Evidence map›Paper›PMID 30787232›Full record

ArticleNeurologia medico-chirurgica2019

EGFRvIII Is Expressed in Cellular Areas of Tumor in a Subset of Glioblastoma.

Takanori Nozawa, Masayasu Okada, Manabu Natsumeda, Takeyoshi Eda, Hideaki Abe, Yoshihiro Tsukamoto, Kouichirou Okamoto, Makoto Oishi, Hitoshi Takahashi, Yukihiko Fujii and 1 more

Open access · goldAbstract read
In one paragraph

Article in Neurologia medico-chirurgica, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 26% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

  1. Pooled it
  2. Review
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  5. Review
  6. Article
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  8. Article
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  10. Article
  11. Highly Sensitive EGFRvIII Detection in Circulating Extracellular Vesicle RNA of Glioma Patients.Clinical cancer research : an official journal of the American Association for Cancer Research · 2022
    Article
  12. GZ17-6.02 Inhibits the Growth of EGFRvIII+ Glioblastoma.International journal of molecular sciences · 2022
    Article
  13. Article
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

11 authors at 1 institution in 1 country.

Takanori NozawaDepartment of Neurosurgery, Brain Research Institute, University of Niigata.
Masayasu OkadaDepartment of Neurosurgery, Brain Research Institute, University of Niigata.
Manabu NatsumedaDepartment of Neurosurgery, Brain Research Institute, University of Niigata.
Takeyoshi EdaDepartment of Neurosurgery, Brain Research Institute, University of Niigata.
Hideaki AbeDepartment of Neurosurgery, Brain Research Institute, University of Niigata.
Yoshihiro TsukamotoDepartment of Neurosurgery, Brain Research Institute, University of Niigata.
Kouichirou OkamotoDepartment of Neurosurgery, Brain Research Institute, University of Niigata.
Makoto OishiDepartment of Neurosurgery, Brain Research Institute, University of Niigata.
Hitoshi TakahashiDepartment of Pathology, Brain Research Institute, University of Niigata.
Yukihiko FujiiDepartment of Neurosurgery, Brain Research Institute, University of Niigata.
Akiyoshi KakitaDepartment of Pathology, Brain Research Institute, University of Niigata.
Niigata University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epidermal growth factor receptor variant III (EGFRvIII) is a tumor-specific cell surface antigen often expressed in glioblastoma and has drawn much attention as a possible therapeutic target. We performed immunohistochemistry on histology sections of surgical specimens taken from 67 cases with glioblastoma, isocitrate dehydrogenase-wild type, and evaluated the morphological characteristics and distribution of the EGFRvIII-positive tumor cells. We then evaluated the localization of EGFRvIII-expression within the tumor and peritumoral areas. EGFRvIII immunopositivity was detected in 15 specimens taken from 13 patients, including two recurrent specimens taken from the same patient at relapse. Immunofluorescence staining demonstrated that EGFRvIII-positive cells were present in cells positive for glial fibrillary acidic protein (GFAP), and some showed astrocytic differentiation with multiple fine processes and others did not shown. The EGFRvIII-positive cells were located in cellular areas of the tumor, but not in the invading zone. In the two recurrent cases, EGFRvIII-positive cells were markedly decreased in one case and retained in the other. With regard to overall survival, univariate analysis indicated that EGFRvIII-expression in patients with glioblastoma was not significantly associated with a favorable outcome. Double-labeling immunofluorescence staining of EGFRvIII and GFAP showed that processes of large, well differentiated, GFAP-positive glia extend to and surround less differentiated, EGFRvIII-positive glial cells in cellular areas of tumor. However, in the tumor periphery, EGFRvIII-positive tumor cells were not observed. This finding suggests that EGFRvIII is involved in tumor proliferation, but that invading glioma cells lose their EGFRvIII expression.

Indexed as

AgedAged, 80 and overBrain NeoplasmsCohort StudiesErbB ReceptorsFemaleGlioblastomaHumansMaleMiddle AgedSurvival Rateepidermal growth factor receptor VIIIErbB ReceptorsdistributionEGFRvIIIglioblastomamorphologyprognosis

Identifiers

PMID30787232
PMCPMC6434422
OpenAlexW2917468161

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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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.