Evidence map›Paper›PMID 34150029›Full record

ArticleAmerican journal of translational research2021

Next generation sequencing of glioblastoma circulating tumor cells: non-invasive solution for disease monitoring.

Katarina Kolostova, Eliska Pospisilova, Vladimira Pavlickova, Robert Bartos, Martin Sames, Ireneusz Pawlak, Vladimir Bobek

Open access · greenAbstract read
In one paragraph

Article in American journal of translational research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 25% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Molecular and Circulating Biomarkers in Patients with Glioblastoma.International journal of molecular sciences · 2022
    Review
  9. Review
  10. Article
  11. Review
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 3 institutions in 2 countries.

Katarina KolostovaDepartment of Personalized Medicine, University Hospital Kralovske Vinohrady Srobarova 50, 100 34 Prague, Czech Republic.
Eliska PospisilovaDepartment of Personalized Medicine, University Hospital Kralovske Vinohrady Srobarova 50, 100 34 Prague, Czech Republic.
Vladimira PavlickovaDepartment of Personalized Medicine, University Hospital Kralovske Vinohrady Srobarova 50, 100 34 Prague, Czech Republic.
Robert BartosDepartment of Neurosurgery of The J.E. Purkinje University, Masaryk Hospital Sociální péče 12A, Ústí nad Labem, 40113, Czech Republic.
Martin SamesDepartment of Neurosurgery of The J.E. Purkinje University, Masaryk Hospital Sociální péče 12A, Ústí nad Labem, 40113, Czech Republic.
Ireneusz PawlakDepartment of Thoracic Surgery, Wroclaw Medical University, Grabiszynska 105, 53-439 Wroclaw, Poland and Department of Thoracic Surgery, Lower Silesian Cancer Center Wroclaw, Plac Ludwika Hirszfelda 12, 53-413 Wrocław, Poland.
Vladimir BobekDepartment of Personalized Medicine, University Hospital Kralovske Vinohrady Srobarova 50, 100 34 Prague, Czech Republic.
University Hospital Kralovske Vinohrady · CZJan Evangelista Purkyně University in Ústí nad Labem · CZWroclaw Medical University · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Treatment of aggressive glioblastoma multiforme (GBM) must be based on very precise histological and molecular diagnostic of GBM type. According to the WHO guidelines, only tissue biopsy is a relevant source of cellular material evaluated in the diagnostic process to specify the tumor features. Nevertheless, obtaining a GBM biopsy is complicated and relies mostly on resection surgery. Evaluating circulating free DNA and/or circulating tumor cells (CTCs) in the clinic, using a liquid biopsy could represent a non-invasive cancer care optimization. In the present study, the peripheral blood of patients undergoing GBM resection (n = 18) was collected and examined for CTCs. The feasibility of GBM molecular diagnostics from a simple non-invasive peripheral blood withdrawal was evaluated. The size-based enriched CTCs were analyzed using cytomorphology and their origin confirmed based on mutational analysis. In addition, shared DNA mutations in CTCs and in primary tumor tissue were searched. For the identification of CTCs, next generation sequencing (NGS) was used. The GeneReader™ sequencing platform enables targeted sequencing of a 12-gene panel and direct evaluation of detected gene variations using QIAGEN Clinical Insight Analyze (QCI-A) software with a special algorithm for liquid biopsy sequencing analysis. Herein, we present a standard operating procedure for CTC enrichment in GBM patients, CTC

Indexed as

CTCsculturinggene expressionglioblastomain vitroliquid biopsymetacellsequencing

Identifiers

PMID34150029
PMCPMC8205800
OpenAlexW3176783920

What OpenQuestion holds

Textmetadata
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.