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首页> 外文期刊>Anticancer Research: International Journal of Cancer Research and Treatment >Prospective study of chemotherapy in combination with cytokine-induced killer cells in patients suffering from advanced non-small cell lung cancer.
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Prospective study of chemotherapy in combination with cytokine-induced killer cells in patients suffering from advanced non-small cell lung cancer.

机译:晚期非小细胞肺癌患者化疗联合细胞因子诱导的杀伤细胞的前瞻性研究。

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The present study evaluated the clinical efficacy of chemotherapy in combination with cytokine-induced killer (CIK) biotherapy compared to the chemotherapy alone. Fifty-nine advanced non-small cell lung cancer (NSCLC) patients were randomly divided into two groups, group A (chemotherapy alone, including docetaxel 75 mg/m2, day 1; cisplatin, 25 mg/m2, days 1-4, tri-weekly) and group B (chemotherapy plus CIK cell transfusion). Autologous CIK cells were induced from the patients'peripheral mononuclear cells in vitro and separated by cytometry and then transfused back the patients. The host cellular immune function, clinical curative effects and quality of life (QOL) were examined and were compared between the two groups. The host immune function was enhanced and QOL was improved in the patients treated by chemotherapy plus CIK biotherapy compared to the patients treated by chemotherapy alone. The overall response rate (ORR) was 43.3% and 44.8% in groups A and B, respectively. The disease control rate (DCR) was higher in group B than in group A (89.7% vs. 65.5%, p = 0.030). The time to progression was 4.67 months (95% CI 3.98-6.02 months) in group A and 6.65 months (95% CI 4.70-7.30 months) in group B and the median survival time was 11.0 months (95% CI 7.88-14.1 months) in group A and 15.0 months (95% CI 11.04-18.96 months) in group B. Compared to patients in group A, the patients in group B had significantly longer progression-free survival (p = 0.042) and overall survival (p = 0.029). No severe side-effects occurred in the CIK cell transfusion patients. It was concluded that chemotherapy plus CIK cells has potential benefits compared to chemotherapy alone in patients suffering from advanced NSCLC and autologous CIK cell transfusion has no obvious side-effects.
机译:本研究评估了化学疗法与细胞因子诱导的杀手(CIK)生物疗法相结合的临床疗效,与单纯化疗相比。 59例晚期非小细胞肺癌(NSCLC)患者随机分为两组,即A组(仅化疗,包括多西他赛75 mg / m2,第1天;顺铂,25 mg / m2,第1-4天,三-每周一次)和B组(化疗加CIK细胞输注)。从患者的外周单个核细胞中体外诱导自体CIK细胞,并通过细胞计数术分离,然后回输给患者。检查并比较了两组的宿主细胞免疫功能,临床疗效和生活质量(QOL)。与单纯化学疗法治疗的患者相比,化学疗法+ CIK生物疗法治疗的患者的宿主免疫功能得到增强,生活质量得到改善。 A组和B组的总缓解率(ORR)分别为43.3%和44.8%。 B组的疾病控制率(DCR)高于A组(89.7%对65.5%,p = 0.030)。 A组的进展时间为4.67个月(95%CI 3.98-6.02个月),B组为6.65个月(95%CI 4.70-7.30个月),中位生存时间为11.0个月(95%CI 7.88-14.1个月) A组)和15.0个月(95%CI 11.04-18.96个月)。与A组患者相比,B组患者的无进展生存期(p = 0.042)和总生存期(p = 0.029)。在CIK细胞输注患者中没有发生严重的副作用。结论是,与单纯化疗相比,化疗加CIK细胞在患有晚期NSCLC的患者中具有潜在的益处,自体CIK细胞输注没有明显的副作用。

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