Choy H, MacRae R
Center for Radiation Oncology, Vanderbilt University Medical Center, Nashville, Tennessee 37232-5671, USA.
Oncology (Williston Park). 2001 Jul;15(7 Suppl 8):22-8.
Irinotecan (CPT-11, Camptosar) is a camptothecin derivative that is thought to exert its cytotoxic effects by targeting topoisomerase I. It is believed that irinotecan stabilizes a DNA-topoisomerase I cleavable complex, and that interactions between this complex and the replication machinery may lead to cell death. There is a significant volume of in vitro and in vivo data demonstrating that irinotecan acts as a radiosensitizer. The exact mechanism of this radiosensitization is currently unknown. The increasing amount of data demonstrating improved outcomes with concurrent chemoradiation treatment of malignancies like lung cancer and head and neck cancer provide impetus for pursuing the addition of other drugs as radiosensitizers to improve local control further. Irinotecan is undergoing early clinical trials in the combined-modality setting in several disease sites. This article will provide an overview of the current status of irinotecan used concurrently with radiotherapy in the treatment of a variety of solid tumors.
伊立替康(CPT - 11,开普拓)是一种喜树碱衍生物,被认为通过作用于拓扑异构酶I发挥其细胞毒性作用。据信,伊立替康可稳定DNA - 拓扑异构酶I可裂解复合物,并且该复合物与复制机制之间的相互作用可能导致细胞死亡。有大量的体外和体内数据表明伊立替康可作为放射增敏剂。目前尚不清楚这种放射增敏的确切机制。越来越多的数据表明,对于肺癌和头颈癌等恶性肿瘤,同步放化疗可改善治疗效果,这为寻求添加其他药物作为放射增敏剂以进一步提高局部控制率提供了动力。伊立替康正在多个疾病部位的联合治疗环境中进行早期临床试验。本文将概述伊立替康与放疗同时用于治疗多种实体瘤的现状。