The application of adjuvant autologous antravesical macrophage cell therapy vs. BCG in non-muscle invasive bladder cancer: a multicenter, randomized trial

<p>Abstract</p> <p>Introduction</p> <p>While adjuvant immunotherapy with Bacille Calmette Guérin (BCG) is effective in non-muscle-invasive bladder cancer (BC), adverse events (AEs) are considerable. Monocyte-derived activated killer cells (MAK) are discussed as essentia...

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Main Authors: Kiss Tamas, Thüroff Joachim W, Romics Imre, Grimm Marc O, Zsolt Domján, Szabo Zoltán, Kisbenedek Laszlo, Jimenz-Cruz Fernando J, Chapado Manuel S, Benoit Gerard, Kondas Jozsef, Denzinger Stefan, Thiounn Nicolas, Burger Maximilian, Tombal Bertrand, Wirth Manfred, Munsell Marc, Mills Bonnie, Koh Tung, Sherman Jeff
Format: Article
Language:English
Published: BMC 2010-06-01
Series:Journal of Translational Medicine
Online Access:http://www.translational-medicine.com/content/8/1/54
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spelling doaj-8849abdd2f3c48baa732e4f10218db742020-11-24T23:39:29ZengBMCJournal of Translational Medicine1479-58762010-06-01815410.1186/1479-5876-8-54The application of adjuvant autologous antravesical macrophage cell therapy vs. BCG in non-muscle invasive bladder cancer: a multicenter, randomized trialKiss TamasThüroff Joachim WRomics ImreGrimm Marc OZsolt DomjánSzabo ZoltánKisbenedek LaszloJimenz-Cruz Fernando JChapado Manuel SBenoit GerardKondas JozsefDenzinger StefanThiounn NicolasBurger MaximilianTombal BertrandWirth ManfredMunsell MarcMills BonnieKoh TungSherman Jeff<p>Abstract</p> <p>Introduction</p> <p>While adjuvant immunotherapy with Bacille Calmette Guérin (BCG) is effective in non-muscle-invasive bladder cancer (BC), adverse events (AEs) are considerable. Monocyte-derived activated killer cells (MAK) are discussed as essential in antitumoural immunoresponse, but their application may imply risks. The present trial compared autologous intravesical macrophage cell therapy (BEXIDEM<sup>®</sup>) to BCG in patients after transurethral resection (TURB) of BC.</p> <p>Materials and methods</p> <p>This open-label trial included 137 eligible patients with TaG1-3, T1G1-2 plurifocal or unifocal tumours and ≥ 2 occurrences within 24 months and was conducted from June 2004 to March 2007. Median follow-up for patients without recurrence was 12 months. Patients were randomized to BCG or mononuclear cells collected by apheresis after ex vivo cell processing and activation (BEXIDEM). Either arm treatment consisted of 6 weekly instillations and 2 cycles of 3 weekly instillations at months 3 and 6. Toxicity profile (primary endpoint) and prophylactic effects (secondary endpoint) were assessed.</p> <p>Results</p> <p>Patient characteristics were evenly distributed. Of 73 treated with BCG and 64 with BEXIDEM, 85% vs. 45% experienced AEs and 26% vs. 14% serious AEs (SAE), respectively (p < 0.001). Recurrence occurred significantly less frequent with BCG than with BEXIDEM (12% vs. 38%; p < 0.001).</p> <p>Discussion</p> <p>This initial report of autologous intravesical macrophage cell therapy in BC demonstrates BEXIDEM treatment to be safe. Recurrence rates were significantly lower with BCG however. As the efficacy of BEXIDEM remains uncertain, further data, e.g. marker lesions studies, are warranted.</p> <p>Trial registration</p> <p>The trial has been registered in the ISRCTN registry <url>http://isrctn.org</url> under the registration number ISRCTN35881130.</p> http://www.translational-medicine.com/content/8/1/54
collection DOAJ
language English
format Article
sources DOAJ
author Kiss Tamas
Thüroff Joachim W
Romics Imre
Grimm Marc O
Zsolt Domján
Szabo Zoltán
Kisbenedek Laszlo
Jimenz-Cruz Fernando J
Chapado Manuel S
Benoit Gerard
Kondas Jozsef
Denzinger Stefan
Thiounn Nicolas
Burger Maximilian
Tombal Bertrand
Wirth Manfred
Munsell Marc
Mills Bonnie
Koh Tung
Sherman Jeff
