Evidence map›Paper›PMID 23837761›Full record

ReviewFuture oncology (London, England)2013

Antibody, T-cell and dendritic cell immunotherapy for malignant brain tumors.

Vidyalakshmi Chandramohan, Duane A Mitchell, Laura A Johnson, John H Sampson, Darell D Bigner

Open access · greenAbstract readReview
In one paragraph

Review in Future oncology (London, England), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

15 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. Harnessing the immune system in glioblastoma.British journal of cancer · 2018
    Review
  8. Review
  9. Article
  10. Recent advances and future of immunotherapy for glioblastoma.Expert opinion on biological therapy · 2016
    Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. 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 at 3 institutions in 1 country.

Vidyalakshmi ChandramohanDuke University Medical Center, Department of Pathology, Durham, NC 27710, USA.
Duane A Mitchell
Laura A Johnson
John H Sampson
Darell D Bigner
Duke Medical Center · USDuke University · USUniversity of Pennsylvania · US

Funding

TUMOR SUPPRESSOR GENES IN HUMAN MEDULLOBLASTOMAP50NS020023 · NINDS · DUKE UNIVERSITY · PI SAMPSON, JOHN H. · 1985 to 2013
$17.3M
BRAIN TUMORS: IMMUNOLOGICAL AND BIOLOGICAL STUDIESR37CA011898 · NCI · DUKE UNIVERSITY · PI BIGNER, DARELL D · 1988 to 2012
$8.1M
Gene-engineered adoptive T cell immunotherapy of GBMDP2CA174502 · NCI · UNIVERSITY OF PENNSYLVANIA · PI JOHNSON, LAURA A · 2012 to 2015
$2.5M
Clinical Brain Tumor Development of a Cytomegalovirus-targeted Therapeutic with Vaccine pre-conditioning to Validate Novel Predictors of Vaccine EfficacyR01CA235612 · NCI · DUKE UNIVERSITY · PI SAMPSON, JOHN H. · 2019 to 2022
$2.0M
NCI NIH HHS DP2 CA174502NCI NIH HHS R01 CA235612NCI NIH HHS R37 CA011898NCI NIH HHS R37 CA 011898‑38NINDS NIH HHS 5P50 NS20023‑25NINDS NIH HHS P50 NS020023
6 · The paper itself

Abstract

Modest improvement in brain tumor patient survival has been achieved through advances in surgical, adjuvant radiation and chemotherapeutic strategies. However, these traditional approaches have been unsuccessful in permanently controlling these aggressive tumors, with recurrence being quite common. Hence, there is a need for novel therapeutic approaches that specifically target the molecularly diverse brain tumor cell population. The ability of the immune system to recognize altered tumor cells while avoiding surrounding normal cells offers an enormous advantage over the nonspecific nature of the conventional treatment schemes. Therefore, immunotherapy represents a promising approach that may supplement the standard therapies in eliminating the residual brain tumor cells. This review summarizes different immunotherapeutic approaches currently being tested for malignant brain tumor treatment.

Indexed as

Antibodies, MonoclonalBrain NeoplasmsDendritic CellsErbB ReceptorsGenetic EngineeringHumansImmunotherapyImmunotoxinsRadioimmunotherapyReceptors, Antigen, T-CellRecombinant ProteinsT-LymphocytesAntibodies, Monoclonalepidermal growth factor receptor VIIIErbB ReceptorsImmunotoxinsReceptors, Antigen, T-CellRecombinant Proteins

Identifiers

PMID23837761
PMCPMC3904373
OpenAlexW2153597760

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.