Molecular Diagnostics of Lung Cancer in Serous Effusion Samples

J. Fassunke, R. Büttner, M. Engels
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引用次数: 1

Abstract

For molecular diagnostics of lung cancer samples, often only a small amount of material is available. The ever-increasing number of biomarker testing is in contrast to the amount of material obtained. In that case, cytological specimens, such as serous effusion samples, are one possible option. Effusion samples were prepared as sediment smears or cytospins or as a cell block if needed. Suitable tumor cells areas were marked by a cytopathologist and used for molecular diagnostics, including fast track analysis, parallel sequencing, and/or fluorescence in situ hybridization. In 62 cases of malignant effusion with cells of pulmonary adenocarcinoma, molecular diagnostics were carried out. A fast-track result with the high-resolution melting method for hotspot mutation of KRAS Exon 2 and EGFR exon 21 and fragment length analysis of EGFR exon 19 was available for 43 out of 47 samples (92%). Parallel sequencing was successful for 56 out of 60 samples (93.3%). In the same period, 108 FISH analyses were performed for MET amplification, followed by ROS1, RET, and ALK translocation analysis. If only a limited amount of tissue/biopsy is available, a malignant effusion is advisable to perform on the molecular diagnostics with a high success rate.
肺癌浆液标本的分子诊断
对于肺癌样本的分子诊断,通常只有少量的材料可用。不断增加的生物标志物检测数量与获得的材料数量形成对比。在这种情况下,细胞学标本,如浆液样本,是一个可能的选择。积液样品制备为沉积物涂片或细胞自旋,或作为细胞块,如果需要的话。合适的肿瘤细胞区域由细胞病理学家标记,并用于分子诊断,包括快速通道分析,平行测序和/或荧光原位杂交。本文对62例肺腺癌细胞恶性积液进行了分子诊断。KRAS外显子2和EGFR外显子21热点突变的高分辨率熔融方法和EGFR外显子19片段长度分析在47个样本中有43个(92%)获得了快速通道结果。60份样品中56份平行测序成功(93.3%)。在同一时期,对MET扩增进行了108次FISH分析,随后进行了ROS1、RET和ALK易位分析。如果只有有限数量的组织/活检可用,恶性积液建议进行分子诊断,成功率高。
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