Evidence map›Paper›PMID 25425467›Full record

ReviewDiscovery medicine2014

Challenges to chimeric antigen receptor (CAR)-T cell therapy for cancer.

Michael S Magee, Adam E Snook

Open access · greenAbstract readReview
In one paragraph

Review in Discovery medicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

25 citing papers in PubMed, 50 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Review
  11. Adverse Effects Associated with Clinical Applications of CAR Engineered T Cells.Archivum immunologiae et therapiae experimentalis · 2018
    Review
  12. Article
  13. Article
  14. Review
  15. Review
  16. Chimeric antigen receptor-engineered natural killer and natural killer T cells for cancer immunotherapy.Translational research : the journal of laboratory and clinical medicine · 2017
    Review
  17. Review
  18. Article
  19. The Antitumor Efficacy of IL2/IL21-Cultured Polyfunctional Neu-Specific T Cells Is TNFα/IL17 Dependent.Clinical cancer research : an official journal of the American Association for Cancer Research · 2016
    Article
  20. 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 at 1 institution in 1 country.

Michael S MageeDepartment of Pharmacology and Experimental Therapeutics, Thomas Jefferson University, 1020 Locust Street, JAH 368, Philadelphia, PA 19107, USA.
Adam E Snook
Thomas Jefferson University · US

Funding

GUCY2C targeted adoptive T cell therapy to treat metastatic colorectal cancerF31CA171672 · NCI · THOMAS JEFFERSON UNIVERSITY · PI MAGEE, MICHAEL S. · 2012 to 2013
$84k
NCI NIH HHS F31 CA171672
6 · The paper itself

Abstract

Chimeric antigen receptor (CAR)-expressing T cells have demonstrated potent clinical efficacy in patients with B cell malignancies. However, the use of CAR-T cell therapy targeting other cancers has, in part, been limited by both the induction of antigen-specific toxicities targeting normal tissues expressing the target-antigen, and the extreme potency of CAR-T cell treatments resulting in life-threatening cytokine-release syndromes. Herein, we discuss toxicities associated with CAR-T cell therapy in the clinic. Further, we discuss potential clinical interventions to ameliorate these toxicities and the application of preclinical animal models to predict the clinical utility of CAR-T cell therapy.

Indexed as

Immunotherapy, AdoptiveAnimalsClinical Trials as TopicHumansModels, ImmunologicalNeoplasmsReceptors, Antigen, T-CellT-LymphocytesReceptors, Antigen, T-Cell

Identifiers

PMID25425467
PMCPMC12321268
OpenAlexW2263192387

What OpenQuestion holds

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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.