Chen Ran, Chen Qi-Tian, Dong You-Hong
Department of Oncology, Xiangyang No. 1 People's Hospital, Huibei University of Medicine, Xiangyang, Hubei 441000, P.R. China.
Oncol Lett. 2019 Jun;17(6):5447-5452. doi: 10.3892/ol.2019.10270. Epub 2019 Apr 18.
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.
研究了阿帕替尼治疗转移性胃癌的临床疗效及其对血清白细胞介素 -17(IL-17)水平的影响。对2012年2月至2015年2月在襄阳市第一人民医院接受一线化疗后发生转移性胃癌的129例患者进行回顾性分析。其中,78例接受阿帕替尼口服并被分配至试验组;51例接受替吉奥口服并被分配至对照组。比较两组的临床疗效,并检测所有患者的血清IL-17水平。试验组的治疗有效率为52.56%,对照组为31.37%。显然,试验组的治疗有效率高于对照组,差异具有统计学意义(P<0.05)。试验组药物不良反应的发生率显著低于对照组(P<0.05)。两组在一个疗程用药后血清IL-17水平均显著低于用药前(P<0.05)。组间比较,试验组在一个疗程用药后的血清IL-17水平明显低于对照组(P<0.05)。结果表明,与替吉奥方案相比,阿帕替尼方案在治疗转移性胃癌时具有较小的毒副作用,提示阿帕替尼具有良好的安全性。此外,阿帕替尼可下调IL-17表达,有助于减弱肿瘤增殖并提高临床疗效。因此,阿帕替尼在广泛的临床应用中具有潜在用途。