Cancer Research UK Cancer Therapeutics Unit, The Institute of Cancer Research, London, SM2 5NG, UK.
Curr Opin Pharmacol. 2013 Aug;13(4):486-96. doi: 10.1016/j.coph.2013.06.004. Epub 2013 Jun 28.
Extraordinary progress has been made in our detailed understanding of the genetic and epigenetic mechanisms responsible for oncogenesis and cancer progression. Empowered by next-generation sequencing, many new targets and pathways have been identified to exploit oncogene and non-oncogene addiction and synthetic lethality. Kinase inhibitors feature strongly in the druggable cancer genome and 19 have been approved in oncology. While survival gains are valuable, drug resistance has emerged as the major challenge. The clonal heterogeneity and evolution of cancers is an intrinsic problem, together with feedback loops, kinase switching and activation of alternative targets and pathways. The solution to drug resistance will require the use of rationally targeted combinational regimens. The application of adaptive treatment cycles based on ongoing multi-technology profiling will be the key to long-term therapeutic success.
在深入了解导致肿瘤发生和癌症进展的遗传和表观遗传机制方面已经取得了非凡的进展。借助下一代测序技术,已经确定了许多新的靶点和途径来利用致癌基因和非致癌基因成瘾以及合成致死性。激酶抑制剂在可药物治疗的癌症基因组中占有重要地位,已有 19 种激酶抑制剂在肿瘤学中获得批准。虽然生存获益是有价值的,但耐药性已成为主要挑战。癌症的克隆异质性和进化是一个内在问题,加上反馈回路、激酶转换以及替代靶点和途径的激活。解决耐药性问题需要合理靶向联合治疗方案。基于持续的多技术分析的适应性治疗周期的应用将是长期治疗成功的关键。