Cohen Deirdre J, Hochster Howard S
Department of Medicine, NYU Clinical Cancer Center, New York, NY 10016, USA.
Clin Colorectal Cancer. 2007 Dec;7 Suppl 1:S21-7. doi: 10.3816/ccc.2008.s.004.
As a result of the development of novel chemotherapeutic drugs and targeted biologic agents, the treatment of colon cancer has changed significantly over the past 10 years. Today, we have more active agents to use in colon cancer than ever before. The better understanding underlying the pathogenesis of this disease at the molecular level has allowed us to take advantage of 2 key pathways, the angiogenic and epidermal growth factor (EGF) signaling pathways. The combination of traditional chemotherapy drugs with agents that inhibit these pathways has led to a significant improvement in survival. At present, patients with metastatic colon cancer routinely achieve a median survival time > 2 years. The numerous agents available have made the choice of initial treatment more difficult for a newly diagnosed patient. Herein, we review the 2 main molecular targets of biologic therapy in colon cancer and examine the clinical evidence for regimens that inhibit angiogenesis and EGF receptor alone or in combination for newly diagnosed metastatic colorectal cancer.
由于新型化疗药物和靶向生物制剂的发展,在过去10年中,结肠癌的治疗发生了显著变化。如今,我们用于结肠癌治疗的活性药物比以往任何时候都更多。对该疾病分子水平发病机制的深入了解,使我们能够利用两条关键途径,即血管生成和表皮生长因子(EGF)信号通路。传统化疗药物与抑制这些途径的药物联合使用,已使生存率得到显著提高。目前,转移性结肠癌患者的中位生存时间通常超过2年。众多可用药物使新诊断患者的初始治疗选择更加困难。在此,我们综述了结肠癌生物治疗的两个主要分子靶点,并研究了单独或联合抑制血管生成和EGF受体的方案用于新诊断转移性结直肠癌的临床证据。