Division of Allergy, Pulmonary and Critical Care Medicine, Department of Medicine, Vanderbilt University Medical Center.
Department of Chemistry, Vanderbilt University.
Curr Opin Pulm Med. 2021 Jul 1;27(4):240-248. doi: 10.1097/MCP.0000000000000780.
Lung cancer remains the leading cause of cancer-related death in the United States, with poor overall 5-year survival. Early detection and diagnosis are key to survival as demonstrated in lung cancer screening trials. However, with increasing implementation of screening guidelines and use of computed tomography, there has been a sharp rise in the incidence of indeterminate pulmonary nodules (IPNs). Risk stratification of IPNs, particularly those in the intermediate-risk category, remains challenging in clinical practice. Individual risk factors, imaging characteristics, biomarkers, and prediction models are currently used to assist in risk stratifying patients, but such strategies remain suboptimal. This review focuses on established risk stratification methods, current areas of research, and future directions.
The multitude of yearly incidental and screening-detected IPNs, its management-related healthcare costs, and risk of invasive procedures provides a strong rationale for risk stratification efforts. The development of new molecular and imaging biomarkers to discriminate benign from malignant lung nodules shows great promise. Yet, risk stratification methods need integration into the diagnostic workflow and await validation in prospective, biomarker-driven clinical trials.
Novel biomarkers and new imaging analysis, including radiomics and deep-learning methods, have been developed to optimize the risk stratification of IPNs. While promising, additional validation and clinical studies are needed before they can be part of routine clinical practice.
肺癌仍然是美国癌症相关死亡的主要原因,整体 5 年生存率较差。正如肺癌筛查试验所证明的那样,早期发现和诊断是生存的关键。然而,随着筛查指南的不断实施和计算机断层扫描的广泛应用,未定性肺结节(IPN)的发病率急剧上升。IPN 的风险分层,特别是那些处于中危类别的,在临床实践中仍然具有挑战性。个体危险因素、影像学特征、生物标志物和预测模型目前用于协助患者进行风险分层,但这些策略仍不理想。本综述重点介绍了已确立的风险分层方法、当前的研究领域和未来的方向。
每年偶然发现和筛查发现的 IPN 数量众多,其管理相关的医疗保健费用以及侵袭性操作的风险,为风险分层工作提供了强有力的理由。开发新的分子和成像生物标志物来区分良性和恶性肺结节显示出巨大的前景。然而,风险分层方法需要整合到诊断工作流程中,并需要在前瞻性、基于生物标志物的临床试验中进行验证。
新的生物标志物和新的成像分析,包括放射组学和深度学习方法,已经被开发出来以优化 IPN 的风险分层。虽然有希望,但在它们成为常规临床实践的一部分之前,还需要进一步的验证和临床研究。