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Clinical efficacy of apatinib in treating metastatic gastric cancer and its effect on IL-17
Clinical efficacy of apatinib in treating metastatic gastric cancer and its effect on the levels of serum IL-17 were investigated. A retrospective analysis was performed on 129 patients who had metastatic gastric cancer after first-line chemotherapy and were treated in Xiangyang No. 1 People's...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6507486/ https://www.ncbi.nlm.nih.gov/pubmed/31186764 http://dx.doi.org/10.3892/ol.2019.10270 |
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author | Chen, Ran Chen, Qi-Tian Dong, You-Hong |
author_facet | Chen, Ran Chen, Qi-Tian Dong, You-Hong |
author_sort | Chen, Ran |
collection | PubMed |
description | Clinical efficacy of apatinib in treating metastatic gastric cancer and its effect on the levels of serum IL-17 were investigated. A retrospective analysis was performed on 129 patients who had metastatic gastric cancer after first-line chemotherapy and were treated in Xiangyang No. 1 People's Hospital from February 2012 to February 2015. Of these patients, 78 received oral apatinib and were assigned to experimental group; and 51 received oral tegafur-gimeracil-oteracil and were assigned to control group. Clinical efficacy was compared between the two groups, and the levels of serum IL-17 were measured for all the patients. The treatment response rate in the experimental group was 52.56% and in the control group 31.37%. Apparently, the treatment response rate in the experimental group was higher than that in the control group, and the difference was statistically significant (P<0.05). The incidence of adverse drug reactions in the experimental group was significantly lower than that in the control group (P<0.05). The serum level of IL-17 after one course of medication was significantly lower than that before medication in both groups (P<0.05). In comparison between groups, the serum level of IL-17 after one course of medication was clearly lower in the experimental group than that in the control group (P<0.05). Apatinib regimen was demonstrated to have less toxic side-effects in the treatment of metastatic gastric cancer than tegafur-gimeracil-oteracil regimen, indicating that apatinib has favorable safety. In addition, apatinib can downregulate IL-17 expression, which is helpful in attenuating tumor proliferation and improving the clinical efficacy. Therefore, apatinib has potential use in a wide range of clinical applications. |
format | Online Article Text |
id | pubmed-6507486 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-65074862019-06-11 Clinical efficacy of apatinib in treating metastatic gastric cancer and its effect on IL-17 Chen, Ran Chen, Qi-Tian Dong, You-Hong Oncol Lett Articles Clinical efficacy of apatinib in treating metastatic gastric cancer and its effect on the levels of serum IL-17 were investigated. A retrospective analysis was performed on 129 patients who had metastatic gastric cancer after first-line chemotherapy and were treated in Xiangyang No. 1 People's Hospital from February 2012 to February 2015. Of these patients, 78 received oral apatinib and were assigned to experimental group; and 51 received oral tegafur-gimeracil-oteracil and were assigned to control group. Clinical efficacy was compared between the two groups, and the levels of serum IL-17 were measured for all the patients. The treatment response rate in the experimental group was 52.56% and in the control group 31.37%. Apparently, the treatment response rate in the experimental group was higher than that in the control group, and the difference was statistically significant (P<0.05). The incidence of adverse drug reactions in the experimental group was significantly lower than that in the control group (P<0.05). The serum level of IL-17 after one course of medication was significantly lower than that before medication in both groups (P<0.05). In comparison between groups, the serum level of IL-17 after one course of medication was clearly lower in the experimental group than that in the control group (P<0.05). Apatinib regimen was demonstrated to have less toxic side-effects in the treatment of metastatic gastric cancer than tegafur-gimeracil-oteracil regimen, indicating that apatinib has favorable safety. In addition, apatinib can downregulate IL-17 expression, which is helpful in attenuating tumor proliferation and improving the clinical efficacy. Therefore, apatinib has potential use in a wide range of clinical applications. D.A. Spandidos 2019-06 2019-04-18 /pmc/articles/PMC6507486/ /pubmed/31186764 http://dx.doi.org/10.3892/ol.2019.10270 Text en Copyright: © Chen 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 Chen, Ran Chen, Qi-Tian Dong, You-Hong Clinical efficacy of apatinib in treating metastatic gastric cancer and its effect on IL-17 |
title | Clinical efficacy of apatinib in treating metastatic gastric cancer and its effect on IL-17 |
title_full | Clinical efficacy of apatinib in treating metastatic gastric cancer and its effect on IL-17 |
title_fullStr | Clinical efficacy of apatinib in treating metastatic gastric cancer and its effect on IL-17 |
title_full_unstemmed | Clinical efficacy of apatinib in treating metastatic gastric cancer and its effect on IL-17 |
title_short | Clinical efficacy of apatinib in treating metastatic gastric cancer and its effect on IL-17 |
title_sort | clinical efficacy of apatinib in treating metastatic gastric cancer and its effect on il-17 |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6507486/ https://www.ncbi.nlm.nih.gov/pubmed/31186764 http://dx.doi.org/10.3892/ol.2019.10270 |
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