TY - JOUR
T1 - Pulmonary vein dose and risk of atrial fibrillation in patients with non-small cell lung cancer following definitive radiotherapy: an NI-HEART analysis
AU - Walls, Gerard M
AU - McCann, Conor
AU - O'Connor, John
AU - O'Sullivan, Anna
AU - I Johnston, David
AU - McAleese, Jonathan
AU - McGarry, Conor K
AU - Cole, Aidan J
AU - Jain, Suneil
AU - Butterworth, Karl T
AU - Hanna, Gerard G
N1 - Copyright © 2024. Published by Elsevier B.V.
PY - 2024/3
Y1 - 2024/3
N2 - Symptomatic arrhythmia is common following radiotherapy for non-small cell lung cancer (NSCLC), frequently resulting in morbidity and hospitalization. Modern treatment planning technology theoretically allows sparing of cardiac substructures. Atrial fibrillation (AF) comprises the majority of post-radiotherapy arrhythmias, but efforts to prevent this cardiotoxicity have been limited as the causative cardiac substructure is not known. In this study we investigated if incidental radiation dose to the pulmonary veins (PVs) is associated with AF. A single-centre study of patients completing contemporary (chemo)radiation for NSCLC, with modern planning techniques. Oncology, cardiology and death records were examined, and AF events were verified by a cardiologist. Cardiac substructures were contoured on planning scans for retrospective dose analysis. In 420 eligible patients with NSCLC treated with intensity-modulated (70%) or 3D-conformal (30%) radiotherapy with a median OS of 21.8 months (IQR 10.8-35.1), there were 26 cases of new AF (6%). All cases were grade 3 except two cases of grade 4. Dose metrics for both the left (V55) and right (V10) PVs were associated with the incidence of new AF. Metrics remained statistically significant after accounting for the competing risk of death and cardiovascular covariables for both the left (HR 1.02, 95%CI 1.00-1.03, p=0.005) and right (HR 1.01 (95%CI 1.00-1.02, p=0.033) PVs. Radiation dose to the PVs during treatment of NSCLC was associated with the onset of AF. Actively sparing the PVs during treatment planning could reduce the incidence of AF during follow-up. [Abstract copyright: Copyright © 2024. Published by Elsevier B.V.]
AB - Symptomatic arrhythmia is common following radiotherapy for non-small cell lung cancer (NSCLC), frequently resulting in morbidity and hospitalization. Modern treatment planning technology theoretically allows sparing of cardiac substructures. Atrial fibrillation (AF) comprises the majority of post-radiotherapy arrhythmias, but efforts to prevent this cardiotoxicity have been limited as the causative cardiac substructure is not known. In this study we investigated if incidental radiation dose to the pulmonary veins (PVs) is associated with AF. A single-centre study of patients completing contemporary (chemo)radiation for NSCLC, with modern planning techniques. Oncology, cardiology and death records were examined, and AF events were verified by a cardiologist. Cardiac substructures were contoured on planning scans for retrospective dose analysis. In 420 eligible patients with NSCLC treated with intensity-modulated (70%) or 3D-conformal (30%) radiotherapy with a median OS of 21.8 months (IQR 10.8-35.1), there were 26 cases of new AF (6%). All cases were grade 3 except two cases of grade 4. Dose metrics for both the left (V55) and right (V10) PVs were associated with the incidence of new AF. Metrics remained statistically significant after accounting for the competing risk of death and cardiovascular covariables for both the left (HR 1.02, 95%CI 1.00-1.03, p=0.005) and right (HR 1.01 (95%CI 1.00-1.02, p=0.033) PVs. Radiation dose to the PVs during treatment of NSCLC was associated with the onset of AF. Actively sparing the PVs during treatment planning could reduce the incidence of AF during follow-up. [Abstract copyright: Copyright © 2024. Published by Elsevier B.V.]
UR - http://www.scopus.com/inward/record.url?scp=85183945679&partnerID=8YFLogxK
U2 - 10.1016/j.radonc.2024.110085
DO - 10.1016/j.radonc.2024.110085
M3 - Article
C2 - 38184145
SN - 0167-8140
VL - 192
SP - 1
EP - 39
JO - Radiotherapy and Oncology
JF - Radiotherapy and Oncology
M1 - 110085
ER -