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Bevacizumab for the treatment of non-small cell lung cancer patients with synchronous brain metastases

Bevacizumab is FDA-approved in the treatment of primary brain tumors, but its efficacy in patients with brain metastases could be better-studied. This study examines a population of non-small cell lung cancer (NSCLC) patients with synchronous brain metastases to identify predictors of the decision t...

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Autores principales: Ascha, Mustafa S., Wang, Jacqueline Fang, Kumthekar, Priya, Sloan, Andrew E., Kruchko, Carol, Barnholtz-Sloan, Jill S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6882803/
https://www.ncbi.nlm.nih.gov/pubmed/31780762
http://dx.doi.org/10.1038/s41598-019-54513-3
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author Ascha, Mustafa S.
Wang, Jacqueline Fang
Kumthekar, Priya
Sloan, Andrew E.
Kruchko, Carol
Barnholtz-Sloan, Jill S.
author_facet Ascha, Mustafa S.
Wang, Jacqueline Fang
Kumthekar, Priya
Sloan, Andrew E.
Kruchko, Carol
Barnholtz-Sloan, Jill S.
author_sort Ascha, Mustafa S.
collection PubMed
description Bevacizumab is FDA-approved in the treatment of primary brain tumors, but its efficacy in patients with brain metastases could be better-studied. This study examines a population of non-small cell lung cancer (NSCLC) patients with synchronous brain metastases to identify predictors of the decision to use bevacizumab and survival following bevacizumab treatment. Primary cancer registry data were used to determine which NSCLC patients diagnosed in the years 2010 through 2012 had synchronous brain metastases at the time of diagnosis, and Medicare claims used to identify a population of patients treated with bevacizumab. Record of bevacizumab treatment was found for 81 and 666 patients with and without brain metastases, respectively. After adjusting for clinical and demographic characteristics, bevacizumab was associated with 0.88 times the hazard of mortality in the elderly NSCLC population (95% CI: 0.81–0.96, p: 0.003) and a corresponding hazard ratio of 0.75 in the population of elderly NSCLC patients with synchronous brain metastases (95% CI: 0.59–0.96, p: 0.020). Bevacizumab may benefit NSCLC patients with synchronous brain metastases more than it does patients without intracranial disease, possibly as a result of its multiple potential mechanisms of action simultaneously inhibiting angiogenesis and minimizing vasogenic edema.
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spelling pubmed-68828032019-12-06 Bevacizumab for the treatment of non-small cell lung cancer patients with synchronous brain metastases Ascha, Mustafa S. Wang, Jacqueline Fang Kumthekar, Priya Sloan, Andrew E. Kruchko, Carol Barnholtz-Sloan, Jill S. Sci Rep Article Bevacizumab is FDA-approved in the treatment of primary brain tumors, but its efficacy in patients with brain metastases could be better-studied. This study examines a population of non-small cell lung cancer (NSCLC) patients with synchronous brain metastases to identify predictors of the decision to use bevacizumab and survival following bevacizumab treatment. Primary cancer registry data were used to determine which NSCLC patients diagnosed in the years 2010 through 2012 had synchronous brain metastases at the time of diagnosis, and Medicare claims used to identify a population of patients treated with bevacizumab. Record of bevacizumab treatment was found for 81 and 666 patients with and without brain metastases, respectively. After adjusting for clinical and demographic characteristics, bevacizumab was associated with 0.88 times the hazard of mortality in the elderly NSCLC population (95% CI: 0.81–0.96, p: 0.003) and a corresponding hazard ratio of 0.75 in the population of elderly NSCLC patients with synchronous brain metastases (95% CI: 0.59–0.96, p: 0.020). Bevacizumab may benefit NSCLC patients with synchronous brain metastases more than it does patients without intracranial disease, possibly as a result of its multiple potential mechanisms of action simultaneously inhibiting angiogenesis and minimizing vasogenic edema. Nature Publishing Group UK 2019-11-28 /pmc/articles/PMC6882803/ /pubmed/31780762 http://dx.doi.org/10.1038/s41598-019-54513-3 Text en © The Author(s) 2019 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Ascha, Mustafa S.
Wang, Jacqueline Fang
Kumthekar, Priya
Sloan, Andrew E.
Kruchko, Carol
Barnholtz-Sloan, Jill S.
Bevacizumab for the treatment of non-small cell lung cancer patients with synchronous brain metastases
title Bevacizumab for the treatment of non-small cell lung cancer patients with synchronous brain metastases
title_full Bevacizumab for the treatment of non-small cell lung cancer patients with synchronous brain metastases
title_fullStr Bevacizumab for the treatment of non-small cell lung cancer patients with synchronous brain metastases
title_full_unstemmed Bevacizumab for the treatment of non-small cell lung cancer patients with synchronous brain metastases
title_short Bevacizumab for the treatment of non-small cell lung cancer patients with synchronous brain metastases
title_sort bevacizumab for the treatment of non-small cell lung cancer patients with synchronous brain metastases
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6882803/
https://www.ncbi.nlm.nih.gov/pubmed/31780762
http://dx.doi.org/10.1038/s41598-019-54513-3
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