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非小细胞肺癌中EML4-ALK融合及临床治疗进展
by
吴获 于鸿
in
LC患者
/ receptor
/ 临床治疗
/ 分子靶向药物治疗
/ 基因突变
/ 表皮生长因子受体
/ 酪氨酸激酶抑制剂
/ 非小细胞肺癌
2011
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非小细胞肺癌中EML4-ALK融合及临床治疗进展
by
吴获 于鸿
in
LC患者
/ receptor
/ 临床治疗
/ 分子靶向药物治疗
/ 基因突变
/ 表皮生长因子受体
/ 酪氨酸激酶抑制剂
/ 非小细胞肺癌
2011
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Journal Article
非小细胞肺癌中EML4-ALK融合及临床治疗进展
2011
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Overview
肺癌的死亡率居恶性肿瘤的首位。其中,非小细胞肺癌(non-small cell lung cancer,NSCLC)约占80%,被确诊时多为晚期。传统的化疗能改善近期疗效,对生存期的改善有限,故中位生存时间为12个月左右,预后差[1]。近年来,分子靶向药物治疗正在成为肺癌治疗的热点,如10%,30%的NSCLC患者携带活化的表皮生长因子受体(epidermal growth factor receptor,EGFR)基因突变,70%以上的EGFR突变患者对小分子酪氨酸激酶抑制剂(tyrosine kinase inhibitors,TKIs)高度敏感,有明显的生存获益。因此,发现和确认肺癌患者的分子亚型,寻找有效的分子靶向治疗靶点是当前需要迫切解决的问题[2]。
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