Denis Marc G, Bennouna Jaafar
Department of Biochemistry and Molecular Biology, Nantes University Hospital, Nantes, France.
INSERM U1232, CRCINA, Nantes, France.
Cancer Manag Res. 2020 Dec 8;12:12593-12602. doi: 10.2147/CMAR.S218751. eCollection 2020.
Non-small cell lung cancer (NSCLC) is one of the most efficient models for precision medicine in oncology. The most appropriate therapeutic for the patient is chosen according to the molecular characteristics of the tumor, schematically distributed between immunogenicity and oncogenic addiction. For this last concept, advanced NSCLC with epidermal growth factor receptor () mutation is one of the most illustrative models. EGFR-tyrosine kinase inhibitors (TKIs) are the therapeutic backbone for this type of tumor. The recent development of a third-generation TKI, osimertinib, has been a new step forward in the treatment of NSCLC patients. In this article, we first review the clinical development of osimertinib and highlight its efficacy results. We then present the most frequent tumor escape mechanisms when osimertinib is prescribed in first line: off-target ( amplification, amplification, mutation, gene fusions, histologic transformation) and on-target mechanisms ( mutation). Finally, we discuss subsequent biomarker-driven treatment strategies.
非小细胞肺癌(NSCLC)是肿瘤学中精准医学最有效的模型之一。根据肿瘤的分子特征为患者选择最合适的治疗方法,这些分子特征大致分布在免疫原性和致癌成瘾性之间。就后一个概念而言,具有表皮生长因子受体()突变的晚期NSCLC是最具代表性的模型之一。表皮生长因子受体酪氨酸激酶抑制剂(TKIs)是这类肿瘤的治疗支柱。第三代TKI奥希替尼的最新研发是NSCLC患者治疗的新进展。在本文中,我们首先回顾奥希替尼的临床研发情况并突出其疗效结果。然后我们介绍一线使用奥希替尼时最常见的肿瘤逃逸机制:脱靶(扩增、扩增、突变、基因融合、组织学转化)和靶上机制(突变)。最后,我们讨论后续的生物标志物驱动的治疗策略。