Evidence map›Paper›PMID 20953324›Full record

ReviewClinical & developmental immunology2010

Overview of cellular immunotherapy for patients with glioblastoma.

Elodie Vauleon, Tony Avril, Brigitte Collet, Jean Mosser, Véronique Quillien

Abstract readReview
In one paragraph

Review in Clinical & developmental immunology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 1 pooled it
–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

40 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Influence of Lipoxygenase Inhibition on Glioblastoma Cell Biology.International journal of molecular sciences · 2020
    Article
  3. Article
  4. Article
  5. Article
  6. Advances in Immunotherapy for Glioblastoma Multiforme.Journal of immunology research · 2017
    Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Effects of dendritic cell-activated and cytokine-induced killer cell therapy on 22 children with acute myeloid leukemia after chemotherapy.Journal of Huazhong University of Science and Technology. Medical sciences = Hua zhong ke ji da xue xue bao. Yi xue Ying De wen ban = Huazhong keji daxue xuebao. Yixue Yingdewen ban · 2015
    Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. The progress of immunotherapy for glioblastoma.Human vaccines & immunotherapeutics · 2015
    Review
  18. Vaccine therapies for patients with glioblastoma.Journal of neuro-oncology · 2014
    Review
  19. Clinical application of adoptive T cell therapy in solid tumors.Medical science monitor : international medical journal of experimental and clinical research · 2014
    Review
  20. Current Studies of Immunotherapy on Glioblastoma.Journal of neurology and neurosurgery · 2014
    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

5 authors.

Elodie VauleonDépartement de Biologie, Centre Eugène Marquis, Rennes, France. e.vauleon@rennes.fnclcc.fr
Tony Avril
Brigitte Collet
Jean Mosser
Véronique Quillien

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

High grade gliomas (HGG) including glioblastomas (GBM) are the most common and devastating primary brain tumours. Despite important progresses in GBM treatment that currently includes surgery combined to radio- and chemotherapy, GBM patients' prognosis remains very poor. Immunotherapy is one of the new promising therapeutic approaches that can specifically target tumour cells. Such an approach could also maintain long term antitumour responses without inducing neurologic defects. Since the past 25 years, adoptive and active immunotherapies using lymphokine-activated killer cells, cytotoxic T cells, tumour-infiltrating lymphocytes, autologous tumour cells, and dendritic cells have been tested in phase I/II clinical trials with HGG patients. This paper inventories these cellular immunotherapeutic strategies and discusses their efficacy, limits, and future perspectives for optimizing the treatment to achieve clinical benefits for GBM patients.

Indexed as

AnimalsBrain NeoplasmsClinical Trials, Phase I as TopicClinical Trials, Phase II as TopicGlioblastomaHumansImmunotherapy, ActiveImmunotherapy, AdoptiveKiller Cells, Lymphokine-ActivatedLymphocytes, Tumor-InfiltratingT-Lymphocytes, CytotoxicTreatment Outcome

Identifiers

PMID20953324
PMCPMC2952949

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.