<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Hung RJ</submitter><funding>CTSA</funding><funding>U.S. Army Medical Research</funding><funding>NCATS</funding><funding>FIS-FEDER</funding><funding>NCATS NIH HHS</funding><funding>World Health Organization</funding><funding>NCRR NIH HHS</funding><funding>FICYT</funding><funding>Materiel Command Program</funding><funding>Department of Defense</funding><funding>Asturias</funding><funding>NCI NIH</funding><funding>CIHR</funding><funding>NCRR</funding><funding>Medical Research Council</funding><funding>NCI NIH HHS</funding><funding>Vanderbilt University</funding><funding>UK Biobank</funding><funding>Canadian Cancer Society Research Institute</funding><pagination>1607-1615</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7969419</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>81(6)</volume><pubmed_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 (&lt;i>N&lt;/i> = 335,931). Absolute risk was estimated on the basis of age-specific lung cancer incidence and all-cause mo</pubmed_abstract><journal>Cancer research</journal><pubmed_title>Assessing Lung Cancer Absolute Risk Trajectory Based on a Polygenic Risk Model.</pubmed_title><pmcid>PMC7969419</pmcid><funding_grant_id>FIS-01/310</funding_grant_id><funding_grant_id>10153006</funding_grant_id><funding_grant_id>P20 RR018787</funding_grant_id><funding_grant_id>UL1 TR000117</funding_grant_id><funding_grant_id>U01 CA209414</funding_grant_id><funding_grant_id>K07 CA172294</funding_grant_id><funding_grant_id>FIS-07-BI060604</funding_grant_id><funding_grant_id>P30 CA177558</funding_grant_id><funding_grant_id>FICYT PB02-67</funding_grant_id><funding_grant_id>23261</funding_grant_id><funding_grant_id>P50 CA090578</funding_grant_id><funding_grant_id>P20 CA090578</funding_grant_id><funding_grant_id>020214</funding_grant_id><funding_grant_id>S10 RR025141</funding_grant_id><funding_grant_id>U01 CA063464</funding_grant_id><funding_grant_id>MC_QA137853</funding_grant_id><funding_grant_id>P30 CA076292</funding_grant_id><funding_grant_id>R01 CA074386</funding_grant_id><funding_grant_id>U19 CA148127</funding_grant_id><funding_grant_id>MC_PC_17228</funding_grant_id><funding_grant_id>U01 CA164973</funding_grant_id><funding_grant_id>R35 CA197449</funding_grant_id><funding_grant_id>UL1TR000445</funding_grant_id><funding_grant_id>U01-CA063673</funding_grant_id><funding_grant_id>UL1 TR000445</funding_grant_id><funding_grant_id>U01 CA167462</funding_grant_id><funding_grant_id>1S10RR025141-01</funding_grant_id><funding_grant_id>P50 CA119997</funding_grant_id><funding_grant_id>P01 CA033619</funding_grant_id><funding_grant_id>R01 CA092824</funding_grant_id><funding_grant_id>FIS-PI03-0365</funding_grant_id><funding_grant_id>FICYT IB09-133</funding_grant_id><funding_grant_id>001</funding_grant_id><funding_grant_id>R01 CA063464</funding_grant_id><funding_grant_id>U01-CA167462</funding_grant_id><funding_grant_id>UM1 CA167462</funding_grant_id><funding_grant_id>W81XWH-11-1-0781</funding_grant_id><funding_grant_id>FDN 167273</funding_grant_id><funding_grant_id>U01 CA063673</funding_grant_id><funding_grant_id>U19 CA203654</funding_grant_id><funding_grant_id>UM1 CA164973</funding_grant_id><funding_grant_id>UM1-CA167462</funding_grant_id><pubmed_authors>Zienolddiny S</pubmed_authors><pubmed_authors>Chatterjee N</pubmed_authors><pubmed_authors>Christiani DC</pubmed_authors><pubmed_authors>Brhane Y</pubmed_authors><pubmed_authors>Amos CI</pubmed_authors><pubmed_authors>Aldrich MC</pubmed_authors><pubmed_authors>Bojesen SE</pubmed_authors><pubmed_authors>Hung RJ</pubmed_authors><pubmed_authors>Caporaso NE</pubmed_authors><pubmed_authors>Lazarus P</pubmed_authors><pubmed_authors>Warkentin MT</pubmed_authors><pubmed_authors>McKay JD</pubmed_authors><pubmed_authors>Kiemeney LA</pubmed_authors><pubmed_authors>Brennan P</pubmed_authors><pubmed_authors>Tardon A</pubmed_authors><pubmed_authors>Bickeboller H</pubmed_authors><pubmed_authors>Chen C</pubmed_authors><pubmed_authors>Risch A</pubmed_authors><pubmed_authors>Arnold SM</pubmed_authors><pubmed_authors>Rennert G</pubmed_authors><pubmed_authors>Albanes D</pubmed_authors><pubmed_authors>Landi MT</pubmed_authors><pubmed_authors>Lam S</pubmed_authors><pubmed_authors>Marchand LL</pubmed_authors><pubmed_authors>Johansson M</pubmed_authors><pubmed_authors>Andrew AS</pubmed_authors><pubmed_authors>Field JK</pubmed_authors><pubmed_authors>Liu G</pubmed_authors><pubmed_authors>Schabath MB</pubmed_authors></additional><is_claimable>false</is_claimable><name>Assessing Lung Cancer Absolute Risk Trajectory Based on a Polygenic Risk Model.</name><description>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 (&lt;i>N&lt;/i> = 335,931). Absolute risk was estimated on the basis of age-specific lung cancer incidence and all-cause mo</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Mar</publication><modification>2026-06-04T04:31:32.188Z</modification><creation>2022-02-11T10:53:54.445Z</creation></dates><accession>S-EPMC7969419</accession><cross_references><pubmed>33472890</pubmed><doi>10.1158/0008-5472.CAN-20-1237</doi><doi>10.1158/0008-5472.can-20-1237</doi></cross_references></HashMap>