Evidence map›Paper›PMID 28586395›Full record

Trial reportPloS one2017

The HER2 phenotype of circulating tumor cells in HER2-positive early breast cancer: A translational research project of a prospective randomized phase III trial.

B A S Jaeger, J Neugebauer, U Andergassen, C Melcher, F Schochter, D Mouarrawy, G Ziemendorff, M Clemens, E V Abel, G Heinrich and 11 more

Registry-linked trialOpen access · goldAbstract readClinical Trial, Phase IIIRandomized Controlled Trial
In one paragraph

Trial report in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03979339 (Feasibility of a New Technology for Isolating Circulating Tumour Cells in Selected Cancer Patients and Healthy Volunteers), which is not on this map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.5field-weighted citation impact, top 9% 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.

NCT03979339 naunknown statusnot on this mapstarted 2020, after this paper: background citation

Feasibility of a New Technology for Isolating Circulating Tumour Cells in Selected Cancer Patients and Healthy Volunteers

TypeinterventionalSponsorCentre Oscar LambretRan2020 to 2023Enrolled76ConditionsHER2-positive Metastatic Breast Cancer, Ovarian Cancer, Hormone-resistant Prostate Cancer, Circulating Tumor CellArmsBlood sample collection
3 · Its place in the literature

Who cites it

32 citing papers in PubMed, 52 citations in OpenAlex.

  1. Trial
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  9. The journal of liquid biopsy · 2023
    Review
  10. Article
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  12. Review
  13. Article
  14. Review
  15. Article
  16. Circulating tumor cells: biology and clinical significance.Signal transduction and targeted therapy · 2021
    Review
  17. Review
  18. Review
  19. Review
  20. 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

21 authors at 13 institutions in 1 country.

B A S JaegerDepartment of Gynecology and Obstetrics, Heinrich-Heine-University Hospital, Duesseldorf, Germany.
J NeugebauerDepartment of Gynecology and Obstetrics, Ludwig-Maximilians-University Hospital, Munich, Germany.
U AndergassenDepartment of Gynecology and Obstetrics, Ludwig-Maximilians-University Hospital, Munich, Germany.
C MelcherDepartment of Gynecology and Obstetrics, Heinrich-Heine-University Hospital, Duesseldorf, Germany.
F SchochterDepartment of Gynecology and Obstetrics, University Hospital Ulm, Ulm, Germany.
D MouarrawyHospital Bremerhaven-Reinkenheide, Bremerhaven, Germany.
G ZiemendorffHospital Ludwigsburg, Ludwigsburg, Germany.
M ClemensKrankenanstalten Mutterhaus der Borromäerinnen, Trier, Germany.
E V AbelHospital Schwäbisch Gmuend, Mutlangen, Germany.
G HeinrichPraxis Dr. Heinrich, Fuerstenwalde, Germany.
K SchuellerStat-up Statistische Beratung und Dienstleistung, Munich, Germany.
A SchneeweissDepartment of Gynecology and Obstetrics in the National Center for Tumor Disease, University Hospital Heidelberg, Heidelberg, Germany.
P FaschingDepartment of Gynecology and Obstetrics, University Hospital Erlangen, Friedrich-Alexander University Erlangen-Nuremberg, Comprehensive Cancer Center Erlangen-EMN, Erlangen, Germany.
M W BeckmannDepartment of Gynecology and Obstetrics, University Hospital Erlangen, Friedrich-Alexander University Erlangen-Nuremberg, Comprehensive Cancer Center Erlangen-EMN, Erlangen, Germany.
Ch ScholzDepartment of Gynecology and Obstetrics, University Hospital Ulm, Ulm, Germany.
T W P FriedlDepartment of Gynecology and Obstetrics, University Hospital Ulm, Ulm, Germany.
K FrieseHospital Bad Trissl, Bad Trissl, Germany.
K PantelInstitute for Tumor Biology, Center of Experimental Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
T FehmDepartment of Gynecology and Obstetrics, Heinrich-Heine-University Hospital, Duesseldorf, Germany.
W JanniDepartment of Gynecology and Obstetrics, University Hospital Ulm, Ulm, Germany.
B RackDepartment of Gynecology and Obstetrics, Ludwig-Maximilians-University Hospital, Munich, Germany.
University Hospital Ulm · DELudwig-Maximilians-Universität München · DEComprehensive Cancer Center Erlangen · DEDüsseldorf University Hospital · DEHeidelberg University · DEHeinrich Heine University Düsseldorf · DEHNO-Praxis · DEKlinikum Bremerhaven-Reinkenheide · DEKlinikum Ludwigsburg · DEKlinikum Mutterhaus der Borromäerinnen · DEStatistisches Bundesamt · DEUniversity Medical Center Hamburg-Eppendorf · DEUniversity of Education Schwaebisch Gmuend · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHER2 is one of the predominant therapeutic targets in breast cancer. The metastatic selection process may lead to discrepancies between the HER2 status of the primary tumor and circulating tumor cells (CTCs). This study analyzed the HER2 status of CTCs in patients with HER2-positive primary breast cancer at the time of diagnosis. Aim of the study was to assess potential discordance of HER2 status between primary tumor and CTCs, as this may have important implications for the use of HER2-targeted therapy.

methodsThe number and HER2 status of CTCs out of 30ml peripheral blood were assessed in 642 patients using the CellSearch System (Janssen Diagnostics, USA). The cutoff for CTC positivity was the presence of at least 1 CTC, and the cutoff for HER2 positivity of CTCs was the presence of at least 1 CTC with a strong HER2 staining.

results258 (40.2%) of the 642 patients were positive for CTCs (median 2; range 1-1,689). 149 (57.8%) of these 258 patients had at least 1 CTC with strong HER2 staining. The presence of HER2-positive CTCs was not associated with tumor size (p = 0.335), histopathological grading (p = 0.976), hormone receptor status (ER: p = 0.626, PR: p = 0.263) or axillary lymph node involvement (p = 0.430). Overall, 83 (32.2%) of the CTC-positive patients exclusively had CTCs with strong HER2 staining, whereas 31 (12.0%) had only CTCs with negative HER2 staining. Within-sample variation in the HER2 status of CTCs was found in 86 (57.8%) of the 149 patients with more than 1 CTC.

conclusionThis study demonstrated that discordance between the HER2 expression of CTCs and that of the primary tumor frequently occurs in early breast cancer. Future follow-up evaluation will assess whether this discrepancy may contribute to trastuzumab resistance.

Indexed as

AdultAgedBiomarkers, TumorBreast NeoplasmsErb-b2 Receptor Tyrosine KinasesFemaleGene Expression Regulation, NeoplasticHumansMiddle AgedNeoplasm StagingNeoplastic Cells, CirculatingTranslational Research, BiomedicalTrastuzumabBiomarkers, TumorERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesTrastuzumab

Identifiers

PMID28586395
PMCPMC5460789
OpenAlexW2622009279

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Registered trials

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.