Evidence map›Paper›PMID 24800234›Full record

Trial reportBioMed research international2014

Evaluation of two different analytical methods for circulating tumor cell detection in peripheral blood of patients with primary breast cancer.

B A S Jaeger, J Jueckstock, U Andergassen, J Salmen, F Schochter, V Fink, M Alunni-Fabbroni, M Rezai, Th Beck, M W Beckmann and 4 more

Open access · hybridAbstract readClinical Trial, Phase IIIComparative StudyMulticenter Study
In one paragraph

Trial report in BioMed research international, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

9 citing papers in PubMed, 19 citations in OpenAlex.

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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

14 authors at 5 institutions in 1 country.

B A S JaegerDepartment of Gynecology and Obstetrics, University Hospital Ulm, 89075 Ulm, Germany.
J JueckstockDepartment of Gynecology and Obstetrics, University Hospital Munich, Ludwig-Maximilians-University, 80337 Munich, Germany.
U AndergassenDepartment of Gynecology and Obstetrics, University Hospital Munich, Ludwig-Maximilians-University, 80337 Munich, Germany.
J SalmenDepartment of Gynecology and Obstetrics, University Hospital Ulm, 89075 Ulm, Germany.
F SchochterDepartment of Gynecology and Obstetrics, University Hospital Ulm, 89075 Ulm, Germany.
V FinkDepartment of Gynecology and Obstetrics, University Hospital Ulm, 89075 Ulm, Germany.
M Alunni-FabbroniDepartment of Gynecology and Obstetrics, University Hospital Munich, Ludwig-Maximilians-University, 80337 Munich, Germany.
M RezaiLuisen Hospital, 40235 Duesseldorf, Germany.
Th BeckRoMed Hospital Rosenheim, 83022 Rosenheim, Germany.
M W BeckmannDepartment of Gynecology and Obstetrics, University Hospital Erlangen, Friedrich-Alexander University Erlangen-Nuremberg, Comprehensive Cancer Center Erlangen-EMN, 91054 Erlangen, Germany.
K FrieseDepartment of Gynecology and Obstetrics, University Hospital Munich, Ludwig-Maximilians-University, 80337 Munich, Germany.
T W P FriedlDepartment of Gynecology and Obstetrics, University Hospital Ulm, 89075 Ulm, Germany.
W JanniDepartment of Gynecology and Obstetrics, University Hospital Ulm, 89075 Ulm, Germany.
B RackDepartment of Gynecology and Obstetrics, University Hospital Munich, Ludwig-Maximilians-University, 80337 Munich, Germany.
University Hospital Ulm · DELudwig-Maximilians-Universität München · DELuisenkrankenhaus · DERoMed Kliniken · DEUniversitätsklinikum Erlangen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEvidence is accumulating that circulating tumor cells (CTC) out of peripheral blood can serve as prognostic marker not only in metastatic but also in early breast cancer (BC). Various methods are available to detect CTC. Comparisons between the different techniques, however, are rare. MATERIAL AND

methodsWe evaluate two different methods for CTC enrichment and detection in primary BC patients: the FDA-approved CellSearch System (CSS; Veridex, Warren, USA) and a manual immunocytochemistry (MICC). The cut-off value for positivity was ≥1 CTC.

resultsThe two different nonoverlapping patient cohorts evaluated with one or the other method were well balanced regarding common clinical parameters. Before adjuvant CHT 21.1% (416 out of 1972) and 20.6% (247 out of 1198) of the patients were CTC-positive, while after CHT 22.5% (359 out of 1598) and 16.6% (177 out of 1066) of the patients were CTC-positive using CSS or MICC, respectively. CTC positivity rate before CHT was thus similar and not significantly different (P = 0.749), while CTC positivity rate immediately after CHT was significantly lower using MICC compared to CSS (P < 0.001).

conclusionUsing CSS or MICC for CTC detection, we found comparable prevalence of CTC before but not after adjuvant CHT.

Indexed as

AdultAgedBreast NeoplasmsCell CountCytodiagnosisFemaleGermanyHumansImmunohistochemistryImmunomagnetic SeparationMiddle AgedNeoplastic Cells, CirculatingReproducibility of ResultsSensitivity and Specificity

Identifiers

PMID24800234
PMCPMC3997081
OpenAlexW2091083280

What OpenQuestion holds

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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.