Wu Hong-Gyun, Choy Hak
Center for Radiation Oncology, Vanderbilt University Medical Center, Nashville, Tennessee 37232-5671, USA.
Oncology (Williston Park). 2002 Sep;16(9 Suppl 9):13-8.
Lung cancer is the leading cause of cancer-related death in the United States. There was rapidprogress in the treatment of lung cancer duringpast decades, but local control and survival rates are still poor. Radiation therapy has been an indispensable part of the management of lung cancer, and a recent paradigm is concurrent chemoradiation therapy. Many novel chemotherapeutic agents were recently developed to improve both local and systemic control of cancer, including camptothecin derivatives, which are topoisomerase I inhibitors. Irinotecan (CPT-11, Camptosar) is a semisynthetic water-soluble derivative of camptothecin. Irinotecan is active as a single agent against lung cancer, and is also a potent radiosensitizing agent in human lung cancer cell lines and xenografts. There have been many phase I and II clinical trials demonstrating promising results of single-agent irinotecan and combination with concurrent therapy. This article reviews irinotecan's mechanism of action of cytotoxicity and of radiation-sensitizing effects, as well as recent clinical data regarding combining radiation therapy and irinotecan for both non-small-cell and small-cell lung cancer.
肺癌是美国癌症相关死亡的主要原因。在过去几十年中,肺癌治疗取得了快速进展,但局部控制和生存率仍然很低。放射治疗一直是肺癌治疗中不可或缺的一部分,最近的一种模式是同步放化疗。最近开发了许多新型化疗药物以改善癌症的局部和全身控制,包括喜树碱衍生物,它们是拓扑异构酶I抑制剂。伊立替康(CPT-11,开普拓)是喜树碱的半合成水溶性衍生物。伊立替康作为单一药物对肺癌有活性,并且在人肺癌细胞系和异种移植模型中也是一种有效的放射增敏剂。已经有许多I期和II期临床试验证明了单药伊立替康以及与同步治疗联合使用的 promising 结果。本文综述了伊立替康的细胞毒性作用机制和放射增敏作用,以及关于将放射治疗与伊立替康联合用于非小细胞肺癌和小细胞肺癌的最新临床数据。 注:“promising”直译为“有希望的”,结合语境这里可意译为“令人鼓舞的” 。