Medical Oncology Unit, University Hospital of Parma, Italy.
Lung Cancer. 2011 Feb;71(2):241-3. doi: 10.1016/j.lungcan.2010.11.014. Epub 2010 Dec 18.
The fusion gene EML4-ALK (echinoderm microtubule-associated protein-like 4 gene and the anaplastic lymphoma kinase gene) was recently identified as a novel genetic alteration in non-small cell lung cancer (NSCLC). EML4-ALK translocations correlate with specific clinical and pathological features, in particular lack of EGFR and K-ras mutations, and may be associated with resistance to EGFR tyrosine-kinase inhibitors (TKIs). Here, we report a case of a patient with a concomitant EGFR mutation and ALK translocation resistant to erlotinib. Considering this report, ALK status should be investigated in unexplained cases of EGFR-TKI-resistance of EGFR mutated NSCLCs.
棘皮动物微管相关蛋白样 4 基因(EML4)与间变性淋巴瘤激酶(ALK)的融合基因最近被确定为非小细胞肺癌(NSCLC)中的一种新型遗传改变。EML4-ALK 易位与特定的临床和病理特征相关,特别是缺乏 EGFR 和 K-ras 突变,并且可能与 EGFR 酪氨酸激酶抑制剂(TKI)的耐药性相关。在这里,我们报告了一例同时存在 EGFR 突变和 ALK 易位的患者,对厄洛替尼耐药。考虑到这一报告,在 EGFR 突变的 NSCLC 对 EGFR-TKI 耐药的原因不明的情况下,应检测 ALK 状态。