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癌症治疗中药物遗传学的最新进展及其临床意义。

Recent progress and clinical importance on pharmacogenetics in cancer therapy.

机构信息

Department of Hematology-Oncology, National University Cancer Institute, Singapore.

出版信息

Clin Chem Lab Med. 2011 Oct;49(10):1621-32. doi: 10.1515/CCLM.2011.715. Epub 2011 Sep 28.

Abstract

Recent advances have provided unprecedented opportunities to identify prognostic and predictive markers of efficacy of cancer therapy. Genetic markers can be used to exclude patients who will not benefit from therapy, exclude patients at high risk of severe toxicity and adjust dosing. Genomic approaches for marker discovery now include genome-wide association studies and tumor DNA sequencing. The challenge is now to select markers for which there is enough evidence to transition them to the clinic. The hurdles include the inherent low frequency of many of these markers, the lengthy validation process through trials, as well as legislative and economic hurdles. Attempts to answer questions about certain markers more quickly have led to an increased popularity of trials with enrichment design, especially in light of the dramatic phase I results seen in recent months. Personalized medicine in oncology is a step closer to reality.

摘要

近年来的进展为识别癌症治疗疗效的预后和预测标志物提供了前所未有的机会。遗传标志物可用于排除不会从治疗中获益的患者,排除有严重毒性高风险的患者,并调整剂量。目前用于标志物发现的基因组方法包括全基因组关联研究和肿瘤 DNA 测序。现在的挑战是选择有足够证据将其转化为临床应用的标志物。这些障碍包括许多此类标志物的固有低频率、通过试验进行的漫长验证过程以及立法和经济障碍。为了更快地回答某些标志物的问题,人们尝试了富集设计试验,尤其是考虑到最近几个月看到的戏剧性的 I 期结果。肿瘤学的个性化医学更接近现实。

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