机构地区:[1]新疆维吾尔自治区人民医院放疗一科,乌鲁木齐830000 [2]新疆维吾尔自治区人民医院肿瘤中心,乌鲁木齐830000
出 处:《中华细胞与干细胞杂志(电子版)》2021年第1期34-39,共6页Chinese Journal of Cell and Stem Cell(Electronic Edition)
基 金:吴阶平医学基金会临床科研专项资助(320.6799.1143)。
摘 要:目的探讨血管内皮抑制素联合调强放疗在老年中晚期非小细胞肺癌(NSCLC)中的放疗增敏作用及对T细胞、NK细胞的影响。方法选取2015年3月至2016年8月新疆维吾尔自治区人民医院NSCLC患者106例,依据简单随机数字表法分为对照组(采取调强放疗)与研究组(在对照组基础上使用血管内皮抑制素),每组53例。分析两组临床疗效、治疗前后NK细胞、T细胞水平、血清肿瘤标志物水平、EPO mRNA、EPO-R mRNA水平、毒副反应,随访3年后统计两组生存情况[中位总生存期(OS)、中位无进展生存期(PFS)]。两组比较采用独立样本t检验,组内治疗前后比较采用配对t检验,临床疗效、毒副反应发生率等采用c2检验。结果对照组肿瘤控制率低于研究组(69.81%比86.79%)(P<0.05);与治疗前比较,两组治疗后NK细胞、CD3±、CD4^+、CD4^+/CD8^+水平,血清CA199、CA125、CEA、CY211水平,EPO mRNA,EPO-R mRNA水平均降低,CD8^+水平增高,差异有统计学意义(P均<0.05);与对照组治疗后比较,研究组治疗后NK细胞[(8.01±1.64)%比(10.44±2.13)%]、CD3±[(53.51±6.02)%比(59.33±5.15)%],CD4^+[(32.31±4.01)%比(36.40±3.86)%]、CD4^+/CD8^+[(0.94±0.28)%比(1.23±0.30)%],中位PFS(5个月比8个月)、中位OS(18个月比23个月)升高,CD8^+[(34.22±3.08)%比(29.56±2.50)%],CA199[(35.20±4.46)kU/L比(30.15±4.14)kU/L]、CA125[(34.91±6.03)kU/L比(29.77±5.30)kU/L]、CEA[(22.50±3.97)μg/L比(17.97±4.10)μg/L]、CY211[(7.19±2.01)μg/L比(4.56±1.34)μg/L],EPO mRNA水平(0.85±0.08比0.80±0.06)、EPO-RmRNA水平(0.88±0.09比0.81±0.08)降低,差异具有统计学意义(P均<0.05);与对照组比较,研究组血红蛋白减少、肝肾功能损伤、恶心呕吐、中性粒细胞减少发生率之间比较差异无统计学意义(P>0.05)。结论联合采取调强放疗及血管内皮抑制素治疗老年中晚期NSCLC,可有效提高肿瘤控制率,改善患者生存状况,可能是因其能降低血清肿瘤标志物水平,减轻对免疫功能的�Objective To investigate the radiosensitization effect of endostatin combined with intensity-modulated radiotherapy in elderly patients with advanced non-small cell lung cancer NSCLC)and its effect on T cells and natural killer(NK)cells.Methods A total of 106 patients with NSCLC in our hospital from March 2015 to August 2016 were selected and divided into a study group and a control group according to a simple random number table method,53 cases in each group.The control group took intensity-modulated radiotherapy,and the study group took endostatin on the basis of the control group.The clinical efficacy,levels of NK cells and T cells,serum tumor marker levels,erythropoieth(EPO)mRNA,EPO-receptor mRNA levels before and after treatment,toxic and side effects were counted in the two groups.After 3 years of follow-up,the survival[median overall survival(OS),median progression-free survival(PFS)]of the two groups was counted.Results The tumor control rate of the study group(86.79%)was higher than that of the control group(69.81%)(P<0.05);after treatment,the NK cells,CD3±,CD4^+,CD4^+/CD8^+in the two groups were lower than before treatment,and CD8^+was higher than before treatment.However,NK cells(10.44±2.13)%,CD3±(59.33±5.15)%,CD4^+(36.40±3.86)%,and CD4^+/CD8^+(1.23±0.30)in the study group were higher than those in the control group,CD8^+(29.56±2.50)%was lower than the control group(P<0.05);after treatment,the serum levels of CA199,CA125,CEA and CY211 in the two groups were lower than before treatment.And the CA199(30.15±4.14)kU/L,CA125(29.77±5.30)kU/L,CEA(17.97±4.10)μg/L,CY211(4.56±1.34)μg/L of the study group were lower than those of the control group(P<0.05);after treatment,the levels of EPO mRNA and EPO-R mRNA in the two groups were lower than before treatment.EPO mRNA(0.80±0.06)and EPO-R mRNA(0.81±0.08)in the study group were lower than those in the control group(P<0.05);the incidence of hemoglobin reduction,liver and kidney function damage,vomiting and nausea,neutropenia between the study group and
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