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A proof-of-concept study with the tyrosine kinase inhibitor nilotinib in spondyloarthritis
BACKGROUND: To evaluate the immunomodulating and clinical effects of nilotinib, a tyrosine kinase inhibitor, in a proof-of-concept study in spondyloarthritis (SpA) assessing the mast cell as potential novel therapeutic target in this disease. METHODS: Twenty eight patients with active peripheral (pS...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5081668/ https://www.ncbi.nlm.nih.gov/pubmed/27784336 http://dx.doi.org/10.1186/s12967-016-1050-2 |
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author | Paramarta, Jacqueline E. Turina, Maureen C. Noordenbos, Troy Heijda, Tanja F. Blijdorp, Iris C. Yeremenko, Nataliya Baeten, Dominique |
author_facet | Paramarta, Jacqueline E. Turina, Maureen C. Noordenbos, Troy Heijda, Tanja F. Blijdorp, Iris C. Yeremenko, Nataliya Baeten, Dominique |
author_sort | Paramarta, Jacqueline E. |
collection | PubMed |
description | BACKGROUND: To evaluate the immunomodulating and clinical effects of nilotinib, a tyrosine kinase inhibitor, in a proof-of-concept study in spondyloarthritis (SpA) assessing the mast cell as potential novel therapeutic target in this disease. METHODS: Twenty eight patients with active peripheral (pSpA) and/or axial SpA (axSpA) were included in a randomized, double-blind, placebo-controlled clinical trial (Trial registration: Trialregister.nl NTR2834). Patients were treated 1:1 with nilotinib or placebo for 12 weeks, followed by an open label extension for another 12 weeks. Paired synovial tissue biopsies, serum sampling and assessment of clinical symptoms were performed serially. RESULTS: In pSpA (n = 13) synovial inflammation appeared to diminish after 12 weeks of nilotinib treatment as evidenced by histopathology (decrease in number of infiltrating CD68+ and CD163+ macrophages and mast cells). Compared to placebo mRNA expression of c-Kit as mast cell marker (p = 0.037) and of pro-inflammatory cytokines such as IL-6 (p = 0.024) were reduced. The reduction of synovial inflammation was paralleled by a decrease in serum biomarkers of inflammation such as C-reactive protein (p = 0.024) and calprotectin (p = 0.055). Also clinical parameters such as patient’s global assessment of disease activity (p = 0.031) and ankylosing spondylitis disease activity score (p = 0.031) showed improvement upon 12 weeks of nilotinib but not placebo treatment. This improvement was further augmented at week 24. In contrast to pSpA, neither serum biomarkers of inflammation nor clinical parameters improved upon nilotinib treatment in axSpA. During the trial one serious adverse event occurred, which was considered unrelated to the study drug. CONCLUSIONS: This small proof-of-concept study suggests that nilotinib treatment modulates inflammation and clinical symptoms in pSpA. A similar effect was not seen in axSpA. Trial registration: trialregister.nl registration code NTR2834 registered 31 March 2011 |
format | Online Article Text |
id | pubmed-5081668 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-50816682016-10-31 A proof-of-concept study with the tyrosine kinase inhibitor nilotinib in spondyloarthritis Paramarta, Jacqueline E. Turina, Maureen C. Noordenbos, Troy Heijda, Tanja F. Blijdorp, Iris C. Yeremenko, Nataliya Baeten, Dominique J Transl Med Research BACKGROUND: To evaluate the immunomodulating and clinical effects of nilotinib, a tyrosine kinase inhibitor, in a proof-of-concept study in spondyloarthritis (SpA) assessing the mast cell as potential novel therapeutic target in this disease. METHODS: Twenty eight patients with active peripheral (pSpA) and/or axial SpA (axSpA) were included in a randomized, double-blind, placebo-controlled clinical trial (Trial registration: Trialregister.nl NTR2834). Patients were treated 1:1 with nilotinib or placebo for 12 weeks, followed by an open label extension for another 12 weeks. Paired synovial tissue biopsies, serum sampling and assessment of clinical symptoms were performed serially. RESULTS: In pSpA (n = 13) synovial inflammation appeared to diminish after 12 weeks of nilotinib treatment as evidenced by histopathology (decrease in number of infiltrating CD68+ and CD163+ macrophages and mast cells). Compared to placebo mRNA expression of c-Kit as mast cell marker (p = 0.037) and of pro-inflammatory cytokines such as IL-6 (p = 0.024) were reduced. The reduction of synovial inflammation was paralleled by a decrease in serum biomarkers of inflammation such as C-reactive protein (p = 0.024) and calprotectin (p = 0.055). Also clinical parameters such as patient’s global assessment of disease activity (p = 0.031) and ankylosing spondylitis disease activity score (p = 0.031) showed improvement upon 12 weeks of nilotinib but not placebo treatment. This improvement was further augmented at week 24. In contrast to pSpA, neither serum biomarkers of inflammation nor clinical parameters improved upon nilotinib treatment in axSpA. During the trial one serious adverse event occurred, which was considered unrelated to the study drug. CONCLUSIONS: This small proof-of-concept study suggests that nilotinib treatment modulates inflammation and clinical symptoms in pSpA. A similar effect was not seen in axSpA. Trial registration: trialregister.nl registration code NTR2834 registered 31 March 2011 BioMed Central 2016-10-27 /pmc/articles/PMC5081668/ /pubmed/27784336 http://dx.doi.org/10.1186/s12967-016-1050-2 Text en © The Author(s) 2016 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. 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 Paramarta, Jacqueline E. Turina, Maureen C. Noordenbos, Troy Heijda, Tanja F. Blijdorp, Iris C. Yeremenko, Nataliya Baeten, Dominique A proof-of-concept study with the tyrosine kinase inhibitor nilotinib in spondyloarthritis |
title | A proof-of-concept study with the tyrosine kinase inhibitor nilotinib in spondyloarthritis |
title_full | A proof-of-concept study with the tyrosine kinase inhibitor nilotinib in spondyloarthritis |
title_fullStr | A proof-of-concept study with the tyrosine kinase inhibitor nilotinib in spondyloarthritis |
title_full_unstemmed | A proof-of-concept study with the tyrosine kinase inhibitor nilotinib in spondyloarthritis |
title_short | A proof-of-concept study with the tyrosine kinase inhibitor nilotinib in spondyloarthritis |
title_sort | proof-of-concept study with the tyrosine kinase inhibitor nilotinib in spondyloarthritis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5081668/ https://www.ncbi.nlm.nih.gov/pubmed/27784336 http://dx.doi.org/10.1186/s12967-016-1050-2 |
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