Evidence map›Paper›PMID 38441358›Full record

ArticleCancer reports (Hoboken, N.J.)2024

Targeting HER2/HER3 co-mutations in metastatic breast cancer: Case reports of exceptional responders to trastuzumab and pertuzumab therapy.

Page E Blas, Esther San Roman Rodriguez, Heather L Williams, Maren K Levin, Joshua S K Bell, Mariaelena Pierobon, Alexander S Barrett, Emanuel F Petricoin, Joyce A O'Shaughnessy

Open access · goldAbstract readCase Reports
In one paragraph

Article in Cancer reports (Hoboken, N.J.), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 41% of its field
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

2 citing papers in PubMed, 1 citations in OpenAlex.

  1. Review
  2. 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

9 authors at 4 institutions in 1 country.

Page E BlasClinical Oncology Research Coordination, Baylor Scott and White Research Institute, Dallas, Texas, USA.ORCID 0009-0008-5044-1169
Esther San Roman RodriguezClinical Oncology Research Coordination, Baylor Scott and White Research Institute, Dallas, Texas, USA.
Heather L WilliamsClinical Oncology Research Coordination, Baylor Scott and White Research Institute, Dallas, Texas, USA.
Maren K LevinClinical Oncology Research Coordination, Baylor Scott and White Research Institute, Dallas, Texas, USA.
Joshua S K BellDepartment of Translational Science, Tempus Labs Inc., Chicago, Illinois, USA.
Mariaelena PierobonCenter for Applied Proteomics and Molecular Medicine, George Mason University, Manassas, Virginia, USA.
Alexander S BarrettDepartment of Translational Science, Tempus Labs Inc., Chicago, Illinois, USA.
Emanuel F PetricoinCenter for Applied Proteomics and Molecular Medicine, George Mason University, Manassas, Virginia, USA.
Joyce A O'ShaughnessyBreast Cancer Research Program, Baylor University Medical Center, Texas Oncology, US Oncology, Dallas, Texas, USA.
Baylor Scott & White Health · USGeorge Mason University · USTempus Labs (United States) · USTexas Oncology · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOverexpression of HER2 plays an important role in cancer progression and is the target of multiple therapies in HER2-positive breast cancer. Recent studies have also highlighted the presence of activating mutations in HER2, and HER3 that are predicted to enhance HER2 downstream pathway activation in a HER2-dependent manner.

methodsIn this report, we present two exceptional responses in hormone receptor-positive, HER2-nonamplified, HER2/HER3 co-mutated metastatic breast cancer patients who were treated with the anti-HER2-directed monoclonal antibodies, trastuzumab and pertuzumab.

resultsBoth patients acheived exceptional responses to treatment, suggesting that combined trastuzumab, pertuzumab, and endocrine therapy could be a highly effective therapy for these patients and our observations could help prioritize trastuzumab deruxtecan as an early therapeutic choice for patients whose cancers have activating mutations in HER2.

Indexed as

Breast NeoplasmsAntibodies, Monoclonal, HumanizedErb-b2 Receptor Tyrosine KinasesFemaleHumansMutationReceptor, ErbB-3TrastuzumabAntibodies, Monoclonal, HumanizedERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesERBB3 protein, humanpertuzumabReceptor, ErbB-3Trastuzumabcancer biologyexceptional responderHER2/HER3 co-mutationsmetastatic breast cancer

Identifiers

PMID38441358
PMCPMC10913072
OpenAlexW4392460429

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

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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.