Evidence map›Paper›PMID 19348609›Full record

ReviewCritical reviews in immunology2009

Immunotherapeutic approaches for glioma.

Hideho Okada, Gary Kohanbash, Xinmei Zhu, Edward R Kastenhuber, Aki Hoji, Ryo Ueda, Mitsugu Fujita

Open access · greenAbstract readReview
In one paragraph

Review in Critical reviews in immunology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 74 papers.

0numbers the graph read from it
0cells of the map it votes in
74citing papers in PubMed
6.7field-weighted citation impact, top 3% 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

74 citing papers in PubMed, 157 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Genetically Modified Cellular Therapies for Malignant Gliomas.International journal of molecular sciences · 2021
    Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Conventional and advanced magnetic resonance imaging in patients with high-grade glioma.The quarterly journal of nuclear medicine and molecular imaging : official publication of the Italian Association of Nuclear Medicine (AIMN) [and] the International Association of Radiopharmacology (IAR), [and] Section of the Society of... · 2018
    Review
  16. Article
  17. Article
  18. Review
  19. Review
  20. Imaging in neuro-oncology.Therapeutic advances in neurological disorders · 2018
    Review

14 more citing papers are in PubMed but not listed here.

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

7 authors at 1 institution in 1 country.

Hideho OkadaBrain Tumor Program, University of Pittsburgh Cancer Institute, Pittsburgh, PA 15213, USA. okadah@upmc.edu
Gary Kohanbash
Xinmei Zhu
Edward R Kastenhuber
Aki Hoji
Ryo Ueda
Mitsugu Fujita
UPMC Hillman Cancer Center · US

Funding

Vector delivery to modify the brain tumor and its microenvironmentP01NS040923 · NINDS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI GLORIOSO, JOSEPH C · 2002 to 2012
$12.7M
VECTOR COREP01CA100327 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI STORKUS, WALTER J. · 2005 to 2009
$4.5M
Novel Immunotherapy of Glioma using miR-17-92 Transfected T CellsR01NS055140 · NINDS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI OKADA, HIDEHO · 2007 to 2015
$2.6M
NCI NIH HHS 1P01CA100327NCI NIH HHS P01 CA100327NINDS NIH HHS 1R01NS055140-01NINDS NIH HHS 2P01NS40923NINDS NIH HHS P01 NS040923NINDS NIH HHS R01 NS055140
6 · The paper itself

Abstract

The development of effective immunotherapy strategies for glioma requires adequate understanding of the unique immunological microenvironment in the central nervous system (CNS) and CNS tumors. Although the CNS is often considered to be an immunologically privileged site and poses unique challenges for the delivery of effector cells and molecules, recent advances in technology and discoveries in CNS immunology suggest novel mechanisms that may significantly improve the efficacy of immunotherapy against gliomas. In this review, we first summarize recent advances in the CNS and CNS tumor immunology. We address factors that may promote immune escape of gliomas. We also review advances in passive and active immunotherapy strategies for glioma, with an emphasis on lessons learned from recent early-phase clinical trials. We also discuss novel immunotherapy strategies that have been recently tested in non-CNS tumors and show great potential for application to gliomas. Finally, we discuss how each of these promising strategies can be combined to achieve clinical benefit for patients with gliomas.

Indexed as

AnimalsCentral Nervous SystemCentral Nervous System NeoplasmsCytokinesDendritic CellsGliomaHumansImmunotherapySuppressor Factors, ImmunologicT-Lymphocyte SubsetsCytokinesSuppressor Factors, Immunologic

Identifiers

PMID19348609
PMCPMC2713019
OpenAlexW2065319085

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.