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DC-CIK联合化疗治疗非小细胞肺癌的临床疗效评价(英文) 被引量:3

The clinical effects of DC-CIK cells combined with chemotherapy in the treatment of advanced NSCLC
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摘要 Objective: The aim of the study was to evaluate the safety and therapeutic effects of autologous dendritic cells co-cultured with cytokine-induced killer cells (DC-CIK) combined with chemotherapy in advanced non-small cell lung cancer (NSCLC) patients. Methods: Fifty patients with advanced NSCLC (stages III to IV), who had received therapies in our Center (Department of Biotherapy, Affiliated to Cancer Hospital of Shanxi Medical University, Taiyuan, China) from August 2008 to January 2010, were treated by DC-CIK + chemotherapy as the combined treatment group; fifty advanced NSCLC patients treated with chemotherapy at the same time served as controls. The immunologic function, short-term therapeutic effects, the 1-year survival rate, the life quality, the chemotherapy side effects were compared between the two groups, the safety and therapeutic effects of DC-CIK cells therapy were observed too. Results: There was no obvious change of subsets of T cells in peripheral blood before and after therapy in DC-CIK + chemotherapy group, and IFN-γ was improved after therapy in this group (P < 0.05); in chemotherapy alone group, the ratios of CD3+CD4+, CD3+CD8+, CD3-CD56+ cells and the secretion of IL-2, TNF-α decreased significantly after therapy (P < 0.05); the ratios of CD3+CD8+, CD3+CD56+ were improved after cell culture (P < 0.05). The disease control rate (DCR) of DC-CIK + chemotherapy group was higher than that in the chemotherapy alone group (78.0% vs 56.0%, P < 0.05); the 1-year survival rates of DC-CIK + chemotherapy group and chemotherapy alone group were 50% and 44% respectively, had no significant difference. Compared with chemotherapy alone group, the occurrence of chemotherapy side effects (including bone marrow suppression, nausea and vomiting, peripheral nerve toxicity) was less in the DC-CIK + chemotherapy group (P < 0.05). The physical and appetite were better in DC-CIK + chemotherapy group after therapy. Conclusion: To compare with simple chemotherapy, DC-CIK + chemotherapy for advanced NSCLC is safe and effective, and it can improve patients' life quality and remission rate, and prolong their survival time. Objective: The aim of the study was to evaluate the safety and therapeutic effects of autologous dendritic cells co-cultured with cytokine-induced killer cells (DC-CIK) combined with chemotherapy in advanced non-small cell lung cancer (NSCLC) patients. Methods: Fifty patients with advanced NSCLC (stages III to IV), who had received therapies in our Center (Department of Biotherapy, Affiliated to Cancer Hospital of Shanxi Medical University, Taiyuan, China) from August 2008 to January 2010, were treated by DC-CIK + chemotherapy as the combined treatment group; fifty advanced NSCLC patients treated with chemotherapy at the same time served as controls. The immunologic function, short-term therapeutic effects, the 1-year survival rate, the life quality, the chemotherapy side effects were compared between the two groups, the safety and therapeutic effects of DC-CIK cells therapy were observed too. Results: There was no obvious change of subsets of T cells in peripheral blood before and after therapy in DC-CIK + chemotherapy group, and IFN-γ was improved after therapy in this group (P 0.05); in chemotherapy alone group, the ratios of CD3+CD4+, CD3+CD8+, CD3–CD56+ cells and the secretion of IL-2, TNF-α decreased significantly after therapy (P 0.05); the ratios of CD3+CD8+, CD3+CD56+ were improved after cell culture (P 0.05). The disease control rate (DCR) of DC-CIK + chemotherapy group was higher than that in the chemotherapy alone group (78.0% vs 56.0%, P 0.05); the 1-year survival rates of DC-CIK + chemotherapy group and chemotherapy alone group were 50% and 44% respectively, had no significant difference. Compared with chemotherapy alone group, the occurrence of chemotherapy side effects (including bone marrow suppression, nausea and vomiting, peripheral nerve toxicity) was less in the DC-CIK + chemotherapy group (P 0.05). The physical and appetite were better in DC-CIK + chemotherapy group after therapy. Conclusion: To compare with simple chemotherapy, DC-CIK + chemotherapy for advanced NSCLC is safe and effective, and it can improve patients’ life quality and remission rate, and prolong their survival time.
出处 《The Chinese-German Journal of Clinical Oncology》 CAS 2012年第2期67-71,共5页 中德临床肿瘤学杂志(英文版)
基金 Supported by a grant from the key Scientific Foundation of Shanxi Province (No. 051096-2)
关键词 非小细胞肺癌 生物治疗 化疗 晚期 临床效果 山西医科大学 生活质量 毒副作用 autologous dendritic cells co-cultured with cytokine-induced killer cells (DC-CIK) non-small cell lung cancer (NSCLC) adoptive cellular immunotherapy chemotherapy
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  • 1王金万,孙燕,刘永煜,于起涛,张沂平,李凯,朱允中,周清华,侯梅,管忠震,李维廉,庄武,王东林,梁后杰,秦凤展,卢辉山,刘晓晴,孙红,张燕军,王杰军,罗素霞,杨瑞合,涂远荣,王秀问,宋恕平,周静敏,游丽芬,王竞,姚晨.重组人血管内皮抑素联合NP方案治疗晚期NSCLC随机、双盲、对照、多中心Ⅲ期临床研究[J].中国肺癌杂志,2005,8(4):283-290. 被引量:625
  • 2张金娥,梁长虹,赵振军,林华欢,曾辉,何晖,茹光腾.CT肺灌注在肺结节诊断中的应用研究[J].中华放射学杂志,2005,39(10):1041-1045. 被引量:95
  • 3Rosenberg SA,Restifo NP,Yang JC,et al.Adoptive cell transfer:a clinical path to effective cancer immunotherapy[J].Nat Rev Cancer,2008,8(4):299-308.
  • 4Sumpter K,Harper-Wynne C,Cunningham D,et al.Report of two protocol planned interim analyses in a randomised multicentre phase Ⅲ study comparing capeeitabine with fluomuracil and oxaliplatin with cisplatin in patients with advanced oesophagogastric cancer receiving ECF[J].Br J Cancer,2005,92(11):1976-1983.
  • 5Gao DQ,Li CY,Zhao P,et al.The clinical effects of dendritic cell and cytokine-induced killer cell therapy for lung cancer after surgery[J].Cancer Research,2014,74 Suppl 19:S2812.
  • 6Neeru Khanna,Sudip Sen,Himani Sharma,Neeta Singh.S29 ribosomal protein induces apoptosis in H520 cells and sensitizes them to chemotherapy[J].Biochemical and Biophysical Research Communications.2003(1)
  • 7Liapi E, Geschwind JF. Chemoembolization for primary and meta- static liver cancer[ J]. Cancer J,2010,16 : 156-162.
  • 8Hillingso JG, Wille-Jφrgensen P. Staged or simultaneous resection of synchronous liver metastases from eolorectal cancer-a systematic re- view[J]. Colorectal Dis,2009,11:3-10.
  • 9Yin H, Lu K, Qiao WB, et al. Whole-liver Radiotherapy Concurrent with Chemotherapy as a Palliative Treatment for Colorectal Patients with Massive and Multiple Liver Metastases:a Retrospective Study [ J ]. Asian Pac J Cancer Prey,2014,15 : 1597-602.
  • 10Xu J,Qin X,Wang J. Chinese guidelines for the diagnosis and com- prehensive treatment of hepatic metastasis of colorectal cancer[J].J Cancer Res Clin Oncol,2011,137 : 1379-1396.

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