Santino Butler MD , Hyunsoo No MD , Felicia Guo BA , Gibran Merchant BS , Natalie J. Park BA , Scott Jackson MS , Daniel Eugene Clark MD , Lucas Vitzthum MD , Alex Chin MD, MBA , Kathleen Horst MD , Richard T. Hoppe MD , Billy W. Loo MD, PhD , Maximilian Diehn MD, PhD , Michael Sargent Binkley MD, MS
{"title":"Predictors of Atrial Fibrillation After Thoracic Radiotherapy","authors":"Santino Butler MD , Hyunsoo No MD , Felicia Guo BA , Gibran Merchant BS , Natalie J. Park BA , Scott Jackson MS , Daniel Eugene Clark MD , Lucas Vitzthum MD , Alex Chin MD, MBA , Kathleen Horst MD , Richard T. Hoppe MD , Billy W. Loo MD, PhD , Maximilian Diehn MD, PhD , Michael Sargent Binkley MD, MS","doi":"10.1016/j.jaccao.2024.08.007","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><div>Atrial fibrillation (AF) has been associated with thoracic radiotherapy, but the specific risk with irradiating different cardiac substructures remains unknown.</div></div><div><h3>Objectives</h3><div>This study sought to examine the relationship between irradiation of cardiac substructures and the risk of clinically significant (grade ≥3) AF.</div></div><div><h3>Methods</h3><div>We analyzed data from patients who underwent definitive radiotherapy for localized cancers (non–small cell lung, breast, Hodgkin lymphoma, or esophageal) at our institution between 2004 and 2022. The 2-Gy fraction equivalent dose was calculated for cardiac substructures, including the pulmonary veins (PVs), left atrium, sinoatrial node, and left coronary arteries (the left main, left anterior descending, and left circumflex arteries). Competing risk models (subdistribution HRs [sHRs]) for AF incidence were adjusted for the Mayo AF risk score (MAFRS).</div></div><div><h3>Results</h3><div>Among 539 patients, the median follow-up was 58.8 months. The 5-year cumulative incidence of AF was 11.1% for non–small cell lung cancer, 8.3% for esophageal cancer, 1.3% for breast cancer, and 0.8% for Hodgkin lymphoma. Increased AF risk was associated with a higher PV maximum dose (d<sub>max</sub>) (sHR: 1.22; <em>P <</em> 0.001), larger left atrial volume (sHR: 1.01; <em>P =</em> 0.002), greater smoking history in pack-years (sHR: 1.01; <em>P =</em> 0.010), and higher MAFRS (sHR: 1.16; <em>P <</em> 0.001). PV d<sub>max</sub> remained a significant predictor of AF across different MAFRS subgroups (<em>P</em><sub>interaction</sub> = 0.11), and a PV d<sub>max</sub> >39.7 Gy was linked to a higher AF risk, even when stratified by MAFRS.</div></div><div><h3>Conclusions</h3><div>PV d<sub>max</sub> is a significant predictor of grade ≥3 AF regardless of underlying risk factors. These findings highlight the importance of cardiac substructures in radiation toxicity and suggest that various PV dose metrics should be further validated in clinical settings.</div></div>","PeriodicalId":48499,"journal":{"name":"Jacc: Cardiooncology","volume":"6 6","pages":"Pages 935-945"},"PeriodicalIF":12.0000,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11711808/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Jacc: Cardiooncology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2666087324003405","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CARDIAC & CARDIOVASCULAR SYSTEMS","Score":null,"Total":0}
引用次数: 0
Abstract
Background
Atrial fibrillation (AF) has been associated with thoracic radiotherapy, but the specific risk with irradiating different cardiac substructures remains unknown.
Objectives
This study sought to examine the relationship between irradiation of cardiac substructures and the risk of clinically significant (grade ≥3) AF.
Methods
We analyzed data from patients who underwent definitive radiotherapy for localized cancers (non–small cell lung, breast, Hodgkin lymphoma, or esophageal) at our institution between 2004 and 2022. The 2-Gy fraction equivalent dose was calculated for cardiac substructures, including the pulmonary veins (PVs), left atrium, sinoatrial node, and left coronary arteries (the left main, left anterior descending, and left circumflex arteries). Competing risk models (subdistribution HRs [sHRs]) for AF incidence were adjusted for the Mayo AF risk score (MAFRS).
Results
Among 539 patients, the median follow-up was 58.8 months. The 5-year cumulative incidence of AF was 11.1% for non–small cell lung cancer, 8.3% for esophageal cancer, 1.3% for breast cancer, and 0.8% for Hodgkin lymphoma. Increased AF risk was associated with a higher PV maximum dose (dmax) (sHR: 1.22; P < 0.001), larger left atrial volume (sHR: 1.01; P = 0.002), greater smoking history in pack-years (sHR: 1.01; P = 0.010), and higher MAFRS (sHR: 1.16; P < 0.001). PV dmax remained a significant predictor of AF across different MAFRS subgroups (Pinteraction = 0.11), and a PV dmax >39.7 Gy was linked to a higher AF risk, even when stratified by MAFRS.
Conclusions
PV dmax is a significant predictor of grade ≥3 AF regardless of underlying risk factors. These findings highlight the importance of cardiac substructures in radiation toxicity and suggest that various PV dose metrics should be further validated in clinical settings.
期刊介绍:
JACC: CardioOncology is a specialized journal that belongs to the esteemed Journal of the American College of Cardiology (JACC) family. Its purpose is to enhance cardiovascular care for cancer patients by publishing high-quality, innovative scientific research and sharing evidence-based knowledge.
The journal aims to revolutionize the field of cardio-oncology and actively involve and educate professionals in both cardiovascular and oncology fields. It covers a wide range of topics including pre-clinical, translational, and clinical research, as well as best practices in cardio-oncology. Key areas of focus include understanding disease mechanisms, utilizing in vitro and in vivo models, exploring novel and traditional therapeutics (across Phase I-IV trials), studying epidemiology, employing precision medicine, and investigating primary and secondary prevention.
Amyloidosis, cardiovascular risk factors, heart failure, and vascular disease are some examples of the disease states that are of particular interest to the journal. However, it welcomes research on other relevant conditions as well.