Department of Chemistry and The Vanderbilt Institute for Chemical Biology , Vanderbilt University , Nashville , Tennessee 37235 , United States.
Department of Biostatistics , Vanderbilt University Medical Center , Nashville , Tennessee 37232 , United States.
ACS Comb Sci. 2019 Jun 10;21(6):465-472. doi: 10.1021/acscombsci.9b00022. Epub 2019 May 10.
Diagnosis of lung cancer patients with indeterminate pulmonary nodules (IPNs) presents a significant clinical challenge, with morbidity and management costs of $28 billion/year. We show that a quantitative free-solution assay (FSA), coupled with a compensated interferometric reader (CIR), improves the diagnostic performance of CYFRA 21-1 as a lung cancer biomarker. FSA-CIR is a rapid, mix-and-read, isothermal, label- and enzyme-free, matrix-insensitive, and target and probe-agnostic assay. Operating FSA-CIR at ∼40, 0.75 μL samples/day delivered a serum CYFRA 21-1 limit of quantification (LOQ) of 81 pg/mL with intra-assay and interassay CVs of 4.9% and 9.6% for four-day replicate determinations. Blinded analysis of a 225 patient cohort, consisting of 75 nonmalignant nodules, 45 adenocarcinomas, 44 squamous cell carcinomas, and 61 small cell lung cancers, gave a clear separation of cases and controls, not observed in the Cobas ECL analysis. The area under the curve (AUC) for the Mayo model increased from 0.595 to 0.923 when combined with the FSA-CIR CYFRA 21-1 measurements. In a population with nodules between 6 and 30 mm, the AUC increased from 0.567 to 0.943. In this subgroup, the positive predictive value (PPV) for all tumors by the CYFRA 21-1 assay was 98.7%. Our results demonstrate increased performance of the CYFRA 21-1 assay using FSA-CIR and represents a proof of concept for redefining the performance characteristics of this important candidate biomarker.
肺癌患者肺部不确定结节(IPN)的诊断具有重大的临床挑战,每年的发病率和管理成本为 280 亿美元。我们证明,一种定量游离溶液分析(FSA)与补偿干涉仪读数器(CIR)相结合,可提高 CYFRA 21-1 作为肺癌生物标志物的诊断性能。FSA-CIR 是一种快速、混合读取、等温、无标签和酶、基质不敏感、目标和探针不可知的分析方法。在约 40°C 和 0.75μL/天的条件下运行 FSA-CIR,可实现血清 CYFRA 21-1 的定量下限(LOQ)为 81pg/mL,对于四天重复测定,批内和批间 CV 分别为 4.9%和 9.6%。对 225 名患者队列的盲法分析,包括 75 个非恶性结节、45 个腺癌、44 个鳞状细胞癌和 61 个小细胞肺癌,与 Cobas ECL 分析相比,清楚地区分了病例和对照组。当与 FSA-CIR CYFRA 21-1 测量结果结合时,Mayo 模型的曲线下面积(AUC)从 0.595 增加到 0.923。在结节直径为 6-30mm 的人群中,AUC 从 0.567 增加到 0.943。在该亚组中,CYFRA 21-1 检测的所有肿瘤的阳性预测值(PPV)为 98.7%。我们的结果表明,使用 FSA-CIR 可提高 CYFRA 21-1 检测的性能,这为重新定义这一重要候选生物标志物的性能特征提供了概念验证。