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A placebo-controlled efficacy study of the intravesical immunomodulators TMX-101 and TMX-202 in an orthotopic bladder cancer rat model.

Authors :
Falke J
Hulsbergen-van de Kaa CA
Maj R
Oosterwijk E
Witjes JA
Source :
World journal of urology [World J Urol] 2018 Nov; Vol. 36 (11), pp. 1719-1725. Date of Electronic Publication: 2018 May 16.
Publication Year :
2018

Abstract

Purpose: TMX-101 and TMX-202 are formulations of toll-like receptor 7 (TLR-7) agonists, under investigation for the treatment of urothelial carcinoma. Our goal was to evaluate the efficacy of intravesical instillations of TMX-101 or TMX-202 in an orthotopic bladder cancer rat model.<br />Methods: Four groups of 14 rats received an instillation with isogenic AY-27 tumor cells on day 0, starting tumor development. On day 2 and 5, the rats were treated with an intravesical instillation of TMX-101 0.1%, TMX-202 0.38%, vehicle solution or NaCl. On day 12 the rats were sacrificed and the bladders were evaluated histopathologically.<br />Results: No signs of toxicity were seen. The number of tumor-positive rats was 11 of 14 (79%) in the vehicle control group and in the NaCl control group, versus 9 of 14 (64%) in the TMX-101-treated group, and 8 of 14 (57%) in the TMX-20-treated group. The difference between tumor-bearing rats in the treated and control groups was not significant (pā€‰=ā€‰0.12). Bladder weight was significantly lower for TMX-202-treated rats compared to vehicle (pā€‰=ā€‰0.005).<br />Conclusions: TMX-101 and TMX-202 are TLR-7 agonists with antitumor activity. Treatment with TMX-101 and TMX-202 resulted in less tumor-bearing rats compared to vehicle or saline control groups, although not statistically significant. In this aggressive bladder cancer model, a lower number of tumor-positive rats after treatment with TLR-7 agonists indicates activity for the treatment of non-muscle invasive bladder cancer.

Details

Language :
English
ISSN :
1433-8726
Volume :
36
Issue :
11
Database :
MEDLINE
Journal :
World journal of urology
Publication Type :
Academic Journal
Accession number :
29767328
Full Text :
https://doi.org/10.1007/s00345-018-2334-3