Evidence map›Paper›PMID 22554015›Full record

ArticleBreast cancer research : BCR2012

Biomarkers characterization of circulating tumour cells in breast cancer patients.

Rosa Nadal, Ana Fernandez, Pedro Sanchez-Rovira, Marta Salido, María Rodríguez, José Luis García-Puche, Marta Macià, Josep Maria Corominas, Miguel Delgado-Rodriguez, Lucas Gonzalez and 5 more

Open access · goldAbstract read
In one paragraph

Article in Breast cancer research : BCR, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 2 pooled it
7.3field-weighted citation impact, top 2% 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

41 citing papers in PubMed, 2 syntheses or guidelines pooled it, 100 citations in OpenAlex.

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  13. The Advancing Roles of Exosomes in Breast Cancer.Frontiers in cell and developmental biology · 2021
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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

15 authors at 6 institutions in 1 country.

Rosa NadalPfizer-University of Granada-Andalusian Government Center of Genomics and Oncology (GENyO), Avenida de la Ilustración, 114, Granada, ES-18007, Spain.
Ana Fernandez
Pedro Sanchez-Rovira
Marta Salido
María Rodríguez
José Luis García-Puche
Marta Macià
Josep Maria Corominas
Miguel Delgado-Rodriguez
Lucas Gonzalez
Joan Albanell
Mónica Fernández
Francesc Solé
José Antonio Lorente
María José Serrano
Pfizer-University of Granada-Junta de Andalucía Centre for Genomics and Oncological Research · ESParc de Salut · ESHospital Del Mar · ESUniversidad de Jaén · ESUniversidad de Granada · ESUniversitat Autònoma de Barcelona · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionIncreasing evidence supports the view that the detection of circulating tumor cells (CTCs) predicts outcomes of nonmetastatic breast cancer patients. CTCs differ genetically from the primary tumor and may contribute to variations in prognosis and response to therapy. As we start to understand more about the biology of CTCs, we can begin to address how best to treat this form of disease.

methodsNinety-eight nonmetastatic breast cancer patients were included in this study. CTCs were isolated by immunomagnetic techniques using magnetic beads labelled with a multi-CK-specific antibody (CK3-11D5) and CTC detection through immunocytochemical methods. Estrogen receptor, progesterone receptor and epidermal growth factor receptor (EGFR) were evaluated by immunofluorescence experiments and HER2 and TOP2A by fluorescence in situ hybridization. We aimed to characterize this set of biomarkers in CTCs and correlate it with clinical-pathological characteristics.

resultsBaseline detection rate was 46.9% ≥ 1 CTC/30 ml threshold. CTC-positive cells were more frequent in HER2-negative tumors (p = 0.046). In patients younger than 50 years old, HER2-amplified and G1-G2 tumors had a higher possibility of being nondetectable CTCs. Heterogeneous expression of hormonal receptors (HRs) in samples from the same patients was found. Discordances between HR expression, HER2 and TOP2A status in CTCs and their primary tumor were found in the sequential blood samples. Less that 35% of patients switched their CTC status after receiving chemotherapy. EGFR-positive CTCs were associated with Luminal tumors (p = 0.03).

conclusionsThis is the largest exploratory CTC biomarker analysis in nonmetastatic BC patients. Our study suggests that CTC biomarkers profiles might be useful as a surrogate marker for therapeutic selection and monitoring since heterogeneity of the biomarker distribution in CTCs and the lack of correlation with the primary tumor biomarker status were found. Further exploration of the association between EGFR-positive CTCs and Luminal tumors is warranted.

Indexed as

Antigens, NeoplasmBiomarkers, TumorBreast NeoplasmsCell Line, TumorDNA-Binding ProteinsDNA Topoisomerases, Type IIErb-b2 Receptor Tyrosine KinasesFemaleHumansKeratinsMiddle AgedNeoplastic Cells, CirculatingPoly-ADP-Ribose Binding ProteinsPrognosisReceptors, EstrogenReceptors, ProgesteroneAntigens, NeoplasmBiomarkers, TumorDNA-Binding ProteinsDNA Topoisomerases, Type IIERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesKeratinsPoly-ADP-Ribose Binding ProteinsReceptors, EstrogenReceptors, ProgesteroneTOP2A protein, human

Identifiers

PMID22554015
PMCPMC3446333
OpenAlexW2106271594

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.