PMID- 25268709 OWN - NLM STAT- MEDLINE DCOM- 20150616 LR - 20220408 IS - 1932-6203 (Electronic) IS - 1932-6203 (Linking) VI - 9 IP - 9 DP - 2014 TI - Effectiveness and safety of chemotherapy combined with dendritic cells co-cultured with cytokine-induced killer cells in the treatment of advanced non-small-cell lung cancer: a systematic review and meta-analysis. PG - e108958 LID - 10.1371/journal.pone.0108958 [doi] LID - e108958 AB - BACKGROUND: Lung cancer, particularly non-small-cell lung cancer (NSCLC) is the leading cause of cancer mortality. Chemotherapy combined dendritic cells co-cultured with cytokine-induced killer cells (DC-CIK) immunotherapy has been applied in advanced NSCLC patients' treatment, but couldn't provide consistent beneficial results. Therefore, it is necessary to evaluate the efficiency and safety of combination therapy to promote the application. METHODS: A literature search for randomized controlled trials of NSCLC was conducted in PubMed database. Before meta-analysis was performed, studies were evaluated heterogeneity. Pooled risk ratios (RRs) were estimated and 95% confidence intervals (CIs) were calculated using a fixed-effect model. Sensitivity analysis was also performed. RESULTS: Six eligible trials were enrolled. Efficiency and safety of chemotherapy followed by DC-CIK immunotherapy (experimental group) and chemotherapy alone (control group) were compared. 1-year overall survival (OS) (P = 0.02) and progression free survival (PFS) (P = 0.005) in the experimental group were significantly increased compared with the control. Disease control rate (DCR) (P = 0.006) rose significantly in experimental group. However, no significant differences between the two groups were observed in 2-year OS (P = 0.21), 2-year PFS (P = 0.10), overall response rate (ORR) (P = 0.76) and partial response (PR) (P = 0.22). Temporary fever, anemia, leukopenia and nausea were the four major adverse events (AEs) treated by chemotherapy. The incidence of anemia, leukopenia and nausea in the experimental group was obviously lower than the control group. Temporary fever rate was higher in experimental group than that in the control, but could be alleviated by taking sufficient rest. CONCLUSIONS: Chemotherapy combined with DC-CIK immunotherapy showed superiority in DCR, 1-year OS and PFS, and no more AEs appeared, however, there was no significant improvement in ORR, PR, 2-year OS and PFS. As a whole, the combination therapy is safer but modest in efficacy for advanced NSCLC patients. FAU - Han, Rui-xian AU - Han RX AD - First Teaching Hospital of Tianjin University of Traditional Chinese Medicine, Tianjin, China; Tianjin University of Traditional Chinese Medicine, Tianjin, China. FAU - Liu, Xu AU - Liu X AD - First Teaching Hospital of Tianjin University of Traditional Chinese Medicine, Tianjin, China. FAU - Pan, Pan AU - Pan P AD - First Teaching Hospital of Tianjin University of Traditional Chinese Medicine, Tianjin, China; Tianjin University of Traditional Chinese Medicine, Tianjin, China. FAU - Jia, Ying-jie AU - Jia YJ AD - First Teaching Hospital of Tianjin University of Traditional Chinese Medicine, Tianjin, China. FAU - Yu, Jian-chun AU - Yu JC AD - First Teaching Hospital of Tianjin University of Traditional Chinese Medicine, Tianjin, China. LA - eng PT - Journal Article PT - Meta-Analysis PT - Research Support, Non-U.S. Gov't PT - Review PT - Systematic Review DEP - 20140930 PL - United States TA - PLoS One JT - PloS one JID - 101285081 RN - 0 (Antineoplastic Agents) SB - IM MH - Antineoplastic Agents/therapeutic use MH - Carcinoma, Non-Small-Cell Lung/drug therapy/mortality/*therapy MH - Coculture Techniques MH - Cytokine-Induced Killer Cells/*cytology MH - Databases, Factual MH - Dendritic Cells/cytology/*transplantation MH - Disease-Free Survival MH - Humans MH - Immunotherapy MH - Lung Neoplasms/drug therapy/mortality/*therapy MH - Remission Induction MH - Survival Rate PMC - PMC4182599 COIS- Competing Interests: The authors have declared that no competing interests exist. EDAT- 2014/10/01 06:00 MHDA- 2015/06/17 06:00 PMCR- 2014/09/30 CRDT- 2014/10/01 06:00 PHST- 2013/12/30 00:00 [received] PHST- 2014/09/06 00:00 [accepted] PHST- 2014/10/01 06:00 [entrez] PHST- 2014/10/01 06:00 [pubmed] PHST- 2015/06/17 06:00 [medline] PHST- 2014/09/30 00:00 [pmc-release] AID - PONE-D-13-54665 [pii] AID - 10.1371/journal.pone.0108958 [doi] PST - epublish SO - PLoS One. 2014 Sep 30;9(9):e108958. doi: 10.1371/journal.pone.0108958. eCollection 2014.