Department of Medical Oncology and Hematology, University Health Network, Princess Margaret Hospital and the University of Toronto, Toronto, Ontario, Canada.
J Thorac Oncol. 2011 Oct;6(10):1763-73. doi: 10.1097/JTO.0b013e31822e28fc.
Non-small cell lung cancer (NSCLC) is often diagnosed in advanced stages and is associated with poor outcomes. Existing standards of care for NSCLC result in low overall cure rates, suggesting that novel treatment approaches are needed. In this review, we provide an updated look at the clinical data on immunotherapeutic interventions, which potentiate the immune system's response to lung tumor cells.
We searched articles on PubMed and abstracts from recent oncology meetings for publications on immunotherapies with clinical applicability to the treatment of NSCLC.
Results from phase 2 trials show vaccine therapies, which target either tumor cells themselves or aberrantly expressed tumor markers (mucin 1, melanoma-associated antigen 3, or epidermal growth factor), may be promising immunotherapeutics for NSCLC. Antigen-independent immunotherapies, such as anti-cytotoxic T-lymphocyte antigen-4 monoclonal antibodies, talactoferrin alfa, and toll-like receptor 9 agonists, act on a stimulated immune system regardless of the tumor antigen and may be feasible interventions for metastatic NSCLC. Several immunotherapies are undergoing phase 3 studies to assess optimal treatment settings and to determine clinical benefit compared with current standard treatments for NSCLC.
A growing body of evidence suggests that immune responses to lung tumors are present. Immunotherapeutic interventions, including vaccine therapy and antigen-independent immunomodulatory strategies, may improve outcomes in NSCLC. Furthermore, treatments that enhance antitumor immune responses may prove to be synergistic with chemotherapy. Identification of biomarkers and further elucidation of immunotherapeutic mechanisms of action will be essential in determining which patients will experience the greatest benefit from immunotherapy.
非小细胞肺癌(NSCLC)常被诊断为晚期,预后不良。现有的 NSCLC 治疗标准导致总体治愈率较低,这表明需要新的治疗方法。在这篇综述中,我们提供了对免疫治疗干预的临床数据的最新评估,这些干预措施增强了免疫系统对肺肿瘤细胞的反应。
我们在 PubMed 上搜索了与免疫疗法相关的文章,并查阅了最近肿瘤学会议的摘要,以寻找对 NSCLC 治疗具有临床应用价值的免疫疗法出版物。
2 期试验结果表明,针对肿瘤细胞本身或异常表达的肿瘤标志物(黏蛋白 1、黑色素瘤相关抗原 3 或表皮生长因子)的疫苗疗法可能是 NSCLC 有前途的免疫疗法。非抗原依赖性免疫疗法,如抗细胞毒性 T 淋巴细胞抗原-4 单克隆抗体、乳铁蛋白 alpha 和 Toll 样受体 9 激动剂,作用于受刺激的免疫系统,而不考虑肿瘤抗原,可能是转移性 NSCLC 的可行干预措施。几种免疫疗法正在进行 3 期研究,以评估最佳治疗方案,并确定与 NSCLC 目前标准治疗相比的临床获益。
越来越多的证据表明,针对肺肿瘤的免疫反应是存在的。免疫治疗干预,包括疫苗治疗和非抗原依赖性免疫调节策略,可能改善 NSCLC 的结局。此外,增强抗肿瘤免疫反应的治疗方法可能与化疗具有协同作用。确定生物标志物并进一步阐明免疫治疗的作用机制对于确定哪些患者将从免疫治疗中获得最大益处至关重要。