Clinical Efficacy of Tumor Antigen-Pulsed DC Treatment for High-Grade Glioma Patients: Evidence from a Meta-Analysis

被引:37
作者
Cao, Jun-Xia [1 ,2 ]
Zhang, Xiao-Yan [1 ]
Liu, Jin-Long [1 ]
Li, Duo [1 ]
Li, Jun-Li [1 ]
Liu, Yi-Shan [1 ]
Wang, Min [1 ]
Xu, Bei-Lei [1 ]
Wang, Hai-Bo [1 ]
Wang, Zheng-Xu [1 ]
机构
[1] Gen Hosp Beijing Mil Command, Biotherapy Ctr, Beijing Mil Command, Beijing, Peoples R China
[2] Tsinghua Univ, Sch Life Sci, Tsinghua Peking Ctr Life Sci, Lab Dynam Immunobiol, Beijing 100084, Peoples R China
基金
中国国家自然科学基金;
关键词
DENDRITIC CELL VACCINATION; GLIOBLASTOMA-MULTIFORME; PEPTIDE VACCINATION; RECURRENT GLIOMA; IMMUNOTHERAPY; IMMUNE; TRIAL; RESPONSES; THERAPY; CANCER;
D O I
10.1371/journal.pone.0107173
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: The effectiveness of immunotherapy for high-grade glioma (HGG) patients remains controversial. To evaluate the therapeutic efficacy of dendritic cells (DCs) alone in the treatment of HGG, we performed a systematic review and meta-analysis in terms of patient survival with relevant published clinical studies. Materials and methods: A total of 409 patients, including historical cohorts, nonrandomized and randomized controls with HGG, were selected for the meta-analysis. Results: The treatment of HGG with DCs was associated with a significantly improved one-year survival (OS) (p<0.001) and 1.5-, 2-, 3-, 4-, and 5-year OS (p<0.001) compared with the non-DC group. A meta-analysis of the patient outcome data revealed that DC immunotherapy has a significant influence on progression-free survival (PFS) in HGG patients, who showed significantly improved 1-, 1.5-, 2-, 3-and 4-year PFS (p<0.001). The analysis of Karnofsky performance status (KPS) demonstrated no favorable results for DC cell therapy arm (p = 0.23). The percentages of CD3(+) CD8(+) and CD3(+) CD4(+) T cells and CD16(+) lymphocyte subset were not significantly increased in the DC group compared with the baseline levels observed before treatment (p. 0.05), whereas CD56(+) lymphocyte subset were significantly increased after DC treatment (p = 0.0001). Furthermore, the levels of IFN-gamma in the peripheral blood of HGG patients, which reflect the immune function of the patients, were significantly increased after DC immunotherapy (p<0.001). Conclusions: Thus, our meta-analysis showed that DC immunotherapy markedly prolongs survival rates and progression-free time, enhances immune function, and improves the efficacy of the treatment of HGG patients.
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页数:12
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