Evidence map›Paper›PMID 37761848›Full record

ArticleGenes2023

The Prediction Analysis of Microarray 50 (PAM50) Gene Expression Classifier Utilized in Indeterminate-Risk Breast Cancer Patients in Hungary: A Consecutive 5-Year Experience.

Magdolna Dank, Dorottya Mühl, Annamária Pölhös, Renata Csanda, Magdolna Herold, Attila Kristof Kovacs, Lilla Madaras, Janina Kulka, Timea Palhazy, Anna-Maria Tokes and 4 more

Abstract read
In one paragraph

Article in Genes, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Precision medicine in breast cancer (Review).Molecular and clinical oncology · 2024
    Review
  4. Review
  5. 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

14 authors.

Magdolna DankDivision of Oncology, Department of Internal Medicine and Oncology, Semmelweis University, H-1083 Budapest, Hungary.ORCID 0000-0002-4694-3624
Dorottya MühlDivision of Oncology, Department of Internal Medicine and Oncology, Semmelweis University, H-1083 Budapest, Hungary.
Annamária PölhösDivision of Oncology, Department of Internal Medicine and Oncology, Semmelweis University, H-1083 Budapest, Hungary.
Renata CsandaDivision of Oncology, Department of Internal Medicine and Oncology, Semmelweis University, H-1083 Budapest, Hungary.
Magdolna HeroldDivision of Oncology, Department of Internal Medicine and Oncology, Semmelweis University, H-1083 Budapest, Hungary.ORCID 0000-0002-1036-6343
Attila Kristof KovacsDepartment of Pathology, Forensic and Insurance Medicine, Semmelweis University, H-1091 Budapest, Hungary.
Lilla MadarasDepartment of Pathology, Forensic and Insurance Medicine, Semmelweis University, H-1091 Budapest, Hungary.
Janina KulkaDepartment of Pathology, Forensic and Insurance Medicine, Semmelweis University, H-1091 Budapest, Hungary.
Timea PalhazyDepartment of Surgery, Transplantation and Gastroenterology, Semmelweis University, H-1082 Budapest, Hungary.
Anna-Maria TokesDepartment of Pathology, Forensic and Insurance Medicine, Semmelweis University, H-1091 Budapest, Hungary.
Monika TothDepartment of Radiology, Semmelweis University, H-1082 Budapest, Hungary.
Mihaly UjhelyiTritonLife Medical Center, H-1135 Budapest, Hungary.ORCID 0000-0001-7164-563X
Attila Marcell SzaszDivision of Oncology, Department of Internal Medicine and Oncology, Semmelweis University, H-1083 Budapest, Hungary.ORCID 0000-0003-2739-4196
Zoltan HeroldDivision of Oncology, Department of Internal Medicine and Oncology, Semmelweis University, H-1083 Budapest, Hungary.ORCID 0000-0001-5990-4889

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBreast cancer has been categorized into molecular subtypes using immunohistochemical staining (IHC) and fluorescence in situ hybridization (FISH) since the early 2000s. However, recent research suggests that gene expression testing, specifically Prosigna

resultsWe analyzed 42 unilateral breast cancer samples, with 18 classified as luminal A, 10 as luminal B, 8 as Human epidermal growth factor receptor 2 (HER2)-positive, and 6 as basal-like using PAM50. Interestingly, 17 out of the 42 samples (40.47%) showed discordant results between histopathological assessment and the PAM50 classifier. While routine IHC/FISH resulted in classification differences for a quarter to a third of samples within each subtype, all basal-like tumors were misclassified. Hormone receptor-positive tumors (hazard rate: 8.7803;

conclusionsOur study supports the existing understanding of molecular subtypes in breast cancer and emphasizes the overlap between clinical characteristics and molecular subtyping. These findings underscore the value of gene expression profiling, such as PAM50, in improving treatment decisions for breast cancer patients.

Indexed as

Breast NeoplasmsFemaleGene ExpressionHumansHungaryIn Situ Hybridization, FluorescenceRetrospective Studiesbreast carcinomagene expressionimmunohistochemistryintrinsic subtypePAM50subtype

Identifiers

PMID37761848
PMCPMC10530528

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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.