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EGFR and K-ras mutations in cytologic samples from fine-needle aspirates in NSCLC patients

机译:NSCLC患者细针穿刺细胞学样本中的EGFR和K-ras突变

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Mutations in the epidermal growth factor receptor (EGFR) gene in patients with nonsmall cell lung cancer (NSCLC) have been correlated with tumour response to treatment with targeted tyrosine kinase inhibitors (TKIs), especially gefitinib and erlotinib [1, 2]. A large number of studies have reported a significantly higher overall response rate, overall survival and time-to-progression in patients with EGFR-activating mutations compared with those with wild-type tumours [3-5].
机译:非小细胞肺癌(NSCLC)患者的表皮生长因子受体(EGFR)基因突变与肿瘤对靶向酪氨酸激酶抑制剂(TKIs)治疗的反应相关,尤其是吉非替尼和厄洛替尼[1,2]。大量研究表明,与野生型肿瘤患者相比,EGFR激活突变患者的总体缓解率,总体生存率和进展时间显着提高[3-5]。

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