The development of camptothecin analogs in childhood cancers.
نویسندگان
چکیده
Camptothecin analogs, agents that target the intranuclear enzyme topoisomerase I, represent a promising new class of anticancer drugs for the treatment of childhood cancer. In preclinical studies, camptothecins, such as topotecan and irinotecan, are highly active against a variety of pediatric malignancies including neuroblastomas, rhabdomyosarcomas, gliomas, and medulloblastomas. In this paper, we review the status of completed and ongoing clinical trials and pharmacokinetic studies of camptothecin analogs in children. These and future planned studies of this novel class of cytotoxic agents are critical to defining the ultimate role of topoisomerase I poisons in the treatment of childhood cancer.
منابع مشابه
Camptothecin and Its Analogs Antitumor Activity by Poisoning Topoisomerase I, Their Structure Activity Relationship and Clinical Development Perspective of Analogs
Camptothecin or CPT and its analogs appear to employ anticancer action by poisoning topoisomerase I (topo I) enzyme. As a result topo I activity inhibited and have established important role against a wide range of tumors. CPT was extracted from bark of Chinese plant Camptotheca acuminate but now a large number of synthetic and semi-synthetics are identified. After activity, researchers organiz...
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ورودعنوان ژورنال:
- The oncologist
دوره 6 6 شماره
صفحات -
تاریخ انتشار 2001