Advani Sunil J, Weichselbaum Ralph R, Chmura Steven J
Department of Radiation and Cellular Oncology, Center for Molecular Medicine, University of Chicago, Chicago, IL, USA.
J Clin Oncol. 2007 Sep 10;25(26):4090-5. doi: 10.1200/JCO.2007.12.2739.
Concurrent radiotherapy and chemotherapy have been used to treat a variety of tumors to improve local control and overall survival. Gene therapy strategies represent a novel means to further improve the therapeutic ratio of ionizing radiation. Cancer gene therapy strategies in clinical trials include the use of replication-defective shuttle vectors to deliver exogenous genes and replication-competent oncolytic viruses. This review focuses on these approaches in the context of radiotherapy and radiochemotherapy. In the shuttle vector approach, exogenous gene products that enhance ionizing radiation-mediated tumor cell destruction have been selected. Moreover, the expression of exogenous genes encoding therapeutic proteins can be regulated through the use of ionizing radiation-enhanced promoters. Also, genetically engineered attenuated replication-competent viruses have been investigated in clinical trials. Preclinical data indicate that ionizing radiation interacts with replication-competent oncolytic viruses to enhance viral replication and tumor destruction. Here, we review the background preclinical and current clinical data utilizing gene therapy with radiotherapy.
同步放化疗已被用于治疗多种肿瘤,以提高局部控制率和总生存率。基因治疗策略是进一步提高电离辐射治疗增益比的一种新方法。临床试验中的癌症基因治疗策略包括使用复制缺陷型穿梭载体来递送外源基因以及具有复制能力的溶瘤病毒。本综述聚焦于放疗和放化疗背景下的这些方法。在穿梭载体方法中,已筛选出可增强电离辐射介导的肿瘤细胞破坏的外源基因产物。此外,编码治疗性蛋白质的外源基因的表达可通过使用电离辐射增强型启动子来调控。同时,具有复制能力的基因工程减毒病毒也已在临床试验中得到研究。临床前数据表明,电离辐射与具有复制能力的溶瘤病毒相互作用可增强病毒复制和肿瘤破坏。在此,我们综述利用基因治疗联合放疗的临床前背景及当前临床数据。