Evidence map›Paper›PMID 42591577›Full record

ReviewTranslational cancer research2026

Emerging role of human epidermal growth factor 2-low status in the prognosis and management of triple-negative breast cancer: a narrative review.

Nathan Oelschlagel, Hamid Mithoowani, Emily A Goebel, Farhad Ghasemi, Sarah Knowles, Allison Maciver, Muriel Brackstone, Armen Parsyan

Abstract readReview
In one paragraph

Review in Translational cancer research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Nathan Oelschlagel *Faculty of Medicine, Schulich School of Medicine & Dentistry, Western University, London, ON, Canada.
Hamid Mithoowani *Department of Oncology, Schulich School of Medicine & Dentistry, Western University, London, ON, Canada.
Emily A GoebelDepartment of Pathology and Laboratory Medicine, London Health Sciences Centre and Western University, London, ON, Canada.
Farhad GhasemiDepartment of Surgery, Schulich School of Medicine & Dentistry, Canada and St Joseph's Health Care, London, ON, Canada.
Sarah KnowlesDepartment of Oncology, Schulich School of Medicine & Dentistry, Western University, London, ON, Canada.
Allison MaciverDepartment of Oncology, Schulich School of Medicine & Dentistry, Western University, London, ON, Canada.
Muriel BrackstoneDepartment of Oncology, Schulich School of Medicine & Dentistry, Western University, London, ON, Canada.
Armen ParsyanDepartment of Oncology, Schulich School of Medicine & Dentistry, Western University, London, ON, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Objective: Triple-negative breast cancer (TNBC) remains one of the most aggressive and therapeutically challenging breast cancer subtypes. Lack of targeted therapies in TNBC mandates identification of novel molecular and therapeutic vulnerabilities. Human epidermal growth factor 2 (HER2)-low breast cancer, defined by immunohistochemistry (IHC) score 1+ or 2+ with negative Methods: We queried the PubMed database, Google Scholar and other databases for studies published in English (up to April 2026) and available online, using search terms (such as TNBC, breast cancer, HER2-low, HER2-ultralow, trastuzumab deruxtecan, T-DXd, T-DM1), and selected publications based on their relevance to the topic. We also hand-searched reference lists of relevant papers to provide the most updated and comprehensive review of the topic, and utilized "ClinicalTrials.gov" to identify studies exploring anti-HER2 directed treatments in HER2-low and HER2-ultralow breast cancers, with an emphasis on TNBC. Key Content and Findings: HER2-low TNBC represents a relatively large proportion of TNBC cases, and is gaining recognition as a distinct therapeutic and biological subtype, affecting clinical management. In HER2-low TNBC patients, utilization of anti-HER2 targeted therapies, similar to those in HER2-positive breast cancer patients, has been recently shown to offer clinical advantages. Namely, antibody-drug conjugate (ADC) trastuzumab deruxtecan (T-DXd), confers survival benefits in patients with HER2-low breast cancer, including HER2-low TNBC patients with metastatic disease. Ongoing clinical trials investigate T-DXd in various clinical settings as a monotherapy or in combination with chemotherapeutic, immunotherapeutic and targeted drugs in patients with hormone (HR) receptor-negative and HER2-low expressing breast cancer. New HER2-directed ADCs are also being developed, with several being investigated in clinical trials. Conclusions: The development of new HER2-directed treatments is revolutionizing the management of TNBC patients, and mandates further research to better detect and target clinically meaningful HER2-positive signals. This manuscript provides analysis and synthesis of current literature to potentially guide future research and clinical efforts directed at improving outcomes of patients with TNBC.

Indexed as

antibody-drug conjugate (ADC)Human epidermal growth factor 2-low (HER2-low)trastuzumab deruxtecan (T-DXd)triple-negative breast cancer (TNBC)

Identifiers

PMID42591577
PMCPMC13462145

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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.