. R. China.ORCID 0000-0002-2883-1282
Yu-Wen CaiDepartment of Breast Surgery, Fudan University Shanghai Cancer Center, Shanghai, 200032, P. R. China.
Song-Yang WuShanghai Medical College, Fudan University, Shanghai, 200032, P. R. China.
Ruo-Hong ShuiDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, 200032, P. R. China.
Zhi-Ming ShaoDepartment of Breast Surgery, Fudan University Shanghai Cancer Center, Shanghai, 200032, P. R. China.

Funding

2018 Shanghai Youth Excellent Academic LeaderFudan ZHUOSHI ProjectNational Natural Science Foundation of China 81672600National Natural Science Foundation of China 81722032National Natural Science Foundation of China 82072916
6 · The paper itself

Abstract

Hormone receptor testing mainly serves the purpose of guiding treatment choices for breast cancer patients. Patients with estrogen receptor (ER)-positive breast cancers show significant response to endocrine therapy. However, the methods to define ER status and eligibility for treatment remain controversial. Despite recent guidelines considering staining ≥1% of tumor nuclei by immunohistology as ER-positive, it has raised concerns on the benefit of endocrine therapy for tumors with ER 1%-10% expression, termed "ER-low positive". This subgroup accounts for 3% to 9% of all patients and is likely to have unique molecular features, and therefore distinct therapeutic response to endocrine therapy compared with ER-high positive tumors. The latest guidelines did not provide detailed descriptions for those patients, resulting in inconsistent treatment strategies. Consequently, we aimed to resolve this dilemma comprehensively. This review discusses molecular traits and recent ER-low positive breast cancer innovations, highlighting molecular-targeted treatment rather than traditional unified endocrine therapy for future basic and clinical research.

Indexed as

Breast NeoplasmsReceptors, EstrogenBiologyCarrier ProteinsFemaleHumansCarrier ProteinsReceptors, Estrogenbreast cancerendocrine therapyestrogen receptor-lowimmunohistochemistryintrinsic subtype

Identifiers

PMID34251757
PMCPMC8504145

What OpenQuestion holds

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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.