The Integrative Analysis of Lung Cancer Etiology and Risk (INTEGRAL) program is an NCI-funded initiative with an objective to develop tools to optimize low-dose CT (LDCT) lung cancer screening. Here, we de-scribe the rationale and design for the Risk Biomarker and Nodule Malignancy projects within INTEGRAL.The overarching goal of these projects is to systematically investigate circulating protein markers to include on a panel for use (i) pre-LDCT, to identify people likely to benefit from screening, and (ii) post-LDCT, to differentiate benign versus malignant nodules. To identify informative proteins, the Risk Biomarker project measured 1161 proteins in a nested-case control study within 2 prospective cohorts (n = 252 lung cancer cases and 252 controls) and replicated associations for a subset of proteins in 4 cohorts (n = 479 cases and 479 controls). Eligible participants had a current or former history of smok-ing and cases were diagnosed up to 3 years following blood draw. The Nodule Malignancy project mea-sured 1078 proteins among participants with a heavy smoking history within four LDCT screening stud-ies (n = 425 cases diagnosed up to 5 years following blood draw, 430 benign-nodule controls, and 398 nodule-free controls).The INTEGRAL panel will enable absolute quantification of 21 proteins. We will evaluate its perfor-mance in the Risk Biomarker project using a case-cohort study including 14 cohorts (n = 1696 cases and 2926 subcohort representatives), and in the Nodule Malignancy project within five LDCT screening studies (n = 675 cases, 680 benign-nodule controls, and 648 nodule-free controls). Future progress to advance lung cancer early detection biomarkers will require carefully designed validation, translational, and comparative studies.(c) 2022 Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND IGO license ( http://creativecommons.org/licenses/by-nc-nd/3.0/igo/ )

Design and methodological considerations for biomarker discovery and validation in the Integrative Analysis of Lung Cancer Etiology and Risk (INTEGRAL) Program / Robbins, Hilary A; Alcala, Karine; Moez, Elham Khodayari; Guida, Florence; Thomas, Sera; Zahed, Hana; Warkentin, Matthew T; Smith-Byrne, Karl; Brhane, Yonathan; Muller, David; Feng, Xiaoshuang; Albanes, Demetrius; Aldrich, Melinda C; Arslan, Alan A; Bassett, Julie; Berg, Christine D; Cai, Qiuyin; Chen, Chu; Davies, Michael P A; Diergaarde, Brenda; Field, John K; Freedman, Neal D; Huang, Wen-Yi; Johansson, Mikael; Jones, Michael; Koh, Woon-Puay; Lam, Stephen; Lan, Qing; Langhammer, Arnulf; Liao, Linda M; Liu, Geoffrey; Malekzadeh, Reza; Milne, Roger L; Montuenga, Luis M; Rohan, Thomas; Sesso, Howard D; Severi, Gianluca; Sheikh, Mahdi; Sinha, Rashmi; Shu, Xiao-Ou; Stevens, Victoria L; Tammemägi, Martin C; Tinker, Lesley F; Visvanathan, Kala; Wang, Ying; Wang, Renwei; Weinstein, Stephanie J; White, Emily; Wilson, David; Yuan, Jian-Min; Zhang, Xuehong; Zheng, Wei; Amos, Christopher I; Brennan, Paul; Johansson, Mattias; Hung, Rayjean J. - In: ANNALS OF EPIDEMIOLOGY. - ISSN 1873-2585. - STAMPA. - 77:(2023), pp. 1-12. [10.1016/j.annepidem.2022.10.014]

Design and methodological considerations for biomarker discovery and validation in the Integrative Analysis of Lung Cancer Etiology and Risk (INTEGRAL) Program

Severi, Gianluca;
2023

Abstract

The Integrative Analysis of Lung Cancer Etiology and Risk (INTEGRAL) program is an NCI-funded initiative with an objective to develop tools to optimize low-dose CT (LDCT) lung cancer screening. Here, we de-scribe the rationale and design for the Risk Biomarker and Nodule Malignancy projects within INTEGRAL.The overarching goal of these projects is to systematically investigate circulating protein markers to include on a panel for use (i) pre-LDCT, to identify people likely to benefit from screening, and (ii) post-LDCT, to differentiate benign versus malignant nodules. To identify informative proteins, the Risk Biomarker project measured 1161 proteins in a nested-case control study within 2 prospective cohorts (n = 252 lung cancer cases and 252 controls) and replicated associations for a subset of proteins in 4 cohorts (n = 479 cases and 479 controls). Eligible participants had a current or former history of smok-ing and cases were diagnosed up to 3 years following blood draw. The Nodule Malignancy project mea-sured 1078 proteins among participants with a heavy smoking history within four LDCT screening stud-ies (n = 425 cases diagnosed up to 5 years following blood draw, 430 benign-nodule controls, and 398 nodule-free controls).The INTEGRAL panel will enable absolute quantification of 21 proteins. We will evaluate its perfor-mance in the Risk Biomarker project using a case-cohort study including 14 cohorts (n = 1696 cases and 2926 subcohort representatives), and in the Nodule Malignancy project within five LDCT screening studies (n = 675 cases, 680 benign-nodule controls, and 648 nodule-free controls). Future progress to advance lung cancer early detection biomarkers will require carefully designed validation, translational, and comparative studies.(c) 2022 Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND IGO license ( http://creativecommons.org/licenses/by-nc-nd/3.0/igo/ )
2023
77
1
12
Robbins, Hilary A; Alcala, Karine; Moez, Elham Khodayari; Guida, Florence; Thomas, Sera; Zahed, Hana; Warkentin, Matthew T; Smith-Byrne, Karl; Brhane, Yonathan; Muller, David; Feng, Xiaoshuang; Albanes, Demetrius; Aldrich, Melinda C; Arslan, Alan A; Bassett, Julie; Berg, Christine D; Cai, Qiuyin; Chen, Chu; Davies, Michael P A; Diergaarde, Brenda; Field, John K; Freedman, Neal D; Huang, Wen-Yi; Johansson, Mikael; Jones, Michael; Koh, Woon-Puay; Lam, Stephen; Lan, Qing; Langhammer, Arnulf; Liao, Linda M; Liu, Geoffrey; Malekzadeh, Reza; Milne, Roger L; Montuenga, Luis M; Rohan, Thomas; Sesso, Howard D; Severi, Gianluca; Sheikh, Mahdi; Sinha, Rashmi; Shu, Xiao-Ou; Stevens, Victoria L; Tammemägi, Martin C; Tinker, Lesley F; Visvanathan, Kala; Wang, Ying; Wang, Renwei; Weinstein, Stephanie J; White, Emily; Wilson, David; Yuan, Jian-Min; Zhang, Xuehong; Zheng, Wei; Amos, Christopher I; Brennan, Paul; Johansson, Mattias; Hung, Rayjean J
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/1343345
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