spellingShingle Kiss Tamas
Thüroff Joachim W
Romics Imre
Grimm Marc O
Zsolt Domján
Szabo Zoltán
Kisbenedek Laszlo
Jimenz-Cruz Fernando J
Chapado Manuel S
Benoit Gerard
Kondas Jozsef
Denzinger Stefan
Thiounn Nicolas
Burger Maximilian
Tombal Bertrand
Wirth Manfred
Munsell Marc
Mills Bonnie
Koh Tung
Sherman Jeff
The application of adjuvant autologous antravesical macrophage cell therapy vs. BCG in non-muscle invasive bladder cancer: a multicenter, randomized trial
Journal of Translational Medicine
author_facet Kiss Tamas
Thüroff Joachim W
Romics Imre
Grimm Marc O
Zsolt Domján
Szabo Zoltán
Kisbenedek Laszlo
Jimenz-Cruz Fernando J
Chapado Manuel S
Benoit Gerard
Kondas Jozsef
Denzinger Stefan
Thiounn Nicolas
Burger Maximilian
Tombal Bertrand
Wirth Manfred
Munsell Marc
Mills Bonnie
Koh Tung
Sherman Jeff
author_sort Kiss Tamas
title The application of adjuvant autologous antravesical macrophage cell therapy vs. BCG in non-muscle invasive bladder cancer: a multicenter, randomized trial
title_short The application of adjuvant autologous antravesical macrophage cell therapy vs. BCG in non-muscle invasive bladder cancer: a multicenter, randomized trial
title_full The application of adjuvant autologous antravesical macrophage cell therapy vs. BCG in non-muscle invasive bladder cancer: a multicenter, randomized trial
title_fullStr The application of adjuvant autologous antravesical macrophage cell therapy vs. BCG in non-muscle invasive bladder cancer: a multicenter, randomized trial
title_full_unstemmed The application of adjuvant autologous antravesical macrophage cell therapy vs. BCG in non-muscle invasive bladder cancer: a multicenter, randomized trial
title_sort application of adjuvant autologous antravesical macrophage cell therapy vs. bcg in non-muscle invasive bladder cancer: a multicenter, randomized trial
publisher BMC
series Journal of Translational Medicine
issn 1479-5876
publishDate 2010-06-01
description <p>Abstract</p> <p>Introduction</p> <p>While adjuvant immunotherapy with Bacille Calmette Guérin (BCG) is effective in non-muscle-invasive bladder cancer (BC), adverse events (AEs) are considerable. Monocyte-derived activated killer cells (MAK) are discussed as essential in antitumoural immunoresponse, but their application may imply risks. The present trial compared autologous intravesical macrophage cell therapy (BEXIDEM<sup>®</sup>) to BCG in patients after transurethral resection (TURB) of BC.</p> <p>Materials and methods</p> <p>This open-label trial included 137 eligible patients with TaG1-3, T1G1-2 plurifocal or unifocal tumours and ≥ 2 occurrences within 24 months and was conducted from June 2004 to March 2007. Median follow-up for patients without recurrence was 12 months. Patients were randomized to BCG or mononuclear cells collected by apheresis after ex vivo cell processing and activation (BEXIDEM). Either arm treatment consisted of 6 weekly instillations and 2 cycles of 3 weekly instillations at months 3 and 6. Toxicity profile (primary endpoint) and prophylactic effects (secondary endpoint) were assessed.</p> <p>Results</p> <p>Patient characteristics were evenly distributed. Of 73 treated with BCG and 64 with BEXIDEM, 85% vs. 45% experienced AEs and 26% vs. 14% serious AEs (SAE), respectively (p < 0.001). Recurrence occurred significantly less frequent with BCG than with BEXIDEM (12% vs. 38%; p < 0.001).</p> <p>Discussion</p> <p>This initial report of autologous intravesical macrophage cell therapy in BC demonstrates BEXIDEM treatment to be safe. Recurrence rates were significantly lower with BCG however. As the efficacy of BEXIDEM remains uncertain, further data, e.g. marker lesions studies, are warranted.</p> <p>Trial registration</p> <p>The trial has been registered in the ISRCTN registry <url>http://isrctn.org</url> under the registration number ISRCTN35881130.</p>
url http://www.translational-medicine.com/content/8/1/54
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