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首页> 外文期刊>Experimental and therapeutic medicine >Evaluation of 29 indicators for the prognosis of advanced non-small cell lung cancer with cytokine-induced killer cell therapy combined with chemotherapy
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Evaluation of 29 indicators for the prognosis of advanced non-small cell lung cancer with cytokine-induced killer cell therapy combined with chemotherapy

机译:细胞因子诱导的杀伤细胞疗法联合化疗对晚期非小细胞肺癌29项指标的评价

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The aim of the present study was to evaluate 29 whole blood or serum indicators to identify factors able to predict clinical outcome following cytokine-induced killer (CIK) cell therapy combined with chemotherapy in patients with advanced non-small cell lung cancer (NSCLC), and to evaluate the 5-year prognosis of the patients. From March 2008 to October 2013, 42 patients with advanced NSCLC (stages III and IV) were enrolled in the study. These patients were from a single hospital, and had been treated with CIK therapy combined with chemotherapy. Evaluation of the correlation between prognosis and age, gender, tumor stage, surgery resection status, number of CIK therapy cycles, tumor subtype, and the differential whole blood or serum indicators were analyzed by Kaplan-Meier methods and the log-rank test. The prognostic factors were analyzed by Cox proportional models. The median progression-free survival (mPFS) time of patients with high expression levels of albumin [20.0 months; 95% confidence interval (CI): 17.4-22.6 months] was significantly longer than the mPFS for patients with low expression levels of albumin (36.0 months; 95% CI: 24.7-47.3 months) (P= 0.034). Other factors demonstrated no significant difference. Following analysis using the Cox proportional hazards regression model, the number of CIK therapy cycles (P = 0.041) and the expression level of albumin (P = 0.038) were revealed to be independent prognostic factors following the use of CIK cell therapy combined with chemotherapy for patients with advanced NSCLC. The risk of adverse outcomes in patients receiving >= 4 CIK therapy cycles and in patients with increased expression levels of albumin were 0.38 (95% CI: 0.14-1.13) and 0.32 (95% CI: 0.10-1.24) -fold those of patients receiving <4 CIK therapy cycles and with decreased expression levels of albumin, respectively. The serum albumin concentration may therefore be a predictor of the 5-year survival rate of patients with advanced NSCLC treated with CIK cell therapy combined with chemotherapy; patients with high expression levels of albumin may have a better prognosis in comparison with patients with low expression levels of albumin.
机译:本研究的目的是评估29种全血或血清指标,以鉴定能够预测细胞因子诱导的杀伤(CIK)细胞疗法与化学疗法联合治疗的晚期非小细胞肺癌(NSCLC)患者临床预后的因素,并评估患者的5年预后。从2008年3月至2013年10月,共有42例晚期NSCLC患者(III和IV期)入选了该研究。这些患者来自一家医院,并接受了CIK疗法和化学疗法的治疗。通过Kaplan-Meier方法和对数检验分析了预后与年龄,性别,肿瘤分期,手术切除状态,CIK治疗周期数,肿瘤亚型以及全血或血清指标差异之间的相关性。通过Cox比例模型分析预后因素。白蛋白高表达水平患者的中位无进展生存时间(mPFS)[20.0个月;对于白蛋白表达水平低的患者(36.0个月; 95%CI:24.7-47.3个月),“ 95%置信区间(CI):17.4-22.6个月]明显比mPFS长(P = 0.034)。其他因素无明显差异。使用Cox比例风险回归模型进行分析后,发现CIK细胞疗法与化学疗法联合用于CIK治疗后,CIK治疗周期数(P = 0.041)和白蛋白表达水平(P = 0.038)是独立的预后因素。晚期NSCLC患者。接受> = 4 CIK治疗周期的患者和白蛋白表达水平升高的患者产生不良结局的风险是患者的0.38(95%CI:0.14-1.13)和0.32(95%CI:0.10-1.24)-分别接受<4个CIK治疗周期和白蛋白表达水平降低。因此,血清白蛋白浓度可能是CIK细胞疗法联合化疗治疗晚期NSCLC患者5年生存率的预测指标。与白蛋白低表达水平的患者相比,白蛋白高表达水平的患者预后更好。

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