Medical Oncology Service, ICMHO, Hospital Clinic Barcelona, Barcelona, Spain;
Cancer Manag Res. 2010 Jun 1;2:143-56. doi: 10.2147/cmar.s5398.
Erlotinib hydrochloride (Tarceva(®)) is a member of a class of small molecule inhibitors that targets the tyrosine kinase domain of the epidermal growth factor receptor (EGFR), with anti-tumor activity in preclinical models. Erlotinib represents a new-generation of agents known as "targeted therapies" designed to act upon cancer cells by interfering with aberrant specific activated pathways needed for tumor growth, angiogenesis and cell survival. Since its approval in November 2004 for the treatment of locally advanced or metastatic non-small cell lung cancer (NSCLC) after the failure of at least one prior chemotherapy regimen and with a view to improving patients' outcomes and prevent symptoms, the scientific community has evaluated the potential role of erlotinib in other scenarios such as in maintenance therapy and, in first-line setting for a selected population based on biological markers of response such as mutations of the EGFR. The convenient once-a-day pill administration and the good toxicity profile of erlotinib make it a reasonable candidate for testing in this context. This report provides a review of the role of erlotinib therapy in advanced NSCLC. It summarizes current data and perspectives of erlotinib in upfront treatment and maintenance for advanced NSCLC as well as looking at candidate biomarkers of response to these new targeted-agents.
盐酸厄洛替尼(特罗凯(®))是一类小分子抑制剂中的一种,其作用靶点是表皮生长因子受体(EGFR)的酪氨酸激酶结构域,在临床前模型中具有抗肿瘤活性。厄洛替尼代表了新一代被称为“靶向治疗”的药物,旨在通过干扰肿瘤生长、血管生成和细胞存活所需的异常特定激活途径来作用于癌细胞。自 2004 年 11 月批准用于至少一种先前化疗方案失败后的局部晚期或转移性非小细胞肺癌(NSCLC)的治疗,旨在改善患者的预后和预防症状以来,科学界一直在评估厄洛替尼在其他情况下的潜在作用,例如维持治疗,以及在基于 EGFR 突变等反应生物标志物的选定人群中作为一线治疗。厄洛替尼每天服用一次的便利给药方式和良好的毒性特征使其成为在这种情况下进行测试的合理候选药物。本报告回顾了厄洛替尼治疗晚期 NSCLC 的作用。它总结了厄洛替尼在晚期 NSCLC 一线治疗和维持治疗中的当前数据和观点,并探讨了这些新型靶向药物的反应候选生物标志物。