Vaccines for the treatment of non-small cell lung cancer: Investigational approaches and clinical experience

被引:46
作者
Mellstedt, Hakan [1 ]
Vansteenkiste, Johan [2 ]
Thatcher, Nick [3 ]
机构
[1] Karolinska Univ Hosp, Dept Oncol, Canc Ctr Karolinska, SE-17176 Stockholm, Sweden
[2] Univ Hosp Gasthuisberg, Resp Oncol Unit Pulmonol, B-3000 Leuven, Belgium
[3] Christie Hosp NHS Trust, Dept Med Oncol, Manchester M20 4BX, Lancs, England
关键词
NSCLC; Therapeutic cancer vaccine; Immunotherapy; Clinical trials; Tumor antigen; Immune response; PHASE-III TRIAL; BLP25 LIPOSOME VACCINE; DENDRITIC CELLS; OPEN-LABEL; ANTITUMOR IMMUNITY; TUMOR-ANTIGENS; SIPULEUCEL-T; MUC1; IMMUNOTHERAPY; CHEMOTHERAPY;
D O I
10.1016/j.lungcan.2011.02.023
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Globally, lung cancer remains the most common malignancy and the leading cause of cancer-related death. Whilst resection is a therapeutic option for patients with early stage non-small cell lung cancer (NSCLC), most patients have locally advanced or metastatic disease at diagnosis, the treatment of which still presents a considerable challenge for medical oncologists. Therapeutic cancer vaccines offer a novel approach for the treatment of patients with NSCLC in both the adjuvant and advanced disease settings. Although early attempts to use such technologies were of limited success, increased knowledge of the molecular pathology of tumors, of the immune system in general, and of tumor immunity in particular, has facilitated the production of more sophisticated anticancer vaccines. A number of promising vaccine candidates based on different types of antigenic stimulus have now been evaluated in clinical studies. These include belagenpumatucel-L, a vaccine derived from four genetically modified, irradiated NSCLC cell lines and target protein-specific vaccines designed to induce responses against epidermal growth factor (EGF), melanoma-associated antigen A3 (MAGE-A3) and mucin 1 (MUC1). The purpose of this review is to describe the mode of action of the vaccine candidates that are most advanced in their clinical development for the treatment of NSCLC, and to summarize the most recent data from clinical studies of these vaccines. (C) 2011 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:11 / 17
页数:7
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