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EGFR T790M mutation after chemotherapy for small cell lung cancer transformation of EGFR-positive non-small cell lung cancer

机译:化疗后的EGFR T790M突变用于小细胞肺癌EGFR阳性非小细胞肺癌的转化

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In non-small cell lung cancer (NSCLC) with an epidermal growth factor receptor (EGFR) mutation, 50%–65% of cases acquire resistance after treatment with EGFR-tyrosine kinase inhibitors (EGFR-TKIs) because of an EGFR T790M point mutation and 3%–14% of these cases transformed to small cell lung cancer (SCLC). Generally, the EGFR T790M secondary mutation develops with ongoing ATP competitive inhibition. We present a case of a 76-year-old woman with lung adenocarcinoma harboring an EGFR-L858R mutation who received first-line gefitinib and developed SCLC transformation. She was administered several chemotherapy agents, including a platinum doublet. The primary lesion that showed SCLC transformation had reconverted to adenocarcinoma with EGFR L858R and T790M mutations at the time of a second re-biopsy. Therefore, she was administered osimertinib, which resulted in clinical remission. This case suggested that serial biopsies are necessary even after SCLC transformation.
机译:在具有表皮生长因子受体(EGFR)突变的非小细胞肺癌(NSCLC)中,由于EGFR T790M点突变,在使用EGFR-酪氨酸激酶抑制剂(EGFR-TKIs)治疗后50%–65%的病例获得了耐药性这些病例中有3%–14%转化为小细胞肺癌(SCLC)。通常,EGFR T790M继发突变会伴随持续的ATP竞争性抑制而发展。我们介绍了一个患有EGFR-L858R突变并携带一线吉非替尼并发展为SCLC的肺腺癌的76岁女性的病例。她接受了几种化疗药物的治疗,包括铂金双峰治疗。在第二次再次活检时,显示出SCLC转化的原发灶已转变为具有EGFR L858R和T790M突变的腺癌。因此,她被给予奥西替尼,导致临床缓解。这种情况表明,即使在SCLC转化后也需要进行连续活检。

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