Screening approaches for lung cancer by blood-based biomarkers: Challenges and opportunities.

Q3 Biochemistry, Genetics and Molecular Biology
Tumor Biology Pub Date : 2024-01-01 DOI:10.3233/TUB-230004
Daniel van den Broek, Harry J M Groen
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引用次数: 0

Abstract

Lung cancer (LC) is one of the leading causes for cancer-related deaths in the world, accounting for 28% of all cancer deaths in Europe. Screening for lung cancer can enable earlier detection of LC and reduce lung cancer mortality as was demonstrated in several large image-based screening studies such as the NELSON and the NLST. Based on these studies, screening is recommended in the US and in the UK a targeted lung health check program was initiated. In Europe lung cancer screening (LCS) has not been implemented due to limited data on cost-effectiveness in the different health care systems and questions on for example the selection of high-risk individuals, adherence to screening, management of indeterminate nodules, and risk of overdiagnosis. Liquid biomarkers are considered to have a high potential to address these questions by supporting pre- and post- Low Dose CT (LDCT) risk-assessment thereby improving the overall efficacy of LCS. A wide variety of biomarkers, including cfDNA, miRNA, proteins and inflammatory markers have been studied in the context of LCS. Despite the available data, biomarkers are currently not implemented or evaluated in screening studies or screening programs. As a result, it remains an open question which biomarker will actually improve a LCS program and do this against acceptable costs. In this paper we discuss the current status of different promising biomarkers and the challenges and opportunities of blood-based biomarkers in the context of lung cancer screening.

通过血液生物标记物筛查肺癌的方法:挑战与机遇。
肺癌(LC)是全球癌症相关死亡的主要原因之一,占欧洲癌症死亡总数的 28%。肺癌筛查可以更早地发现肺癌并降低肺癌死亡率,这一点已在 NELSON 和 NLST 等多项大型图像筛查研究中得到证实。基于这些研究,美国建议进行筛查,英国则启动了一项有针对性的肺部健康检查计划。在欧洲,肺癌筛查(LCS)尚未实施,原因是不同医疗系统的成本效益数据有限,而且在高危人群的选择、筛查的依从性、不确定结节的处理以及过度诊断的风险等方面也存在问题。液体生物标记物被认为很有可能通过支持低剂量 CT(LDCT)前后的风险评估来解决这些问题,从而提高 LCS 的整体疗效。在 LCS 的背景下,人们研究了多种生物标记物,包括 cfDNA、miRNA、蛋白质和炎症标记物。尽管已有数据,但生物标志物目前尚未在筛查研究或筛查计划中应用或评估。因此,哪种生物标记物能真正改善 LCS 计划,并以可接受的成本实现这一目标,仍是一个未决问题。在本文中,我们将讨论各种有前景的生物标志物的现状,以及在肺癌筛查中基于血液的生物标志物所面临的挑战和机遇。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Tumor Biology
Tumor Biology 医学-肿瘤学
CiteScore
5.40
自引率
0.00%
发文量
18
审稿时长
1 months
期刊介绍: Tumor Biology is a peer reviewed, international journal providing an open access forum for experimental and clinical cancer research. Tumor Biology covers all aspects of tumor markers, molecular biomarkers, tumor targeting, and mechanisms of tumor development and progression. Specific topics of interest include, but are not limited to: Pathway analyses, Non-coding RNAs, Circulating tumor cells, Liquid biopsies, Exosomes, Epigenetics, Cancer stem cells, Tumor immunology and immunotherapy, Tumor microenvironment, Targeted therapies, Therapy resistance Cancer genetics, Cancer risk screening. Studies in other areas of basic, clinical and translational cancer research are also considered in order to promote connections and discoveries across different disciplines. The journal publishes original articles, reviews, commentaries and guidelines on tumor marker use. All submissions are subject to rigorous peer review and are selected on the basis of whether the research is sound and deserves publication. Tumor Biology is the Official Journal of the International Society of Oncology and BioMarkers (ISOBM).
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