Mileshkin Linda, Shah Bhaumik, Michael Michael
Division of Cancer Medicine, Peter MacCallum Cancer Centre, St. Andrews Place, East Melbourne, VIC 3002, Australia.
Chemother Res Pract. 2012;2012:838509. doi: 10.1155/2012/838509. Epub 2012 May 14.
There have been many exciting new breakthroughs in understanding tumour biology. This has opened up the possibility of personalized treatment for people with certain tumours. The epidermal growth factor receptor (EGFR) and K-ras are two such targets that can help classify tumours on a molecular basis and guide treatment decisions. However, there are still questions about how best to implement new molecular tests like these to characterize tumours in clinical practice. Potential obstacles include availability of good quality tissue specimens, access to the right test, and consensus about interpretation, funding, and availability. In this paper, we review these issues, by discussing these two examples in detail and suggest some actions for addressing potential barriers.
在肿瘤生物学的理解方面已经有了许多令人兴奋的新突破。这为特定肿瘤患者的个性化治疗开辟了可能性。表皮生长因子受体(EGFR)和K-ras就是这样两个靶点,它们可以帮助在分子基础上对肿瘤进行分类并指导治疗决策。然而,关于如何在临床实践中最好地应用这类新的分子检测来表征肿瘤,仍然存在问题。潜在的障碍包括高质量组织标本的可获得性、获得正确检测的途径、关于解读、资金和可获得性的共识。在本文中,我们通过详细讨论这两个例子来审视这些问题,并提出一些应对潜在障碍的行动建议。