• 中国核心期刊(遴选)数据库收录期刊
  • 中文科技期刊数据库收录期刊
  • 中国期刊全文数据库收录期刊
  • 中国学术期刊综合评价数据库统计源期刊等

中国药物评价 ›› 2023, Vol. 40 ›› Issue (3): 266-270.

• 药品评价 • 上一篇    下一篇

安罗替尼联合TP化疗治疗晚期卵巢癌的疗效观察及对肿瘤标志物的影响

李文静   

  1. 新乡市第二人民医院, 河南 新乡 453000
  • 收稿日期:2023-02-13 修回日期:2023-05-23 出版日期:2023-06-28 发布日期:2023-07-24

Effect of Antirotinib Combined with TP Chemotherapy on Advanced Ovarian Cancer and its Effect on Tumor Markers

  1. The Second People′s Hospital of Xinxiang, Henan Xinxiang 453000, China
  • Received:2023-02-13 Revised:2023-05-23 Online:2023-06-28 Published:2023-07-24

摘要:  目的:探讨安罗替尼联合紫杉醇+顺铂(TP)化疗治疗晚期卵巢癌的临床疗效,分析其对肿瘤标志物、血管生成的影响。方法:选取2019年2月至2022年2月本院收治的80例晚期卵巢癌患者为研究对象,依据治疗方案不同分为对照组(n=40)、研究组(n=40)。对照组予以TP化疗,研究组予以安罗替尼+TP化疗。对比分析两组疗效及治疗前、治疗1个疗程、3个疗程后肿瘤标志物[人附睾蛋白4(HE4)、转铁蛋白(SF)、糖类抗原125(CA125)、糖类抗原199(CA199)]、血管生成相关因子[基质金属蛋白酶-2(MMP-2)、血管内皮生长因子(VEGF)、人血管生成素2(Ang-2)]、肿瘤生长转移相关因子水平[肝素结合性表皮生长因子(HB-EGF)、胸苷激酶1(TK1)、生长分化因子15(GDF15)]。结果:研究组总有效率67.50%,高于对照组45.00%(P<0.05);治疗1个疗程、3个疗程后研究组HE4、SF、CA125、CA199、MMP-2、VEGF、Ang-2、HB-EGF、TK1、GDF15水平低于对照组(P<0.05);治疗3个疗程后两组毒副反应发生率比较,差异无统计学意义(P>0.05)。结论:安罗替尼联合TP化疗方案治疗晚期卵巢癌的疗效确切,可抑制肿瘤标志物表达,抑制肿瘤血管生成,促进病情改善。

关键词: font-size:medium, ">卵巢癌;安罗替尼;紫杉醇;顺铂;血管生成

Abstract: Objective:To investigate the clinical efficacy of anrotinib combined with paclitaxel + cisplatin (TP) in the treatment of advanced ovarian cancer, and to analyze its effect on tumor markers and angiogenesis. Methods: A total of 80 patients with advanced ovarian cancer admitted to our hospital from February 2019 to February 2022 were selected as research objects and divided into control group (n=40) and study group (n=40) according to different treatment regimens. The control group was given TP chemotherapy, and the study group was given antirotinib +TP chemotherapy. The efficacy of the two groups and tumor markers [human epididymal protein 4 (HE4), transferrin (SF), carbohydrate antigen 125 (CA125), carbohydrate antigen 199 (CA199)], angiogenesis related factors [matrix metalloproteinase-2 (MMP-2), vascular endothelial growth factor (VE) were compared before treatment, after 1 course of treatment, and after 3 courses of treatment GF), human Ang-2], tumor growth and metastasis related factors [heparin-binding epidermal growth factor (HB-EGF), thymidine kinase 1 (TK1), growth differentiation factor 15 (GDF15)]. Results: The total effective rate of the study group was 67.50% higher than that of the control group (45.00%) (P<0.05). The levels of HE4, SF, CA125, CA199, MMP-2, VEGF, Ang-2, HB-EGF, TK1 and GDF15 in the study group were lower than those in the control group after 1 course of treatment and 3 courses of treatment (P<0.05). There was no significant difference in the incidence of toxic and side effects between the two groups after 3 courses of treatment (P>0.05). Conclusion: Androtinib combined with TP chemotherapy is effective in the treatment of advanced ovarian cancer. It can inhibit the expression of tumor markers, inhibit tumor angiogenesis and promote the improvement of the disease.

Key words: font-size:medium, ">Ovarian cancer; Anrotinib; Paclitaxel; Cisplatin

中图分类号: