Evidence map›Paper›PMID 35884366›Full record

ReviewCancers2022

Targeted Therapeutic Options and Future Perspectives for HER2-Positive Breast Cancer.

Angelica Ferrando-Díez, Eudald Felip, Anna Pous, Milana Bergamino Sirven, Mireia Margelí

Open access · goldAbstract readReview
In one paragraph

Review in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
4.2field-weighted citation impact, top 4% 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

23 citing papers in PubMed, 42 citations in OpenAlex.

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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 at 1 institution in 1 country.

Angelica Ferrando-DíezMedical Oncology Department, Catalan Institute of Oncology-Badalona, Hospital Universitari Germans Trias i Pujol (HGTiP), 08916 Badalona, Spain.ORCID 0000-0003-0206-7498
Eudald FelipMedical Oncology Department, Catalan Institute of Oncology-Badalona, Hospital Universitari Germans Trias i Pujol (HGTiP), 08916 Badalona, Spain.ORCID 0000-0002-3812-1313
Anna PousMedical Oncology Department, Catalan Institute of Oncology-Badalona, Hospital Universitari Germans Trias i Pujol (HGTiP), 08916 Badalona, Spain.
Milana Bergamino SirvenMedical Oncology Department, Catalan Institute of Oncology-Badalona, Hospital Universitari Germans Trias i Pujol (HGTiP), 08916 Badalona, Spain.
Mireia MargelíMedical Oncology Department, Catalan Institute of Oncology-Badalona, Hospital Universitari Germans Trias i Pujol (HGTiP), 08916 Badalona, Spain.ORCID 0000-0003-3594-4530
Universitat Autònoma de Barcelona · ES

Funding

Rio Hortega grant from the Instituto de Salud Carlos III ISCIII- CM20/00027
6 · The paper itself

Abstract

Despite the improvement achieved by the introduction of HER2-targeted therapy, up to 25% of early human epidermal growth factor receptor 2-positive (HER2+) breast cancer (BC) patients will relapse. Beyond trastuzumab, other agents approved for early HER2+ BC include the monoclonal antibody pertuzumab, the antibody-drug conjugate (ADC) trastuzumab-emtansine (T-DM1) and the reversible HER2 inhibitor lapatinib. New agents, such as trastuzumab-deruxtecan or tucatinib in combination with capecitabine and trastuzumab, have also shown a significant improvement in the metastatic setting. Other therapeutic strategies to overcome treatment resistance have been explored in HER2+ BC, mainly in HER2+ that also overexpress estrogen receptors (ER+). In ER+ HER2+ patients, target therapies such as phosphoinositide-3-kinase (PI3K) pathway inhibition or cyclin-dependent kinases 4/6 blocking may be effective in controlling downstream of HER2 and many of the cellular pathways associated with resistance to HER2-targeted therapies. Multiple trials have explored these strategies with some promising results, and probably, in the next years conclusive results will succeed. In addition, HER2+ BC is known to be more immunogenic than other BC subgroups, with high variability between tumors. Different immunotherapeutic agents such as HER-2 therapy plus checkpoint inhibitors, or new vaccines approaches have been investigated in this setting, with promising but controversial results obtained to date.

Indexed as

breast cancerestrogen receptor positiveHER2-positiveHER2-targeted therapyimmunotherapytriple-positive

Identifiers

PMID35884366
PMCPMC9320771
OpenAlexW4284895135

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.