Evidence map›Paper›PMID 29040782›Full record

ReviewNeuro-oncology2018

EGFR heterogeneity and implications for therapeutic intervention in glioblastoma.

Eskil Eskilsson, Gro V Røsland, Gergely Solecki, Qianghu Wang, Patrick N Harter, Grazia Graziani, Roel G W Verhaak, Frank Winkler, Rolf Bjerkvig, Hrvoje Miletic

Open access · bronzeAbstract readReview
In one paragraph

Review in Neuro-oncology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 188 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
188citing papers in PubMed, 2 pooled it
8.3field-weighted citation impact, top 2% 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

188 citing papers in PubMed, 2 syntheses or guidelines pooled it, 325 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
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  7. The functional imperative in high-grade glioma.Experimental & molecular medicine · 2026
    Review
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  9. Article
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  17. Tumor heterogeneity and resistance in glioblastoma: the role of stem cells.Apoptosis : an international journal on programmed cell death · 2025
    Review
  18. Article
  19. Review
  20. Article

128 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

10 authors at 8 institutions in 5 countries.

Eskil EskilssonDepartment of Genomic Medicine, The University of Texas M.D. Anderson Cancer Center, Houston, Texas, USA.
Gro V RøslandDepartment of Biomedicine, University of Bergen, Norway.
Gergely SoleckiDepartment of Neurooncology, University Hospital Heidelberg, Germany.
Qianghu WangDepartment of Genomic Medicine, The University of Texas M.D. Anderson Cancer Center, Houston, Texas, USA.
Patrick N HarterEdinger-Institute, Goethe-University Medical School, Frankfurt am Main, Germany.
Grazia GrazianiDepartment of Systems Medicine, University of Rome Tor Vergata, Rome, Italy.
Roel G W VerhaakDepartment of Genomic Medicine, The University of Texas M.D. Anderson Cancer Center, Houston, Texas, USA.
Frank WinklerDepartment of Neurooncology, University Hospital Heidelberg, Germany.
Rolf BjerkvigDepartment of Biomedicine, University of Bergen, Norway.
Hrvoje MileticDepartment of Biomedicine, University of Bergen, Norway.
The University of Texas MD Anderson Cancer Center · USUniversity of Bergen · NOGoethe University Frankfurt · DEHeidelberg University · DEJackson Laboratory · USLuxembourg Institute of Health · LUUniversity Hospital Heidelberg · DEUniversity of Rome Tor Vergata · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Patients with glioblastoma (GBM) have a universally poor prognosis and are in urgent need of effective treatment strategies. Recent advances in sequencing techniques unraveled the complete genomic landscape of GBMs and revealed profound heterogeneity of individual tumors even at the single cell level. Genomic profiling has detected epidermal growth factor receptor (EGFR) gene alterations in more than half of GBMs. Major genetic events include amplification and mutation of EGFR. Yet, treatment strategies targeting EGFR have thus far failed in clinical trials. In this review, we discuss the clonal and functional heterogeneity of EGFRs in GBM development and critically reassess the potential of EGFRs as therapeutic targets.

Indexed as

Molecular Targeted TherapyMutationErbB ReceptorsGlioblastomaHumansPrognosisProtein Kinase InhibitorsEGFR protein, humanErbB ReceptorsProtein Kinase Inhibitors

Identifiers

PMID29040782
PMCPMC5961011
OpenAlexW2763129844

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.