Evidence map›Paper›PMID 32924014›Full record

ArticleNovel approaches in cancer study2020

Glioblastoma: Targeting Angiogenesis and Tyrosine Kinase Pathways.

Ali S Arbab, Meser M Ali

Open access · diamondAbstract read
In one paragraph

Article in Novel approaches in cancer study, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

8 citing papers in PubMed, 15 citations in OpenAlex.

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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

2 authors at 1 institution in 1 country.

Ali S ArbabTumor Angiogenesis Laboratory, Georgia Cancer Center, Augusta University, USA.
Meser M AliCellular and Molecular Imaging Lab, Department of Neurosurgery, Henry Ford Hospital, USA.
Henry Ford Hospital · US

Funding

Treatment of glioma with nanocombretastatin with MRI monitoringR01CA206190 · NCI · HENRY FORD HEALTH SYSTEM · PI ALI, MESER M. · 2016 to 2019
$1.4M
NCI NIH HHS R01 CA206190
6 · The paper itself

Abstract

Angiogenesis is a hallmark of glioblastoma (GBM) and remains an important therapeutic target in its treatment, especially for recurrent GBM. GBMs are characterized by the release of vascular endothelial growth factor (VEGF), an important regulator and promoter of angiogenesis. Therefore, antiangiogenic therapies (AATs) targeting VEGF or VEGF receptors (VEGFRs) were designed and thought to be an effective tool for controlling the growth of GBM. However, recent results of different clinical trials using humanized monoclonal antibodies against VEGF (bevacizumab), as well as tyrosine kinase inhibitors (TKIs) that target different VEGFRs alone or in combination with other therapeutic agents demonstrated mixed results, with the majority of reports indicating that GBM developed resistance against antiangiogenic treatments.

Indexed as

AngiogenesisGlioblastomaTyrosine kinase inhibitors

Identifiers

PMID32924014
PMCPMC7486014
OpenAlexW3084868799

What OpenQuestion holds

Textmetadata
LicenceTDM
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.