间变性淋巴瘤激酶
肺癌
医学
可药性
表皮生长因子受体
靶向治疗
癌症研究
酪氨酸激酶
ROS1型
肿瘤科
埃罗替尼
癌症
克里唑蒂尼
吉非替尼
精密医学
内科学
腺癌
病理
生物
受体
基因
恶性胸腔积液
生物化学
作者
Mercedes Herrera,Cristina Serrano‐Gómez,Helena Bote,Luís Paz-Ares
出处
期刊:Cancer
[Wiley]
日期:2023-04-19
卷期号:129 (12): 1803-1820
被引量:32
摘要
Precision oncology comprises the set of strategies that aim to design the best cancer treatment based on tumor biology. A recognized subset of patients with non-small cell lung cancer (NSCLC) harbor actionable genomic aberrations that can benefit from targeted therapy. In lung cancer, epidermal growth factor receptor (EGFR) mutations and anaplastic lymphoma kinase (ALK) rearrangements are well characterized oncogenic drivers for which the therapeutic use of tyrosine kinase inhibitors has demonstrated improved outcomes compared with chemotherapy. Other druggable targets are also well characterized, and effective inhibitors have been developed and commercialized, leading to a paradigm shift in NSCLC treatment. Here, the authors provide a review of the oncogenic role of the most relevant molecular alterations in NSCLC and emerging treatments in this setting beyond EGFR-driven and ALK-driven diseases.
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