Evidence map›Paper›PMID 30562956›Full record

ArticleCancers2018

EphA3 Pay-Loaded Antibody Therapeutics for the Treatment of Glioblastoma.

Carolin Offenhäuser, Fares Al-Ejeh, Simon Puttick, Kathleen S Ensbey, Zara C Bruce, Paul R Jamieson, Fiona M Smith, Brett W Stringer, Benjamin Carrington, Adrian V Fuchs and 6 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

24 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Review
  10. Eph Receptors in Cancer.Biomedicines · 2023
    Review
  11. Review
  12. Article
  13. Article
  14. Review
  15. Review
  16. Review
  17. Review
  18. Review
  19. Antibody Targeting of Eph Receptors in Cancer.Pharmaceuticals (Basel, Switzerland) · 2020
    Review
  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

16 authors at 5 institutions in 1 country.

Carolin OffenhäuserDepartment of Cell and Molecular Biology, QIMR Berghofer Medical Research Institute, Brisbane 4006, Australia. Carolin.Offenhauser@qimrberghofer.edu.au.
Fares Al-EjehDepartment of Cell and Molecular Biology, QIMR Berghofer Medical Research Institute, Brisbane 4006, Australia. Fares.Al-Ejeh@qimrberghofer.edu.au.ORCID 0000-0002-1553-0077
Simon PuttickAustralian Institute for Bioengineering and Nanotechnology, The University of Queensland, Brisbane 4072, Australia. S.Puttick@uq.edu.au.
Kathleen S EnsbeyDepartment of Cell and Molecular Biology, QIMR Berghofer Medical Research Institute, Brisbane 4006, Australia. Kathleen.Ensbey@qimrberghofer.edu.au.
Zara C BruceDepartment of Cell and Molecular Biology, QIMR Berghofer Medical Research Institute, Brisbane 4006, Australia. Zara.Bruce@qimrberghofer.edu.au.
Paul R JamiesonDepartment of Cell and Molecular Biology, QIMR Berghofer Medical Research Institute, Brisbane 4006, Australia. Jamieson.P@wehi.edu.au.
Fiona M SmithDepartment of Cell and Molecular Biology, QIMR Berghofer Medical Research Institute, Brisbane 4006, Australia. Fiona.Smith@qimrberghofer.edu.au.
Brett W StringerDepartment of Cell and Molecular Biology, QIMR Berghofer Medical Research Institute, Brisbane 4006, Australia. Brett.W.Stringer@gmail.com.ORCID 0000-0003-4552-9736
Benjamin CarringtonDepartment of Cell and Molecular Biology, QIMR Berghofer Medical Research Institute, Brisbane 4006, Australia. Ben.Carrington@hansonwade.com.
Adrian V FuchsAustralian Institute for Bioengineering and Nanotechnology, The University of Queensland, Brisbane 4072, Australia. adrianfuchs1@hotmail.com.
Craig A BellAustralian Institute for Bioengineering and Nanotechnology, The University of Queensland, Brisbane 4072, Australia. C.Bell1@uq.edu.au.ORCID 0000-0002-8986-2795
Rosalind JeffreeKenneth G. Jamieson Department of Neurosurgery, Royal Brisbane and Women's Hospital, Brisbane 4029, Australia. Lindy.Jeffree@health.qld.gov.au.ORCID 0000-0001-7663-2694
Stephen RoseCommonwealth Scientific and Industrial Research Organisation (CSIRO), Brisbane 4006, Australia. Stephen.Rose@csiro.au.
Kristofer J ThurechtAustralian Institute for Bioengineering and Nanotechnology, The University of Queensland, Brisbane 4072, Australia. K.Thurecht@uq.edu.au.
Andrew W BoydDepartment of Cell and Molecular Biology, QIMR Berghofer Medical Research Institute, Brisbane 4006, Australia. Andrew.Boyd@qimrberghofer.edu.au.
Bryan W DayDepartment of Cell and Molecular Biology, QIMR Berghofer Medical Research Institute, Brisbane 4006, Australia. Bryan.Day@qimrberghofer.edu.au.
QIMR Berghofer Medical Research Institute · AUThe University of Queensland · AUCommonwealth Scientific and Industrial Research Organisation · AUQueensland University of Technology · AURoyal Brisbane and Women's Hospital · AU

Funding

National Health and Medical Research Council 1078893
6 · The paper itself

Abstract

The EphA3 receptor has recently emerged as a functional tumour-specific therapeutic target in glioblastoma (GBM). EphA3 is significantly elevated in recurrent disease, is most highly expressed on glioma stem cells (GSCs), and has a functional role in maintaining self-renewal and tumourigenesis. An unlabelled EphA3-targeting therapeutic antibody is currently under clinical assessment in recurrent GBM patients. In this study, we assessed the efficacy of EphA3 antibody drug conjugate (ADC) and radioimmunotherapy (RIT) approaches using orthotopic animal xenograft models. Brain uptake studies, using positron emission tomography/computed tomography (PET/CT) imaging, show EphA3 antibodies are effectively delivered across the blood-tumour barrier and accumulate at the tumour site with no observed normal brain reactivity. A robust anti-tumour response, with no toxicity, was observed using EphA3, ADC, and RIT approaches, leading to a significant increase in overall survival. Our current research provides evidence that GBM patients may benefit from pay-loaded EphA3 antibody therapies.

Indexed as

antibody drug conjugateEphA3glioblastomaradioimmunotherapystem cells

Identifiers

PMID30562956
PMCPMC6316644
OpenAlexW2904927807

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.