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首页> 外文期刊>Cancer: A Journal of the American Cancer Society >EGFR Gene Status in Cytological Samples of Nonsmall Cell Lung Carcinoma Controversies and Opportunities
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EGFR Gene Status in Cytological Samples of Nonsmall Cell Lung Carcinoma Controversies and Opportunities

机译:非小细胞肺癌细胞学样本中EGFR基因状态的争议和机会

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BACKGROUND: In nonsmall cell lung cancer (NSCLC), the development and clinical application of tyrosine kinase inhibitors (TKIs) targeting the epidermal growth factor receptor (EGFR) has required the investigation of EGFR status by gene copy number and/or mutation analysis. This review aimed to present the current knowledge of the use of cytological specimens for EGFR testing in lung cancer. METHODS: A systematic computerized search was performed of the MEDLINE(R) and EMBASE databases to identify articles reporting the use of cytological samples for determining EGFR status in NSCLC. RESULTS: Data were extracted from 30 original articles. An additional 19 reviews, consensus statements, and editorials were selected from 175 retrieved papers. Different techniques using cell blocks, scraped cells from archival slides, and fresh cells have shown promising results and include fluorescent in situ hybridization (FISH), direct sequencing, and quantitative polymerase chain reaction (PCR), with similar or higher accuracy and sensitivity than surgical specimens. Preservation and quality of the extracted DNA seem to matter more than the actual number of tumor cells present in the samples. However, major issues still reside in the amount of material, the interference from background non-neoplastic cells, and standardization of parameters for cytological samples. CONCLUSIONS: This analysis provided evidence that cytological material is suitable for detecting EGFR status using several different methodologies and preparations. New prospective, clinical studies are encouraged for collection and handling of cytological samples as well as for validation of novel techniques in large cohorts.
机译:背景:在非小细胞肺癌(NSCLC)中,靶向表皮生长因子受体(EGFR)的酪氨酸激酶抑制剂(TKI)的开发和临床应用要求通过基因拷贝数和/或突变分析来研究EGFR的状态。这篇综述旨在介绍在肺癌中使用细胞学标本进行EGFR检测的最新知识。方法:对MEDLINE(R)和EMBASE数据库进行了系统的计算机搜索,以鉴定报告使用细胞学样本确定NSCLC中EGFR状态的文章。结果:数据摘自30篇原始文章。从175篇检索的论文中另外选择了19条评论,共识声明和社论。使用细胞块,从载玻片上刮下的细胞和新鲜细胞的不同技术已显示出令人鼓舞的结果,包括荧光原位杂交(FISH),直接测序和定量聚合酶链反应(PCR),其准确性和敏感性均高于外科手术标本。提取的DNA的保存和质量似乎比样品中存在的肿瘤细胞的实际数量更为重要。但是,主要问题仍然在于材料的数量,来自背景非肿瘤细胞的干扰以及细胞学样品参数的标准化。结论:该分析提供了证据,表明细胞学材料适合使用几种不同的方法和制剂检测EGFR状态。鼓励进行新的前瞻性临床研究,以收集和处理细胞学样品,以及验证大批研究中的新技术。

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