Evidence map›Paper›PMID 20546782›Full record

ReviewPharmacology & therapeutics2010

Experimental approaches for the treatment of malignant gliomas.

Leopold Arko, Igor Katsyv, Grace E Park, William Patrick Luan, John K Park

Registry-linked trialOpen access · greenAbstract readReview
In one paragraph

Review in Pharmacology & therapeutics, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01413438 (Prospective, Randomized Controlled Trial of Surgical Resection Prior to Bevacizumab Therapy for Recurrent Glioblastoma Multiforme), which is not on this map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
3.8field-weighted citation impact, top 7% 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.

NCT01413438 phase2withdrawnnot on this mapstarted 2011, after this paper: background citation

Prospective, Randomized Controlled Trial of Surgical Resection Prior to Bevacizumab Therapy for Recurrent Glioblastoma Multiforme

TypeinterventionalSponsorNational Institute of Neurological Disorders and Stroke (NINDS)Ran2011 to 2013Enrolled0ConditionsGlioblastoma, Brain NeoplasmArmsCraniotomy
3 · Its place in the literature

Who cites it

36 citing papers in PubMed, 79 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. si-PDGFROxidative medicine and cellular longevity · 2022
    Article
  6. Frontiers in molecular biosciences · 2021
    Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Dihydroartemisinin suppresses glioma proliferation and invasion via inhibition of the ADAM17 pathway.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2015
    Article
  17. Review
  18. Article
  19. Article
  20. 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

5 authors at 3 institutions in 1 country.

Leopold ArkoSurgical and Molecular Neuro-oncology Unit, National Institute of Neurological Disorders and Stroke, NIH, Bethesda, MD 20892, USA.
Igor Katsyv
Grace E Park
William Patrick Luan
John K Park
National Institute of Neurological Disorders and Stroke · USHoward Hughes Medical Institute · USNational Institute of Arthritis and Musculoskeletal and Skin Diseases · US

Funding

Mechanisms of Brain Tumor ChemoresistanceZIANS003100 · NINDS · NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE · PI PARK, JOHN · 2009 to 2013
$2.6M
Mechanisms of Brain Tumor Stem Cell Growth and DifferentiationZIANS003026 · NINDS · NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE · PI PARK, JOHN · 2009 to 2012
$2.3M
Howard Hughes Medical InstituteIntramural NIH HHS ZIA NS003100
6 · The paper itself

Abstract

Malignant gliomas, which include glioblastomas and anaplastic astrocytomas, are the most common primary tumors of the brain. Over the past 30 years, the standard treatment for these tumors has evolved to include maximal safe surgical resection, radiation therapy and temozolomide chemotherapy. While the median survival of patients with glioblastomas has improved from 6 months to 14.6 months, these tumors continue to be lethal for the vast majority of patients. There has, however, been recent substantial progress in our mechanistic understanding of tumor development and growth. The translation of these genetic, epigenetic and biochemical findings into therapies that have been tested in clinical trials is the subject of this review.

Indexed as

Angiogenesis InhibitorsAntineoplastic AgentsApoptosisBiological TherapyClinical Trials as TopicDisease ProgressionEpigenomicsGliomaHumansImmunotherapyProtein Kinase InhibitorsSignal TransductionAngiogenesis InhibitorsAntineoplastic AgentsProtein Kinase Inhibitors

Identifiers

PMID20546782
PMCPMC2939300
OpenAlexW1991623686

What OpenQuestion holds

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Read underepoch 390

Registered trials

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.