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Efficacy of RetroNectin-activated cytokine-induced killer cell therapy in the treatment of advanced hepatocelluar carcinoma

机译:RetroNectin激活的细胞因子诱导的杀伤细胞治疗在晚期肝细胞癌中的疗效

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摘要

The present study aimed to investigate the efficacy of RetroNectin-activated cytokine-induced killer cell (R-CIK) therapy in advanced hepatocellular carcinoma patients as compared with conventional chemotherapy, a comparison that has not yet been thoroughly studied. From January 2010 to October 2013, 74 patients with an initial diagnosis of advanced hepatocelluar carcinoma were enrolled in the study. Patients were assigned to one of two treatment arms: patients in arm 1 (n=37) received R-CIK treatment as the first line therapy, whereas those in arm 2 (n=37) received chemotherapy as the first line treatment. The primary end point measured in this study was median overall survival (mOS). Median progression-free survival time (mPFS) and 1- and 2-year survival rates were recorded as secondary end points. Kaplan-Meier analysis was performed on all mOS and mPFS data, and treatment hazard ratios were established using the Cox proportional hazards model. The 1-year survival rate in treatment arm 1 was 42.47% vs. 24.89% in arm 2 (95% CI, 24.91–59.01% vs. 12.10–40.02%, P=0.066); the 2-year survival rates were 21.24 and 5.53% (95% CI, 4.60–45.86 vs. 0.46–21.06%, P=0.106) in arms 1 and 2, respectively; the mPFS in arm 1 was 4.37 vs. 3.90 (x2=0.182, P=0.670) in arm 2; and the mOS in arm 1 was 14.03 months vs. 9.46 months(x2=4.406, P=0.036) in arm 2. Calculations of univariate analyses of arm 1, R-CIK cycles ≥6, KPS >70, AFP ≤400 ng/ml, and findings of no vascular invasion and no extra-hepatic metastasis were potential predictive factors (P<0.05). Calculations from multivariate analyses similarly identified these factors as potentially having predictive value (P<0.05). The main adverse effects of R-CIK therapy included fever and headache pain. R-CIK treatment may prolong mOS in advanced hepatocellular carcinoma patients compared with conventional chemotherapy. Patients who underwent ≥6 cycles of R-CIK, had KPS scores >70, AFP ≤400 ng/ml, displayed no evidence of vascular invasion, and no extra-hepatic metastasis appeared to have longer survival times compared with other cohorts in the present study.
机译:本研究旨在研究与传统化学疗法相比,RetroNectin激活的细胞因子诱导的杀伤细胞(R-CIK)治疗在晚期肝细胞癌患者中的疗效,这一比较尚未进行深入研究。从2010年1月至2013年10月,本研究招募了74例初步诊断为晚期肝细胞癌的患者。将患者分配到两个治疗组中的一个:第1组(n = 37)的患者接受R-CIK治疗作为一线治疗,而第2组(n = 37)的患者接受化疗作为一线治疗。在这项研究中测量的主要终点是中位总生存期(mOS)。中位无进展生存时间(mPFS)和1年和2年生存率记录为次要终点。对所有mOS和mPFS数据进行Kaplan-Meier分析,并使用Cox比例风险模型建立治疗风险比。治疗组1的1年生存率为42.47%,而治疗组2为24.89%(95%CI,24.91–59.01%vs. 12.10–40.02%,P = 0.066);第一组和第二组的2年生存率分别为21.24和5.53%(95%CI,4.60-45.86 vs. 0.46-21.06%,P = 0.106);手臂1的mPFS为4.37 vs.3.90(x 2 = 0.182,P = 0.670);并且第1组的mOS为14.03个月,而第2组的9.46个月(x 2 = 4.406,P = 0.036)与第1组的单因素分析计算得出,R-CIK周期≥6,KPS > 70,AFP≤400ng / ml,无血管侵犯和无肝外转移的发现是潜在的预测因素(P <0.05)。来自多变量分析的计算类似地将这些因素确定为可能具有预测价值(P <0.05)。 R-CIK治疗的主要不良反应包括发烧和头痛。与常规化学疗法相比,R-CIK治疗可延长晚期肝细胞癌患者的mOS。与当前其他队列相比,接受R-CIK≥6周期,KPS评分> 70,AFP≤400ng / ml,无血管侵犯迹象,无肝外转移的患者生存时间更长的患者研究。

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