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首页> 外文期刊>Current breast cancer reports. >Topoisomerase inhibitors in metastatic breast cancer: Overview of current practice and future development
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Topoisomerase inhibitors in metastatic breast cancer: Overview of current practice and future development

机译:转移性乳腺癌中的拓扑异构酶抑制剂:当前实践和未来发展概述

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摘要

Topoisomerases are enzymes involved in the replication of DNA and they are the target of the topoisomerase inhibitors 1 and 2. This class of anticancer agents forms the backbone of chemotherapeutic regimens in several solid tumors including breast cancer. This review focuses on their role in the treatment of metastatic breast cancer. While anthracyclines (topoisomerase 2 inhibitors) are commonly used in metastatic breast cancer, other agents such as the topoisomerase 1 inhibitors and etoposide have reached some level of clinical development. New formulations of doxorubicin are frequently used in the clinic and a new formulation of irinotecan, and etirinotecan pegol, has recently reached phase 3 development. An overview of their mechanism of action, toxicity, and clinical use (single agent or combination settings) is provided.
机译:拓扑异构酶是参与DNA复制的酶,它们是拓扑异构酶抑制剂1和2的靶标。这类抗癌剂形成了包括乳腺癌在内的几种实体瘤中化疗方案的骨干。这篇综述着重于它们在转移性乳腺癌治疗中的作用。尽管蒽环类药物(拓扑异构酶2抑制剂)通常用于转移性乳腺癌,但其他药物(例如拓扑异构酶1抑制剂和依托泊苷)已达到一定的临床开发水平。新的阿霉素制剂在临床中经常使用,伊立替康和依替立替康聚乙二醇的新制剂最近已进入3期开发。概述了它们的作用机理,毒性和临床用途(单药或联合用药设置)。

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