Gastrointestinal Tumor Program, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL 33612, USA.
Cancer Control. 2010 Jan;17(1):7-15. doi: 10.1177/107327481001700102.
Several molecular targeting agents are available and being used in patients with colorectal cancer, and many others are being tested clinically.
The authors review and present the biology and use, including predictive testing, of the agents currently approved for use in colorectal cancer as well as current data on several newer tyrosine kinase inhibitors that are undergoing clinical trials.
The angiogenesis inhibitor bevacizumab and the two EGFR inhibitors cetuximab and panitumumab are currently the three targeted agents approved in colorectal cancer. Recent studies show that the combined use of bevacizumab and EGFR inhibitors may lead to increased toxicity and inferior outcome. Much remains to be understood regarding these drugs and other targeted therapies as well as the underlying mechanism of tumor resistance or responsiveness to treatment. Their optimal use and sequencing with other treatment modalities such as surgery need to be further refined.
There is a crucial need for identification of predictive markers of response and identification of possible negative interactions between targeted agents so that we can better select patients likely to respond to treatment.
有几种分子靶向药物可用于结直肠癌患者,并且有许多其他药物正在进行临床测试。
作者回顾并介绍了目前批准用于结直肠癌的药物的生物学特性和用途,包括预测性检测,以及正在进行临床试验的几种新型酪氨酸激酶抑制剂的最新数据。
血管生成抑制剂贝伐单抗和两种 EGFR 抑制剂西妥昔单抗和帕尼单抗是目前在结直肠癌中批准使用的三种靶向药物。最近的研究表明,贝伐单抗和 EGFR 抑制剂的联合使用可能会导致毒性增加和预后不良。这些药物以及其他靶向治疗方法以及肿瘤对治疗的耐药性或敏感性的潜在机制仍有许多需要了解的地方。它们的最佳使用和与手术等其他治疗方式的序贯应用需要进一步完善。
迫切需要识别反应的预测标志物,并识别靶向药物之间可能存在的负相互作用,以便我们能够更好地选择可能对治疗有反应的患者。