BL-MOL-AR项目,液体活检的初步结果:肿瘤环境中的分子方法经验和研究活动。

IF 1.2 Q4 GENETICS & HEREDITY Global Medical Genetics Pub Date : 2023-09-01 DOI:10.1055/s-0043-1771193
Alessandro Pancrazzi, Francesco Bloise, Alice Moncada, Roberta Perticucci, Stefania Vecchietti, Francesca Pompili, Francesca Ricciarini, Silvia Lenzi, Cristina Gatteschi, Sabrina Giusti, Maria Pia Rosito, Sabrina Del Buono, Paola Belardi, Alessandra Bruni, Filippo Borri, Andrea Campione, Lorella Laurini, Rossella Occhini, Loretta Presenti, Viviana Viticchi, Maja Rossi, Sara Bardi, Antonio D'Urso, Simona Dei, Duccio Venezia, Raffaele Scala, Carmelo Bengala, Nicola Libertà Decarli, Andrea Carnevali, Carlo Milandri, Agostino Ognibene
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引用次数: 0

摘要

背景液体活检主要用于肺肿瘤的肿瘤细胞鉴别。它更多地用于研究而不是临床实践。BL-MOL-AR研究旨在探讨下一代测序(NGS)的有效性和循环游离DNA (cfDNA)水平的临床解释。本研究报告了来自各种肿瘤患者的第一批样本分析的初步结果:肺、肠、乳腺、胃、胆道和皮肤。方法Biopsia liquida - molecular - arezzo研究旨在招募包括肺部、肠道、晚期尿路上皮、胆道、乳腺、皮肤和胃部肿瘤在内的各种恶性肿瘤患者。本初步报告纳入了39例患者。在时间零点,进行液体活检,并进行两种类型的NGS小组,小组1包括17个基因,已经在常规组织设置中使用,小组2包括52个基因。从入组后第7个月开始,连续进行10次液体活检,直至第17个月。测定每个血浆样品的变异等位基因频率(%)和cfDNA水平(ng/mL)。结果不同小组的NGS结果相似,但肺病变的突变数更为一致。在已确定的变体的可操作性水平上没有显着差异。大多数液体活检的分子谱反映了组织数据。结论:本研究的初步数据证实有必要澄清肺外液体活检的局限性和潜力。总之,与cfDNA水平和变异等位基因频率相关的参数可以为预后和疾病监测提供重要的指标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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BL-MOL-AR Project, Preliminary Results about Liquid Biopsy: Molecular Approach Experience and Research Activity in Oncological Settings.

Background  Liquid biopsy is mainly used to identify tumor cells in pulmonary neoplasms. It is more often used in research than in clinical practice. The BL-MOL-AR study aims to investigate the efficacy of next-generation sequencing (NGS) and clinical interpretation of the circulating free DNA (cfDNA) levels. This study reports the preliminary results from the first samples analyzed from patients affected by various neoplasms: lung, intestinal, mammary, gastric, biliary, and cutaneous. Methods  The Biopsia Liquida-Molecolare-Arezzo study aims to enroll cancer patients affected by various malignancies, including pulmonary, intestinal, advanced urothelial, biliary, breast, cutaneous, and gastric malignancies. Thirty-nine patients were included in this preliminary report. At time zero, a liquid biopsy is executed, and two types of NGS panels are performed, comprising 17 genes in panel 1, which is already used in the routine tissue setting, and 52 genes in panel 2. From the 7th month after enrollment, 10 sequential liquid biopsies are performed up to the 17th month. The variant allele frequency (%) and cfDNA levels (ng/mL) are measured in every plasmatic sample. Results  The NGS results obtained by different panels are similar even though the number of mutations is more concordant for lung pathologies. There are no significant differences in the actionability levels of the identified variants. Most of the molecular profiles of liquid biopsies reflect tissue data. Conclusions  Preliminary data from this study confirm the need to clarify the limitations and potential of liquid biopsy beyond the lung setting. Overall, parameters related to cfDNA levels and variant allele frequency could provide important indications for prognosis and disease monitoring.

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来源期刊
Global Medical Genetics
Global Medical Genetics GENETICS & HEREDITY-
自引率
11.80%
发文量
30
审稿时长
14 weeks
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