Lung cancer continues to be the most common cancer and reduction of lung cancer related death is a global priority. The National Lung Screening Trial (NLST) reported that the low-dose computed tomography (LDCT) screening reduced the lung cancer mortality by 20%, with a trade-off of more than 95% of false positive results. This underlined our need for a much improved risk prediction model and higher screening efficiency to balance the benefits and potential harms. Although there have been substantial efforts in establishing lung cancer risk prediction models, none have taken all aspects into account and the joint performance of all predictors remains unknown. For those with CT nodules, currently there is a wide range of clinical protocols on how they are managed, from watchful waiting to invasive diagnostic procedures. With the usage of LDCT scans rapidly growing following the NLST report, there is an urgent need to address the issues of (i) who should be recommended for screening and (ii) what to do when a nodule is found. Our research team is in the unique position to conduct this much needed work as we have already established extensive resources for the data elements needed being the lead investigators of the three lung cancer consortia (International Lung Cancer Consortium, Transdisciplinary Research in Cancer of Lung, and Lung Cancer Cohort Consortium), and have established collaborations with the lung cancer CT screening programs in the US, Canada and Europe. The overall goal of this project is to translate the epidemiological, molecular and clinical data into lung cancer risk assessment and to improve nodule assessment. Specifically, we will (i) establish an integrated risk prediction model to identify individuals at high risk of lung cancer, combining personal health and exposure history, targeted molecular and genomic profile and lung function data based lung cancer CT screening populations in US, Canada and Europe based on a total of 950 CT-detected lung cancer patients from cohorts of 46,057 screening individuals; and (ii) establish a comprehensive nodule assessment models for individuals with LDCT-detected non-calcified pulmonary nodules based on both 2 dimensional-based and 3D volume and radiomics-based probability models. We will compare the model performance with the existing classification system such as Lung-RADS and conduct net benefit and decision curve analysis to assess their clinical usefulness. These models will be very valuable for the general public, clinicians, researchers and health administrators. It will increase the efficiency of lung cancer LDCT screening, and reduce unnecessary workup (and patient anxiety) for those who were found to have LDCT-detected pulmonary non-calcified nodules. The impact of this project will be wide-spread in our community.

Public Health Relevance

Lung cancer continues to be the most common cancer and leading cause of cancer death worldwide, and the reduction of lung cancer death remains to be the global priority. Based on the report from NLST showing that low-dose computed tomography (LDCT) can reduce mortality by 20%, several public health agencies have considered population-wide implementation of lung cancer LDCT screening. To balance the potential benefits and harms, our project aims to establish an integrative model for population lung cancer risk assessment for lung cancer screening recommendation, and a nodule assessment model for those with LDCT- detected abnormalities to improve patient management.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program--Cooperative Agreements (U19)
Project #
5U19CA203654-03
Application #
9518758
Study Section
Special Emphasis Panel (ZCA1)
Project Start
Project End
Budget Start
2019-04-01
Budget End
2020-03-31
Support Year
3
Fiscal Year
2019
Total Cost
Indirect Cost
Name
Baylor College of Medicine
Department
Type
DUNS #
051113330
City
Houston
State
TX
Country
United States
Zip Code
77030
Barfield, Richard; Shen, Jincheng; Just, Allan C et al. (2017) Testing for the indirect effect under the null for genome-wide mediation analyses. Genet Epidemiol 41:824-833
Patel, Chirag J; Kerr, Jacqueline; Thomas, Duncan C et al. (2017) Opportunities and Challenges for Environmental Exposure Assessment in Population-Based Studies. Cancer Epidemiol Biomarkers Prev 26:1370-1380
Gauderman, W James; Mukherjee, Bhramar; Aschard, Hugues et al. (2017) Update on the State of the Science for Analytical Methods for Gene-Environment Interactions. Am J Epidemiol 186:762-770
Qian, David C; Molfese, David L; Jin, Jennifer L et al. (2017) Genome-wide imaging association study implicates functional activity and glial homeostasis of the caudate in smoking addiction. BMC Genomics 18:740
McAllister, Kimberly; Mechanic, Leah E; Amos, Christopher et al. (2017) Current Challenges and New Opportunities for Gene-Environment Interaction Studies of Complex Diseases. Am J Epidemiol 186:753-761