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Hypertension as a predictive biomarker in patients with advanced non-small-cell lung cancer treated with apatinib
BACKGROUND: Hypertension (HTN) is a common adverse event of the vascular endothelial growth factor pathway inhibitor apatinib. This study was conducted to evaluate the association of apatinib-induced HTN with clinical outcomes in patients with advanced non-small-cell lung cancer (NSCLC). METHODS: We...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6362948/ https://www.ncbi.nlm.nih.gov/pubmed/30774384 http://dx.doi.org/10.2147/OTT.S189984 |
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author | Fang, Shen-Cun Huang, Wen Zhang, Ying-Ming Zhang, Hai-Tao Xie, Wei-Ping |
author_facet | Fang, Shen-Cun Huang, Wen Zhang, Ying-Ming Zhang, Hai-Tao Xie, Wei-Ping |
author_sort | Fang, Shen-Cun |
collection | PubMed |
description | BACKGROUND: Hypertension (HTN) is a common adverse event of the vascular endothelial growth factor pathway inhibitor apatinib. This study was conducted to evaluate the association of apatinib-induced HTN with clinical outcomes in patients with advanced non-small-cell lung cancer (NSCLC). METHODS: We retrospectively analyzed 110 consecutive patients with advanced NSCLC who were treated with apatinib from August 2014 to January 2018. All patients were classified as normotensive or hypertensive based on blood pressure measurements after initiating therapy. Therapeutic response, progression-free survival (PFS), and overall survival (OS) were evaluated. Univariate and multivariate analyses were performed using the Cox proportional hazards method. RESULTS: A total of 46 patients (42%) were diagnosed with HTN. The median PFS for the hypertensive and normotensive groups were 5.6 months and 4.2 months, respectively (P=0.0027). The median OS times for the hypertensive and normotensive groups were 9.9 months and 7.8 months, respectively (P=0.005). Thirty percent of patients who experienced HTN showed partial response to apatinib as compared with 6.3% of non-hypertensive patients (P=0.002). HTN was independently associated with improved PFS and OS on both univariate and multivariate analyses. CONCLUSION: Apatinib-induced HTN may be an inexpensive, valid, and easily measurable biomarker for apatinib antitumor efficacy in patients with advanced NSCLC. |
format | Online Article Text |
id | pubmed-6362948 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-63629482019-02-15 Hypertension as a predictive biomarker in patients with advanced non-small-cell lung cancer treated with apatinib Fang, Shen-Cun Huang, Wen Zhang, Ying-Ming Zhang, Hai-Tao Xie, Wei-Ping Onco Targets Ther Original Research BACKGROUND: Hypertension (HTN) is a common adverse event of the vascular endothelial growth factor pathway inhibitor apatinib. This study was conducted to evaluate the association of apatinib-induced HTN with clinical outcomes in patients with advanced non-small-cell lung cancer (NSCLC). METHODS: We retrospectively analyzed 110 consecutive patients with advanced NSCLC who were treated with apatinib from August 2014 to January 2018. All patients were classified as normotensive or hypertensive based on blood pressure measurements after initiating therapy. Therapeutic response, progression-free survival (PFS), and overall survival (OS) were evaluated. Univariate and multivariate analyses were performed using the Cox proportional hazards method. RESULTS: A total of 46 patients (42%) were diagnosed with HTN. The median PFS for the hypertensive and normotensive groups were 5.6 months and 4.2 months, respectively (P=0.0027). The median OS times for the hypertensive and normotensive groups were 9.9 months and 7.8 months, respectively (P=0.005). Thirty percent of patients who experienced HTN showed partial response to apatinib as compared with 6.3% of non-hypertensive patients (P=0.002). HTN was independently associated with improved PFS and OS on both univariate and multivariate analyses. CONCLUSION: Apatinib-induced HTN may be an inexpensive, valid, and easily measurable biomarker for apatinib antitumor efficacy in patients with advanced NSCLC. Dove Medical Press 2019-02-01 /pmc/articles/PMC6362948/ /pubmed/30774384 http://dx.doi.org/10.2147/OTT.S189984 Text en © 2019 Fang 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 | Original Research Fang, Shen-Cun Huang, Wen Zhang, Ying-Ming Zhang, Hai-Tao Xie, Wei-Ping Hypertension as a predictive biomarker in patients with advanced non-small-cell lung cancer treated with apatinib |
title | Hypertension as a predictive biomarker in patients with advanced non-small-cell lung cancer treated with apatinib |
title_full | Hypertension as a predictive biomarker in patients with advanced non-small-cell lung cancer treated with apatinib |
title_fullStr | Hypertension as a predictive biomarker in patients with advanced non-small-cell lung cancer treated with apatinib |
title_full_unstemmed | Hypertension as a predictive biomarker in patients with advanced non-small-cell lung cancer treated with apatinib |
title_short | Hypertension as a predictive biomarker in patients with advanced non-small-cell lung cancer treated with apatinib |
title_sort | hypertension as a predictive biomarker in patients with advanced non-small-cell lung cancer treated with apatinib |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6362948/ https://www.ncbi.nlm.nih.gov/pubmed/30774384 http://dx.doi.org/10.2147/OTT.S189984 |
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