Laboratory of Tumor Immunology and Biology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, 10 Center Dr, Rm 8B09, Bethesda, MD 20892, USA.
J Natl Cancer Inst. 2012 Apr 18;104(8):599-613. doi: 10.1093/jnci/djs033. Epub 2012 Mar 6.
Concurrent with U.S. Food and Drug Administration (FDA) approval of the first therapeutic cancer vaccine, a wide spectrum of other cancer vaccine platforms that target a diverse range of tumor-associated antigens is currently being evaluated in randomized phase II and phase III trials. The profound influence of the tumor microenvironment and other immunosuppressive entities, however, can limit the effectiveness of these vaccines. Numerous strategies are currently being evaluated both preclinically and clinically to counteract these immunosuppressive entities, including the combined use of vaccines with immune checkpoint inhibitors, certain chemotherapeutics, small-molecule targeted therapies, and radiation. The potential influence of the appropriate patient population and clinical trial endpoint in vaccine therapy studies is discussed, as well as the potential importance of biomarkers in future directions of this field.
与美国食品和药物管理局 (FDA) 批准首个治疗性癌症疫苗同时,目前正在随机 II 期和 III 期试验中评估针对多种肿瘤相关抗原的广泛的其他癌症疫苗平台。然而,肿瘤微环境和其他免疫抑制实体的深远影响可能会限制这些疫苗的有效性。目前正在临床前和临床评估许多策略来对抗这些免疫抑制实体,包括将疫苗与免疫检查点抑制剂、某些化疗药物、小分子靶向疗法和放射治疗联合使用。讨论了疫苗治疗研究中合适的患者人群和临床试验终点的潜在影响,以及生物标志物在该领域未来发展方向的重要性。