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Pharmacol Rev. 2013 Oct 3;65(4):1351-95. doi: 10.1124/pr.113.007807. Print 2013.
The strategy for discovery and development of new cancer drugs has shifted the field from cytotoxic agents to therapies that selectively target oncogenic drivers. In the last decade, a number of targeted cancer therapies have been discovered and proven effective in a variety of hematological and solid malignancies. In this article, we review clinical pharmacokinetic characteristics of the U.S. Food and Drug Administration-approved targeted therapies and provide an overview of key clinical trials that led to approval of these drugs. The major limiting factor of targeted treatment is the development of resistance. We describe general principles of resistance and specific, clinically confirmed mechanisms of resistance to several therapies in different malignancies.
新癌症药物的发现和开发策略已经将该领域从细胞毒性药物转变为选择性针对致癌驱动因素的治疗方法。在过去的十年中,已经发现了许多靶向癌症疗法,并在各种血液系统恶性肿瘤和实体瘤中证明了其有效性。在本文中,我们回顾了美国食品和药物管理局批准的靶向治疗药物的临床药代动力学特征,并概述了导致这些药物获得批准的关键临床试验。靶向治疗的主要限制因素是耐药性的发展。我们描述了几种不同恶性肿瘤中几种治疗方法的耐药性的一般原则和具体的临床确认的耐药机制。