Evidence map›Paper›PMID 37046648›Full record

ReviewCancers2023

Emerging Targeted Therapies for HER2-Positive Breast Cancer.

María Florencia Mercogliano, Sofía Bruni, Florencia Luciana Mauro, Roxana Schillaci

Open access · goldAbstract readReview
In one paragraph

Review in Cancers, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 96 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
96citing papers in PubMed, 2 pooled it
39.6field-weighted citation impact, top 1% 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

96 citing papers in PubMed, 2 syntheses or guidelines pooled it, 172 citations in OpenAlex.

  1. Pooled it
  2. Guideline
  3. Computationally Derived Spatial Immune Signature Identifies Trastuzumab Responders in HER2+ Breast Cancer: NSABP B-41 Clinical Trial Validation.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
    Trial
  4. Review
  5. Article
  6. In vitro study and in silico reveal Teucrium Polium L. methanolic extract as an apoptosis inducer and a potential Bcl-2 inhibitor for breast cancer.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2026
    Article
  7. Exploring tyrosine kinase inhibitors for HER2-positive breast cancer: comprehensive review on a complete pharmacology-molecular mechanisms, safety profiles, and insights from preclinical and clinical studies.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
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  11. Article
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36 more citing papers are in PubMed but not listed here.

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

4 authors at 1 institution in 1 country.

María Florencia MercoglianoInstituto de Biología y Medicina Experimental (IByME-CONICET), Buenos Aires C1428ADN, Argentina.ORCID 0000-0003-1094-9247
Sofía BruniInstituto de Biología y Medicina Experimental (IByME-CONICET), Buenos Aires C1428ADN, Argentina.ORCID 0000-0001-7429-8039
Florencia Luciana MauroInstituto de Biología y Medicina Experimental (IByME-CONICET), Buenos Aires C1428ADN, Argentina.
Roxana SchillaciInstituto de Biología y Medicina Experimental (IByME-CONICET), Buenos Aires C1428ADN, Argentina.ORCID 0000-0002-7776-3378
Consejo Nacional de Investigaciones Científicas y Técnicas · AR

Funding

Florencio Fiorini Foundation Research Grant awarded to MFMThe National Agency of Scientific Promotion of Argentina IDB/PICT 2017-1517The National Agency of Scientific Promotion of Argentina PICT 2018-2086The National Agency of Scientific Promotion of Argentina PICT aplicación intensiva 2021-023The National Cancer Institute of Argentina INC 2018-2020
6 · The paper itself

Abstract

Breast cancer is the most common cancer in women and the leading cause of death. HER2 overexpression is found in approximately 20% of breast cancers and is associated with a poor prognosis and a shorter overall survival. Tratuzumab, a monoclonal antibody directed against the HER2 receptor, is the standard of care treatment. However, a third of the patients do not respond to therapy. Given the high rate of resistance, other HER2-targeted strategies have been developed, including monoclonal antibodies such as pertuzumab and margetuximab, trastuzumab-based antibody drug conjugates such as trastuzumab-emtansine (T-DM1) and trastuzumab-deruxtecan (T-DXd), and tyrosine kinase inhibitors like lapatinib and tucatinib, among others. Moreover, T-DXd has proven to be of use in the HER2-low subtype, which suggests that other HER2-targeted therapies could be successful in this recently defined new breast cancer subclassification. When patients progress to multiple strategies, there are several HER2-targeted therapies available; however, treatment options are limited, and the potential combination with other drugs, immune checkpoint inhibitors, CAR-T cells, CAR-NK, CAR-M, and vaccines is an interesting and appealing field that is still in development. In this review, we will discuss the highlights and pitfalls of the different HER2-targeted therapies and potential combinations to overcome metastatic disease and resistance to therapy.

Indexed as

cancer vaccinesCAR-M cellsCAR-NK cellsCAR-T cellsHER2-positive breast cancerimmunotherapymonoclonal antibodiestyrosine kinase inhibitors

Identifiers

PMID37046648
PMCPMC10093019
OpenAlexW4361004330

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

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 Socratic graph.