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Axitinib in the treatment of renal cell carcinoma: design, development, and place in therapy
Since 2005, the approved first-line treatment of metastatic renal cell carcinoma consists in tyrosine kinase inhibitors (TKIs) targeting the vascular endothelial growth factor receptors (VEGFRs). Axitinib is an oral second-generation TKI and a potent VEGFR inhibitor with a half maximal inhibitory co...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5614734/ https://www.ncbi.nlm.nih.gov/pubmed/29033542 http://dx.doi.org/10.2147/DDDT.S109640 |
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author | Bellesoeur, Audrey Carton, Edith Alexandre, Jerome Goldwasser, Francois Huillard, Olivier |
author_facet | Bellesoeur, Audrey Carton, Edith Alexandre, Jerome Goldwasser, Francois Huillard, Olivier |
author_sort | Bellesoeur, Audrey |
collection | PubMed |
description | Since 2005, the approved first-line treatment of metastatic renal cell carcinoma consists in tyrosine kinase inhibitors (TKIs) targeting the vascular endothelial growth factor receptors (VEGFRs). Axitinib is an oral second-generation TKI and a potent VEGFR inhibitor with a half maximal inhibitory concentration for the VEGF family receptors 10-fold lower than other TKIs. Axitinib activity in renal cell carcinoma (RCC) patients has been studied in various settings and particularly as second-line treatment. In this setting, axitinib with clinically based dose escalation compared to sorafenib has demonstrated an improvement in progression-free survival in a randomized Phase III trial leading to US Food and Drug Administration approval. In the first-line setting, axitinib failed to demonstrate improved efficacy over sorafenib, but the field of RCC treatment is rapidly changing with novel TKIs as cabozantinib or the emergence of check point inhibitors as nivolumab and the place of axitinib in therapy is therefore challenged. In this review, we focus on axitinib pharmacological and clinical properties in RCC patients and discuss its place in the treatment of patients with RCC. |
format | Online Article Text |
id | pubmed-5614734 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-56147342017-10-13 Axitinib in the treatment of renal cell carcinoma: design, development, and place in therapy Bellesoeur, Audrey Carton, Edith Alexandre, Jerome Goldwasser, Francois Huillard, Olivier Drug Des Devel Ther Review Since 2005, the approved first-line treatment of metastatic renal cell carcinoma consists in tyrosine kinase inhibitors (TKIs) targeting the vascular endothelial growth factor receptors (VEGFRs). Axitinib is an oral second-generation TKI and a potent VEGFR inhibitor with a half maximal inhibitory concentration for the VEGF family receptors 10-fold lower than other TKIs. Axitinib activity in renal cell carcinoma (RCC) patients has been studied in various settings and particularly as second-line treatment. In this setting, axitinib with clinically based dose escalation compared to sorafenib has demonstrated an improvement in progression-free survival in a randomized Phase III trial leading to US Food and Drug Administration approval. In the first-line setting, axitinib failed to demonstrate improved efficacy over sorafenib, but the field of RCC treatment is rapidly changing with novel TKIs as cabozantinib or the emergence of check point inhibitors as nivolumab and the place of axitinib in therapy is therefore challenged. In this review, we focus on axitinib pharmacological and clinical properties in RCC patients and discuss its place in the treatment of patients with RCC. Dove Medical Press 2017-09-21 /pmc/articles/PMC5614734/ /pubmed/29033542 http://dx.doi.org/10.2147/DDDT.S109640 Text en © 2017 Bellesoeur et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Review Bellesoeur, Audrey Carton, Edith Alexandre, Jerome Goldwasser, Francois Huillard, Olivier Axitinib in the treatment of renal cell carcinoma: design, development, and place in therapy |
title | Axitinib in the treatment of renal cell carcinoma: design, development, and place in therapy |
title_full | Axitinib in the treatment of renal cell carcinoma: design, development, and place in therapy |
title_fullStr | Axitinib in the treatment of renal cell carcinoma: design, development, and place in therapy |
title_full_unstemmed | Axitinib in the treatment of renal cell carcinoma: design, development, and place in therapy |
title_short | Axitinib in the treatment of renal cell carcinoma: design, development, and place in therapy |
title_sort | axitinib in the treatment of renal cell carcinoma: design, development, and place in therapy |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5614734/ https://www.ncbi.nlm.nih.gov/pubmed/29033542 http://dx.doi.org/10.2147/DDDT.S109640 |
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