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首页> 外文期刊>Journal of International Medical Research >Transformation of non-small cell lung cancer into small cell lung cancer in a patient with advanced lung cancer: a case report
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Transformation of non-small cell lung cancer into small cell lung cancer in a patient with advanced lung cancer: a case report

机译:用晚期肺癌患者中非小细胞肺癌转化为小细胞肺癌:案例报告

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Targeted therapy in patients with epidermal growth factor receptor ( EGFR )-mutated non-small cell lung cancer (NSCLC) often fails because of drug resistance. Here, we report a 57-year-old male patient with stage IV small cell lung cancer (SCLC) transformation during targeted therapy. Chest computerized tomography (CT), hematoxylin and eosin histological examination, immunohistochemistry, allele refractory mutation system‐based quantitative polymerase chain reaction analysis of EGFR point mutations, and next-generation sequencing were performed for diagnosis and therapeutic efficacy evaluation. A combination of chest CT, histological examination, and immunohistochemistry confirmed the initial NSCLC diagnosis. Next-generation sequencing detected only EGFR exon 19 deletion ( ex19del ) before treatment and later identified EGFR exon20p.T790M point mutation, EGFR amplification, myc proto-oncogene ( MYC) amplification, retinoblastoma 1 ( RB1) mutation, and tumor protein 53 ( TP53) mutation. Histology and immunohistochemistry revealed transformation from NSCLC to SCLC during treatment, which eventually returned to NSCLC. Drug resistance to targeted therapy for patients with NSCLC frequently occurs because of EGFR exon20p.T790M point mutation, TP53 mutation, RB1 mutation, and MYC amplification. These mutations are also the major determining factors of NSCLC outcomes. Therefore, next-generation sequencing should be performed to confirm drug efficacy during targeted therapy for NSCLC.
机译:针对表皮生长因子受体(EGFR)的患者的靶向治疗 - 由于耐药性而导致的非小细胞肺癌(NSCLC)经常发生。在这里,我们在有针对性疗法期间举报了一个57岁的男性患者阶段的阶段小细胞肺癌(SCLC)转化。胸部电脑断层扫描(CT),苏木精和曙红组织学检查,免疫组织化学,等位基因难治性突变体系的基于等级难治性突变的定量聚合酶链反应分析,并进行下一代测序进行诊断和治疗疗效评估。胸部CT,组织学检查和免疫组化的组合证实了初始NSCLC诊断。在治疗前仅检测到EGFR外显子19缺失(EX19DEL),后来鉴定EGFR EXON20P.T790M点突变,EGFR扩增,MYC原癌基因(MYC)扩增,视网膜母细胞瘤1(RB1)突变和肿瘤蛋白53(TP53 )突变。组织学和免疫组织化学揭示了在治疗期间从NSCLC到SCLC的转化,最终返回NSCLC。由于EGFR Exon20P.T790M点突变,TP53突变,RB1突变和MYC扩增,对NSCLC患者的毒性对NSCLC患者的耐药性耐药性经常发生。这些突变也是NSCLC结果的主要决定因素。因此,应进行下一代测序以确认NSCLC靶向治疗期间的药物功效。

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