Evidence map›Paper›PMID 26789903›Full record

ArticleInternational journal of cancer2016

A novel microfluidic platform for size and deformability based separation and the subsequent molecular characterization of viable circulating tumor cells.

G E Hvichia, Z Parveen, C Wagner, M Janning, J Quidde, A Stein, V Müller, S Loges, R P L Neves, N H Stoecklein and 4 more

Registry-linked trialAbstract read
In one paragraph

Article in International journal of cancer, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03427450 (Harvest of Circulating Tumor Cells), which is not on this map. Cited by 95 papers.

0numbers the graph read from it
0cells of the map it votes in
95citing papers in PubMed
–field-weighted citation impact
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.

NCT03427450 completednot on this mapstarted 2018, after this paper: background citation

Harvest of Circulating Tumor Cells (CTCs) From Patients With Metastatic Breast Cancer (MBC) Using the Parsortix™ PC1 System

TypeobservationalSponsorAngle plcRan2018 to 2019Enrolled421ConditionsHealthy Volunteers, Breast Cancer, MetastaticArmsBlood draw
3 · Its place in the literature

Who cites it

95 citing papers in PubMed.

  1. A Novel Workflow to Enrich and Isolate Patient-Matched EpCAMInternational journal of molecular sciences · 2017
    Trial
  2. Review
  3. Feasibility ofGeburtshilfe und Frauenheilkunde · 2026
    Article
  4. Review
  5. Review
  6. Article
  7. Article
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  9. Article
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  19. CIRCUS: CIRCUlating tumour cells in soft tissue Sarcoma - a short report.Cancer drug resistance (Alhambra, Calif.) · 2024
    Article
  20. Article

35 more citing papers are in PubMed but not listed here.

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.

G E HvichiaANGLE North America Inc, Philadelphia, PA.
Z ParveenANGLE North America Inc, Philadelphia, PA.
C WagnerANGLE North America Inc, Philadelphia, PA.
M JanningDepartment of Tumor Biology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
J QuiddeDepartment of Hematology/Oncology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
A SteinDepartment of Hematology/Oncology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
V MüllerGynecology Department and Clinic, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
S LogesDepartment of Tumor Biology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
R P L NevesDepartment of General, Visceral and Pediatric Surgery, University Hospital and Medical Faculty of the Heinrich-Heine University Düsseldorf, Düsseldorf, Germany.
N H StoeckleinDepartment of General, Visceral and Pediatric Surgery, University Hospital and Medical Faculty of the Heinrich-Heine University Düsseldorf, Düsseldorf, Germany.
H WikmanDepartment of Tumor Biology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
S RiethdorfDepartment of Tumor Biology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
K PantelDepartment of Tumor Biology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
T M GorgesDepartment of Tumor Biology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Circulating tumor cells (CTCs) were introduced as biomarkers more than 10 years ago, but capture of viable CTCs at high purity from peripheral blood of cancer patients is still a major technical challenge. Here, we report a novel microfluidic platform designed for marker independent capture of CTCs. The Parsortix™ cell separation system provides size and deformability-based enrichment with automated staining for cell identification, and subsequent recovery (harvesting) of cells from the device. Using the Parsortix™ system, average cell capture inside the device ranged between 42% and 70%. Subsequent harvest of cells from the device ranged between 54% and 69% of cells captured. Most importantly, 99% of the isolated tumor cells were viable after processing in spiking experiments as well as after harvesting from patient samples and still functional for downstream molecular analysis as demonstrated by mRNA characterization and array-based comparative genomic hybridization. Analyzing clinical blood samples from metastatic (n = 20) and nonmetastatic (n = 6) cancer patients in parallel with CellSearch(®) system, we found that there was no statistically significant difference between the quantitative behavior of the two systems in this set of twenty six paired separations. In conclusion, the epitope independent Parsortix™ system enables the isolation of viable CTCs at a very high purity. Using this system, viable tumor cells are easily accessible and ready for molecular and functional analysis. The system's ability for enumeration and molecular characterization of EpCAM-negative CTCs will help to broaden research into the mechanisms of cancer as well as facilitating the use of CTCs as "liquid biopsies."

Indexed as

Lab-On-A-Chip DevicesNeoplastic Cells, CirculatingCell Line, TumorCell SeparationCell ShapeCell SizeCell SurvivalHumanscirculating tumor celldeformabilityepithelial-mesenchymal transitionliquid biopsy

Identifiers

PMID26789903
PMCPMC5069649

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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.