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癌症中表皮生长因子受体酪氨酸激酶的分子成像策略

Strategies for molecular imaging of epidermal growth factor receptor tyrosine kinase in cancer.

作者信息

Mishani Eyal, Hagooly Aviv

机构信息

Cyclotron Unit, Department of Nuclear Medicine, Hadassah Hebrew University Hospital, Jerusalem, Israel.

出版信息

J Nucl Med. 2009 Aug;50(8):1199-202. doi: 10.2967/jnumed.109.062117. Epub 2009 Jul 17.

Abstract

A wealth of research has focused on developing targeted cancer therapies by specifically inhibiting epidermal growth factor receptor tyrosine kinase (EGFR-TK). However, the outcome of most EGFR-TK-targeted drugs that were approved by the Food and Drug Administration or entered clinical trials has been only moderate. Enhancement of EGFR-targeted therapy hinges on a reliable in vivo quantitative molecular imaging method. Such a method would enable monitoring of receptor drug binding and receptor occupancy in vivo; determination of the duration of EGFR inhibition in vivo; and, potentially, identification of a primary or secondary mutation in EGFR leading to drug interaction or loss of EGFR recognition by the drug. This review analyzes the most recent strategies to visualize and quantify EGFR-TK in cancer by nuclear medicine imaging and describes future directions.

摘要

大量研究致力于通过特异性抑制表皮生长因子受体酪氨酸激酶(EGFR-TK)来开发靶向癌症疗法。然而,大多数已获美国食品药品监督管理局批准或进入临床试验的EGFR-TK靶向药物的疗效仅为中等。增强EGFR靶向治疗取决于一种可靠的体内定量分子成像方法。这种方法将能够监测体内受体与药物的结合以及受体占有率;确定体内EGFR抑制的持续时间;并且有可能识别导致药物相互作用或药物无法识别EGFR的EGFR原发性或继发性突变。本综述分析了通过核医学成像可视化和量化癌症中EGFR-TK的最新策略,并描述了未来的方向。

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