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Heterogeneity of epidermal growth factor receptor mutations in lung adenocarcinoma harboring anaplastic lymphoma kinase rearrangements: A case report

机译:携带间变性淋巴瘤激酶重排的肺腺癌中表皮生长因子受体突变的异质性:一例报告

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摘要

Lung cancer is a heterogeneous and complex disease that remains the leading cause of cancer-related mortality worldwide. The identification of epidermal growth factor receptor (EGFR) mutation and anaplastic lymphoma kinase (ALK) rearrangements has changed the treatment of non-small cell lung cancer, creating a personalized treatment era that is based on the appropriate molecular selection of patients. In spite of the efficacy of tyrosine kinase inhibitors (TKIs), acquired resistance remains inevitable due to various mechanisms. The present study reports the case of a 30-year-old patient with stage IV lung adenocarcinoma initially harboring an EGFR mutation. However, following disease progression and a series of treatments, the wild-type EGFR gene was observed and the ALK rearrangements were revealed. Erlotinib administration resulted in a good response in the patient initially, but crizotinib did not. This indicated an association between the secondary mutations in kinases and the drug resistance to TKIs. This case should also highlight the clinical significance of repeat biopsies for the subsequent therapeutic choices at the onset of clinical progression.
机译:肺癌是一种异质性和复杂性疾病,仍然是全球癌症相关死亡率的主要原因。表皮生长因子受体(EGFR)突变和间变性淋巴瘤激酶(ALK)重排的鉴定改变了非小细胞肺癌的治疗方法,从而建立了基于患者适当分子选择的个性化治疗时代。尽管酪氨酸激酶抑制剂(TKIs)的功效,由于各种机制,获得性耐药仍然不可避免。本研究报告了一名30岁的IV期肺腺癌患者,该患者最初携带EGFR突变。然而,在疾病进展和一系列治疗之后,观察到野生型EGFR基因并揭示了ALK重排。最初给予厄洛替尼使患者产生良好的反应,但克唑替尼却没有。这表明激酶的继发突变与对TKI的耐药性相关。在临床进展开始时,该病例还应强调重复活检对随后治疗选择的临床意义。

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