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Long-term efficacy of imatinib mesylate in patients with advanced Tenosynovial Giant Cell Tumor

Tenosynovial giant cell tumors (TGCT), are rare colony stimulating factor-1(CSF-1)-driven proliferative disorders affecting joints. Diffuse-type TGCT often causes significant morbidity due to local recurrences necessitating multiple surgeries. Imatinib mesylate (IM) blocks the CSF-1 receptor. This s...

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Autores principales: Verspoor, F. G. M., Mastboom, M. J. L., Hannink, G., Maki, R. G., Wagner, A., Bompas, E., Desai, J., Italiano, A., Seddon, B. M., van der Graaf, W. T. A., Blay, J.-Y., Brahmi, M., Eberst, L., Stacchiotti, S., Mir, O., van de Sande, M. A. J., Gelderblom, H., Cassier, P. A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6786996/
https://www.ncbi.nlm.nih.gov/pubmed/31601938
http://dx.doi.org/10.1038/s41598-019-51211-y
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author Verspoor, F. G. M.
Mastboom, M. J. L.
Hannink, G.
Maki, R. G.
Wagner, A.
Bompas, E.
Desai, J.
Italiano, A.
Seddon, B. M.
van der Graaf, W. T. A.
Blay, J.-Y.
Brahmi, M.
Eberst, L.
Stacchiotti, S.
Mir, O.
van de Sande, M. A. J.
Gelderblom, H.
Cassier, P. A.
author_facet Verspoor, F. G. M.
Mastboom, M. J. L.
Hannink, G.
Maki, R. G.
Wagner, A.
Bompas, E.
Desai, J.
Italiano, A.
Seddon, B. M.
van der Graaf, W. T. A.
Blay, J.-Y.
Brahmi, M.
Eberst, L.
Stacchiotti, S.
Mir, O.
van de Sande, M. A. J.
Gelderblom, H.
Cassier, P. A.
author_sort Verspoor, F. G. M.
collection PubMed
description Tenosynovial giant cell tumors (TGCT), are rare colony stimulating factor-1(CSF-1)-driven proliferative disorders affecting joints. Diffuse-type TGCT often causes significant morbidity due to local recurrences necessitating multiple surgeries. Imatinib mesylate (IM) blocks the CSF-1 receptor. This study investigated the long term effects of IM in TGCT. We conducted an international multi-institutional retrospective study to assess the activity of IM: data was collected anonymously from individual patients with locally advanced, recurrent or metastatic TGCT. Sixty-two patients from 12 institutions across Europe, Australia and the United States were identified. Four patients with metastatic TGCT progressed rapidly on IM and were excluded for further analyses. Seventeen of 58 evaluable patients achieved complete response (CR) or partial response (PR). One- and five-year progression-free survival rates were 71% and 48%, respectively. Thirty-eight (66%) patients discontinued IM after a median of 7 (range 1–80) months. Reported adverse events in 45 (78%) patients were among other edema (48%) and fatigue (50%), mostly grade 1–2 (89%). Five patients experienced grade 3–4 toxicities. This study confirms, with additional follow-up, the efficacy of IM in TGCT. In responding cases we confirmed prolonged IM activity on TGCT symptoms even after discontinuation, but with high rates of treatment interruption and additional treatments.
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spelling pubmed-67869962019-10-17 Long-term efficacy of imatinib mesylate in patients with advanced Tenosynovial Giant Cell Tumor Verspoor, F. G. M. Mastboom, M. J. L. Hannink, G. Maki, R. G. Wagner, A. Bompas, E. Desai, J. Italiano, A. Seddon, B. M. van der Graaf, W. T. A. Blay, J.-Y. Brahmi, M. Eberst, L. Stacchiotti, S. Mir, O. van de Sande, M. A. J. Gelderblom, H. Cassier, P. A. Sci Rep Article Tenosynovial giant cell tumors (TGCT), are rare colony stimulating factor-1(CSF-1)-driven proliferative disorders affecting joints. Diffuse-type TGCT often causes significant morbidity due to local recurrences necessitating multiple surgeries. Imatinib mesylate (IM) blocks the CSF-1 receptor. This study investigated the long term effects of IM in TGCT. We conducted an international multi-institutional retrospective study to assess the activity of IM: data was collected anonymously from individual patients with locally advanced, recurrent or metastatic TGCT. Sixty-two patients from 12 institutions across Europe, Australia and the United States were identified. Four patients with metastatic TGCT progressed rapidly on IM and were excluded for further analyses. Seventeen of 58 evaluable patients achieved complete response (CR) or partial response (PR). One- and five-year progression-free survival rates were 71% and 48%, respectively. Thirty-eight (66%) patients discontinued IM after a median of 7 (range 1–80) months. Reported adverse events in 45 (78%) patients were among other edema (48%) and fatigue (50%), mostly grade 1–2 (89%). Five patients experienced grade 3–4 toxicities. This study confirms, with additional follow-up, the efficacy of IM in TGCT. In responding cases we confirmed prolonged IM activity on TGCT symptoms even after discontinuation, but with high rates of treatment interruption and additional treatments. Nature Publishing Group UK 2019-10-10 /pmc/articles/PMC6786996/ /pubmed/31601938 http://dx.doi.org/10.1038/s41598-019-51211-y Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Verspoor, F. G. M.
Mastboom, M. J. L.
Hannink, G.
Maki, R. G.
Wagner, A.
Bompas, E.
Desai, J.
Italiano, A.
Seddon, B. M.
van der Graaf, W. T. A.
Blay, J.-Y.
Brahmi, M.
Eberst, L.
Stacchiotti, S.
Mir, O.
van de Sande, M. A. J.
Gelderblom, H.
Cassier, P. A.
Long-term efficacy of imatinib mesylate in patients with advanced Tenosynovial Giant Cell Tumor
title Long-term efficacy of imatinib mesylate in patients with advanced Tenosynovial Giant Cell Tumor
title_full Long-term efficacy of imatinib mesylate in patients with advanced Tenosynovial Giant Cell Tumor
title_fullStr Long-term efficacy of imatinib mesylate in patients with advanced Tenosynovial Giant Cell Tumor
title_full_unstemmed Long-term efficacy of imatinib mesylate in patients with advanced Tenosynovial Giant Cell Tumor
title_short Long-term efficacy of imatinib mesylate in patients with advanced Tenosynovial Giant Cell Tumor
title_sort long-term efficacy of imatinib mesylate in patients with advanced tenosynovial giant cell tumor
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6786996/
https://www.ncbi.nlm.nih.gov/pubmed/31601938
http://dx.doi.org/10.1038/s41598-019-51211-y
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