scholarly journals The Vancouver Lung Cancer Risk Prediction Model: Assessment by Using a Subset of the National Lung Screening Trial Cohort

Radiology ◽  
2017 ◽  
Vol 283 (1) ◽  
pp. 264-272 ◽  
Author(s):  
Charles S. White ◽  
Ekta Dharaiya ◽  
Erin Campbell ◽  
Lilla Boroczky
CHEST Journal ◽  
2019 ◽  
Vol 156 (1) ◽  
pp. 112-119 ◽  
Author(s):  
Heber MacMahon ◽  
Feng Li ◽  
Yulei Jiang ◽  
Samuel G. Armato

2014 ◽  
Vol 23 (11) ◽  
pp. 2462-2470 ◽  
Author(s):  
Randa A. El-Zein ◽  
Mirtha S. Lopez ◽  
Anthony M. D'Amelio ◽  
Mei Liu ◽  
Reginald F. Munden ◽  
...  

2017 ◽  
Author(s):  
Alison L. Van Dyke ◽  
Christine D. Berg ◽  
Neil E. Caporaso ◽  
Hormuzd A. Katki ◽  
Anil K. Chaturvedi ◽  
...  

2016 ◽  
Vol 89 (1060) ◽  
pp. 20160016 ◽  
Author(s):  
Henry Zhao ◽  
Henry M Marshall ◽  
Ian A Yang ◽  
Rayleen V Bowman ◽  
John Ayres ◽  
...  

2017 ◽  
Vol 25 (2) ◽  
pp. 110-112 ◽  
Author(s):  
Paul F Pinsky ◽  
Christina R Bellinger ◽  
David P Miller

Objectives Low-dose computed tomography lung cancer screening has been shown to reduce lung cancer mortality but has a high false-positive rate. The precision medicine approach to low-dose computed tomography screening assesses subjects’ benefits versus harms based on their personal lung cancer risk, where harms include false-positive screens and resultant invasive procedures. We assess the relationship between lung cancer risk and the rate of false-positive LDCT screens. Methods The National Lung Screening Trial randomized high-risk subjects to three annual screens with low-dose computed tomography or chest radiographs. Following the completion of National Lung Screening Trial, the Lung CT Screening Reporting and Data System (Lung-RADS) classification system was developed and retrospectively applied to National Lung Screening Trial low-dose computed tomography findings. The rate of false-positive screens (by Lung-RADS) and the resultant invasive procedures were examined as a function of lung cancer risk estimated by a model. Results Of 26,722 subjects randomized to the low-dose computed tomography arm, 26,309 received a baseline screen and were included in the analysis. The proportion with any false positive over three screening rounds increased from 12.9% to 25.9% from lowest to highest risk decile, and the proportion with an invasive procedure following a false positive also significantly increased from 0.7% to 2.0% from lowest to highest risk decile. Conclusion These findings indicate a need for personalized low-dose computed tomography lung cancer screening decision aids to accurately convey the benefits to harm trade-off.


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