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首页> 外文期刊>Oncology letters >Acquired resistance L747S mutation in an epidermal growth factor receptor-tyrosine kinase inhibitor-na?ve patient: A report of three cases
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Acquired resistance L747S mutation in an epidermal growth factor receptor-tyrosine kinase inhibitor-na?ve patient: A report of three cases

机译:表皮生长因子受体酪氨酸激酶抑制剂初治患者获得性耐药L747S突变:三例报告

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The purpose of the present study was to report cases of epidermal growth factor receptor-tyrosine kinase inhibitor (EGFR-TKI)-na?ve patients carrying a mutation associated with acquired resistance to the drug. Gene alterations in 77 lung carcinoma patients were analyzed by collecting and studying curette lavage fluid at the time of diagnosis. PCRs were performed to amplify mutation hotspot regions in EGFR genes. The PCR products were direct-sequenced and the mutations confirmed by resequencing using different primers. Case 1 was a 78-year-old Japanese male diagnosed with stage IB lung adenocarcinoma who was found to have two EGFR mutations, G719S and L747S. Case 2 was a 73-year-old Japanese male diagnosed with stage IV squamous cell lung carcinoma and bone metastasis who had the EGFR mutation, L747S. Case 3 was an 82-year-old Japanese male diagnosed with hyponatremia due to inappropriate secretion of antidiuretic hormone and stage IIIB small cell lung carcinoma (SCLC) who had the EGFR mutation, L747S. Thus, the EGFR mutation L747S associated with acquired EGFR-TKI resistance was detected in two non-small cell lung carcinoma (NSCLC) patients and one SCLC patient, none of whom had ever received EGFR-TKI. The patients were current smokers with stages at diagnosis ranging from IB to IV, and their initial tumors contained resistant clones carrying L747S. L747S may be associated with primary resistance. To the best of our knowledge, this study is the first report of an EGFR mutation associated with resistance to EGFR-TKI in SCLC patients. The early detection of EGFR-TKI resistance mutations may be beneficial in making treatment decisions for lung carcinoma patients, including those with SCLC.
机译:本研究的目的是报道未发生表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKI)的患者,这些患者携带与获得性耐药相关的突变。在诊断时通过收集和研究刮匙灌洗液来分析77例肺癌患者的基因改变。进行PCR以扩增EGFR基因中的突变热点区域。 PCR产物是直接测序的,并且通过使用不同的引物进行重测序来确认突变。案例1是一名78岁的日本男性,被诊断患有IB期肺腺癌,被发现具有两个EGFR突变,即G719S和L747S。案例2是一名73岁的日本男性,被诊断患有EGFR突变L747S的IV期鳞状细胞肺癌和骨转移。案例3是一名82岁的日本男性,由于抗利尿激素的分泌异常和患有EGFR突变L747S的IIIB期小细胞肺癌(SCLC)而被诊断为低钠血症。因此,在两名非小细胞肺癌(NSCLC)患者和一名SCLC患者中均检测到与获得性EGFR-TKI耐药相关的EGFR突变L747S,他们均未曾接受过EGFR-TKI。这些患者是目前的吸烟者,诊断阶段从IB到IV,其最初的肿瘤包含携带L747S的抗性克隆。 L747S可能与初级电阻有关。据我们所知,这项研究是关于SCLC患者中与EGFR-TKI耐药相关的EGFR突变的首次报道。 EGFR-TKI耐药性突变的早期检测可能有助于制定肺癌患者(包括SCLC患者)的治疗决策。

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