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Axitinib Induces and Aggravates Hypertension Regardless of Prior Treatment With Tyrosine Kinase Inhibitors
Background: Axitinib is a tyrosine kinase inhibitor (TKI) that inhibits vascular endothelial growth factor receptor signaling and is approved for second-line treatment of advanced renal cell carcinoma (RCC). Although the occurrence of hypertension with axitinib use has been documented, it is unclear...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Japanese Circulation Society
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8024013/ https://www.ncbi.nlm.nih.gov/pubmed/33842729 http://dx.doi.org/10.1253/circrep.CR-21-0008 |
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author | Kadowaki, Hiroshi Ishida, Junichi Akazawa, Hiroshi Yagi, Hiroki Saga-Kamo, Akiko Umei, Masahiko Matsuoka, Ryo Liu, Qing Matsunaga, Hiroshi Maki, Hisataka Sato, Yusuke Kume, Haruki Komuro, Issei |
author_facet | Kadowaki, Hiroshi Ishida, Junichi Akazawa, Hiroshi Yagi, Hiroki Saga-Kamo, Akiko Umei, Masahiko Matsuoka, Ryo Liu, Qing Matsunaga, Hiroshi Maki, Hisataka Sato, Yusuke Kume, Haruki Komuro, Issei |
author_sort | Kadowaki, Hiroshi |
collection | PubMed |
description | Background: Axitinib is a tyrosine kinase inhibitor (TKI) that inhibits vascular endothelial growth factor receptor signaling and is approved for second-line treatment of advanced renal cell carcinoma (RCC). Although the occurrence of hypertension with axitinib use has been documented, it is unclear whether a first-line TKI regimen can significantly affect the development of hypertension when axitinib is used as second-line therapy. Methods and Results: In this single-center retrospective study, advanced RCC patients treated with axitinib after first-line chemotherapy were divided into 2 groups according to the use of TKIs as part of first-line treatment before the initiation of axitinib. Clinical outcomes were compared between patients who were treated with (TKI(+); n=11) or without (TKI(–); n=11) a TKI. Although 63.6% of all patients had hypertension at baseline, axitinib-induced hypertension developed in 81.8% of patients, and 36.4% of patients experienced Grade 3 hypertension. After initiation of axitinib, both systolic and diastolic blood pressures and the hypertension grade were significantly elevated both in the TKI(+) and TKI(–) groups, and the number of antihypertensive drugs was significantly increased among all patients. Conclusions: This study suggests the need for proper monitoring and management of blood pressure in RCC patients treated with axitinib, regardless of a prior regimen with or without TKIs. |
format | Online Article Text |
id | pubmed-8024013 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Japanese Circulation Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-80240132021-04-08 Axitinib Induces and Aggravates Hypertension Regardless of Prior Treatment With Tyrosine Kinase Inhibitors Kadowaki, Hiroshi Ishida, Junichi Akazawa, Hiroshi Yagi, Hiroki Saga-Kamo, Akiko Umei, Masahiko Matsuoka, Ryo Liu, Qing Matsunaga, Hiroshi Maki, Hisataka Sato, Yusuke Kume, Haruki Komuro, Issei Circ Rep Original article Background: Axitinib is a tyrosine kinase inhibitor (TKI) that inhibits vascular endothelial growth factor receptor signaling and is approved for second-line treatment of advanced renal cell carcinoma (RCC). Although the occurrence of hypertension with axitinib use has been documented, it is unclear whether a first-line TKI regimen can significantly affect the development of hypertension when axitinib is used as second-line therapy. Methods and Results: In this single-center retrospective study, advanced RCC patients treated with axitinib after first-line chemotherapy were divided into 2 groups according to the use of TKIs as part of first-line treatment before the initiation of axitinib. Clinical outcomes were compared between patients who were treated with (TKI(+); n=11) or without (TKI(–); n=11) a TKI. Although 63.6% of all patients had hypertension at baseline, axitinib-induced hypertension developed in 81.8% of patients, and 36.4% of patients experienced Grade 3 hypertension. After initiation of axitinib, both systolic and diastolic blood pressures and the hypertension grade were significantly elevated both in the TKI(+) and TKI(–) groups, and the number of antihypertensive drugs was significantly increased among all patients. Conclusions: This study suggests the need for proper monitoring and management of blood pressure in RCC patients treated with axitinib, regardless of a prior regimen with or without TKIs. The Japanese Circulation Society 2021-03-10 /pmc/articles/PMC8024013/ /pubmed/33842729 http://dx.doi.org/10.1253/circrep.CR-21-0008 Text en Copyright © 2021, THE JAPANESE CIRCULATION SOCIETY This article is licensed under a Creative Commons [Attribution-NonCommercial-NoDerivatives 4.0 International] license.https://creativecommons.org/licenses/by-nc-nd/4.0/ |
spellingShingle | Original article Kadowaki, Hiroshi Ishida, Junichi Akazawa, Hiroshi Yagi, Hiroki Saga-Kamo, Akiko Umei, Masahiko Matsuoka, Ryo Liu, Qing Matsunaga, Hiroshi Maki, Hisataka Sato, Yusuke Kume, Haruki Komuro, Issei Axitinib Induces and Aggravates Hypertension Regardless of Prior Treatment With Tyrosine Kinase Inhibitors |
title | Axitinib Induces and Aggravates Hypertension Regardless of Prior Treatment With Tyrosine Kinase Inhibitors |
title_full | Axitinib Induces and Aggravates Hypertension Regardless of Prior Treatment With Tyrosine Kinase Inhibitors |
title_fullStr | Axitinib Induces and Aggravates Hypertension Regardless of Prior Treatment With Tyrosine Kinase Inhibitors |
title_full_unstemmed | Axitinib Induces and Aggravates Hypertension Regardless of Prior Treatment With Tyrosine Kinase Inhibitors |
title_short | Axitinib Induces and Aggravates Hypertension Regardless of Prior Treatment With Tyrosine Kinase Inhibitors |
title_sort | axitinib induces and aggravates hypertension regardless of prior treatment with tyrosine kinase inhibitors |
topic | Original article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8024013/ https://www.ncbi.nlm.nih.gov/pubmed/33842729 http://dx.doi.org/10.1253/circrep.CR-21-0008 |
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