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肺癌靶向药物肝脏毒性作用研究进展

Targeted drugs aimed at driver gene, such as Geftinib, Erlotinib and Crizotinib, have an irreplaceable position in the therapy of advanced non-small cell lung cancer. Tese drugs bring beneft to patients, however, higher hepatotoxicity is also presented. Now, drug induced hepatotoxicity and its mecha...

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Detalles Bibliográficos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 中国肺癌杂志编辑部 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6000506/
https://www.ncbi.nlm.nih.gov/pubmed/25248711
http://dx.doi.org/10.3779/j.issn.1009-3419.2014.09.08
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description Targeted drugs aimed at driver gene, such as Geftinib, Erlotinib and Crizotinib, have an irreplaceable position in the therapy of advanced non-small cell lung cancer. Tese drugs bring beneft to patients, however, higher hepatotoxicity is also presented. Now, drug induced hepatotoxicity and its mechanism are reviewed.
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spelling pubmed-60005062018-07-06 肺癌靶向药物肝脏毒性作用研究进展 Zhongguo Fei Ai Za Zhi 综述 Targeted drugs aimed at driver gene, such as Geftinib, Erlotinib and Crizotinib, have an irreplaceable position in the therapy of advanced non-small cell lung cancer. Tese drugs bring beneft to patients, however, higher hepatotoxicity is also presented. Now, drug induced hepatotoxicity and its mechanism are reviewed. 中国肺癌杂志编辑部 2014-09-20 /pmc/articles/PMC6000506/ /pubmed/25248711 http://dx.doi.org/10.3779/j.issn.1009-3419.2014.09.08 Text en 版权所有©《中国肺癌杂志》编辑部2014 https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 3.0) License. See: https://creativecommons.org/licenses/by/3.0/
spellingShingle 综述
肺癌靶向药物肝脏毒性作用研究进展
title 肺癌靶向药物肝脏毒性作用研究进展
title_full 肺癌靶向药物肝脏毒性作用研究进展
title_fullStr 肺癌靶向药物肝脏毒性作用研究进展
title_full_unstemmed 肺癌靶向药物肝脏毒性作用研究进展
title_short 肺癌靶向药物肝脏毒性作用研究进展
title_sort 肺癌靶向药物肝脏毒性作用研究进展
topic 综述
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6000506/
https://www.ncbi.nlm.nih.gov/pubmed/25248711
http://dx.doi.org/10.3779/j.issn.1009-3419.2014.09.08
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