<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Brooks RT</submitter><funding>BLRD VA</funding><funding>Rheumatology Research Foundation</funding><funding>VA Biomedical Laboratory Research and Development</funding><funding>National Institute of General Medical Sciences</funding><funding>Department of Defense</funding><funding>CSRD VA</funding><funding>American Heart Association</funding><funding>VA CSRD</funding><funding>VA BLRD</funding><funding>VA Biomedical Laboratory Research and Development (BLRD)</funding><funding>VA Lung Precision Oncology Program</funding><funding>Great Plains IDeA-CTR Network</funding><funding>VA Clinical Science Research and Development (CSRD)</funding><funding>NIGMS NIH HHS</funding><pagination>1730-1738</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11605274</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>76(12)</volume><pubmed_abstract>&lt;h4>Objective&lt;/h4>We aimed to evaluate lung cancer risk in patients with rheumatoid arthritis (RA) and RA-interstitial lung disease (ILD).&lt;h4>Methods&lt;/h4>We performed a retrospective, matched cohort study of RA and RA-ILD within the Veterans Health Administration (VA) between 2000 and 2019. Patients with RA and RA-ILD were identified with validated administrative-based algorithms, then matched (up to 1:10) on age, gender, and VA enrollment year to individuals without RA. Lung cancers were identified from a VA oncology database and the National Death Index. Conditional Cox regression models assessed lung cancer risk adjusting for race, ethnicity, smoking status, Agent Orange exposure, and comorbidity burden among matched individuals. Several sensitivity analyses were performed.&lt;h4>Results&lt;/h4>We matched 72,795 patients with RA with 633,937 patients without RA (mean age 63 years; 88% male). Over 4,481,323 patient-years, 17,099 incident lung cancers occurred. RA was independently associated with an increased lung cancer risk (adjusted hazard ratio [aHR] 1.58 [95% confidence interval (CI) 1.52-1.64]), which persisted in never smokers (aHR 1.65 [95% CI 1.22-2.24]) and in those with incident RA (aHR 1.54 [95% CI 1.44-1.65]). Compared to non-RA controls, prevalent RA-ILD (n = 757) was more strongly associated with lung cancer risk (aHR 3.25 [95% CI 2.13-4.95]) than RA without ILD (aHR 1.57 [95% CI 1.51-1.64]). Analyses of both prevalent and incident RA-ILD produced similar results (RA-ILD vs non-RA aHR 2.88 [95% CI 2.45-3.40]).&lt;h4>Conclusion&lt;/h4>RA was associated with a >50% increased risk of lung cancer, and those with RA-ILD represented a particularly high-risk group with an approximate three-fold increased risk. Increased lung cancer surveillance in RA, and especially RA-ILD, may be a useful strategy for reducing the burden posed by the leading cause of cancer death.</pubmed_abstract><journal>Arthritis &amp; rheumatology (Hoboken, N.J.)</journal><pubmed_title>The Risk of Lung Cancer in Rheumatoid Arthritis and Rheumatoid Arthritis-Associated Interstitial Lung Disease.</pubmed_title><pmcid>PMC11605274</pmcid><funding_grant_id>I01 CX001703</funding_grant_id><funding_grant_id>PR200793</funding_grant_id><funding_grant_id>U54-GM-115458</funding_grant_id><funding_grant_id>IK2 CX002203</funding_grant_id><funding_grant_id>I01 BX004676</funding_grant_id><funding_grant_id>U54‐GM‐115458</funding_grant_id><funding_grant_id>I01-BX-004676</funding_grant_id><funding_grant_id>I01-BX-004660</funding_grant_id><funding_grant_id>I01 BX004660</funding_grant_id><funding_grant_id>IK2-CX-002203</funding_grant_id><funding_grant_id>I01-CX-001703</funding_grant_id><funding_grant_id>I01-BX-003635</funding_grant_id><funding_grant_id>U54 GM115458</funding_grant_id><funding_grant_id>I50-CU-000163-01</funding_grant_id><funding_grant_id>I01‐BX‐004676</funding_grant_id><pubmed_authors>Roul P</pubmed_authors><pubmed_authors>Wheeler A</pubmed_authors><pubmed_authors>Sauer BC</pubmed_authors><pubmed_authors>Baker JF</pubmed_authors><pubmed_authors>Johnson TM</pubmed_authors><pubmed_authors>Mikuls TR</pubmed_authors><pubmed_authors>England BR</pubmed_authors><pubmed_authors>Brooks RT</pubmed_authors><pubmed_authors>Luedders B</pubmed_authors><pubmed_authors>Yang Y</pubmed_authors><pubmed_authors>Ganti AK</pubmed_authors><pubmed_authors>Singh N</pubmed_authors><pubmed_authors>Cannon GW</pubmed_authors></additional><is_claimable>false</is_claimable><name>The Risk of Lung Cancer in Rheumatoid Arthritis and Rheumatoid Arthritis-Associated Interstitial Lung Disease.</name><description>&lt;h4>Objective&lt;/h4>We aimed to evaluate lung cancer risk in patients with rheumatoid arthritis (RA) and RA-interstitial lung disease (ILD).&lt;h4>Methods&lt;/h4>We performed a retrospective, matched cohort study of RA and RA-ILD within the Veterans Health Administration (VA) between 2000 and 2019. Patients with RA and RA-ILD were identified with validated administrative-based algorithms, then matched (up to 1:10) on age, gender, and VA enrollment year to individuals without RA. Lung cancers were identified from a VA oncology database and the National Death Index. Conditional Cox regression models assessed lung cancer risk adjusting for race, ethnicity, smoking status, Agent Orange exposure, and comorbidity burden among matched individuals. Several sensitivity analyses were performed.&lt;h4>Results&lt;/h4>We matched 72,795 patients with RA with 633,937 patients without RA (mean age 63 years; 88% male). Over 4,481,323 patient-years, 17,099 incident lung cancers occurred. RA was independently associated with an increased lung cancer risk (adjusted hazard ratio [aHR] 1.58 [95% confidence interval (CI) 1.52-1.64]), which persisted in never smokers (aHR 1.65 [95% CI 1.22-2.24]) and in those with incident RA (aHR 1.54 [95% CI 1.44-1.65]). Compared to non-RA controls, prevalent RA-ILD (n = 757) was more strongly associated with lung cancer risk (aHR 3.25 [95% CI 2.13-4.95]) than RA without ILD (aHR 1.57 [95% CI 1.51-1.64]). Analyses of both prevalent and incident RA-ILD produced similar results (RA-ILD vs non-RA aHR 2.88 [95% CI 2.45-3.40]).&lt;h4>Conclusion&lt;/h4>RA was associated with a >50% increased risk of lung cancer, and those with RA-ILD represented a particularly high-risk group with an approximate three-fold increased risk. Increased lung cancer surveillance in RA, and especially RA-ILD, may be a useful strategy for reducing the burden posed by the leading cause of cancer death.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Dec</publication><modification>2026-06-05T20:52:03.563Z</modification><creation>2025-04-06T22:23:57.464Z</creation></dates><accession>S-EPMC11605274</accession><cross_references><pubmed>39073264</pubmed><doi>10.1002/art.42961</doi></cross_references></HashMap>