肺癌合剂联合吉非替尼治疗EGFR敏感突变的非小细胞肺癌的疗效及安全性评价 |
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引用本文: | 周良发,覃双来,胡作为,王珊,骆曼. 肺癌合剂联合吉非替尼治疗EGFR敏感突变的非小细胞肺癌的疗效及安全性评价[J]. 临床和实验医学杂志, 2021, 20(8): 824-827 |
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作者姓名: | 周良发 覃双来 胡作为 王珊 骆曼 |
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作者单位: | 武汉市第一医院肿瘤科 湖北 武汉 430000 |
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基金项目: | 2019年湖北省卫生计生委科研项目(编号:wJ2019h114);武汉市卫生计生委科研项目(编号:WZ19C27)。 |
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摘 要: | 目的 研究肺癌合剂联合吉非替尼治疗表皮生长因子受体(EGFR)敏感突变的非小细胞肺癌的疗效及安全性.方法 回顾性选取2018年1月至2020年1月武汉市第一医院收治的80例EGFR敏感突变的非小细胞肺癌患者为研究对象,根据不同用药方式分为研究组(n=40)与对照组(n=40).对照组单用吉非替尼治疗,研究组联用吉非替尼...
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关 键 词: | 非小细胞肺癌 肺癌合剂 吉非替尼 表皮生长因子受体 肿瘤标志物 |
Efficacy and safety of lung cancer mixture combined with gefeitinib in the treatment of EGFR-sensitive non-small cell lung cancer |
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Affiliation: | (Department of Oncology,Wuhan First Hospital,Wuhan Hubei 430000,China) |
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Abstract: | Objective To study the efficacy and safety of lung cancer combination therapy with gefitinib in the treatment of sensitive non-small cell lung cancer with epidermal growth factor receptor(EGFR).Methods From January 2018 to January 2020,80 cases of non-small cell lung cancer patients with EGFR-sensitive mutations admitted to Wuhan First Hospital were retrospectively selected as the research objects,and divided into study group(n=40)and control group(n=40)according to different medication methods.The control group was treated with gefitinib alone,while the study group was treated with gefitinib combined with lung cancer mixture.Comparing the two groups before and after 4 weeks of treatment of T lymphocyte subsets(CD3+,CD4+,CD8+,CD4+/CD8+),serum tumor markers(neuron specificity enolization enzyme,carcinoembryonic antigen,cancer antigen 125,cytokeratin 19 fragment)level and the total effective rate,incidence of adverse reactions(nausea and vomiting syndrome),anemia,hypertension,skin rashes,hands and feet.Results After 4 weeks of treatment,the content of CD3+,CD4+,CD4+/CD8+in the two groups were higher than before treatment,the content of CD8+and serum neuron-specific enolase,carcinoembryonic antigen,cancer antigen 125,and cytokeratin 19 Fragment were lower than before treatment,and the differences were statistically significant(P<0.05);after 4 weeks of treatment,the content of CD3+,CD4+,CD4+/CD8+in study group[(63.08±5.23)%,(37.52±4.26)%,1.32±0.25]were higher than those in the control group[(30.03±3.56)%,(37.52±4.26)%、0.84±0.22],the content of CD8+and the levels of serum neuron-specific enolase,carcinoembryonic antigen,cancer antigen 125,and cytokeratin 19 fragment[(53.42±4.38)%,(16.12±3.93)ng/mL,(30.24±4.38)ng/mL,(50.23±6.48)U/mL,(6.52±3.09)ng/mL]were lower than those in the control group[(33.28±4.76)%,(21.06±3.86)ng/mL,(59.81±5.18)ng/mL,(78.69±6.76)U/mL,(10.86±3.14)ng/mL],and the differences were statistically significant(P<0.05).The total effective rate of the study group(87.50%)was significantly higher than that of the control group(65.00%),and the difference was statistically significant(P<0.05).There was no significant difference in the incidence of adverse reactions between the study group(10.00%)and the control group(12.50%)(P>0.05).Conclusion Lung cancer mixture combined with gefeitinib in the treatment of EGFR-sensitive non-small cell lung cancer has a significant effect,can improve the immune function of patients and improve the level of tumor markers,with fewer adverse reactions,high safety. |
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Keywords: | Non-small cell lung cancer Lung cancer mixture Gefitinib Epidermal growth factor receptor Tumor marker |
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