He Jin, Ahuja Nita
Department of Surgery, The Johns Hopkins University School of Medicine, 600 North Wolfe Street, Blalock 1202, Baltimore, MD 21287, USA.
Department of Surgery, The Johns Hopkins University School of Medicine, 600 North Wolfe Street, Blalock 685, Baltimore, MD 21287, USA.
Surg Clin North Am. 2015 Oct;95(5):1081-94. doi: 10.1016/j.suc.2015.05.002. Epub 2015 Jun 16.
Cancers are characterized by complex tumor heterogeneity driven by subclones with differential genotypes and phenotypes, which then drives cancer behavior. As genomic strategies become feasible on smaller samples such as biopsies, coupled with decreasing costs of these approaches, clinicians will increasingly use genomic information to drive therapeutic decision making. Early applications of such personalized approaches are discussed. Genetic testing of high-risk family members may identify patients with germline mutations who can have prophylactic surgeries as a cancer prevention strategy. This article discusses examples of successful targeted therapy. Clinical trials need to incorporate genetic testing to stratify patients into different groups.
癌症的特征是由具有不同基因型和表型的亚克隆驱动的复杂肿瘤异质性,进而驱动癌症行为。随着基因组策略在活检等较小样本上变得可行,再加上这些方法成本的降低,临床医生将越来越多地利用基因组信息来推动治疗决策。本文讨论了这种个性化方法的早期应用。对高危家庭成员进行基因检测可能会识别出具有种系突变的患者,这些患者可以通过预防性手术作为癌症预防策略。本文讨论了成功的靶向治疗实例。临床试验需要纳入基因检测,以便将患者分层到不同组中。