索拉非尼
医学
腺癌
肺癌
肿瘤科
癌症研究
ROS1型
内科学
肝细胞癌
靶向治疗
吉非替尼
人口
突变
化疗
癌症
生物
表皮生长因子受体
基因
遗传学
环境卫生
作者
María Sereno,Víctor Moreno,Juan Moreno‐Rubio,César Gómez-Raposo,Sagrario García Sánchez,Rebeca Hernández Jusdado,Sandra Falagán,Francisco Zambrana Tébar,Enrique Casado Sáenz
出处
期刊:Anti-Cancer Drugs
[Lippincott Williams & Wilkins]
日期:2015-08-01
卷期号:26 (9): 1004-1007
被引量:36
标识
DOI:10.1097/cad.0000000000000277
摘要
Lung adenocarcinoma includes recurrent activating oncogenic mutations (EGFR, EML4-ALK, ROS1) that have been associated with response to EGFR and ALK inhibitors. Platinum-based chemotherapy is the standard therapy for non-oncodrivers population. Sorafenib is a small molecule that blocks the activation of C-RAF, B-RAF, c-KIT, FLT-3, RET, VEGFR-2, VEGFR-3 and PDGFR approved for advanced renal cell and hepatocellular carcinoma (b, c). Many studies have evaluated sorafenib in advanced non-small-cell lung cancer (NSCLC), with different results. We present a case report of a patient with NSCLC and the BRAF G469R mutation who showed a dramatic response to sorafenib.
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