Evidence map›Paper›PMID 31277254›Full record

ArticleCancers2019

In Vivo Detection of Circulating Tumor Cells in High-Risk Non-Metastatic Prostate Cancer Patients Undergoing Radiotherapy.

Shukun Chen, Gerlinde Tauber, Tanja Langsenlehner, Linda Maria Schmölzer, Michaela Pötscher, Sabine Riethdorf, Andra Kuske, Gerd Leitinger, Karl Kashofer, Zbigniew T Czyż and 5 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 16% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 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

15 authors at 3 institutions in 3 countries.

Shukun ChenDepartment of Laboratory Medicine, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.ORCID 0000-0003-3346-1420
Gerlinde TauberDepartment of Therapeutic Radiology and Oncology, Medical University of Graz, 8036 Graz, Austria.
Tanja LangsenlehnerDepartment of Therapeutic Radiology and Oncology, Medical University of Graz, 8036 Graz, Austria.
Linda Maria SchmölzerDepartment of Therapeutic Radiology and Oncology, Medical University of Graz, 8036 Graz, Austria.
Michaela PötscherDepartment of Therapeutic Radiology and Oncology, Medical University of Graz, 8036 Graz, Austria.
Sabine RiethdorfInstitute of Tumor Biology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
Andra KuskeInstitute of Tumor Biology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
Gerd LeitingerDepartment of Cell Biology, Histology and Embryology, Gottfried Schatz Research Center, Medical University of Graz, 8010 Graz, Austria.
Karl KashoferDiagnostic and Research Institute of Pathology, Medical University Graz, 8036 Graz, Austria.
Zbigniew T CzyżDivision Personalized Tumor Therapy, Fraunhofer Institute for Toxicology and Experimental Medicine, 93053 Regensburg, Germany.
Bernhard PolzerDivision Personalized Tumor Therapy, Fraunhofer Institute for Toxicology and Experimental Medicine, 93053 Regensburg, Germany.
Klaus PantelInstitute of Tumor Biology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.ORCID 0000-0001-5736-2772
Peter SedlmayrDepartment of Cell Biology, Histology and Embryology, Gottfried Schatz Research Center, Medical University of Graz, 8010 Graz, Austria.
Thomas KroneisDepartment of Cell Biology, Histology and Embryology, Gottfried Schatz Research Center, Medical University of Graz, 8010 Graz, Austria. thomas.kroneis@medunigraz.at.
Amin El-HeliebiDepartment of Cell Biology, Histology and Embryology, Gottfried Schatz Research Center, Medical University of Graz, 8010 Graz, Austria.
Medical University of Graz · ATUniversität Hamburg · DEFraunhofer Institute for Toxicology and Experimental Medicine · DE

Funding

Austrian Science Fund (FWF) I 1220-B19Franz Lanyar-Stiftung at the Medical University Graz #394
6 · The paper itself

Abstract

High-risk non-metastatic prostate cancer (PCa) has the potential to progress into lethal disease. Treatment options are manifold but, given a lack of surrogate biomarkers, it remains unclear which treatment offers the best results. Several studies have reported circulating tumor cells (CTCs) to be a prognostic biomarker in metastatic PCa. However, few reports on CTCs in high-risk non-metastatic PCa are available. Herein, we evaluated CTC detection in high-risk non-metastatic PCa patients using the in vivo CellCollector CANCER01 (DC01) and CellSearch system. CTC counts were analyzed and compared before and after radiotherapy (two sampling time points) in 51 high-risk non-metastatic PCa patients and were further compared according to isolation technique; further, CTC counts were correlated to clinical features. Use of DC01 resulted in a significantly higher percentage of CTC-positive samples compared to CellSearch (33.7% vs. 18.6%;

Indexed as

circulating tumor cellsin vivo detectionnon-metastatic prostate cancerradiotherapy

Identifiers

PMID31277254
PMCPMC6678903
OpenAlexW2953875688

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.