用于肺结节特征描述的新型多分析血浆检验的分析验证。

Biomedical research and reviews Pub Date : 2018-12-01 Epub Date: 2018-11-23 DOI:10.15761/brr.1000123
Neil N Trivedi, James K Brown, Tess Rubenstein, Abigail D Rostykus, Amanda L Fish, Heng Yu, Luis Carbonell, Alice Juang, Sandy Kamer, Bhavin Patel, Manpreet Sidhu, Doris Vuong, Shan Wang, Mike Beggs, Alan Hb Wu, Mehrdad Arjomandi
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引用次数: 0

摘要

背景:在全国肺部筛查试验中,96.4% 的结节为良性病因。为了避免不必要的行动和伤害,必须识别良性疾病患者。我们在此介绍一种多分析物免疫测定法的分析验证,该方法用于确定 CT 发现的肺部结节是恶性的风险。风险较低者可考虑进行连续监测,以避免不必要且可能有害的手术。而那些风险较高的结节可能适合采取更积极的行动:目的:验证用于肺结节特征描述的新型检验中的多重血浆蛋白测定的分析性能:方法:在一家临床检验实验室评估了一种多重免疫检测板,用于测量CT扫描发现肺结节的当前吸烟者的血浆蛋白。通过多次运行、批次和技术人员对表皮生长因子受体(EGFR)、前表面活性蛋白 B(ProSB)和组织金属蛋白酶抑制剂 1(TIMP1)的分析灵敏度、重现性、精确度和回收率进行了评估。评估了干扰物质和样品分析前储存条件对分析物回收率的影响。对多个批次的肺结节风险评分的重现性进行了评估:检测灵敏度分别为 0.10 纳克/毫升表皮生长因子受体、0.02 纳克/毫升 ProSB 和 0.29 纳克/毫升 TIMP1,检测动态范围超过三个数量级。这些检测方法和分析物对分析前的样品处理非常稳定,血浆在新鲜采集或在-80°C长期保存后解冻,可在4°C保存4天。经过 20 天的检测后,所有三种检测方法的总不精确度仍低于 9%。风险评分变异性保持在±10%的风险评分范围内:在临床实验室中,用于肺结节特征描述的多分析血浆检测中的三种蛋白质检测方法的表现都相当不错。
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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Analytical validation of a novel multi-analyte plasma test for lung nodule characterization.

Background: In the National Lung Screening Trial, 96.4% of nodules had benign etiology. To avoid unnecessary actions and exposure to harm, individuals with benign disease must be identified. We describe herein the analytical validation of a multi-analyte immunoassay for characterizing the risk that a lung nodule found on CT is malignant. Those at lower risk may be considered for serial surveillance to avoid unnecessary and potentially harmful procedures. While those nodules characterized at higher risk may be appropriate for more aggressive actions.

Objective: To validate the analytical performance of multiplexed plasma protein assays used in a novel test for lung nodule characterization.

Methods: A multiplexed immunoassay panel for the measurement of plasma proteins in current smokers who present with a lung nodule on CT scan was evaluated in a clinical testing laboratory. Assay analytical sensitivity, reproducibility, precision, and recovery of Epidermal Growth Factor Receptor (EGFR), Prosurfactant protein B (ProSB), and Tissue Inhibitor of Metalloproteinases 1 (TIMP1) from human EDTA plasma samples were evaluated across multiple runs, lots, and technicians. Interfering substances and sample pre-analytical storage conditions were evaluated for their effect on analyte recovery. The lung nodule risk score reproducibility was assessed across multiple lots.

Results: The assay sensitivities were 0.10 ng/mL EGFR, 0.02 ng/mL ProSB, and 0.29 ng/mL TIMP1 with over three orders of magnitude in the assay dynamic ranges. The assays and analytes are robust to pre-analytical sample handling and the plasma can be stored for up to 4 days at 4°C either when freshy collected or thawed after long-term storage at -80°C. Total imprecision after 20 days of testing remained under 9% for all three assays. Risk score variability remained within a ± 10% risk score range.

Conclusions: The three protein assays comprising the multi-analyte plasma test for lung nodule characterization performed quite acceptably in a clinical laboratory.

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