研究动态
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ISO 和 CEN/TS 液体活检标准的临床应用——每个人都想要但没有人愿意付费的信息。

Clinical Application of ISO and CEN/TS Standards for Liquid Biopsies-Information Everybody Wants but Nobody Wants to Pay For.

发表日期:2024 Jul 03
作者: Lilli Bonstingl, Christina Skofler, Christine Ulz, Margret Zinnegger, Katja Sallinger, Julia Schönberger, Katharina Schuch, Karin Pankratz, Anatol Borrás-Cherrier, Visnja Somodi, Peter M Abuja, Lisa Oberauner-Wappis, Tina Moser, Ellen Heitzer, Thomas Bauernhofer, Thomas Kroneis, Amin El-Heliebi
来源: BIOMEDICINE & PHARMACOTHERAPY

摘要:

液体活检正在成为癌症监测的有价值的临床生物标志物。尽管存在国际标准组织 (ISO) 和欧洲标准化委员会 (CEN/TS) 的技术规范标准化工作流程,但它们在临床实践中的实施尚不成熟。我们旨在评估 ISO 和 CEN/TS 标准在现实临床环境中的适用性,特别关注评估分析前参数和溶血对液体活检分析的影响。我们评估了来自晚期前列腺癌患者的 659 份外周血样本符合 ISO 和 CEN/TS 标准,并记录了所有基本标准,包括试管抽取顺序、填充水平、温度以及从血液抽取到储存的时间跟踪。我们评估了溶血及其对循环肿瘤 DNA (ctDNA) 和循环肿瘤细胞 (CTC) 分析的影响。我们的结果显示出较高的合规率,96.2% (634/659) 的样本符合基本 ISO 和 CEN/TS 标准。我们没有观察到溶血和非溶血样本对 ctDNA 或 CTC 检出率的显着影响。在我们的晚期前列腺癌队列中,12.9% (40/311) 的血浆样本中发现溶血,并且在 5 个采血管的抽取顺序中,从第 1 管到第 5 管,溶血并没有显着增加。总共,83.8% (552 /659) 的采血管的填充水平高于标称填充水平的 80%。我们的研究证明了在临床液体活检研究中遵守 ISO 和 CEN/TS 标准的可行性和益处。标准显示,在我们的晚期前列腺癌患者队列中,溶血频繁发生,但并未损害下游 ctDNA 和 CTC 分析。© 诊断协会
Liquid biopsies are emerging as valuable clinical biomarkers for cancer monitoring. Although International Organization for Standards (ISO) and Technical Specifications from the European Committee for Standardization (CEN/TS) standardized workflows exist, their implementation in clinical practice is underdeveloped. We aimed to assess the applicability of ISO and CEN/TS standards in a real-world clinical setting, with a particular focus on evaluating the impact of preanalytical parameters and hemolysis on liquid biopsy analysis.We evaluated 659 peripheral blood samples from advanced prostate cancer patients against ISO and CEN/TS standards and documented all essential criteria, including tube draw order, filling level, temperature, and time tracking from blood draw to storage. We assessed hemolysis and its effect on circulating tumor DNA (ctDNA) and circulating tumor cell (CTC) analysis.Our results demonstrated a high compliance rate, with 96.2% (634/659) of samples meeting essential ISO and CEN/TS criteria. We did not observe a significant impact on ctDNA or CTC detection rates between hemolytic and nonhemolytic samples. Hemolysis was identified in 12.9% (40/311) of plasma samples from our advanced prostate cancer cohort, and within the draw order of 5 blood collection tubes, hemolysis did not significantly increase from tube 1 to 5. In total, 83.8% (552/659) of blood collection tubes had high fill levels above 80% of nominal filling level.Our study demonstrates the feasibility and benefits of adhering to ISO and CEN/TS standards in a clinical liquid biopsy study. The standards revealed that hemolysis occurred frequently but did not impair downstream ctDNA and CTC analysis in our cohort of advanced prostate cancer patients.© Association for Diagnostics & Laboratory Medicine 2024.