Milano G, Spano J-P, Leyland-Jones B
Oncopharmacology Unit, Centre Antoine-Lacassagne, 33 Avenue de Valombrose, Nice 06189, France.
Br J Cancer. 2008 Jul 8;99(1):1-5. doi: 10.1038/sj.bjc.6604373. Epub 2008 May 27.
The clinical experience recently reported with epidermal growth factor receptor (EGFR)-targeting drugs confirms the synergistic interactions observed between these compounds and conventional cytotoxic agents, which were previously established at the preclinical stage. There are, however, examples of major gaps between the bench and the bedside. Particularly demonstrative is the failure of the tyrosine kinase inhibitors (TKIs) (gefitinib and erlotinib) combined with chemotherapy in pretreated nonsmall cell lung cancer patients. These discrepancies can be due to several factors such as the methodology used to evaluate TKI plus cytotoxic agent combinations in preclinical models and the insufficient consideration given to the importance of the drug sequences for the tested combinations. Recent advances in understanding the biologic basis of acquired resistance to these agents have great potential to improve their clinical effectiveness. The purpose of this review is to critically examine the experimental conditions of the preclinical background for anti-EGFR drug-cytotoxic agent combinations and to attempt to explain the gap between clinical observations and preclinical data.
最近报道的表皮生长因子受体(EGFR)靶向药物的临床经验证实了这些化合物与传统细胞毒性药物之间存在协同相互作用,这种相互作用在临床前阶段就已得到证实。然而,基础研究与临床应用之间存在重大差距的例子也不少。特别典型的是,酪氨酸激酶抑制剂(TKIs)(吉非替尼和厄洛替尼)与化疗联合应用于经治的非小细胞肺癌患者时效果不佳。这些差异可能归因于几个因素,如在临床前模型中评估TKI加细胞毒性药物联合应用的方法,以及对测试联合用药中药物顺序重要性的考虑不足。最近在理解这些药物获得性耐药生物学基础方面取得的进展,极有可能提高其临床疗效。本综述的目的是严格审视抗EGFR药物与细胞毒性药物联合应用的临床前背景的实验条件,并试图解释临床观察结果与临床前数据之间的差距。