Evidence map›Paper›PMID 19080742›Full record

ReviewCurrent oncology reports2009

Molecular profiling in glioblastoma: prelude to personalized treatment.

Nikol Mladkova, Arnab Chakravarti

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current oncology reports, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

  1. Review
  2. Synergistic drug combinations for a precision medicine approach to interstitial glioblastoma therapy.Journal of controlled release : official journal of the Controlled Release Society · 2020
    Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. 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

2 authors.

Nikol MladkovaDepartment of Radiation Oncology, Massachusetts General Hospital Cancer Center, Boston, MA 02114, USA.
Arnab Chakravarti

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The purpose of this review is to provide an up-to-date summary of the current knowledge and understanding of the molecular alterations and pathways relevant to the clinical outcome of glioblastoma patients and their potential use in designing personalized treatment for these patients. This article also discusses the potential of molecular profiling as a diagnostic modality, possible therapeutic implications of MGMT promoter methylation, the targeted inhibition of angiogenesis, and assessment of the tumor's molecular background with respect to PI3K/AKT pathway activation and associated molecules (EGFR, EGFRvIII, PTEN).

Indexed as

Antineoplastic AgentsBrain NeoplasmsDNA MethylationDNA Modification MethylasesDNA Repair EnzymesErbB ReceptorsGlioblastomaHumansMedical OncologyModels, BiologicalNeovascularization, PathologicPhosphatidylinositol 3-KinasesPlatelet-Derived Growth FactorPromoter Regions, GeneticSignal TransductionTumor Suppressor ProteinsAntineoplastic AgentsDNA Modification MethylasesDNA Repair EnzymesErbB ReceptorsMGMT protein, humanPhosphatidylinositol 3-KinasesPlatelet-Derived Growth FactorTumor Suppressor ProteinsVascular Endothelial Growth Factor A

Identifiers

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.