肺癌预测模型 "压力测试"

Brent E. Heideman MD , Michael N. Kammer PhD , Rafael Paez MD , Terra Swanson MD , Caroline M. Godfrey MD , See-Wei Low MD , David Xiao MD , Thomas Z. Li BS , Jacob R. Richardson BS , Michael A. Knight BS , Samira Shojaee MD , Stephen A. Deppen PhD , Robert J. Lentz MD , Eric L. Grogan MD, MPH , Fabien Maldonado MD, FCCP
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引用次数: 0

摘要

背景由于恶性病变的延迟诊断和良性病变的过度检查,肺结节给医疗保健带来了日益沉重的负担。临床预测模型的开发为医生评估结节恶性概率提供了依据,但尚未在最终进行活检的高风险结节队列中进行验证。研究问题当指南推荐的预测模型应用于通过导航支气管镜转诊进行活检的病例时,是否能充分区分良性结节和恶性结节?研究设计和方法我们收集了2017年至2019年期间转诊至一家三级医疗中心进行导航支气管镜诊断的282名患者中322个不确定肺结节的前瞻性队列。我们使用布洛克模型、梅奥诊所模型和退伍军人事务(VA)模型计算了每个结节的恶性概率。在活检前还进行了 PET-CT 扫描的 168 例患者子集中,我们还使用 Herder 模型计算了恶性肿瘤的概率。通过计算每个模型的接收者操作特征曲线下面积(AUC)来评估模型的性能。结果研究队列中有 185 个恶性结节和 137 个良性结节(恶性发生率为 57%)。恶性和良性结节的大小相似,良性和恶性结节的中位最长直径分别为 15 毫米和 16 毫米。布洛克模型、梅奥诊所模型和 VA 模型在整个队列中显示出相似的性能(布洛克 AUC,0.70;95% CI,0.64-0.76;梅奥诊所 AUC,0.70;95% CI,0.64-0.76;VA AUC,0.67;95% CI,0.62-0.74)。对于有 PET-CT 扫描资料的 168 个结节,Herder 模型的 AUC 为 0.77(95% CI,0.68-0.85)。
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The Lung Cancer Prediction Model “Stress Test”

Background

Pulmonary nodules represent a growing health care burden because of delayed diagnosis of malignant lesions and overtesting for benign processes. Clinical prediction models were developed to inform physician assessment of pretest probability of nodule malignancy but have not been validated in a high-risk cohort of nodules for which biopsy was ultimately performed.

Research Question

Do guideline-recommended prediction models sufficiently discriminate between benign and malignant nodules when applied to cases referred for biopsy by navigational bronchoscopy?

Study Design and Methods

We assembled a prospective cohort of 322 indeterminate pulmonary nodules in 282 patients referred to a tertiary medical center for diagnostic navigational bronchoscopy between 2017 and 2019. We calculated the probability of malignancy for each nodule using the Brock model, Mayo Clinic model, and Veterans Affairs (VA) model. On a subset of 168 patients who also had PET-CT scans before biopsy, we also calculated the probability of malignancy using the Herder model. The performance of the models was evaluated by calculating the area under the receiver operating characteristic curves (AUCs) for each model.

Results

The study cohort contained 185 malignant and 137 benign nodules (57% prevalence of malignancy). The malignant and benign cohorts were similar in terms of size, with a median longest diameter for benign and malignant nodules of 15 and 16 mm, respectively. The Brock model, Mayo Clinic model, and VA model showed similar performance in the entire cohort (Brock AUC, 0.70; 95% CI, 0.64-0.76; Mayo Clinic AUC, 0.70; 95% CI, 0.64-0.76; VA AUC, 0.67; 95% CI, 0.62-0.74). For 168 nodules with available PET-CT scans, the Herder model had an AUC of 0.77 (95% CI, 0.68-0.85).

Interpretation

Currently available clinical models provide insufficient discrimination between benign and malignant nodules in the common clinical scenario in which a patient is being referred for biopsy, especially when PET-CT scan information is not available.

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