肺结节危险分层的多变量细胞液体活检:分析验证和早期临床评估

Jason D. Berndt , Fergal J. Duffy , Mark D. D'Ascenzo , Leslie R. Miller , Yijun Qi , G. Adam Whitney , Samuel A. Danziger , Anil Vachani , Pierre P. Massion , Stephen A. Deppen , Robert J. Lipshutz , John D. Aitchison , Jennifer J. Smith
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引用次数: 0

摘要

指示细胞分析平台(iCAP)是一种基于血液诊断的新工具,它使用活细胞作为生物传感器来整合和放大患者血清中存在的微弱、多价疾病信号。在该平台中,标准化细胞暴露于少量患者血清中,并使用机器学习工具分析由此产生的转录组反应,以开发疾病分类器。方法:我们开发了肺癌特异性iCAP (LC-iCAP),作为低剂量CT筛查发现的不确定肺结节的排除试验。这包括分析参数化,分析重复性测试,以及为未来临床验证和监管开发选择固定的85个基因特征集。临床表现评估采用前瞻性标本收集,回顾性盲法评估(PRoBE)研究设计,包括176个样本。分类器变体通过使用85个基因子集的嵌套交叉验证进行训练,选定的变体通过使用39个对照和40个病例样本(72%为I期癌症,22%为II期癌症)的时间盲验证进行评估。结果该实验在各种条件和细胞系中显示出良好的再现性,并且缺氧反应基因的病例对照转录组信号丰富,与已知的肺癌生物学一致。两个模型在盲验证中表现出区分能力,其中一个模型的AUC = 0.64 (95% CI: 0.51-0.76)。与CT成像特征的事后整合产生了一个联合模型,其灵敏度为90%,特异性为64%,在25%的患病率下,阴性预测值为95%,表明了临床实用性,并且超越了现有的排除测试。结论本研究建立了LC-iCAP的分析重复性和生物学相关性。虽然临床验证是初步的,但结果支持该检测在肺结节管理中的潜在效用。该研究引入了一种使用可扩展且具有成本效益的基于细胞的生物传感器检测液体活检的新范例。该平台具有多元读数,适用于多种癌症早期检测等精准医疗应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A multivariate cell-based liquid biopsy for lung nodule risk stratification: Analytical validation and early clinical evaluation

Background

The Indicator Cell Assay Platform (iCAP) is a novel tool for blood-based diagnostics that uses living cells as biosensors to integrate and amplify weak, multivalent disease signals present in patient serum. In the platform, standardized cells are exposed to small volumes of patient serum, and the resulting transcriptomic response is analyzed using machine learning tools to develop disease classifiers.

Methods

We developed a lung cancer-specific iCAP (LC-iCAP) as a rule-out test for the management of indeterminate pulmonary nodules detected by low-dose CT screening. This included assay parameterization, analytical reproducibility testing, and selection of a fixed 85-gene feature set for future clinical validation and regulatory development. Clinical performance was estimated using a prospective-specimen-collection, retrospective-blinded-evaluation (PRoBE) study design comprising 176 samples. Classifier variants were trained by nested cross validation using subsets of the 85 genes, and selected variants were evaluated by temporal blind validation using 39 control and 40 case samples (72 % Stage I, 22 % Stage II cancer).

Results

The assay showed excellent reproducibility across various conditions and cell lineages, and case versus control transcriptomic signals were enriched for hypoxia-responsive genes, consistent with known lung cancer biology. Two models demonstrated discriminative ability in blind validation, one with AUC = 0.64 (95 % CI: 0.51–0.76). Post hoc integration with CT imaging features yielded a combined model with 90 % sensitivity, 64 % specificity, and 95 % negative predictive value at 25 % prevalence, suggesting clinical utility and surpassing performance of existing rule-out tests.

Conclusion

This study establishes the analytical reproducibility and biological relevance of the LC-iCAP. While clinical validation is preliminary, the results support the assay's potential utility in lung nodule management. The study introduces a new paradigm of using scalable and cost-effective cell-based biosensor assays for liquid biopsies. With a multivariate readout, the platform is amenable to precision medicine applications such as multi-cancer early detection.
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