Evidence map›Paper›PMID 23977426›Full record

ReviewCNS oncology2013

Exploitation of adaptive evolution in glioma treatment.

Ryan Cordner, Keith L Black, Christopher J Wheeler

Open access · greenAbstract readReview
In one paragraph

Review in CNS oncology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

10 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. The miR-200 family: multiple effects on gliomas.Cancer management and research · 2018
    Review
  10. 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

3 authors at 1 institution in 1 country.

Ryan Cordner
Keith L Black
Christopher J Wheeler
Cedars-Sinai Medical Center · US

Funding

EGFR activity in T cell-influenced glioma invasiveness & chemosensitivityR21NS054162 · NINDS · CEDARS-SINAI MEDICAL CENTER · PI WHEELER, CHRISTOPHER JAY · 2006 to 2007
$380k
NINDS NIH HHS 1 R21 NS054162-01NINDS NIH HHS R21 NS054162
6 · The paper itself

Abstract

Glioblastoma multiforme (GBM) is a malignant neoplasm of the CNS with almost uniform lethality. Even with standard-of-care treatments, the prognosis for patients remains dismal. GBM, as with other malignancies, often acquires treatment resistance after an initial response to therapy. Treatment resistance may come about through the adaptive evolution of tumors in response to selection pressures from treatment interventions and the microenvironment. This review discusses how adaptive evolution might potentially be exploited as a new paradigm in GBM treatment.

Indexed as

Biological EvolutionCentral Nervous System NeoplasmsDrug TherapyGlioblastomaHumansImmunotherapy, Adoptive

Identifiers

PMID23977426
PMCPMC3746825
OpenAlexW2030600298

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.