Section of Medical Oncology, Department of Surgical and Oncological Sciences, Universita di Palermo, Via del Vespro 129, 90127 Palermo, Italy.
Curr Drug Metab. 2011 Dec;12(10):944-55. doi: 10.2174/138920011798062346.
The treatment of solid malignancies includes various target drugs, such as monoclonal antibodies and tyrosine kinase inhibitors, which exert their effect alone or in combination with chemotherapy. The main part of these molecules have a target on proteins of EGFR and VEGF pathways. The particular toxicity profile and the financial impact, deriving from the application of these agents in cancer treatment, prompted a lot of researches to define predictive factors of their efficacy. Various biomarker were identified among the components of the targeted pathways. However just few studies allowed to identify specific factors to predict the toxicity of these drugs. In this review EGFR and VEGF-related pathways are described, most relevant clinical findings about target therapy applications are exposed and the clinical impact of predictive factors of efficacy and toxicity are discussed.
实体恶性肿瘤的治疗包括各种靶向药物,如单克隆抗体和酪氨酸激酶抑制剂,它们单独或与化疗联合发挥作用。这些分子的主要部分在 EGFR 和 VEGF 途径的蛋白质上有靶点。这些药物在癌症治疗中的应用所带来的特殊毒性谱和经济影响,促使许多研究来定义其疗效的预测因素。在靶向途径的组成部分中确定了各种生物标志物。然而,只有少数研究能够确定特定的因素来预测这些药物的毒性。在这篇综述中,描述了 EGFR 和 VEGF 相关途径,阐述了靶向治疗应用的最相关的临床发现,并讨论了疗效和毒性预测因素的临床影响。