Hakan Yalman, Ilayda Yalman, Mehmet Semih Belpinar, Murat Cimci, Halil Cumhur Yildirim, Fazilet Oner Dincbas, Kivanc Yalin
{"title":"Association of Cardiac Conduction System Radiation Doses with Incident Atrial Fibrillation in Lung Cancer.","authors":"Hakan Yalman, Ilayda Yalman, Mehmet Semih Belpinar, Murat Cimci, Halil Cumhur Yildirim, Fazilet Oner Dincbas, Kivanc Yalin","doi":"10.1007/s12012-026-10198-5","DOIUrl":null,"url":null,"abstract":"<p><p>Thoracic radiotherapy (RT) is linked to cardiovascular toxicity, but its impact on the cardiac conduction system, particularly the sinoatrial (SA) node, is poorly defined. We examined whether SA node radiation dose is associated with new-onset atrial fibrillation (AF), accounting for the competing risk of death. We retrospectively studied 84 lung cancer patients undergoing thoracic RT, stratified by maximum SA node dose (D<sub>max</sub>) using an exploratory, data-derived threshold of 17.23 Gy. Cumulative incidence functions and Fine-Gray regression, treating death as a competing event, assessed AF risk. Median age was 68.5 years; median follow-up was 12.0 months. AF occurred in 9 patients (10.7%). The high-dose SA node group (>17.23 Gy) was significantly younger (65.5 vs. 70.0 years; P=0.010) with similar Mayo AF Risk Scores (P=0.821), yet had a higher 24-month cumulative incidence of AF (18.8% vs. 4.1%; Gray's test P=0.038). AV node D<sub>max</sub> was not associated with AF but correlated with post-radiotherapy PR-interval prolongation (+14.1 ms; Spearman ρ=0.47, P=0.006). In an exploratory multivariable model adjusting for age, SA node D<sub>max</sub> remained associated with AF (adjusted sHR 1.04 per 1-Gy; 95% CI 1.01-1.06; P=0.008), warranting cautious interpretation given the limited event number. In this hypothesis-generating, single-center cohort, higher SA node dose was associated with increased AF incidence independent of age, while AV node dose was linked to PR prolongation rather than AF. These preliminary findings require validation in larger, prospective, multicenter cohorts before the SA node can be considered a formal organ at risk in RT planning.</p>","PeriodicalId":9570,"journal":{"name":"Cardiovascular Toxicology","volume":"26 10","pages":""},"PeriodicalIF":3.3000,"publicationDate":"2026-09-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cardiovascular Toxicology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s12012-026-10198-5","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CARDIAC & CARDIOVASCULAR SYSTEMS","Score":null,"Total":0}
引用次数: 0
Abstract
Thoracic radiotherapy (RT) is linked to cardiovascular toxicity, but its impact on the cardiac conduction system, particularly the sinoatrial (SA) node, is poorly defined. We examined whether SA node radiation dose is associated with new-onset atrial fibrillation (AF), accounting for the competing risk of death. We retrospectively studied 84 lung cancer patients undergoing thoracic RT, stratified by maximum SA node dose (Dmax) using an exploratory, data-derived threshold of 17.23 Gy. Cumulative incidence functions and Fine-Gray regression, treating death as a competing event, assessed AF risk. Median age was 68.5 years; median follow-up was 12.0 months. AF occurred in 9 patients (10.7%). The high-dose SA node group (>17.23 Gy) was significantly younger (65.5 vs. 70.0 years; P=0.010) with similar Mayo AF Risk Scores (P=0.821), yet had a higher 24-month cumulative incidence of AF (18.8% vs. 4.1%; Gray's test P=0.038). AV node Dmax was not associated with AF but correlated with post-radiotherapy PR-interval prolongation (+14.1 ms; Spearman ρ=0.47, P=0.006). In an exploratory multivariable model adjusting for age, SA node Dmax remained associated with AF (adjusted sHR 1.04 per 1-Gy; 95% CI 1.01-1.06; P=0.008), warranting cautious interpretation given the limited event number. In this hypothesis-generating, single-center cohort, higher SA node dose was associated with increased AF incidence independent of age, while AV node dose was linked to PR prolongation rather than AF. These preliminary findings require validation in larger, prospective, multicenter cohorts before the SA node can be considered a formal organ at risk in RT planning.
期刊介绍:
Cardiovascular Toxicology is the only journal dedicated to publishing contemporary issues, timely reviews, and experimental and clinical data on toxicological aspects of cardiovascular disease. CT publishes papers that will elucidate the effects, molecular mechanisms, and signaling pathways of environmental toxicants on the cardiovascular system. Also covered are the detrimental effects of new cardiovascular drugs, and cardiovascular effects of non-cardiovascular drugs, anti-cancer chemotherapy, and gene therapy. In addition, Cardiovascular Toxicology reports safety and toxicological data on new cardiovascular and non-cardiovascular drugs.