Evidence map›Paper›PMID 41881067›Full record

ArticleJCO precision oncology2026

Real-World Study Assessing Characteristics and Treatment Patterns of Patients With Human Epidermal Growth Factor Receptor 2 Immunohistochemistry 0 and Human Epidermal Growth Factor Receptor 2-Low Stage IV Breast Cancer: A Multicenter Retrospective Study.

Chia Jie Tan, Connor Willis, Trang Au, Matthew B Schabath, Chenghui Li, Kristen Kelley, Xiaoqing Xu, Leah Park, Clara Lam, Sandhya Mehta and 3 more

Abstract readMulticenter Study
In one paragraph

Article in JCO precision oncology, 2026. 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. Review
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

13 authors.

Chia Jie TanPharmacotherapy Outcomes Research Centre, University of Utah, Salt Lake City, UT.ORCID 0000-0003-2452-0556
Connor WillisPharmacotherapy Outcomes Research Centre, University of Utah, Salt Lake City, UT.ORCID 0000-0001-7895-2747
Trang AuPharmacotherapy Outcomes Research Centre, University of Utah, Salt Lake City, UT.ORCID 0000-0002-0149-0115
Matthew B SchabathH. Lee Moffitt Cancer Center and Research Institute, Tampa, FL.ORCID 0000-0003-3241-3216
Chenghui LiDivision of Pharmaceutical Evaluation and Policy, University of Arkansas for Medical Sciences, Little Rock, AR.ORCID 0000-0002-2778-5149
Kristen KelleyHuntsman Cancer Institute, Salt Lake City, UT.ORCID 0000-0002-2310-510X
Xiaoqing XuAstraZeneca Oncology Outcomes Research, Gaithersburg, MD.ORCID 0000-0001-8209-6963
Leah ParkAstraZeneca Oncology Outcomes Research, Gaithersburg, MD.
Clara LamAstraZeneca Oncology Outcomes Research, Gaithersburg, MD.
Sandhya MehtaDaiichi Sankyo, Basking Ridge, NJ.
Jackie KwongDaiichi Sankyo, Basking Ridge, NJ.
Diana BrixnerPharmacotherapy Outcomes Research Centre, University of Utah, Salt Lake City, UT.ORCID 0000-0001-6637-6359
David StenehjemPharmacotherapy Outcomes Research Centre, University of Utah, Salt Lake City, UT.ORCID 0000-0002-1831-285X

Funding

TRANSLATIONAL RESEARCHP30CA076292 · NCI · UNIVERSITY OF SOUTH FLORIDA · PI KENNETH Lynn WRIGHT · 1998 to 2026
$93.5M
NCI NIH HHS P30 CA076292
6 · The paper itself

Abstract

purposeTo describe and compare patient characteristics, treatment patterns, and survival outcomes of patients with human epidermal growth factor receptor 2 (HER2)-low and HER2 immunohistochemistry 0 (IHC 0) stage IV breast cancer.

methodsA retrospective study was conducted across three academic centers in the United States. Adult patients diagnosed with stage IV breast cancer between 1-1-2010 and 12-31-2020 and classified as having either HER2-low (immunohistochemistry 1+/2+ with negative fluorescence in situ hybridization) or HER2 IHC 0 disease were followed through 12-31-2021. Patient characteristics, treatments received, and treatment discontinuation were analyzed and survival analyses were conducted using Kaplan-Meier methods.

resultsAmong 501 eligible patients, 385 were classified as HER2-low (76.8%) and 116 as HER2 IHC 0 (23.2%). No statistically significant differences were found for demographic characteristics, but

conclusionPatient characteristics were similar between HER2-low and HER2 IHC 0 subgroups except for some differences in genetic alterations. Deterioration of PFS in later lines of therapy highlights a potential unmet need. Given the high patient attrition, the most effective treatments should be used as early as indicated as some patients may not proceed to subsequent lines of therapy.

Indexed as

Breast NeoplasmsErb-b2 Receptor Tyrosine KinasesAdultAgedFemaleHumansImmunohistochemistryMiddle AgedNeoplasm StagingRetrospective StudiesERBB2 protein, humanErb-b2 Receptor Tyrosine Kinases

Identifiers

PMID41881067
PMCPMC13043224

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.