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分子靶向药物的发展前景。

Perspectives on the development of a molecularly targeted agent.

作者信息

Druker Brian J

机构信息

Leukemia Center, Oregon Health & Science University Cancer Institute, 3181 SW Sam Jackson Park Road, Portland 97201, USA.

出版信息

Cancer Cell. 2002 Feb;1(1):31-6. doi: 10.1016/s1535-6108(02)00025-9.

Abstract

STI571 (Gleevec, imatinib mesylate) exemplifies the successful development of a rationally designed, molecularly targeted therapy for the treatment of a specific cancer. This article reviews the identification of Bcr-Abl as a therapeutic target in chronic myelogenous leukemia and the steps in the development of an agent to specifically inactivate this abnormality. Issues related to clinical trials of molecularly targeted agents are discussed, including dose and patient selection, as are possible mechanisms of resistance to STI571. Lastly, the potential use of STI571 in other malignancies and the translation of this paradigm to other malignancies is explored.

摘要

STI571(格列卫,甲磺酸伊马替尼)是成功研发出的针对特定癌症进行合理设计的分子靶向治疗药物的典范。本文回顾了将Bcr - Abl鉴定为慢性粒细胞白血病治疗靶点的过程,以及开发一种能特异性灭活该异常靶点药物的各个步骤。文中讨论了与分子靶向药物临床试验相关的问题,包括剂量和患者选择,以及对STI571产生耐药性的可能机制。最后,探讨了STI571在其他恶性肿瘤中的潜在用途,以及将这种模式应用于其他恶性肿瘤的可能性。

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