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Icotinib and pemetrexed in treatment of lung adenocarcinoma and the effects on prognostic survival rate of patients

Efficacy comparison of icotinib and pemetrexed in the treatment of lung adenocarcinoma and the effects on the prognostic survival rate of patients were investigated. A retrospective analysis was performed in 132 lung adenocarcinoma patients who were treated in the Affiliated Hospital of Weifang Medi...

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Autores principales: Zhou, Xueheng, Hua, Defeng, Gao, Chengpeng, Zhang, Yixiang, Qiu, Lijie, Wang, Leqiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6732991/
https://www.ncbi.nlm.nih.gov/pubmed/31516614
http://dx.doi.org/10.3892/ol.2019.10763
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author Zhou, Xueheng
Hua, Defeng
Gao, Chengpeng
Zhang, Yixiang
Qiu, Lijie
Wang, Leqiang
author_facet Zhou, Xueheng
Hua, Defeng
Gao, Chengpeng
Zhang, Yixiang
Qiu, Lijie
Wang, Leqiang
author_sort Zhou, Xueheng
collection PubMed
description Efficacy comparison of icotinib and pemetrexed in the treatment of lung adenocarcinoma and the effects on the prognostic survival rate of patients were investigated. A retrospective analysis was performed in 132 lung adenocarcinoma patients who were treated in the Affiliated Hospital of Weifang Medical University from July 2010 to July 2015. Among them, 69 patients were treated with icotinib (icotinib group), and 63 patients were treated with pemetrexed (pemetrexed group). In the icotinib group, 125 mg icotinib was orally administered continuously, 3 times a day, until progressive disease or intolerable adverse reactions occurred. In the pemetrexed group, 500 mg/m(2) pemetrexed was intravenously dripped for a total of 4 cycles, 21 days for 1 cycle, until progressive disease or intolerable adverse reactions occurred. The efficacy, toxic and side effects, and survival rate of the two groups were evaluated. There was a statistically significant difference in toxic and side effects between the two groups of drugs after the treatment of lung adenocarcinoma (P<0.05). The median survival time of patients was 16 months in the icotinib group and 10 months in the pemetrexed group, with a statistically significant difference (P<0.05). The 1-year survival rate was higher in the icotinib group than that in the pemetrexed group (P<0.05). There was no difference in 2- and 3-year survival rates between the two groups (P>0.05). In conclusion, the clinical efficacy of icotinib is similar to that of pemetrexed in the treatment of lung adenocarcinoma, but icotinib has less adverse reactions, with better improvement in disease control.
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spelling pubmed-67329912019-09-12 Icotinib and pemetrexed in treatment of lung adenocarcinoma and the effects on prognostic survival rate of patients Zhou, Xueheng Hua, Defeng Gao, Chengpeng Zhang, Yixiang Qiu, Lijie Wang, Leqiang Oncol Lett Articles Efficacy comparison of icotinib and pemetrexed in the treatment of lung adenocarcinoma and the effects on the prognostic survival rate of patients were investigated. A retrospective analysis was performed in 132 lung adenocarcinoma patients who were treated in the Affiliated Hospital of Weifang Medical University from July 2010 to July 2015. Among them, 69 patients were treated with icotinib (icotinib group), and 63 patients were treated with pemetrexed (pemetrexed group). In the icotinib group, 125 mg icotinib was orally administered continuously, 3 times a day, until progressive disease or intolerable adverse reactions occurred. In the pemetrexed group, 500 mg/m(2) pemetrexed was intravenously dripped for a total of 4 cycles, 21 days for 1 cycle, until progressive disease or intolerable adverse reactions occurred. The efficacy, toxic and side effects, and survival rate of the two groups were evaluated. There was a statistically significant difference in toxic and side effects between the two groups of drugs after the treatment of lung adenocarcinoma (P<0.05). The median survival time of patients was 16 months in the icotinib group and 10 months in the pemetrexed group, with a statistically significant difference (P<0.05). The 1-year survival rate was higher in the icotinib group than that in the pemetrexed group (P<0.05). There was no difference in 2- and 3-year survival rates between the two groups (P>0.05). In conclusion, the clinical efficacy of icotinib is similar to that of pemetrexed in the treatment of lung adenocarcinoma, but icotinib has less adverse reactions, with better improvement in disease control. D.A. Spandidos 2019-10 2019-08-16 /pmc/articles/PMC6732991/ /pubmed/31516614 http://dx.doi.org/10.3892/ol.2019.10763 Text en Copyright: © Zhou et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Zhou, Xueheng
Hua, Defeng
Gao, Chengpeng
Zhang, Yixiang
Qiu, Lijie
Wang, Leqiang
Icotinib and pemetrexed in treatment of lung adenocarcinoma and the effects on prognostic survival rate of patients
title Icotinib and pemetrexed in treatment of lung adenocarcinoma and the effects on prognostic survival rate of patients
title_full Icotinib and pemetrexed in treatment of lung adenocarcinoma and the effects on prognostic survival rate of patients
title_fullStr Icotinib and pemetrexed in treatment of lung adenocarcinoma and the effects on prognostic survival rate of patients
title_full_unstemmed Icotinib and pemetrexed in treatment of lung adenocarcinoma and the effects on prognostic survival rate of patients
title_short Icotinib and pemetrexed in treatment of lung adenocarcinoma and the effects on prognostic survival rate of patients
title_sort icotinib and pemetrexed in treatment of lung adenocarcinoma and the effects on prognostic survival rate of patients
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6732991/
https://www.ncbi.nlm.nih.gov/pubmed/31516614
http://dx.doi.org/10.3892/ol.2019.10763
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