Evidence map›Paper›PMID 30595972›Full record

ReviewCurrent pathobiology reports2018

Liquid Biopsy Preservation Solutions for Standardized Pre-Analytical Workflows-Venous Whole Blood and Plasma.

Daniel Grölz, Siegfried Hauch, Martin Schlumpberger, Kalle Guenther, Thorsten Voss, Markus Sprenger-Haussels, Uwe Oelmüller

Abstract readReview
In one paragraph

Review in Current pathobiology reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing 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.

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

48 citing papers in PubMed.

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  15. Network approach in liquidomics landscape.Journal of experimental & clinical cancer research : CR · 2023
    Review
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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.

Daniel GrölzQIAGEN GmbH, Research & Development, QIAGEN Strasse 1, 40724 Hilden, Germany.
Siegfried HauchQIAGEN GmbH, Research & Development, QIAGEN Strasse 1, 40724 Hilden, Germany.
Martin SchlumpbergerQIAGEN GmbH, Research & Development, QIAGEN Strasse 1, 40724 Hilden, Germany.
Kalle GuentherQIAGEN GmbH, Research & Development, QIAGEN Strasse 1, 40724 Hilden, Germany.
Thorsten VossQIAGEN GmbH, Research & Development, QIAGEN Strasse 1, 40724 Hilden, Germany.
Markus Sprenger-HausselsQIAGEN GmbH, Research & Development, QIAGEN Strasse 1, 40724 Hilden, Germany.
Uwe OelmüllerQIAGEN GmbH, Research & Development, QIAGEN Strasse 1, 40724 Hilden, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purpose of reviewLiquid biopsy analyses based on circulating cell-free nucleic acids, circulating tumor cells or other diseased cells from organs, and exosomes or other microvesicles in blood offer new means for non-invasive diagnostic applications. The main goal of this review is to explain the importance of preserving whole blood specimens after blood draw for use as liquid biopsies, and to summarize preservation solutions that are currently available. RECENT

findingsDespite the great potential of liquid biopsies for diagnostics and disease management, besides non-invasive prenatal testing (NIPT), only a few liquid biopsy applications are fully implemented for routine in vitro diagnostic testing. One major barrier is the lack of standardized pre-analytical workflows, including the collection of consistent quality blood specimens and the generation of good-quality plasma samples therefrom. Broader use of liquid biopsies in clinical routine applications therefore requires improved pre-analytical procedures to enable high-quality specimens to obtain unbiased analyte profiles (DNA, RNA, proteins, etc.) as they are in the patient's body. SUMMARY: A growing number of stabilizing reagents and dedicated blood collection tubes are available for the post-collection preservation of circulating cell-free DNA (ccfDNA) profiles in whole blood. In contrast, solutions for the preservation of circulating tumor cells (CTC) that enable both, enumeration and molecular analyses are rare. Solutions for extracellular vesicle (EV) populations, including exosomes, do not yet exist.

Indexed as

Circulating cell-free DNA (ccfDNA)Circulating tumor cells (CTC)Exosomes, pre-analyticsExtracellular vesiclesLiquid biopsyPre-analytical workflows, standardization

Identifiers

PMID30595972
PMCPMC6290703

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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.