Govindan Ramaswamy
Alvin J. Siteman Cancer Center, Washington University School of Medicine, St. Louis, Missouri, USA.
Clin Cancer Res. 2004 Jun 15;10(12 Pt 2):4241s-4244s. doi: 10.1158/1078-0432.CCR-040015.
The epidermal growth factor receptor (EGFR) is frequently overexpressed in non-small cell lung cancer (NSCLC). EGFR activation results in phosphorylation of several downstream intracellular substrates involved in cell proliferation, angiogenesis, and inhibition of apoptosis. Cetuximab (C225, Erbitux), a monoclonal antibody directed against ligand binding in the extracellular domain of EGFR, inhibits tumor growth and is synergistic with chemotherapy and radiation. Cetuximab has been studied in combination with chemotherapy in previously untreated metastatic NSCLC. The response rates in preliminary reports range from 29% to 53%. In patients with refractory/recurrent NSCLC, the combination of docetaxel and cetuximab resulted in a promising response rate of 28%, higher than the typical response rates seen with docetaxel monotherapy in this setting. Addition of cetuximab to chemotherapy is generally well tolerated. Molecular mechanisms predicting response to cetuximab therapy are currently not well understood. Studies are ongoing to assess the single-agent activity of cetuximab in metastatic NSCLC.
表皮生长因子受体(EGFR)在非小细胞肺癌(NSCLC)中常过度表达。EGFR激活导致参与细胞增殖、血管生成和抑制细胞凋亡的几种下游细胞内底物磷酸化。西妥昔单抗(C225,爱必妥)是一种针对EGFR细胞外结构域配体结合的单克隆抗体,可抑制肿瘤生长,并与化疗和放疗具有协同作用。西妥昔单抗已在先前未治疗的转移性NSCLC中与化疗联合进行研究。初步报告中的缓解率为29%至53%。在难治性/复发性NSCLC患者中,多西他赛与西妥昔单抗联合使用产生了28%的良好缓解率,高于在此情况下多西他赛单药治疗的典型缓解率。在化疗中添加西妥昔单抗通常耐受性良好。目前对预测西妥昔单抗治疗反应的分子机制了解不足。正在进行研究以评估西妥昔单抗在转移性NSCLC中的单药活性。