Cotton Lindsey B, Bach Peter B, Cisar Chris, Schonewolf Caitlin A, Tennefoss Demetria, Vachani Anil, Carter-Bawa Lisa, Zaidi Ali H
DELFI Diagnostics, Inc., Baltimore, MD 21224, USA.
Pulmonary, Allergy, and Critical Care Division, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA 19104, USA.
J Clin Med. 2024 Aug 20;13(16):4911. doi: 10.3390/jcm13164911.
Lung cancer mortality rates, particularly non-small cell lung cancer (NSCLC), continue to present a significant global health challenge, and the adoption of lung cancer screening remains limited, often influenced by inequities in access to healthcare. Despite clinical evidence demonstrating the efficacy of annual screening with low-dose computed tomography (LDCT) and recommendations from medical organizations including the U.S. Preventive Services Task Force (USPSTF), the national lung cancer screening uptake remains around 5% among eligible individuals. Advancements in the clinical management of NSCLC have recently become more personalized with the implementation of blood-based biomarker testing. Extensive research into tumor-derived cell-free DNA (cfDNA) through fragmentation offers a novel method for improving early lung cancer detection. This review assesses the screening landscape, explores obstacles to lung cancer screening, and discusses how a plasma whole genome fragmentome test (pWGFrag-Lung) can improve lung cancer screening participation and adherence.
肺癌死亡率,尤其是非小细胞肺癌(NSCLC)的死亡率,仍然是一项重大的全球健康挑战,肺癌筛查的采用率仍然有限,这通常受到医疗保健可及性不平等的影响。尽管有临床证据表明年度低剂量计算机断层扫描(LDCT)筛查的有效性以及包括美国预防服务工作组(USPSTF)在内的医学组织的建议,但符合条件的人群中全国肺癌筛查的接受率仍约为5%。随着基于血液的生物标志物检测的实施,NSCLC的临床管理最近变得更加个性化。通过片段化对肿瘤衍生的游离DNA(cfDNA)进行的广泛研究为改善早期肺癌检测提供了一种新方法。本综述评估了筛查现状,探讨了肺癌筛查的障碍,并讨论了血浆全基因组片段组测试(pWGFrag-Lung)如何提高肺癌筛查的参与度和依从性。