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Data from Assessing Lung Cancer Absolute Risk Trajectory Based on a Polygenic Risk Model

Posted on 2023-03-31 - 04:24
Abstract

Lung cancer is the leading cause of cancer-related death globally. An improved risk stratification strategy can increase efficiency of low-dose CT (LDCT) screening. Here we assessed whether individual's genetic background has clinical utility for risk stratification in the context of LDCT screening. On the basis of 13,119 patients with lung cancer and 10,008 controls with European ancestry in the International Lung Cancer Consortium, we constructed a polygenic risk score (PRS) via 10-fold cross-validation with regularized penalized regression. The performance of risk model integrating PRS, including calibration and ability to discriminate, was assessed using UK Biobank data (N = 335,931). Absolute risk was estimated on the basis of age-specific lung cancer incidence and all-cause mortality as competing risk. To evaluate its potential clinical utility, the PRS distribution was simulated in the National Lung Screening Trial (N = 50,772 participants). The lung cancer ORs for individuals at the top decile of the PRS distribution versus those at bottom 10% was 2.39 [95% confidence interval (CI) = 1.92–3.00; P = 1.80 × 10−14] in the validation set (Ptrend = 5.26 × 10−20). The OR per SD of PRS increase was 1.26 (95% CI = 1.20–1.32; P = 9.69 × 10−23) for overall lung cancer risk in the validation set. When considering absolute risks, individuals at different PRS deciles showed differential trajectories of 5-year and cumulative absolute risk. The age reaching the LDCT screening recommendation threshold can vary by 4 to 8 years, depending on the individual's genetic background, smoking status, and family history. Collectively, these results suggest that individual's genetic background may inform the optimal lung cancer LDCT screening strategy.

Significance:

Three large-scale datasets reveal that, after accounting for risk factors, an individual's genetics can affect their lung cancer risk trajectory, thus may inform the optimal timing for LDCT screening.

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FUNDING

UK Biobank

FIS-FEDER

FICYT

Asturias

NCI

NIH

Canadian Cancer Society Research Institute

Vanderbilt University

CTSA

NCATS

NCRR

U.S. Army Medical Research

Materiel Command Program

Department of Defense

CIHR

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Cancer Research

AUTHORS (29)

  • Rayjean J. Hung
    Matthew T. Warkentin
    Yonathan Brhane
    Nilanjan Chatterjee
    David C. Christiani
    Maria Teresa Landi
    Neil E. Caporaso
    Geoffrey Liu
    Mattias Johansson
    Demetrius Albanes
    Loic Le Marchand
    Adonina Tardon
    Gad Rennert
    Stig E. Bojesen
    Chu Chen
    John K. Field
    Lambertus A. Kiemeney
    Philip Lazarus
    Shanbeth Zienolddiny
    Stephen Lam

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