University of Colorado Cancer Center, 12801 East 17th Avenue, Aurora, CO 80045, USA.
Clin Cancer Res. 2010 Aug 1;16(15):3811-8. doi: 10.1158/1078-0432.CCR-09-2283. Epub 2010 Jun 16.
Initial experience with the epidermal growth factor receptor monoclonal antibodies (EGFR MoAb) in unselected patients with metastatic colorectal cancer (mCRC) showed that most of the treated patients did not derive therapeutic benefit. This outcome has driven the search for biomarkers for this population. Recent advances have further shown the heterogeneous nature of this disease with multiple interlinked pathways being implicated. Two such pathways downstream to the EGFR, mitogen-activated protein kinase (MAPK) and (phosphoinositide 3-kinase) PI3K, have gained increasing attention and become targets for development of novel biomarkers and therapeutic agents. Here, we highlight recent progress.
在未选择的转移性结直肠癌 (mCRC) 患者中使用表皮生长因子受体单克隆抗体 (EGFR MoAb) 的初步经验表明,大多数接受治疗的患者并未从中获得治疗益处。这一结果促使人们寻找此类人群的生物标志物。最近的进展进一步表明,这种疾病具有异质性,涉及多个相互关联的途径。EGFR 下游的两条途径,丝裂原活化蛋白激酶 (MAPK) 和 (磷酸肌醇 3-激酶) PI3K,引起了越来越多的关注,并成为开发新型生物标志物和治疗药物的靶点。在这里,我们重点介绍最近的进展。