Evidence map›Paper›PMID 22240799›Full record

ArticleBritish journal of cancer2012

Combination of a fusogenic glycoprotein, pro-drug activation and oncolytic HSV as an intravesical therapy for superficial bladder cancer.

G R Simpson, A Horvath, N E Annels, T Pencavel, S Metcalf, R Seth, P Peschard, T Price, R S Coffin, H Mostafid and 3 more

Open access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

22 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
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  3. Article
  4. Review
  5. Article
  6. Review
  7. Oncolytic HSV Therapy Modulates Vesicular Trafficking Inducing Cisplatin Sensitivity and Antitumor Immunity.Clinical cancer research : an official journal of the American Association for Cancer Research · 2021
    Article
  8. Review
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  10. Article
  11. Article
  12. Review
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  14. Cowpox Virus: A New and Armed Oncolytic Poxvirus.Molecular therapy oncolytics · 2017
    Article
  15. Deletion ofEMBO molecular medicine · 2017
    Article
  16. Article
  17. Review
  18. Article
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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

13 authors at 6 institutions in 2 countries.

G R SimpsonOncology, Faculty of Health and Medical Sciences, University of Surrey, Guildford, UK. g.simpson@surrey.ac.uk
A Horvath
N E Annels
T Pencavel
S Metcalf
R Seth
P Peschard
T Price
R S Coffin
H Mostafid
A A Melcher
K J Harrington
H S Pandha
University of Surrey · GBInstitute of Cancer Research · GBBasingstoke and North Hampshire Hospital · GBNeuroBioTex (United States) · USSt James's University Hospital · GBVivex Biologics (United States) · US

Funding

Cancer Research UK 13244
6 · The paper itself

Abstract

backgroundThere are still no effective treatments for superficial bladder cancer (SBC)/non-muscle invasive bladder cancer. Following treatment, 20% of patients still develop metastatic disease. Superficial bladder cancer is often multifocal, has high recurrences after surgical resection and recurs after intravesical live Bacillus Calmette-Guérin. Oncovex(GALV/CD), an oncolytic herpes simplex virus-1, has shown enhanced local tumour control by combining oncolysis with the expression of a highly potent pro-drug activating gene and the fusogenic glycoprotein.

methodsIn vitro fusion/prodrug/apoptotic cell-based assays. In vivo orthotopic bladder tumour model, visualised by computed microtomography.

resultsTreatment of seven human bladder carcinoma cell lines with the virus resulted in tumour cell killing through oncolysis, pro-drug activation and glycoprotein fusion. Oncovex(GALV/CD) and mitomycin C showed a synergistic effect, whereas the co-administration with cisplatin or gemcitabine showed an antagonistic effect in vitro. Transitional cell cancer (TCC) cells follow an apoptotic cell death pathway after infection with Oncovex(GALV/CD) with or without 5-FC. In vivo results showed that intravesical treatment with Oncovex(GALV/CD) + prodrug (5-FC) reduced the average tumour volume by over 95% compared with controls. DISCUSSION: Our in vitro and in vivo results indicate that Oncovex(GALV/CD) can improve local tumour control within the bladder, and potentially alter its natural history.

Indexed as

Oncolytic VirotherapyAdministration, IntravesicalAnimalsApoptosisCarcinoma, Transitional CellCell Line, TumorCricetinaeDisease Models, AnimalFemaleFluorouracilGlycoproteinsHerpesvirus 1, HumanHumansLeukemia Virus, Gibbon ApeNeoplasm Recurrence, LocalProdrugsFluorouracilGlycoproteinsProdrugs

Identifiers

PMID22240799
PMCPMC3273343
OpenAlexW2045179871

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.