| Literature DB >> 28331076 |
Henry M Marshall1, Henry Zhao1, Rayleen V Bowman1, Linda H Passmore1, Elizabeth M McCaul1, Ian A Yang1, Kwun M Fong1.
Abstract
High false-positive (FP) scan rates associated with low-dose computed tomography (LDCT) lung cancer screening result in unnecessary follow-up tests and exposure to harm. The definition of a 'positive' scan can impact FP rates and screening performance. We explored the effect of Lung Imaging Reporting and Data System (Lung-RADS) criteria, PanCan Nodule Malignancy Probability Model and varying nodule size thresholds (≥4 mm, ≥6 mm, ≥8 mm) on diagnostic accuracy and screening performance compared with original trial definitions (National Lung Screening Trial (NLST) criteria) in a secondary analysis of a lung cancer screening cohort. We found Lung-RADS criteria and the PanCan Nodule Malignancy Probability Model could substantially improve screening performance and reduce FP scan rates compared with NLST definitions of positivity but that this needs to be balanced against possible risk of false-negative results. TRIAL REGISTRATION NUMBER: Australian New Zealand Clinical Trials Registry, ACTRN12610000007033. Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/.Entities:
Keywords: Imaging/CT MRI etc; Lung Cancer
Mesh:
Year: 2017 PMID: 28331076 DOI: 10.1136/thoraxjnl-2016-209624
Source DB: PubMed Journal: Thorax ISSN: 0040-6376 Impact factor: 9.139