首页|替雷利珠单抗联合化疗治疗晚期NSCLC患者的疗效及对血清肿瘤标志物和T淋巴细胞亚群水平的影响

替雷利珠单抗联合化疗治疗晚期NSCLC患者的疗效及对血清肿瘤标志物和T淋巴细胞亚群水平的影响

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目的 探讨对晚期非小细胞肺癌(NSCLC)患者采取替雷利珠单抗联合化疗治疗的疗效以及对患者血清肿瘤标志物、T淋巴细胞亚群水平的影响.方法 选择 44 例晚期NSCLC患者,以随机数表方式分为对照组与研究组,每组 22 例.对照组患者予化疗治疗,研究组患者则在对照组化疗基础上再予替雷利珠单抗治疗.对比两组患者近期客观疗效、不良反应发生情况及治疗前后的血清肿瘤标志物[癌胚抗原(CEA)、糖类抗原 125(CA125)、细胞角蛋白 19 片段抗原 21-1(CYFRA21-1)、神经元特异性烯醇化酶(NSE)]、T淋巴细胞亚群(CD3+、CD4+、CD8+、CD4+/CD8+)水平、生存质量.结果 研究组客观缓解率为 59.09%、疾病控制率为 95.45%,对照组分别为 27.27%、72.73%.相较于对照组,研究组的客观缓解率与疾病控制率均明显更高(P<0.05).治疗后,研究组CEA(28.24±2.91)ng/ml、CA125(41.56±4.33)U/ml、CYFRA21-1(18.39±1.62)μg/L、NSE(15.39±1.61)ng/ml均低于对照组的(37.67±3.88)ng/ml、(60.62±6.17)U/ml、(25.21±2.60)μg/L、(20.19±2.62)ng/ml(P<0.05).治疗后,研究组CD3+(45.82±3.95)%、CD4+(34.62±3.11)%、CD4+/CD8+(1.04±0.12)均大于对照组的(37.17±2.89)%、(28.68±2.48)%、(0.91±0.10),CD8+(22.38±2.31)%小于对照组的(27.62±2.82)%(P<0.05).研究组不良反应发生率为 40.91%,与对照组的 50.00%比较无差异(P>0.05).治疗后,研究组患者的生存质量评分(84.82±8.62)分大于对照组的(73.59±7.84)分(P<0.05).结论 对晚期NSCLC患者采用替雷利珠单抗联合化疗治疗的疗效可靠,能降低血清肿瘤标志物水平,并调节患者免疫功能,改善生存质量水平.
Therapeutic effect of tislelizumab combined with chemotherapy on patients with advanced NSCLC and its influence on serum tumor markers and T lymphocyte subsets
Objective To explore the therapeutic effect of tislelizumab combined with chemotherapy on patients with advanced non small cell lung cancer(NSCLC)and its influence on serum tumor markers and T lymphocyte subsets.Methods 44 patients with advanced NSCLC were divided into a control group and a study group according to random numerical table,with 22 cases in each group.Patients in the control group were treated with chemotherapy,and patients in the study group were treated with tislelizumab on the basis of chemotherapy in the control group.Patients in both groups were compared in terms of short-term objective curative effect,adverse reactions,serum tumor markers[carcinoembryonic antigen(CEA),carbohydrate antigen 125(CA125),cytokeratin fragment antigen 21-1(CYFRA21-1),neuron specific enolase(NSE)]and T lymphocyte subsets(CD3+,CD4+,CD8+,CD4+/CD8+),and quality of life.Results The objective remission rate and disease control rate of the study group were 59.09%and 95.45%,and those of the control group were 27.27%and 72.73%.Compared with the control group,the objective remission rate and disease control rate of the study group were obviously higher(P<0.05).After treatment,the study group had CEA of(28.24±2.91)ng/ml,CA125 of(41.56±4.33)U/ml,CYFRA21-1 of(18.39±1.62)μg/L,and NSE of(15.39±1.61)ng/ml,which were lower than(37.67±3.88)ng/ml,(60.62±6.17)U/ml,(25.21±2.60)μg/L,and(20.19±2.62)ng/ml of the control group(P<0.05).After treatment,the study group had CD3+of(45.82±3.95)%,CD4+of(34.62±3.11)%,and CD4+/CD8+of(1.04±0.12),which were higher than(37.17±2.89)%,(28.68±2.48)%,and(0.91±0.10)of the control group;the study group had lower CD8+of(22.38±2.31)%than(27.62±2.82)%of the control group(P<0.05).The incidence of adverse reactions in the study group was 40.91%,which was not different form 50.00%in the control group(P>0.05).After treatment,the quality of life score of the study group was(84.82±8.62)points,which was higher than(73.59±7.84)points of the control group(P<0.05).Conclusion The curative effect of the combination of tislelizumab and chemotherapy in patients with advanced NSCLC is reliable,which can reduce the level of serum tumor markers,regulate the immune function of patients and improve their quality of life.

TislelizumabChemotherapyAdvanced non small cell lung cancerSerum tumor markersT lymphocyte subsets

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272200 金乡县人民医院肿瘤科

替雷利珠单抗 化疗 晚期非小细胞肺癌 血清肿瘤标志物 T淋巴细胞亚群水平

2024

中国实用医药
中国康复医学会

中国实用医药

影响因子:0.797
ISSN:1673-7555
年,卷(期):2024.19(13)