TY - JOUR
T1 - Interstitial Lung Abnormalities and Lung Cancer Risk in the National Lung Screening Trial
AU - Whittaker Brown, Stacey Ann
AU - Padilla, Maria
AU - Mhango, Grace
AU - Powell, Charles
AU - Salvatore, Mary
AU - Henschke, Claudia
AU - Yankelevitz, David
AU - Sigel, Keith
AU - de-Torres, Juan P.
AU - Wisnivesky, Juan
N1 - Funding Information:
Author contributions: All authors contributed to conception and design; manuscript writing; and collection, assembly, analysis, and interpretation of data. All authors gave final approval of the manuscript as submitted. Financial/nonfinancial disclosures: The authors have reported to CHEST the following: M. P. has served as a consultant to Boehringer Ingelheim. She has also served as faculty presenter on lectures supported by Genentech and the France Foundation ; and has been an investigator on several multisite clinical trials on idiopathic pulmonary fibrosis sponsored by various pharmaceutical companies. M. S. has been a speaker for Genentech, Boehringer Ingelheim, and Eastern Pulmonary Conference; and a consultant for Genentech and Boehringer Ingelheim. C. H. is a named inventor on a number of patents and patent applications relating to the evaluation of pulmonary nodules on CT scans of the chest which are owned by Cornell Research Foundation. Since 2009, she does not accept any financial benefit from these patents, including royalties and any other proceeds related to the patents or patent applications owned by Cornell Research Foundation. She is President and serves on the board of the Early Diagnosis and Treatment Research Foundation and receives no compensation from the Foundation. The Foundation is established to provide grants for projects, conferences, and public databases for research on early diagnosis and treatment of diseases. Recipients include the International Early Lung Cancer Action Program, among others. The funding comes from a variety of sources, including philanthropic donations, grants and contracts with agencies (federal and nonfederal), imaging, and pharmaceutical companies relating to image processing assessments. The various sources of funding exclude any funding from tobacco companies or tobacco-related sources. D. Y. is an equity owner in Accumetra, a privately held technology company committed to improving the science and practice of image-based decision-making. He also serves on the advisory board of GRAIL. In addition, he is a named inventor on a number of patents and patent applications relating to the evaluation of diseases of the chest, including measurement of nodules. Some of these, which are owned by Cornell Research Foundation, are nonexclusively licensed to General Electric. As an inventor of these patents, he is entitled to a share of any compensation that Cornell Research Foundation may receive from its commercialization of these patents. J. W. has received consulting honorarium from Sanofi and Banook and research grants from Sanofi and Quorum . None declared (S.-A. W. B., G. M., C. P., K. S., J. P. d.-T.). Role of sponsors : The sponsor had no role in the design of the study, the collection and analysis of the data, or the preparation of the manuscript. Other contributions: The authors are grateful to the National Cancer Institute for providing access to data from the NLST. The analysis and manuscript are solely the responsibility of the authors. Additional information: The e-Tables can be found in the Supplemental Materials section of the online article.
Funding Information:
FUNDING/SUPPORT: This study was partially supported by the Stony Wold Herbert Inc. Foundation Fellowship Award.Author contributions: All authors contributed to conception and design; manuscript writing; and collection, assembly, analysis, and interpretation of data. All authors gave final approval of the manuscript as submitted. Financial/nonfinancial disclosures: The authors have reported to CHEST the following: M. P. has served as a consultant to Boehringer Ingelheim. She has also served as faculty presenter on lectures supported by Genentech and the France Foundation; and has been an investigator on several multisite clinical trials on idiopathic pulmonary fibrosis sponsored by various pharmaceutical companies. M. S. has been a speaker for Genentech, Boehringer Ingelheim, and Eastern Pulmonary Conference; and a consultant for Genentech and Boehringer Ingelheim. C. H. is a named inventor on a number of patents and patent applications relating to the evaluation of pulmonary nodules on CT scans of the chest which are owned by Cornell Research Foundation. Since 2009, she does not accept any financial benefit from these patents, including royalties and any other proceeds related to the patents or patent applications owned by Cornell Research Foundation. She is President and serves on the board of the Early Diagnosis and Treatment Research Foundation and receives no compensation from the Foundation. The Foundation is established to provide grants for projects, conferences, and public databases for research on early diagnosis and treatment of diseases. Recipients include the International Early Lung Cancer Action Program, among others. The funding comes from a variety of sources, including philanthropic donations, grants and contracts with agencies (federal and nonfederal), imaging, and pharmaceutical companies relating to image processing assessments. The various sources of funding exclude any funding from tobacco companies or tobacco-related sources. D. Y. is an equity owner in Accumetra, a privately held technology company committed to improving the science and practice of image-based decision-making. He also serves on the advisory board of GRAIL. In addition, he is a named inventor on a number of patents and patent applications relating to the evaluation of diseases of the chest, including measurement of nodules. Some of these, which are owned by Cornell Research Foundation, are nonexclusively licensed to General Electric. As an inventor of these patents, he is entitled to a share of any compensation that Cornell Research Foundation may receive from its commercialization of these patents. J. W. has received consulting honorarium from Sanofi and Banook and research grants from Sanofi and Quorum. None declared (S.-A. W. B. G. M. C. P. K. S. J. P. d.-T.). Role of sponsors: The sponsor had no role in the design of the study, the collection and analysis of the data, or the preparation of the manuscript. Other contributions: The authors are grateful to the National Cancer Institute for providing access to data from the NLST. The analysis and manuscript are solely the responsibility of the authors. Additional information: The e-Tables can be found in the Supplemental Materials section of the online article.
