Evidence map›Paper›PMID 40526089›Full record

ArticleOncotarget2025

Molecular landscape of HER2-mutated non-small cell lung cancer in Northeastern Brazil: Clinical, histopathological, and genomic insights.

Cleto Dantas Nogueira, Samuel Frota, Huylmer Lucena Chaves, Juliana Cordeiro de Sousa, Guilherme de Sousa Veloso, Francisco Jonathan Dos Santos Araujo, Gabriel Barbosa Silva, Samuel Silva Ferreira, Marclesson Santos Alves, Fabio Nasser and 5 more

Abstract read
In one paragraph

Article in Oncotarget, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. 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

15 authors.

Cleto Dantas Nogueira *Postgraduate Program in Pathology, Federal University of Ceará, Fortaleza, Brazil.
Samuel Frota *Argos Pathology Laboratory, Fortaleza, Brazil.
Huylmer Lucena ChavesThoracic Division, São Carlos Imagem Hospital, Fortaleza, Brazil.
Juliana Cordeiro de SousaPostgraduate Program in Natural Resources Biotechnology, Center for Agricultural Sciences, Federal University of Ceará, Fortaleza, Brazil.
Guilherme de Sousa VelosoPostgraduate Program in Pathology, Federal University of Ceará, Fortaleza, Brazil.
Francisco Jonathan Dos Santos AraujoPostgraduate Program in Natural Resources Biotechnology, Center for Agricultural Sciences, Federal University of Ceará, Fortaleza, Brazil.
Gabriel Barbosa SilvaPostgraduate Program in Pathology, Federal University of Ceará, Fortaleza, Brazil.
Samuel Silva FerreiraArgos Pathology Laboratory, Fortaleza, Brazil.
Marclesson Santos AlvesDepartment of Pathology, Messejana Heart and Lung Hospital, Fortaleza, Brazil.
Fabio NasserInstitute D'Or for Research and Education, Fortaleza, Brazil.
Ezequiel RangelDepartment of Pathology, Messejana Heart and Lung Hospital, Fortaleza, Brazil.
Francisco Martins NetoDepartment of Pathology, Messejana Heart and Lung Hospital, Fortaleza, Brazil.
Iusta CaminhaPostgraduate Program in Pathology, Federal University of Ceará, Fortaleza, Brazil.
Ellen NascimentoInCor-HCFMUSP, São Paulo, Brazil.
Fabio TavoraPostgraduate Program in Pathology, Federal University of Ceará, Fortaleza, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

HER2 genomic alterations characterize a specific subset of NSCLC with potential therapeutic relevance. While most studies focus on populations from high-income countries, data from Latin America remains scarce. We retrospectively analyzed 13 HER2-mutated NSCLC cases from a single institution in Northeastern Brazil, integrating clinical, histopathological, immunohistochemical, and molecular findings. Predominant histological patterns included acinar and lepidic subtypes, with HER2 mutations primarily involving exon 20 insertions (A775_G776insYVMA) and frequent co-alterations in TP53, KRAS, and STK11. HER2 protein expression assessed by IHC showed low scores (0-2+) in most cases, while HER2 gene amplification was confirmed in one case by D-DISH and NGS. Tumor mutation burden was universally low. Treatment responses varied, with one patient receiving trastuzumab deruxtecan. Our findings highlight the molecular diversity and diagnostic challenges of HER2-mutated NSCLC in underrepresented populations, emphasizing the need for comprehensive molecular profiling and expanded access to targeted therapies.

Indexed as

Carcinoma, Non-Small-Cell LungErb-b2 Receptor Tyrosine KinasesLung NeoplasmsMutationAdultAgedBiomarkers, TumorBrazilFemaleGenomicsHumansMaleMiddle AgedRetrospective StudiesBiomarkers, TumorERBB2 protein, humanErb-b2 Receptor Tyrosine Kinasesgenomic profilingHER2 mutationlung cancerNSCLCtargeted therapy

Identifiers

PMID40526089
PMCPMC12173199

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.