Evidence map›Paper›PMID 32787900›Full record

ArticleBreast cancer research : BCR2020

HER2 expression on tumor-derived extracellular vesicles and circulating tumor cells in metastatic breast cancer.

Afroditi Nanou, Leonie Laura Zeune, Francois-Clement Bidard, Jean-Yves Pierga, Leonardus Wendelinus Mathias Marie Terstappen

Open access · goldAbstract read
In one paragraph

Article in Breast cancer research : BCR, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
2.7field-weighted citation impact, top 8% 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

35 citing papers in PubMed, 55 citations in OpenAlex.

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  16. Circulating tumor cellsTranslational breast cancer research : a journal focusing on translational research in breast cancer · 2024
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  17. The journal of liquid biopsy · 2023
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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 3 institutions in 2 countries.

Afroditi NanouDepartment of Medical Cell BioPhysics, Faculty of Science and Technology, University of Twente, Carré Room CR4433, Hallenweg 23, 7522 NH, Enschede, The Netherlands. a.nanou@utwente.nl.ORCID 0000-0002-8682-3133
Leonie Laura ZeuneDepartment of Medical Cell BioPhysics, Faculty of Science and Technology, University of Twente, Carré Room CR4433, Hallenweg 23, 7522 NH, Enschede, The Netherlands.
Francois-Clement BidardDepartment of Medical Oncology, Institut Curie, PSL Research University, Paris and Saint Cloud, France.
Jean-Yves PiergaDepartment of Medical Oncology, Institut Curie, PSL Research University, Paris and Saint Cloud, France.
Leonardus Wendelinus Mathias Marie TerstappenDepartment of Medical Cell BioPhysics, Faculty of Science and Technology, University of Twente, Carré Room CR4437, Hallenweg 23, 7522 NH, Enschede, The Netherlands. l.w.m.m.terstappen@utwente.nl.
University of Twente · NLDélégation Paris 5 · FRUniversité de Versailles Saint-Quentin-en-Yvelines · FR

Funding

FP7 Ideas: European Research Council 115749-1Innovative Medicines Initiative 305341Nederlandse Organisatie voor Wetenschappelijk Onderzoek 14190
6 · The paper itself

Abstract

backgroundTumor-derived extracellular vesicles (tdEVs) and circulating tumor cells (CTCs) in the blood of metastatic cancer patients associate with poor outcomes. In this study, we explored the human epidermal growth factor receptor 2 (HER2) expression on CTCs and tdEVs of metastatic breast cancer patients.

methodsBlood samples from 98 patients (CLCC-IC-2006-04 study) were originally processed with the CellSearch® system using the CTC kit and anti-HER2 as an additional marker in the staining cocktail. CTCs and tdEVs were automatically enumerated from the generated CellSearch images using the open-source ACCEPT software.

resultsCTCs and tdEVs were subdivided based on their cytokeratin (CK) and HER2 phenotype into CK+HER2-, CK-HER2+, and CK+HER2+. The inclusion of anti-HER2 increased the percentage of informative samples with ≥ 1 detectable CTC from 89 to 95%. CK- CTCs and tdEVs correlated equally well with the clinical outcome as CK+ CTCs and tdEVs. Inter- and intra-patient heterogeneity was found for the CTC/tdEV phenotypes, and the presence of 2 or 3 classes of CTCs/tdEVs was associated with worse prognosis compared to a uniform CTC/tdEV phenotype present (1 class). The use of ≥ 7% HER2+CK+ tdEVs can predict HER2 expression of the tissue with 74% sensitivity and specificity using the HER2 amplification status of the primary tumor as a classification variable.

conclusionsHER2 can be detected on CTCs and tdEVs not expressing CK, and these CK- CTCs/tdEVs have similar clinical relevance to CTCs and tdEVs expressing CK. tdEVs perform better than CTCs in predicting the HER2 status of the primary tissue. CTC and tdEV heterogeneity in the blood of patients is inversely associated with overall survival.

Indexed as

Biomarkers, TumorBreast NeoplasmsErb-b2 Receptor Tyrosine KinasesExtracellular VesiclesFemaleHumansKeratinsNeoplasm MetastasisNeoplastic Cells, CirculatingPrognosisROC CurveSurvival RateBiomarkers, TumorERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesKeratinsACCEPTCellSearchCirculating tumor cellsHER2Human epidermal growth factor receptor 2Tumor-derived extracellular vesicles

Identifiers

PMID32787900
PMCPMC7424685
OpenAlexW3048610702

What OpenQuestion 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 OpenQuestion graph.