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Self-adjuvanted mRNA vaccination in advanced prostate cancer patients: a first-in-man phase I/IIa study

BACKGROUND: CV9103 is a prostate-cancer vaccine containing self-adjuvanted mRNA (RNActive®) encoding the antigens PSA, PSCA, PSMA, and STEAP1. This phase I/IIa study evaluated safety and immunogenicity of CV9103 in patients with advanced castration-resistant prostate-cancer. METHODS: 44 Patients rec...

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Autores principales: Kübler, Hubert, Scheel, Birgit, Gnad-Vogt, Ulrike, Miller, Kurt, Schultze-Seemann, Wolfgang, vom Dorp, Frank, Parmiani, Giorgio, Hampel, Christian, Wedel, Steffen, Trojan, Lutz, Jocham, Dieter, Maurer, Tobias, Rippin, Gerd, Fotin-Mleczek, Mariola, von der Mülbe, Florian, Probst, Jochen, Hoerr, Ingmar, Kallen, Karl-Josef, Lander, Thomas, Stenzl, Arnulf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4468959/
https://www.ncbi.nlm.nih.gov/pubmed/26082837
http://dx.doi.org/10.1186/s40425-015-0068-y
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author Kübler, Hubert
Scheel, Birgit
Gnad-Vogt, Ulrike
Miller, Kurt
Schultze-Seemann, Wolfgang
vom Dorp, Frank
Parmiani, Giorgio
Hampel, Christian
Wedel, Steffen
Trojan, Lutz
Jocham, Dieter
Maurer, Tobias
Rippin, Gerd
Fotin-Mleczek, Mariola
von der Mülbe, Florian
Probst, Jochen
Hoerr, Ingmar
Kallen, Karl-Josef
Lander, Thomas
Stenzl, Arnulf
author_facet Kübler, Hubert
Scheel, Birgit
Gnad-Vogt, Ulrike
Miller, Kurt
Schultze-Seemann, Wolfgang
vom Dorp, Frank
Parmiani, Giorgio
Hampel, Christian
Wedel, Steffen
Trojan, Lutz
Jocham, Dieter
Maurer, Tobias
Rippin, Gerd
Fotin-Mleczek, Mariola
von der Mülbe, Florian
Probst, Jochen
Hoerr, Ingmar
Kallen, Karl-Josef
Lander, Thomas
Stenzl, Arnulf
author_sort Kübler, Hubert
collection PubMed
description BACKGROUND: CV9103 is a prostate-cancer vaccine containing self-adjuvanted mRNA (RNActive®) encoding the antigens PSA, PSCA, PSMA, and STEAP1. This phase I/IIa study evaluated safety and immunogenicity of CV9103 in patients with advanced castration-resistant prostate-cancer. METHODS: 44 Patients received up to 5 intra-dermal vaccinations. Three dose levels of total mRNA were tested in Phase I in cohorts of 3–6 patients to determine a recommended dose. In phase II, 32 additional patients were treated at the recommended dose. The primary endpoint was safety and tolerability, the secondary endpoint was induction of antigen specific immune responses monitored at baseline and at weeks 5, 9 and 17. RESULTS: The most frequent adverse events were grade 1/2 injection site erythema, injection site reactions, fatigue, pyrexia, chills and influenza-like illness. Possibly treatment related urinary retention occurred in 3 patients. The recommended dose was 1280 μg. A total of 26/33 evaluable patients treated at 1280 μg developed an immune response, directed against multiple antigens in 15 out of 33 patients. One patient showed a confirmed PSA response. In the subgroup of 36 metastatic patients, the Kaplan-Meier estimate of median overall survival was 31.4 months [95 % CI: 21.2; n.a]. CONCLUSIONS: The self-adjuvanted RNActive® vaccine CV9103 was well tolerated and immunogenic. The technology is a versatile, fast and cost-effective platform allowing for creation of vaccines. The follow-up vaccine CV9104 including the additional antigens prostatic acid phosphatase (PAP) and Muc1 is currently being tested in a randomized phase IIb trial to assess the clinical benefit induced by this new vaccination approach. TRIAL REGISTRATION: EU Clinical Trials Register: EudraCT number 2008-003967-37, registered 27 Jan 2009. