Evidence map›Paper›PMID 27119118›Full record

ArticleMolecular therapy oncolytics2016

Preclinical evaluation of VAX-IP, a novel bacterial minicell-based biopharmaceutical for nonmuscle invasive bladder cancer.

Shingo Tsuji, Xuguang Chen, Bryan Hancock, Veronica Hernandez, Barbara Visentin, Katherine Reil, Roger Sabbadini, Matthew Giacalone, W T Godbey

Open access · goldAbstract read
In one paragraph

Article in Molecular therapy oncolytics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.5field-weighted citation impact, top 8% 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

16 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
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  8. Using nanoparticles forInternational journal of hyperthermia : the official journal of European Society for Hyperthermic Oncology, North American Hyperthermia Group · 2020
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  15. Enzyme/Prodrug Systems for Cancer Gene Therapy.Current pharmacology reports · 2016
    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

9 authors at 2 institutions in 1 country.

Shingo TsujiVaxiion Therapeutics , San Diego, California, USA.
Xuguang ChenDepartment of Chemical & Biomolecular Engineering, Tulane University , New Orleans, Louisiana, USA.
Bryan HancockVaxiion Therapeutics , San Diego, California, USA.
Veronica HernandezVaxiion Therapeutics , San Diego, California, USA.
Barbara VisentinVaxiion Therapeutics , San Diego, California, USA.
Katherine ReilVaxiion Therapeutics , San Diego, California, USA.
Roger SabbadiniVaxiion Therapeutics , San Diego, California, USA.
Matthew GiacaloneVaxiion Therapeutics , San Diego, California, USA.
W T GodbeyDepartment of Chemical & Biomolecular Engineering, Tulane University , New Orleans, Louisiana, USA.
Vaxiion Therapeutics (United States) · USTulane University · US

Funding

Immunotherapeutic minicells for use in intermediate and high-risk non-muscle invaR43CA180403 · NCI · VAXIION THERAPEUTICS, INC. · PI GIACALONE, MATTHEW, SABBADINI, ROGER ALLEN · 2013 to 2014
$214k
NCI NIH HHS R43 CA180403
6 · The paper itself

Abstract

The development of new therapies that can prevent recurrence and progression of nonmuscle invasive bladder cancer remains an unmet clinical need. The continued cost of monitoring and treatment of recurrent disease, along with its high prevalence and incidence rate, is a strain on healthcare economics worldwide. The current work describes the characterization and pharmacological evaluation of VAX-IP as a novel bacterial minicell-based biopharmaceutical agent undergoing development for the treatment of nonmuscle invasive bladder cancer and other oncology indications. VAX-IP minicells selectively target two oncology-associated integrin heterodimer subtypes to deliver a unique bacterial cytolysin protein toxin, perfringolysin O, specifically to cancer cells, rapidly killing integrin-expressing murine and human urothelial cell carcinoma cells with a unique tumorlytic mechanism. The in vivo pharmacological evaluation of VAX-IP minicells as a single agent administered intravesically in two clinically relevant variations of a syngeneic orthotopic model of superficial bladder cancer results in a significant survival advantage with 28.6% (P = 0.001) and 16.7% (P = 0.003) of animals surviving after early or late treatment initiation, respectively. The results of these preclinical studies warrant further nonclinical and eventual clinical investigation in underserved nonmuscle invasive bladder cancer patient populations where complete cures are achievable.

Identifiers

PMID27119118
PMCPMC4824562
OpenAlexW2298505006

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.