Cargando…

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

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. METHODS: Four gr...

Descripción completa

Detalles Bibliográficos
Autores principales: Falke, Johannes, Hulsbergen-van de Kaa, Christina A., Maj, Roberto, Oosterwijk, Egbert, Witjes, J. Alfred
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6208681/
https://www.ncbi.nlm.nih.gov/pubmed/29767328
http://dx.doi.org/10.1007/s00345-018-2334-3
_version_ 1783366751208079360
author Falke, Johannes
Hulsbergen-van de Kaa, Christina A.
Maj, Roberto
Oosterwijk, Egbert
Witjes, J. Alfred
author_facet Falke, Johannes
Hulsbergen-van de Kaa, Christina A.
Maj, Roberto
Oosterwijk, Egbert
Witjes, J. Alfred
author_sort Falke, Johannes
collection PubMed
description 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. 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. 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 (p = 0.12). Bladder weight was significantly lower for TMX-202-treated rats compared to vehicle (p = 0.005). 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. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00345-018-2334-3) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-6208681
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Springer Berlin Heidelberg
record_format MEDLINE/PubMed
spelling pubmed-62086812018-11-09 A placebo-controlled efficacy study of the intravesical immunomodulators TMX-101 and TMX-202 in an orthotopic bladder cancer rat model Falke, Johannes Hulsbergen-van de Kaa, Christina A. Maj, Roberto Oosterwijk, Egbert Witjes, J. Alfred World J Urol Topic Paper 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. 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. 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 (p = 0.12). Bladder weight was significantly lower for TMX-202-treated rats compared to vehicle (p = 0.005). 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. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00345-018-2334-3) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2018-05-16 2018 /pmc/articles/PMC6208681/ /pubmed/29767328 http://dx.doi.org/10.1007/s00345-018-2334-3 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Topic Paper
Falke, Johannes
Hulsbergen-van de Kaa, Christina A.
Maj, Roberto
Oosterwijk, Egbert
Witjes, J. Alfred
A placebo-controlled efficacy study of the intravesical immunomodulators TMX-101 and TMX-202 in an orthotopic bladder cancer rat model
title A placebo-controlled efficacy study of the intravesical immunomodulators TMX-101 and TMX-202 in an orthotopic bladder cancer rat model
title_full A placebo-controlled efficacy study of the intravesical immunomodulators TMX-101 and TMX-202 in an orthotopic bladder cancer rat model
title_fullStr A placebo-controlled efficacy study of the intravesical immunomodulators TMX-101 and TMX-202 in an orthotopic bladder cancer rat model
title_full_unstemmed A placebo-controlled efficacy study of the intravesical immunomodulators TMX-101 and TMX-202 in an orthotopic bladder cancer rat model
title_short A placebo-controlled efficacy study of the intravesical immunomodulators TMX-101 and TMX-202 in an orthotopic bladder cancer rat model
title_sort placebo-controlled efficacy study of the intravesical immunomodulators tmx-101 and tmx-202 in an orthotopic bladder cancer rat model
topic Topic Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6208681/
https://www.ncbi.nlm.nih.gov/pubmed/29767328
http://dx.doi.org/10.1007/s00345-018-2334-3
work_keys_str_mv AT falkejohannes aplacebocontrolledefficacystudyoftheintravesicalimmunomodulatorstmx101andtmx202inanorthotopicbladdercancerratmodel
AT hulsbergenvandekaachristinaa aplacebocontrolledefficacystudyoftheintravesicalimmunomodulatorstmx101andtmx202inanorthotopicbladdercancerratmodel
AT majroberto aplacebocontrolledefficacystudyoftheintravesicalimmunomodulatorstmx101andtmx202inanorthotopicbladdercancerratmodel
AT oosterwijkegbert aplacebocontrolledefficacystudyoftheintravesicalimmunomodulatorstmx101andtmx202inanorthotopicbladdercancerratmodel
AT witjesjalfred aplacebocontrolledefficacystudyoftheintravesicalimmunomodulatorstmx101andtmx202inanorthotopicbladdercancerratmodel
AT falkejohannes placebocontrolledefficacystudyoftheintravesicalimmunomodulatorstmx101andtmx202inanorthotopicbladdercancerratmodel
AT hulsbergenvandekaachristinaa placebocontrolledefficacystudyoftheintravesicalimmunomodulatorstmx101andtmx202inanorthotopicbladdercancerratmodel
AT majroberto placebocontrolledefficacystudyoftheintravesicalimmunomodulatorstmx101andtmx202inanorthotopicbladdercancerratmodel
AT oosterwijkegbert placebocontrolledefficacystudyoftheintravesicalimmunomodulatorstmx101andtmx202inanorthotopicbladdercancerratmodel
AT witjesjalfred placebocontrolledefficacystudyoftheintravesicalimmunomodulatorstmx101andtmx202inanorthotopicbladdercancerratmodel