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40425-015-0068-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-44689592015-06-17 Self-adjuvanted mRNA vaccination in advanced prostate cancer patients: a first-in-man phase I/IIa study Kübler, Hubert Scheel, Birgit Gnad-Vogt, Ulrike Miller, Kurt Schultze-Seemann, Wolfgang vom Dorp, Frank Parmiani, Giorgio Hampel, Christian Wedel, Steffen Trojan, Lutz Jocham, Dieter Maurer, Tobias Rippin, Gerd Fotin-Mleczek, Mariola von der Mülbe, Florian Probst, Jochen Hoerr, Ingmar Kallen, Karl-Josef Lander, Thomas Stenzl, Arnulf J Immunother Cancer Research Article BACKGROUND: CV9103 is a prostate-cancer vaccine containing self-adjuvanted mRNA (RNActive®) encoding the antigens PSA, PSCA, PSMA, and STEAP1. This phase I/IIa study evaluated safety and immunogenicity of CV9103 in patients with advanced castration-resistant prostate-cancer. METHODS: 44 Patients received up to 5 intra-dermal vaccinations. Three dose levels of total mRNA were tested in Phase I in cohorts of 3–6 patients to determine a recommended dose. In phase II, 32 additional patients were treated at the recommended dose. The primary endpoint was safety and tolerability, the secondary endpoint was induction of antigen specific immune responses monitored at baseline and at weeks 5, 9 and 17. RESULTS: The most frequent adverse events were grade 1/2 injection site erythema, injection site reactions, fatigue, pyrexia, chills and influenza-like illness. Possibly treatment related urinary retention occurred in 3 patients. The recommended dose was 1280 μg. A total of 26/33 evaluable patients treated at 1280 μg developed an immune response, directed against multiple antigens in 15 out of 33 patients. One patient showed a confirmed PSA response. In the subgroup of 36 metastatic patients, the Kaplan-Meier estimate of median overall survival was 31.4 months [95 % CI: 21.2; n.a]. CONCLUSIONS: The self-adjuvanted RNActive® vaccine CV9103 was well tolerated and immunogenic. The technology is a versatile, fast and cost-effective platform allowing for creation of vaccines. The follow-up vaccine CV9104 including the additional antigens prostatic acid phosphatase (PAP) and Muc1 is currently being tested in a randomized phase IIb trial to assess the clinical benefit induced by this new vaccination approach. TRIAL REGISTRATION: EU Clinical Trials Register: EudraCT number 2008-003967-37, registered 27 Jan 2009. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40425-015-0068-y) contains supplementary material, which is available to authorized users. BioMed Central 2015-06-16 /pmc/articles/PMC4468959/ /pubmed/26082837 http://dx.doi.org/10.1186/s40425-015-0068-y Text en © Kübler et al. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Kübler, Hubert
Scheel, Birgit
Gnad-Vogt, Ulrike
Miller, Kurt
Schultze-Seemann, Wolfgang
vom Dorp, Frank
Parmiani, Giorgio
Hampel, Christian
Wedel, Steffen
Trojan, Lutz
Jocham, Dieter
Maurer, Tobias
Rippin, Gerd
Fotin-Mleczek, Mariola
von der Mülbe, Florian
Probst, Jochen
Hoerr, Ingmar
Kallen, Karl-Josef
Lander, Thomas
Stenzl, Arnulf
Self-adjuvanted mRNA vaccination in advanced prostate cancer patients: a first-in-man phase I/IIa study
title Self-adjuvanted mRNA vaccination in advanced prostate cancer patients: a first-in-man phase I/IIa study
title_full Self-adjuvanted mRNA vaccination in advanced prostate cancer patients: a first-in-man phase I/IIa study
title_fullStr Self-adjuvanted mRNA vaccination in advanced prostate cancer patients: a first-in-man phase I/IIa study
title_full_unstemmed Self-adjuvanted mRNA vaccination in advanced prostate cancer patients: a first-in-man phase I/IIa study
title_short Self-adjuvanted mRNA vaccination in advanced prostate cancer patients: a first-in-man phase I/IIa study
title_sort self-adjuvanted mrna vaccination in advanced prostate cancer patients: a first-in-man phase i/iia study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4468959/
https://www.ncbi.nlm.nih.gov/pubmed/26082837
http://dx.doi.org/10.1186/s40425-015-0068-y
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