Washington University in St Louis, Division of Oncology, 660 South Euclid Ave - Campus Box 8069, St Louis, MO 63110, USA.
Expert Rev Clin Pharmacol. 2008 Jan;1(1):73-80. doi: 10.1586/17512433.1.1.73.
Oncology pharmacogenomics has seen a great deal of progress in the past 10 years. The release of the Human Genome Project data and the availability of fast, affordable genotyping platforms has allowed the field to expand and has provided invaluable data for pharmacogenomics research. The introduction of US FDA-approved targeted therapy (trastuzumab), package insert changes (irinotecan and tamoxifen) and the initiation of a genotype-guided clinical trial for cancer therapy (TYMS TSER in rectal cancer), along with panels of DNA and expression markers (Roche AmpliChip(®) and Oncotype Dx™ panel) are paving the way towards the integration of pharmacogenomics into clinical practice.
在过去的 10 年中,肿瘤药理学基因组学取得了很大的进展。人类基因组计划数据的发布和快速、经济实惠的基因分型平台的出现使得该领域得以扩展,并为药物基因组学研究提供了宝贵的数据。美国食品和药物管理局(FDA)批准的靶向治疗药物(曲妥珠单抗)的引入、药品说明书的变更(伊立替康和他莫昔芬)、以及基于基因型的癌症治疗临床试验(直肠癌中的 TYMS TSER)的启动,以及 DNA 和表达标记物的面板(罗氏 AmpliChip(®)和 Oncotype Dx(™) 面板)都为将药物基因组学纳入临床实践铺平了道路。