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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Circulation Society 2021
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.
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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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