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中华养生保健 ›› 2023, Vol. 41 ›› Issue (9): 47-50.

• 临床 • 上一篇    下一篇

安罗替尼靶向疗法对非小细胞肺癌患者免疫功能及CYFRA21-1和CEA的影响

郭岱年1, 方翎2, 徐俊2, 林菲2,*   

  1. 1.汕头大学医学院附属肿瘤医院药物临床试验机构办公室,广东 汕头,515041;
    2.汕头大学医学院附属肿瘤医院静脉用药调配中心,广东 汕头,515041
  • 出版日期:2023-05-01 发布日期:2023-04-23
  • 通讯作者: *林菲,E-mail:fayefly1986@126.com。
  • 作者简介:郭岱年(1989—),女,汉族,籍贯:广东省汕头市,本科,主管药师,研究方向:抗肿瘤药物。

Effect of Anlotinib Targeted Therapy on Immune Function and CYFRA21-1 and CEA in Patients With Non-small Cell Lung Cancer

GUO Dainian1, FANG Ling2, XU Jun2, LIN Fei2,*   

  1. 1. Office of Drug Clinical Trials, Affiliated Cancer Hospital of Shantou University School of MedicineShantou Guangdong 515041, China;
    2. Intravenous Drug Distribution Center, Affiliated Cancer Hospital of Shantou University School of Medicine, Shantou Guangdong 515041, China
  • Online:2023-05-01 Published:2023-04-23

摘要: 目的 探讨与分析安罗替尼靶向疗法对非小细胞肺癌患者免疫功能及细胞角蛋白19片段(CYFRA21-1)和癌胚抗原(CEA)的影响。方法 选取2019年1月—2020年6月在汕头大学医学院附属肿瘤医院诊治的非小细胞肺癌患者87例作为研究对象,根据随机数表法把患者分为安罗替尼组(44例)与对照组(43例)。对照组给予放疗治疗,安罗替尼组在对照组治疗的基础上给予安罗替尼治疗,两组均治疗观察4周,检测患者的免疫功能治疗效果、不良反应、及CYFRA21-1、CEA表达变化情况。结果 治疗后安罗替尼组的总有效率明显高于对照组,差异有统计学意义(P<0.05)。 安罗替尼组放疗期间的放射性肺炎、放射性食管炎的发生率稍低于对照组,差异无统计学意义(P>0.05)。安罗替尼组治疗后的CD3+T淋巴细胞比例、CD4+T淋巴细胞比例明显高于治疗前(P<0.05),安罗替尼组也明显高于对照组,差异有统计学意义(P<0.05)。安罗替尼组治疗后的血清CYFRA21-1和CEA含量明显低于治疗前(P<0.05),安罗替尼组也明显低于对照组,差异有统计学意义(P<0.05)。结论 安罗替尼靶向疗法联合放疗在非小细胞肺癌患者的应用能有效抑制血清CYFRA21-1和CEA的表达,提高患者的免疫功能,能有效提高治疗效果。

关键词: 安罗替尼, 靶向疗法, 放疗, 非小细胞肺癌, 免疫功能

Abstract: Objective To investigate and analysis the effects of anlotinib targeted therapy on immune function and CYFRA21-1 and CEA in patients with non-small cell lung cancer. Methods From January 2019 to June 2020, a total of 87 cases of patients with non-small cell lung cancer who were diagnosed and treated in the Cancer Hospital Affiliated to Shantou University School of Medicine were selected as the research subjects. The patients were divided into anlotinib group of 44 cases and control group group of 43 cases according to the treatment methods. The control group were given radiotherapy, and the anlotinib group were given anlotinib based on the treatment of the control group. Both groups were treated for 4 weeks, and the immune function and the changes of CYFRA21-1 and CEA expression were detected. Results After treatment, the total effective rate of the anlotinib group was significantly higher than that of the control group, and the difference were statistically significant (P<0.05). The incidence rates of radiation pneumonitis and radiation esophagitis during radiotherapy in the anlotinib group was slightly lower than the control group, and the comparison was not statistically significant (P>0.05). The proportion of CD3+T lymphocytes and CD4+T lymphocytes in the anlotinib group after treatment were significantly higher than those before treatment (P<0.05), and the proportions of the two T lymphocytes of the anlotinib group were also significantly higher than those in the control group, and the differences were statistically significant (P<0.05). The serum CYFRA21-1 and CEA levels in the anlotinib group after treatment were significantly lower than those before treatment (P<0.05), and the levels of serum CYFRA21-1 and CEA in anlotinib group were also significantly lower than those in the control group, and the differences were statistically significant (P<0.05). Conclusion The application of anlotinib targeted therapy combined with radiotherapy in patients with non-small cell lung cancer can effectively inhibit the expression of serum CYFRA21-1 and CEA, improve the immune function of patients, effectively improve the treatment effect.

Key words: anlotinib, targeted therapy, radiotherapy, non-small cell lung cancer, immune function

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