Massion Pierre P, Healey Graham F, Peek Laura J, Fredericks Lynn, Sewell Herb F, Murray Andrea, Robertson John F R
Thoracic Program, Vanderbilt-Ingram Cancer Center, Vanderbilt University, Nashville, Tennessee.
Oncimmune, Ltd., Nottingham, United Kingdom.
J Thorac Oncol. 2017 Mar;12(3):578-584. doi: 10.1016/j.jtho.2016.08.143. Epub 2016 Sep 8.
The incidence of pulmonary nodules is increasing with the movement toward screening for lung cancer by low-dose computed tomography. Given the large number of benign nodules detected by computed tomography, an adjunctive test capable of distinguishing malignant from benign nodules would benefit practitioners. The ability of the EarlyCDT-Lung blood test (Oncimmune Ltd., Nottingham, United Kingdom) to make this distinction by measuring autoantibodies to seven tumor-associated antigens was evaluated in a prospective registry.
Of the members of a cohort of 1987 individuals with Health Insurance Portability and Accountability Act authorization, those with pulmonary nodules detected, imaging, and pathology reports were reviewed. All patients for whom a nodule was identified within 6 months of testing by EarlyCDT-Lung were included. The additivity of the test to nodule size and nodule-based risk models was explored.
A total of 451 patients (32%) had at least one nodule, leading to 296 eligible patients after exclusions, with a lung cancer prevalence of 25%. In 4- to 20-mm nodules, a positive test result represented a greater than twofold increased relative risk for development of lung cancer as compared with a negative test result. Also, when the "both-positive rule" for combining binary tests was used, adding EarlyCDT-Lung to risk models improved diagnostic performance with high specificity (>92%) and positive predictive value (>70%).
A positive autoantibody test result reflects a significant increased risk for malignancy in lung nodules 4 to 20 mm in largest diameter. These data confirm that EarlyCDT-Lung may add value to the armamentarium of the practitioner in assessing the risk for malignancy in indeterminate pulmonary nodules.
随着低剂量计算机断层扫描用于肺癌筛查的普及,肺结节的发病率正在上升。鉴于计算机断层扫描检测出大量良性结节,一种能够区分恶性与良性结节的辅助检测方法将使从业者受益。在一项前瞻性登记研究中,评估了EarlyCDT-Lung血液检测(英国诺丁汉的Oncimmune有限公司)通过检测针对七种肿瘤相关抗原的自身抗体来进行这种区分的能力。
在1987名获得《健康保险流通与责任法案》授权的队列成员中,对那些有肺结节检测结果、影像学和病理报告的成员进行了审查。纳入所有在EarlyCDT-Lung检测后6个月内发现结节的患者。探讨了该检测对结节大小和基于结节的风险模型的附加价值。
共有451名患者(32%)至少有一个结节,排除后有296名符合条件的患者,肺癌患病率为25%。在4至20毫米的结节中,与检测结果为阴性相比,检测结果为阳性表明患肺癌的相对风险增加了两倍以上。此外,当使用二元检测组合的“双阳性规则”时,将EarlyCDT-Lung添加到风险模型中可提高诊断性能,特异性高(>92%),阳性预测值高(>70%)。
自身抗体检测结果为阳性反映了直径4至20毫米的肺结节发生恶性病变的风险显著增加。这些数据证实,EarlyCDT-Lung可能为从业者评估不确定肺结节的恶性风险提供更多帮助。