Strengths and Weaknesses of Immunotherapy for Advanced Non-Small-Cell Lung Cancer: A Meta-Analysis of 12 Randomized Controlled Trials

被引:16
作者
Wang, Juan [1 ]
Zou, Ze-Hong [1 ]
Xia, Hong-Lin [1 ]
He, Jian-Xing [1 ]
Zhong, Nan-Shan [1 ]
Tao, Ai-Lin [1 ]
机构
[1] Guangzhou Med Univ, Affiliated Hosp 2, Guangzhou Municipal Key Lab Allergy & Clin Immuno, Allergy Res Branch,State Key Lab Resp Dis, Guangzhou, Guangdong, Peoples R China
来源
PLOS ONE | 2012年 / 7卷 / 03期
基金
中国国家自然科学基金;
关键词
ACTIVE SPECIFIC IMMUNOTHERAPY; INDUCED KILLER-CELLS; PHASE-II TRIAL; CHEMOTHERAPY; VACCINE; CETUXIMAB; THERAPY; QUALITY; INTERLEUKIN-2; CISPLATIN;
D O I
10.1371/journal.pone.0032695
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: Lung cancer is one of the leading causes of cancer death worldwide. Non-small-cell lung cancer (NSCLC) accounts for approximately 85% of all lung cancers. Immunotherapy has yielded no consistent benefit to date for those patients. Assessing the objective efficacy and safety of immunotherapy for advanced NSCLC patients will help to instruct the future development of immunotherapeutic drugs. Methodology and Principal Findings: We performed a meta-analysis of 12 randomized controlled trials including 3134 patients (1570 patients in the immunotherapy group and 1564 patients in the control group) with histologically confirmed stage IIIA, IIIB, or IV NSCLC. The analysis was executed with efficacy end points regarding overall survival (OS), progression-free survival (PFS), complete response (CR), partial response (PR), and total effective rate. Overall unstratified OS, PFS, PR, and total effective rate were significantly improved in advanced NSCLC patients in the immunotherapy group (P = 0.0007, 0.0004, 0.002, 0.003, respectively), whereas CR was not improved (P = 0.97). Subgroup analysis showed that monoclonal antibody (mAb) immunotherapy significantly improved the PFS, PR, and total effective rate and showed a trend of improving OS of advanced NSCLC patients compared with the control group, with one kind of adverse event being significantly dominant. Compared with the control group, the vaccine subgroup showed no significant difference with regard to serious adverse events, whereas cytokine immunotherapy significantly induced three kinds of serious adverse events. Conclusions: Immunotherapy works efficiently on advanced NSCLC patients. Of several immunotherapies, mAb therapy may be a potential immunotherapy for advanced NSCLC patients, and become a standard complementary therapeutic approach in the future if the issues concerning toxicity and allergenicity of mAbs have been overcome.
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页数:12
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