机构地区:[1]新疆医科大学附属肿瘤医院肺内科二病区,新疆乌鲁木齐830011
出 处:《中国肿瘤生物治疗杂志》2016年第1期83-88,共6页Chinese Journal of Cancer Biotherapy
基 金:吴阶平医学基金会资助项目(No.320675012239);新疆医科大学科研创新基金资助项目(No.XYDCX201485)~~
摘 要:目的:探讨自体肿瘤抗原致敏树突状细胞-细胞因子诱导的杀伤细胞(dendritic cell-cytokine induced killer cell,DC-CIK)联合化疗治疗晚期肺腺癌的临床疗效和安全性。方法:选取2013年1月至2013年12月在新疆医科大学附属肿瘤医院治疗的120例晚期肺腺癌患者,60例行自体肿瘤抗原致敏DC-CIK联合化疗(联合组),60例行单纯化疗(化疗组),评价两组患者治疗后免疫功能、毒副反应、临床疗效、生活质量、无进展生存期和总生存期。结果:联合组治疗前后外周血T细胞亚群无明显变化(P>0.05),而化疗组治疗后外周血中CD3^+、CD3^+CD4^+、CD3^+CD8^+、CD3^-CD56^+细胞百分比明显低于治疗前,且较联合组显著下降(P<0.05);联合组较化疗组的恶心呕吐、Ⅲ-Ⅳ度骨髓抑制发生率均降低,差异有统计学意义(P<0.05);联合治疗组患者治疗后体力、食欲、睡眠较单纯化疗组改善明显(P<0.05)。联合组和化疗组患者的无进展生存期比较差异无统计学意义(6个月vs 4.5个月,P>0.05),联合组患者的总生存期较化疗组患者长(16个月vs 11.5个月,P<0.05)。结论:自体肿瘤抗原致敏DC-CIK联合化疗较单纯化疗治疗晚期肺腺癌,可明显改善患者由于化疗毒性导致的免疫功能降低,提高患者生活质量,延长总生存,减轻不良反应,提高总体疗效。Objective:To investigate the clinical efficacy and safety of autologous tumor antigen-pulsed DC-CIK (den- dritic cell-cytokine induced killer cell ) combined with chemotherapy in treatment of advanced lung adenocarcinoma. Methods: 120 patients with advanced lung adenocarcinoma treated in the Affiliated Tumor Hospital of Xinjiang Medical University from Jan 2013 to December 2013 were selected in this study; 60 patients were treated with autologous tumor an- tigen-pulsed DC-CIK combined with chemotherapy (combination group) , the other 60 patients were treated with chemo- therapy only (chemotherapy group) ; the immune function, curative effect, adverse reactions, quality of life (QOL), pro- gression free survival (PFS) and overall survival (OS) after treatment were separately evaluated in the two groups . Re- sults: Compared to the values of pre-treatment, there was no significant difference in peripheral blood T cell subsets in combination group (P 〉 0.05 ) ; Compared to pre-treatment value, the post-treatment percentage of CD3^+ , CD3^+ CD4^+ , CD3^+ CD8^+ and CD3^- CD56^+ in peripheral blood decreased significantly in chemotherapy group, and it was significant lower than that of combination group (P 〈 0.05 ) ; the incidences of nausea and vomiting,Ⅲ-Ⅳ degree myelosuppression in combination group were less than that of chemotherapy group, and the difference was statistically significant (P 〈0. 05) ; after treatment, compared with chemotherapy group, the combination of sleep, appetite and physical strength in combination group was significantly improved (P 〈 0.05 ). There was no significant difference in PFS between combina- tion group and chemotherapy group (6 months vs 4.5 months, P 〉 0.05 ), however, the OS of combination group was lon- ger than that of chemotherapy group ( 16 months vs 11.5 months, P 〈 0.05 ). Conclusion: Autologous tumor antigen- pulsed DC-CIK combination with chemotherapy, compared with chemotherapy alone, ca
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