使用Biocartis Idylla™平台检测非小细胞肺癌和胰腺腺癌患者液基细胞学标本中的表皮生长因子受体、BRAF和KRAS原癌基因突变

Leonie Wheeldon, Mary Jones, B. Probyn, D. Shetty, J. Garvican
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引用次数: 1

摘要

该研究旨在证明使用Biocartis Idylla™对液体细胞学(LBC)样本进行EGFR、KRAS和BRAF突变的快速有效的分子检测。基于与肿瘤亚型的相关性,对非小细胞肺癌(NSCLC)或胰腺导管腺癌(PDAC)患者的LBC样本进行EGFR、KRAS和BRAF突变检测。比较LBC标本与常规福尔马林固定石蜡包埋(FFPE)血块标本的定量值(Cq值)和突变检测情况。与FFPE血块样品相比,ROSE LBC样品(n = 54)显示出更高的保存完好的肿瘤和野生型(WT) DNA产量,这可以通过更低的定量周期、无假阳性或假阴性以及对低等位基因频率突变的更高敏感性来证明。Biocartis Idylla™为LBC样品提供高度敏感、可靠和快速的检测,用于检测EFGR和KRAS突变。在参与者队列中未检测到BRAF突变;然而,所有LBC WT BRAF结果都与FFPE血块样本的结果相关。使用LBC样本进行快速分子检测可以在更接近诊断时间的时候检测到最常见的驱动突变,从而能够更快地选择最有效的一线靶向治疗,减少次优治疗的延误或副作用,减少患者的焦虑和医疗保健系统的成本,同时改善患者的治疗效果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Use of the Biocartis Idylla™ Platform for the Detection of Epidermal Growth Factor Receptor, BRAF and KRAS Proto-Oncogene Mutations in Liquid-Based Cytology Specimens from Patients with Non-Small Cell Lung Carcinoma and Pancreatic Adenocarcinoma
The study aimed to demonstrate rapid and effective molecular testing on liquid-based cytology (LBC) samples for EGFR, KRAS and BRAF mutations using the Biocartis Idylla™. Rapid on-site evaluation (ROSE) LBC samples for patients with non-small cell lung carcinoma (NSCLC) or pancreatic ductal adenocarcinoma (PDAC) were tested for EGFR, KRAS and BRAF mutations based on the relevance to tumour subtype. The quantification values (Cq values) and mutation detection status were compared between LBC samples and routine formalin-fixed paraffin-embedded (FFPE) clot samples. ROSE LBC samples (n = 54) showed a higher yield of well-preserved tumour and wild type (WT) DNA, demonstrated by lower quantification cycles, no false positives or false negatives, and a higher sensitivity for low allele frequency mutations when compared with FFPE clot samples. The Biocartis Idylla™ provides highly sensitive, reliable and rapid testing for LBC samples for the detection of EFGR and KRAS mutations. BRAF mutations were not detected in the participant cohort; however, all LBC WT BRAF results correlated with the results from the FFPE clot samples. Access to rapid molecular testing using LBC samples can detect the most frequent driver mutations closer to the time of diagnosis, enabling the selection of the most effective first-line targeted therapy sooner, reducing delays or side effects from suboptimal treatments, patient anxiety and costs to healthcare systems, whilst improving patient outcomes.
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