Evidence map›Paper›PMID 40048670›Full record

ArticleJCO precision oncology2025

Association Between Human Epidermal Growth Factor Receptor 2-Low Status and Time to Development of Brain Metastases Among Patients With Breast Cancer: A Retrospective Cohort Study.

Kevin Yijun Fan, Rania Chehade, Italo Fernandes, Veronika Moravan, Arjun Sahgal, Ellen Warner, Katarzyna Joanna Jerzak

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Article in JCO precision oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Kevin Yijun FanUniversity of Toronto, Toronto, ON, Canada.ORCID 0000-0002-8233-5626
Rania ChehadeUniversity of Toronto, Toronto, ON, Canada.ORCID 0009-0000-2535-0275
Italo FernandesUniversity of Toronto, Toronto, ON, Canada.ORCID 0000-0002-9254-6136
Veronika MoravanVM Stats, Toronto, ON, Canada.ORCID 0009-0004-2474-8694
Arjun SahgalUniversity of Toronto, Toronto, ON, Canada.
Ellen WarnerUniversity of Toronto, Toronto, ON, Canada.
Katarzyna Joanna JerzakUniversity of Toronto, Toronto, ON, Canada.ORCID 0000-0002-3995-0308

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeHuman epidermal growth factor receptor 2 (HER2)-low is a newly defined subgroup of HER2-negative breast cancer. It is unknown whether HER2-low status is associated with brain metastases (BrM) development. We aimed to determine the association between HER2-low status and the time to developing BrM.

methodsHER2 status was determined in a cohort of 689 women with metastatic breast cancer (MBC) who underwent treatment for BrM at Sunnybrook Odette Cancer Centre from 2008 to 2018. In patients with primary breast cancer (PBC) HER2 subclassification available (subgroup 1), we investigated time from PBC diagnosis to BrM diagnosis (PBC-time to brain metastases [TTBM]). In patients with HER2 subclassification available in any tissue (subgroup 2), we investigated time from MBC diagnosis to BrM diagnosis (MBC-TTBM).

resultsIn subgroup 1 (n = 175), patients with HER2-low disease (n = 42) had a shorter PBC-TTBM compared with those with HER2-zero disease (n = 77; hazard ratio, 2.4;

conclusionOur findings suggest that among patients with HR+ breast cancer, HER2-low status was associated with shorter TTBM compared with HER2-zero status. In a subset of patients for whom HER2 status of the PBC was available, HER2-low status was associated with shorter PBC-TTBM, irrespective of HR status. This study suggests a previously unrecognized association between HER2-low status and timing of BrM development.

Indexed as

Brain NeoplasmsBreast NeoplasmsErb-b2 Receptor Tyrosine KinasesAdultAgedFemaleHumansMiddle AgedRetrospective StudiesTime FactorsERBB2 protein, humanErb-b2 Receptor Tyrosine Kinases

Identifiers

PMID40048670
PMCPMC11895828

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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.