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细胞因子诱导的杀伤细胞/树突状细胞-细胞因子诱导的杀伤细胞免疫疗法联合化疗在中国治疗结直肠癌:一项涉及2610例患者的29项试验的荟萃分析。

Cytokine-induced killer cells/dendritic cells-cytokine induced killer cells immunotherapy combined with chemotherapy for treatment of colorectal cancer in China: a meta-analysis of 29 trials involving 2,610 patients.

作者信息

Zhang Lei, Mu Ying, Zhang Anqi, Xie Jiaping, Chen Shuangfeng, Xu Fang, Wang Weihua, Zhang Yingxin, Ren Shaoda, Zhou Changhui

机构信息

Institute of Hematopathy, Henan Provincial People's Hospital, Zhengzhou, Henan Province, China.

Department of Gastroenterology, Liaocheng People's Hospital, Liaocheng Clinical School of Taishan Medical University, Liaocheng, Shandong Province, China.

出版信息

Oncotarget. 2017 Jul 11;8(28):45164-45177. doi: 10.18632/oncotarget.16665.

DOI:10.18632/oncotarget.16665
PMID:28404886
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5542175/
Abstract

PURPOSE

To systematically evaluate the efficacy and safety of Cytokine-induced killer cells/dendritic cells-cytokine induced killer cells (CIK/DC-CIK) immunotherapy in treating advanced colorectal cancer (CRC) patients.

RESULTS

29 trials including 2,610 CRC patients were evolved. Compared with chemotherapy alone, the combination of chemotherapy with CIK/DC-CIK immunotherapy significantly prolonged the overall survival rate (OS) and disease-free survival rate (DFS) (1-5 year OS, P < 0.01; 1-, 2-, 3- and 5-year DFS, P < 0.01). The combined therapy also improved patients' overall response, disease control rate and life quality (P < 0.05). After immunotherapy, lymphocyte subsets percentages of CD3+, CD3-CD56+, CD3+CD56+ and CD16+CD56+ (P < 0.01) and cytokines levels of IL-2 and IFN-γ (P < 0.05) were increased, while CD4+, CD8+ and CD4+CD25+ and IL-6 and TNF-α did not show significant change (P > 0.05).

MATERIALS AND METHODS

Clinical trials reporting response or safety of CIK/DC-CIK immunotherapy treating advanced CRC patients and published before September 2016 were searched in Cochrane Library, EMBASE, PubMed, Wanfang and CNKI database. Research quality and heterogeneity were evaluated before analysis. Pooled analyses were performed using random or fixed-effect models.

CONCLUSIONS

The combination of CIK/DC-CIK immunotherapy and chemotherapy prolong CRC patients' survival time, enhanced patients' immune function and alleviates the adverse effects caused by chemotherapy.

摘要

目的

系统评价细胞因子诱导的杀伤细胞/树突状细胞 - 细胞因子诱导的杀伤细胞(CIK/DC - CIK)免疫疗法治疗晚期结直肠癌(CRC)患者的疗效和安全性。

结果

纳入29项试验,共2610例CRC患者。与单纯化疗相比,化疗联合CIK/DC - CIK免疫疗法显著延长了总生存率(OS)和无病生存率(DFS)(1 - 5年OS,P < 0.01;1 -、2 -、3 - 和5年DFS,P < 0.01)。联合治疗还改善了患者的总体缓解率、疾病控制率和生活质量(P < 0.05)。免疫治疗后,CD3 +、CD3 - CD56 +、CD3 + CD56 + 和CD16 + CD56 + 的淋巴细胞亚群百分比(P < 0.01)以及IL - 2和IFN - γ的细胞因子水平(P < 0.05)升高,而CD4 +、CD8 + 和CD4 + CD25 + 以及IL - 6和TNF - α未显示出显著变化(P > 0.05)。

材料与方法

在Cochrane图书馆、EMBASE、PubMed、万方和知网数据库中检索2016年9月之前发表的关于CIK/DC - CIK免疫疗法治疗晚期CRC患者的疗效或安全性的临床试验。在分析前评估研究质量和异质性。使用随机或固定效应模型进行汇总分析。

结论

CIK/DC - CIK免疫疗法与化疗联合可延长CRC患者的生存时间,增强患者的免疫功能,并减轻化疗引起的不良反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d70/5542175/f5bf94a251d8/oncotarget-08-45164-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d70/5542175/54dd75c5edaf/oncotarget-08-45164-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d70/5542175/fd7e5b1223a8/oncotarget-08-45164-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d70/5542175/2c8c0ed72a39/oncotarget-08-45164-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d70/5542175/f5152039d73e/oncotarget-08-45164-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d70/5542175/a66e56cbef7c/oncotarget-08-45164-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d70/5542175/f5bf94a251d8/oncotarget-08-45164-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d70/5542175/54dd75c5edaf/oncotarget-08-45164-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d70/5542175/fd7e5b1223a8/oncotarget-08-45164-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d70/5542175/2c8c0ed72a39/oncotarget-08-45164-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d70/5542175/f5152039d73e/oncotarget-08-45164-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d70/5542175/a66e56cbef7c/oncotarget-08-45164-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d70/5542175/f5bf94a251d8/oncotarget-08-45164-g006.jpg

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