Evidence map›Paper›PMID 39472809›Full record

ArticleBMC cancer2024

Potential of PSMA for breast cancer in nuclear medicine: digital quantitative immunohistochemical analysis and implications for a theranostic approach.

Zoé Neviere, Cécile Blanc-Fournier, Anne-Valérie Guizard, Nicolas Elie, Florence Giffard, Justine Lequesne, George Emile, Laurent Poulain, Charline Lasnon

Abstract read
In one paragraph

Article in BMC cancer, 2024. 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. Article
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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

9 authors.

Zoé NeviereDepartment of Medical Oncology, Comprehensive Cancer Centre F. Baclesse, UNICANCER, Caen, France.
Cécile Blanc-FournierDepartment of Bio-Pathology, Comprehensive Cancer Centre F. Baclesse, UNICANCER, Caen, France.
Anne-Valérie GuizardCalvados General Tumour Registry, Cancers & Préventions - U1086 Inserm, Centre François Baclesse, Caen, France.
Nicolas ElieFederative Structure 4207 'Normandie Oncologie', PLATON Services Unit, VIRTUAL'HIS, Université de Caen Normandie, Caen, France.
Florence GiffardFederative Structure 4207 'Normandie Oncologie', PLATON Services Unit, VIRTUAL'HIS, Université de Caen Normandie, Caen, France.
Justine LequesneBiostatistics Department, Comprehensive Cancer Centre François Baclesse, UNICANCER, Caen, France.
George EmileDepartment of Medical Oncology, Comprehensive Cancer Centre F. Baclesse, UNICANCER, Caen, France.
Laurent PoulainInterdisciplinary Research Unit for Cancer Prevention and Treatment, Federative Structure 4207 'Normandie Oncologie', F. Baclesse, Université of Caen Normandie, Inserm U1086 ANTICIPE, Caen, France.
Charline LasnonInterdisciplinary Research Unit for Cancer Prevention and Treatment, Federative Structure 4207 'Normandie Oncologie', F. Baclesse, Université of Caen Normandie, Inserm U1086 ANTICIPE, Caen, France. c.lasnon@baclesse.unicancer.fr.ORCID https://orcid.org/0000-0001-5643-1668

Funding

La Ligue Contre le Cancer de Normandie. Not applicable
6 · The paper itself

Abstract

backgroundFurther research is still needed to fully understand the potential of prostate-specific membrane antigen (PSMA) in breast cancer (BC) and to develop and optimize targeted therapies and imaging modalities. The objective of this study was to present a comprehensive analysis of immunohistochemistry data on PSMA staining in BC and to discuss its potential value in a theranostic approach.

methodsFifty-eight male and female patients were randomly selected from a retrospective database of patients who underwent surgery for breast cancer between January 2012 and December 2017 and for whom a specimen is available in our tumour library. Immunodetection of PSMA and CD31 was performed on serial slides. The digitized slides were reviewed and analysed by an experienced pathologist. Additionally, the corresponding TIFF images were processed to calculate the percentage of positive neovessels.

resultsEighteen patients (31.6%) had no expression, 29 (50.9%) had PSMA neovascular expression scored as "1", and 10 (17.5%) had neovascular expression scored as "2". Digital immunohistochemistry analysis for this last specific group of patients showed a median proportion of positive neovessels equal to 5% (range: 3-19). A multivariable logistic regression demonstrated that the odds of PSMA positivity were 4.55 times higher in non-luminal tumours and decreased by a factor of 0.12 in lobular subtypes. There was no association between sex or the presence of a germline BRCA1/2 mutation and PSMA expression in tumours.

conclusionsOur study highlights generally low neovascular expression of PSMA in specific histopathological subtypes of breast cancer, which will likely hamper the development of an adequate theranostic strategy.

trial registrationThe procedure has been retrospectively registered to the French National Institute for Health Data (N° F20220615153900).

Indexed as

Antigens, SurfaceBreast NeoplasmsGlutamate Carboxypeptidase IIImmunohistochemistryAdultAgedAged, 80 and overBiomarkers, TumorFemaleHumansMaleMiddle AgedNuclear MedicinePrecision MedicineRetrospective StudiesTheranostic NanomedicineAntigens, SurfaceBiomarkers, TumorFOLH1 protein, humanGlutamate Carboxypeptidase IIBreast cancerHuman FOLH1 proteinNuclear medicinePSMA

Identifiers

PMID39472809
PMCPMC11520496

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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.