III. Medical Department, Technische Universität München, Munich, Germany.
J Cell Mol Med. 2010 Apr;14(4):805-17. doi: 10.1111/j.1582-4934.2010.01032.x. Epub 2010 Feb 16.
In the past two decades there has been a tremendous increase in the understanding of the molecular basis of human malignancies. In a variety of neoplasms, specific molecular markers became part of disease classifications and are now routinely used to define specific entities. Molecular analyses discriminate prognostic groups, guide differential treatment strategies and identify targets for molecular defined cancer therapy. A battery of new drugs has been developed to specifically inhibit oncogenic pathways. For an increasing number of solid and haematological malignancies, the availability of molecular targeted drugs has fundamentally changed treatment algorithms. However, the diagnostic, prognostic and therapeutic impact of selected molecular markers is still limited in many cases. After all, the success of a molecular targeted therapy is clearly determined by the significance of the targeted structure for the biology of cancer and the ability of the malignant cell to evade specific inhibition.
在过去的二十年中,人们对人类恶性肿瘤的分子基础有了巨大的认识。在各种肿瘤中,特定的分子标志物已成为疾病分类的一部分,现在通常用于定义特定的实体。分子分析可区分预后组,指导差异化治疗策略,并确定分子定义的癌症治疗靶标。已经开发出一系列新药来特异性抑制致癌途径。对于越来越多的实体瘤和血液系统恶性肿瘤,分子靶向药物的可用性从根本上改变了治疗方案。然而,在许多情况下,选定的分子标志物的诊断、预后和治疗影响仍然有限。毕竟,分子靶向治疗的成功显然取决于靶向结构对癌症生物学的重要性以及恶性细胞逃避特定抑制的能力。