Evidence map›Paper›PMID 27479125›Full record

ArticlePloS one2016

The Use of a New CellCollector to Isolate Circulating Tumor Cells from the Blood of Patients with Different Stages of Prostate Cancer and Clinical Outcomes - A Proof-of-Concept Study.

Gerit Theil, Kersten Fischer, Ekkehard Weber, Rita Medek, Raschid Hoda, Klaus Lücke, Paolo Fornara

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 2 pooled it
4.6field-weighted citation impact, top 4% 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

36 citing papers in PubMed, 2 syntheses or guidelines pooled it, 62 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

7 authors at 2 institutions in 1 country.

Gerit TheilMartin Luther University Halle-Wittenberg, Clinic of Urology and Transplantation, Ernst-Grube-Str.40, 06120, Halle/Saale, Germany.
Kersten FischerMartin Luther University Halle-Wittenberg, Clinic of Urology and Transplantation, Ernst-Grube-Str.40, 06120, Halle/Saale, Germany.
Ekkehard WeberGILUPI-GmbH, Potsdam, Mühlenberg 11, Germany.
Rita MedekMartin Luther University Halle-Wittenberg, Institute of Physiological Chemistry, Hollystr. 1, 06120, Halle/Saale, Germany.
Raschid HodaMartin Luther University Halle-Wittenberg, Clinic of Urology and Transplantation, Ernst-Grube-Str.40, 06120, Halle/Saale, Germany.
Klaus LückeGILUPI-GmbH, Potsdam, Mühlenberg 11, Germany.
Paolo FornaraMartin Luther University Halle-Wittenberg, Clinic of Urology and Transplantation, Ernst-Grube-Str.40, 06120, Halle/Saale, Germany.
Martin Luther University Halle-Wittenberg · DEGILUPI (Germany) · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

methodsCirculating tumor cells (CTCs) constitute a useful approach for personalized medicine. Nevertheless, the isolation of these cells remains very challenging because they rarely circulate in the blood. Another current problem is the cancer-specific characterization of these cells, which requires a method that allows for the molecular and immunocytochemical profiling of all captured cells. The purpose of our proof of concept study was to investigate the use of a medical wire (CellCollector, GILUPI) to isolate CTCs in the blood of prostate cancer (PCa) patients, which allowed CTCs to be counted and molecularly characterized. Forty-three PCa patients in different stages and 11 control subjects were studied. Some randomized samples were used to detect tumor-associated transcripts, such as prostate-specific membrane antigen (PSMA), prostate-specific antigen (PSA) and epidermal growth factor receptor (EGFR), in the isolated CTCs.

resultsThe mean CTC counts were 4.6 CTCs [range, 0-8] in patients with localized PCa, 16.8 CTCs [range, 10-25] in patients with locally advanced PCa, and 26.8 CTCs [range, 0-98] in patients with metastatic PCa. The median follow-up time was 24 months, and there was a significant difference in the cancer-specific survival rates. Patients with CTC counts under 5 CTCs lived significantly longer (p = 0.035) than patients with more than 5 CTCs. We also demonstrated that the captured CTCs could be molecularly characterized. We detected tumor-associated transcripts of EGFR and PSMA in patients with metastatic PCa in 42.8% and 14.3% of the analyzed samples, respectively.

conclusionOur results indicate that the sensitive isolation and molecular characterization of CTCs can be achieved ex vivo using the wire. Patients with more than 5 CTCs had a mortality risk that was 7.0 times greater that of those with fewer than 5 CTCs (hazard ratio 7.0 95%, CI 1.1-29.39). This proof of concept was required for the approval of the use of the CellCollector in a clinical study for the in vivo isolation of CTCs from the blood stream of PCa patients by the Federal Institute for Drugs and Medical devices (Germany, BfArM).

Indexed as

Models, BiologicalNeoplastic Cells, CirculatingAgedAged, 80 and overCase-Control StudiesCell CountCell Line, TumorCell SeparationHumansImmunohistochemistryMaleMicrofluidic Analytical TechniquesMiddle AgedNeoplasm MetastasisNeoplasm StagingProstate-Specific AntigenProstate-Specific Antigen

Identifiers

PMID27479125
PMCPMC4968821
OpenAlexW2484568738

What OpenQuestion holds

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LicenceCC BY
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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.