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Axitinib as a third or further line of treatment in renal cancer: a single institution experience
BACKGROUND: Kidney cancer is a lethal neoplasm that affects several thousands of people every year. Renal cell carcinoma (RCC) is the most common histologic type. Recent developments in the therapeutic approach include antiangiogenic targeted approaches and Immunotherapy. Thus, the therapeutic algor...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7265645/ https://www.ncbi.nlm.nih.gov/pubmed/32487200 http://dx.doi.org/10.1186/s12894-020-00618-1 |
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author | Tsironis, G. Liontos, M. Kyriazoglou, A. Koutsoukos, K. Tsiara, A. Kaparelou, M. Zakopoulou, R. Cohen, A. Skafida, E. Fontara, S. Zagouri, F. Bamias, A. Dimopoulos, M. A. |
author_facet | Tsironis, G. Liontos, M. Kyriazoglou, A. Koutsoukos, K. Tsiara, A. Kaparelou, M. Zakopoulou, R. Cohen, A. Skafida, E. Fontara, S. Zagouri, F. Bamias, A. Dimopoulos, M. A. |
author_sort | Tsironis, G. |
collection | PubMed |
description | BACKGROUND: Kidney cancer is a lethal neoplasm that affects several thousands of people every year. Renal cell carcinoma (RCC) is the most common histologic type. Recent developments in the therapeutic approach include antiangiogenic targeted approaches and Immunotherapy. Thus, the therapeutic algorithm of RCC patients and the survival outcomes have changed dramatically. METHODS: Herein we present a retrospective study of the patients treated in our Department with an antiangiogenic agent -Axitinib, a tyrosine kinase inhibitor- as a third or further line treatment. Statistical analysis was performed with SPSS, including the available clinicopathological data of the patients included. RESULTS: Axitinib was found to be active in patients who received this treatment beyond second line. The toxicity profile of this regimen did not reveal any unknown adverse events. CONCLUSIONS: Our real world data reflect that axitinib is a safe and effective option, even beyond the second line. |
format | Online Article Text |
id | pubmed-7265645 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-72656452020-06-07 Axitinib as a third or further line of treatment in renal cancer: a single institution experience Tsironis, G. Liontos, M. Kyriazoglou, A. Koutsoukos, K. Tsiara, A. Kaparelou, M. Zakopoulou, R. Cohen, A. Skafida, E. Fontara, S. Zagouri, F. Bamias, A. Dimopoulos, M. A. BMC Urol Research Article BACKGROUND: Kidney cancer is a lethal neoplasm that affects several thousands of people every year. Renal cell carcinoma (RCC) is the most common histologic type. Recent developments in the therapeutic approach include antiangiogenic targeted approaches and Immunotherapy. Thus, the therapeutic algorithm of RCC patients and the survival outcomes have changed dramatically. METHODS: Herein we present a retrospective study of the patients treated in our Department with an antiangiogenic agent -Axitinib, a tyrosine kinase inhibitor- as a third or further line treatment. Statistical analysis was performed with SPSS, including the available clinicopathological data of the patients included. RESULTS: Axitinib was found to be active in patients who received this treatment beyond second line. The toxicity profile of this regimen did not reveal any unknown adverse events. CONCLUSIONS: Our real world data reflect that axitinib is a safe and effective option, even beyond the second line. BioMed Central 2020-06-02 /pmc/articles/PMC7265645/ /pubmed/32487200 http://dx.doi.org/10.1186/s12894-020-00618-1 Text en © The Author(s) 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data. |
spellingShingle | Research Article Tsironis, G. Liontos, M. Kyriazoglou, A. Koutsoukos, K. Tsiara, A. Kaparelou, M. Zakopoulou, R. Cohen, A. Skafida, E. Fontara, S. Zagouri, F. Bamias, A. Dimopoulos, M. A. Axitinib as a third or further line of treatment in renal cancer: a single institution experience |
title | Axitinib as a third or further line of treatment in renal cancer: a single institution experience |
title_full | Axitinib as a third or further line of treatment in renal cancer: a single institution experience |
title_fullStr | Axitinib as a third or further line of treatment in renal cancer: a single institution experience |
title_full_unstemmed | Axitinib as a third or further line of treatment in renal cancer: a single institution experience |
title_short | Axitinib as a third or further line of treatment in renal cancer: a single institution experience |
title_sort | axitinib as a third or further line of treatment in renal cancer: a single institution experience |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7265645/ https://www.ncbi.nlm.nih.gov/pubmed/32487200 http://dx.doi.org/10.1186/s12894-020-00618-1 |
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