Publisher Copyright:
© 2019
PY - 2019/12
Y1 - 2019/12
N2 - Background: Some interstitial lung diseases are associated with lung cancer. However, it is unclear whether asymptomatic interstitial lung abnormalities convey an independent risk. Objectives: The goal of this study was to assess whether interstitial lung abnormalities are associated with an increased risk of lung cancer. Methods: Data from all participants in the National Lung Cancer Trial were analyzed, except for subjects with preexisting interstitial lung disease or prevalent lung cancers. The primary analysis included those who underwent low-dose CT imaging; those undergoing chest radiography were included in a confirmatory analysis. Participants with evidence of reticular/reticulonodular opacities, honeycombing, fibrosis, or scarring were classified as having interstitial lung abnormalities. Lung cancer incidence and mortality in participants with and without interstitial lung abnormalities were compared by using Poisson and Cox regression, respectively. Results: Of the 25,041 participants undergoing low-dose CT imaging included in the primary analysis, 20.2% had interstitial lung abnormalities. Participants with interstitial lung abnormalities had a higher incidence of lung cancer (incidence rate ratio, 1.61; 95% CI, 1.30-1.99). Interstitial lung abnormalities were associated with higher lung cancer incidence on adjusted analyses (incidence rate ratio, 1.33; 95% CI, 1.07-1.65). Lung cancer-specific mortality was also greater in participants with interstitial lung abnormalities. Similar findings were obtained in the analysis of participants undergoing chest radiography. Conclusions: Asymptomatic interstitial lung abnormalities are an independent risk factor for lung cancer that can be incorporated into risk score models.
AB - Background: Some interstitial lung diseases are associated with lung cancer. However, it is unclear whether asymptomatic interstitial lung abnormalities convey an independent risk. Objectives: The goal of this study was to assess whether interstitial lung abnormalities are associated with an increased risk of lung cancer. Methods: Data from all participants in the National Lung Cancer Trial were analyzed, except for subjects with preexisting interstitial lung disease or prevalent lung cancers. The primary analysis included those who underwent low-dose CT imaging; those undergoing chest radiography were included in a confirmatory analysis. Participants with evidence of reticular/reticulonodular opacities, honeycombing, fibrosis, or scarring were classified as having interstitial lung abnormalities. Lung cancer incidence and mortality in participants with and without interstitial lung abnormalities were compared by using Poisson and Cox regression, respectively. Results: Of the 25,041 participants undergoing low-dose CT imaging included in the primary analysis, 20.2% had interstitial lung abnormalities. Participants with interstitial lung abnormalities had a higher incidence of lung cancer (incidence rate ratio, 1.61; 95% CI, 1.30-1.99). Interstitial lung abnormalities were associated with higher lung cancer incidence on adjusted analyses (incidence rate ratio, 1.33; 95% CI, 1.07-1.65). Lung cancer-specific mortality was also greater in participants with interstitial lung abnormalities. Similar findings were obtained in the analysis of participants undergoing chest radiography. Conclusions: Asymptomatic interstitial lung abnormalities are an independent risk factor for lung cancer that can be incorporated into risk score models.
KW - interstitial lung abnormalities
KW - lung cancer screening
UR - http://www.scopus.com/inward/record.url?scp=85075265085&partnerID=8YFLogxK
U2 - 10.1016/j.chest.2019.06.041
DO - 10.1016/j.chest.2019.06.041
M3 - Article
C2 - 31404527
AN - SCOPUS:85075265085
SN - 0012-3692
VL - 156
SP - 1195
EP - 1203
JO - Chest
JF - Chest
IS - 6
ER -