D'Amico Thomas A
Department of Surgery, Duke University Medical Center, Durham, North Carolina 27710, USA.
Ann Thorac Surg. 2008 Feb;85(2):S737-42. doi: 10.1016/j.athoracsur.2007.11.047.
Clinical and pathologic staging of lung cancer is suboptimal in achieving the goals of assessing prognosis and selecting therapy. Although the technologic developments that allow the generalized use of proteomic and genomic analyses are relatively recent, major progress in understanding the molecular basis of lung cancer has been made. Predicting survival is only the first step in the use of genomics and proteomics. If a reliable gene array or protein profile can be identified that is associated with poor prognosis, these profiles can then be identified and become potential therapeutic targets. It is not difficult to envision the development of a simple serum test that will diagnose a lung cancer perhaps even before it is clinically apparent and at the same time identify the chemotherapeutic agents to which the tumor is sensitive, allowing individually directed treatment. Eventually, a comprehensive staging system should incorporate the prognostic information of biologic variables.
肺癌的临床和病理分期在实现评估预后和选择治疗方案的目标方面并不理想。尽管允许广泛使用蛋白质组学和基因组分析的技术发展相对较新,但在理解肺癌分子基础方面已取得重大进展。预测生存只是使用基因组学和蛋白质组学的第一步。如果能够识别出与预后不良相关的可靠基因阵列或蛋白质谱,那么就可以识别出这些谱,并将其作为潜在的治疗靶点。不难设想开发一种简单的血清检测方法,甚至在肺癌临床显现之前就能诊断出来,同时还能识别出肿瘤对哪些化疗药物敏感,从而实现个体化治疗。最终,一个全面的分期系统应纳入生物学变量的预后信息。