Division of Pulmonary and Critical Care Medicine, University of Kentucky, Lexington, Kentucky, United States of America.
Division of Medical Oncology, University of Kentucky, Lexington, Kentucky, United States of America.
PLoS One. 2014 Feb 3;9(2):e87947. doi: 10.1371/journal.pone.0087947. eCollection 2014.
Recommendations for lung cancer screening present a tangible opportunity to integrate predictive blood-based assays with radiographic imaging. This study compares performance of autoantibody markers from prior discovery in sample cohorts from two CT screening trials. One-hundred eighty non-cancer and 6 prevalence and 44 incidence cancer cases detected in the Mayo Lung Screening Trial were tested using a panel of six autoantibody markers to define a normal range and assign cutoff values for class prediction. A cutoff for minimal specificity and best achievable sensitivity were applied to 256 samples drawn annually for three years from 95 participants in the Kentucky Lung Screening Trial. Data revealed a discrepancy in quantile distribution between the two apparently comparable sample sets, which skewed the assay's dynamic range towards specificity. This cutoff offered 43% specificity (102/237) in the control group and accurately classified 11/19 lung cancer samples (58%), which included 4/5 cancers at time of radiographic detection (80%), and 50% of occult cancers up to five years prior to diagnosis. An apparent ceiling in assay sensitivity is likely to limit the utility of this assay in a conventional screening paradigm. Pre-analytical bias introduced by sample age, handling or storage remains a practical concern during development, validation and implementation of autoantibody assays. This report does not draw conclusions about other logical applications for autoantibody profiling in lung cancer diagnosis and management, nor its potential when combined with other biomarkers that might improve overall predictive accuracy.
肺癌筛查的建议提供了一个切实可行的机会,可以将基于预测的血液检测与影像学检查相结合。本研究比较了两项 CT 筛查试验的样本队列中先前发现的自身抗体标志物的性能。使用一组 6 种自身抗体标志物对 Mayo 肺癌筛查试验中检测到的 180 例非癌症和 6 例前期及 44 例确诊癌症病例进行了检测,以确定正常范围并为分类预测分配截断值。将最小特异性和最佳可实现灵敏度的截断值应用于从肯塔基州肺癌筛查试验中 95 名参与者每年抽取的三年共 256 份样本。数据显示,两个看似可比的样本集之间存在分位数分布差异,这使得检测的动态范围偏向于特异性。该截定点在对照组中提供了 43%的特异性(102/237),并准确地对 11/19 例肺癌样本进行了分类(58%),其中包括影像学检测时的 4/5 例癌症(80%),以及在诊断前五年的 50%隐匿性癌症。该检测的敏感性上限可能限制了该检测在常规筛查模式中的应用。在自身抗体检测的开发、验证和实施过程中,由样本年龄、处理或储存引起的分析前偏倚仍然是一个实际问题。本报告并未对自身抗体分析在肺癌诊断和管理中的其他逻辑应用或与其他可能提高总体预测准确性的生物标志物联合应用得出结论。