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首页> 外文期刊>Journal of Thoracic Disease >Current evidence in support of the second-generation anaplastic lymphoma kinase ( ALK ) tyrosine kinase inhibitor alectinib for the treatment of non-small cell lung cancer positive for ALK translocation
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Current evidence in support of the second-generation anaplastic lymphoma kinase ( ALK ) tyrosine kinase inhibitor alectinib for the treatment of non-small cell lung cancer positive for ALK translocation

机译:支持第二代间变性间变性淋巴瘤激酶(ALK)酪氨酸激酶抑制剂alectinib用于治疗ALK易位的非小细胞肺癌的最新证据

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Treatment for advanced non-small cell lung cancer (NSCLC) depends on the molecular characteristics of the tumor. Mutations of the epidermal growth factor receptor ( EGFR ) gene are present in ~32% of Asians and ~7% of individuals of other ethnic groups with NSCLC (1), and rearrangements of the anaplastic lymphoma kinase ( ALK ) gene have been detected in ~3% to 5% of NSCLC tumors (2-4). The echinoderm microtubule-associated protein-like 4 ( EML4 ) gene is the most common fusion partner of ALK in NSCLC, and the fusion gene exists in several variants with different breakpoints within EML4 . NSCLC tumors that harbor ALK fusion genes are oncogene addicted and therefore usually sensitive to treatment with ALK tyrosine kinase inhibitors ( ALK -TKIs).
机译:晚期非小细胞肺癌(NSCLC)的治疗取决于肿瘤的分子特征。表皮生长因子受体(EGFR)基因的突变存在于约32%的亚洲人和约7%患有NSCLC的其他种族的个体中(1),并且在美国检测到了间变性淋巴瘤激酶(ALK)基因的重排。 〜3%至5%的NSCLC肿瘤(2-4)。棘皮动物微管相关蛋白样4(EML4)基因是ALK在NSCLC中最常见的融合伴侣,并且该融合基因存在于EML4内具有不同断点的多个变体中。带有ALK融合基因的NSCLC肿瘤致癌基因上瘾,因此通常对用ALK酪氨酸激酶抑制剂(ALK -TKIs)治疗敏感。

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