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Fatal hemoptysis in patients with advanced esophageal cancer treated with apatinib

Targeted therapy is commonly used for treating advanced malignant tumors. Compared with cytotoxic drugs, targeted drugs have the characteristics of good curative results, less adverse effects, and convenient oral administration. Hence, they are especially suitable for patients with cancer who are no...

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Autores principales: Wang, Wei, Zhang, Lin, Xie, Yan, Zhen, Tianchang, Su, Gongzhang, Zang, Qi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5944459/
https://www.ncbi.nlm.nih.gov/pubmed/29765235
http://dx.doi.org/10.2147/OTT.S150555
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author Wang, Wei
Zhang, Lin
Xie, Yan
Zhen, Tianchang
Su, Gongzhang
Zang, Qi
author_facet Wang, Wei
Zhang, Lin
Xie, Yan
Zhen, Tianchang
Su, Gongzhang
Zang, Qi
author_sort Wang, Wei
collection PubMed
description Targeted therapy is commonly used for treating advanced malignant tumors. Compared with cytotoxic drugs, targeted drugs have the characteristics of good curative results, less adverse effects, and convenient oral administration. Hence, they are especially suitable for patients with cancer who are not able to tolerate chemotherapy. Anti-angiogenic therapy can achieve the objective by inhibiting the formation of new blood vessels in tumors. Apatinib is a novel tyrosine kinase inhibitor targeting the intracellular domain of vascular endothelial growth factor receptor-2. It has been proven to be effective and safe in treating patients with gastric carcinoma and gastroesophageal junction carcinoma. So far, no reports are available on the treatment of esophageal cancer with apatinib. Two patients with advanced esophageal cancer were treated with oral apatinib because of their poor physical condition. After treatment, the dyspnea symptoms disappeared and quality of life significantly improved. Chest computed tomography showed massive necrosis of tumor tissues in each patient. The tumors significantly reduced and a cavity was formed locally in each patient. However, both patients died of massive hemoptysis, probably due to the rupture of the bronchial artery eroded by tumors. The results indicated that apatinib was effective in treating some patients with advanced esophageal cancer, and adverse effects were controllable. However, doctors should choose appropriate candidates according to apatinib’s indications. In addition, the use of apatinib should be carefully controlled for patients with esophageal cancer, especially in those with large vessels and trachea or bronchus eroded by tumor, so as to avoid or reduce the occurrence of fatal hemorrhage.
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spelling pubmed-59444592018-05-15 Fatal hemoptysis in patients with advanced esophageal cancer treated with apatinib Wang, Wei Zhang, Lin Xie, Yan Zhen, Tianchang Su, Gongzhang Zang, Qi Onco Targets Ther Case Series Targeted therapy is commonly used for treating advanced malignant tumors. Compared with cytotoxic drugs, targeted drugs have the characteristics of good curative results, less adverse effects, and convenient oral administration. Hence, they are especially suitable for patients with cancer who are not able to tolerate chemotherapy. Anti-angiogenic therapy can achieve the objective by inhibiting the formation of new blood vessels in tumors. Apatinib is a novel tyrosine kinase inhibitor targeting the intracellular domain of vascular endothelial growth factor receptor-2. It has been proven to be effective and safe in treating patients with gastric carcinoma and gastroesophageal junction carcinoma. So far, no reports are available on the treatment of esophageal cancer with apatinib. Two patients with advanced esophageal cancer were treated with oral apatinib because of their poor physical condition. After treatment, the dyspnea symptoms disappeared and quality of life significantly improved. Chest computed tomography showed massive necrosis of tumor tissues in each patient. The tumors significantly reduced and a cavity was formed locally in each patient. However, both patients died of massive hemoptysis, probably due to the rupture of the bronchial artery eroded by tumors. The results indicated that apatinib was effective in treating some patients with advanced esophageal cancer, and adverse effects were controllable. However, doctors should choose appropriate candidates according to apatinib’s indications. In addition, the use of apatinib should be carefully controlled for patients with esophageal cancer, especially in those with large vessels and trachea or bronchus eroded by tumor, so as to avoid or reduce the occurrence of fatal hemorrhage. Dove Medical Press 2018-05-07 /pmc/articles/PMC5944459/ /pubmed/29765235 http://dx.doi.org/10.2147/OTT.S150555 Text en © 2018 Wang 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 Case Series
Wang, Wei
Zhang, Lin
Xie, Yan
Zhen, Tianchang
Su, Gongzhang
Zang, Qi
Fatal hemoptysis in patients with advanced esophageal cancer treated with apatinib
title Fatal hemoptysis in patients with advanced esophageal cancer treated with apatinib
title_full Fatal hemoptysis in patients with advanced esophageal cancer treated with apatinib
title_fullStr Fatal hemoptysis in patients with advanced esophageal cancer treated with apatinib
title_full_unstemmed Fatal hemoptysis in patients with advanced esophageal cancer treated with apatinib
title_short Fatal hemoptysis in patients with advanced esophageal cancer treated with apatinib
title_sort fatal hemoptysis in patients with advanced esophageal cancer treated with apatinib
topic Case Series
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5944459/
https://www.ncbi.nlm.nih.gov/pubmed/29765235
http://dx.doi.org/10.2147/OTT.S150555
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